Genome-wide association study (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Genome-wide association study" in English language version.

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114nih.gov

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1genome.gov

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Strachan T, Read A (2011). Human Molecular Genetics (4th ed.). Garland Science. pp. 467–495. ISBN 978-0-8153-4149-9.

doi.org

Uffelmann E, Huang QQ, Munung NS, de Vries J, Okada Y, Martin AR, Martin HC, Lappalainen T, Posthuma D (26 August 2021). "Genome-wide association studies". Nature Reviews Methods Primers. 1 (1): 1–21. doi:10.1038/s43586-021-00056-9. ISSN 2662-8449.
Manolio TA (July 2010). "Genomewide association studies and assessment of the risk of disease". The New England Journal of Medicine. 363 (2): 166–76. doi:10.1056/NEJMra0905980. PMID 20647212.
Pearson TA, Manolio TA (March 2008). "How to interpret a genome-wide association study". JAMA. 299 (11): 1335–44. doi:10.1001/jama.299.11.1335. PMID 18349094.
Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, et al. (December 2002). "Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction". Nature Genetics. 32 (4): 650–4. doi:10.1038/ng1047. PMID 12426569. S2CID 21414260.
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, et al. (April 2005). "Complement factor H polymorphism in age-related macular degeneration". Science. 308 (5720): 385–9. Bibcode:2005Sci...308..385K. doi:10.1126/science.1109557. PMC 1512523. PMID 15761122.
Bush WS, Moore JH (2012). Lewitter F, Kann M (eds.). "Chapter 11: Genome-wide association studies". PLOS Computational Biology. 8 (12): e1002822. Bibcode:2012PLSCB...8E2822B. doi:10.1371/journal.pcbi.1002822. PMC 3531285. PMID 23300413.
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (November 2001). "Genomewide scans of complex human diseases: true linkage is hard to find". American Journal of Human Genetics. 69 (5): 936–50. doi:10.1086/324069. PMC 1274370. PMID 11565063.
Risch N, Merikangas K (September 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. Bibcode:1996Sci...273.1516R. doi:10.1126/science.273.5281.1516. PMID 8801636. S2CID 5228523.
Greely HT (2007). "The uneasy ethical and legal underpinnings of large-scale genomic biobanks". Annual Review of Genomics and Human Genetics. 8: 343–64. doi:10.1146/annurev.genom.7.080505.115721. PMID 17550341.
The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.
Schena M, Shalon D, Davis RW, Brown PO (October 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. Bibcode:1995Sci...270..467S. doi:10.1126/science.270.5235.467. PMID 7569999. S2CID 6720459.
Wellcome Trust Case Control Consortium, Burton PR (June 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. Bibcode:2007Natur.447..661B. doi:10.1038/nature05911. PMC 2719288. PMID 17554300.
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (February 2011). "Basic statistical analysis in genetic case-control studies". Nature Protocols. 6 (2): 121–33. doi:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. (September 2007). "PLINK: a tool set for whole-genome association and population-based linkage analyses". American Journal of Human Genetics. 81 (3): 559–75. doi:10.1086/519795. PMC 1950838. PMID 17701901.
Llinares-López F, Grimm DG, Bodenham DA, Gieraths U, Sugiyama M, Rowan B, Borgwardt K (June 2015). "Genome-wide detection of intervals of genetic heterogeneity associated with complex traits". Bioinformatics. 31 (12): i240-9. doi:10.1093/bioinformatics/btv263. PMC 4559912. PMID 26072488.
Ayati M, Erten S, Chance MR, Koyutürk M (December 2015). "MOBAS: identification of disease-associated protein subnetworks using modularity-based scoring". EURASIP Journal on Bioinformatics & Systems Biology. 2015 (1): 7. doi:10.1186/s13637-015-0025-6. PMC 5270451. PMID 28194175.
Ayati M, Koyutürk M (1 January 2015). "Assessing the Collective Disease Association of Multiple Genomic Loci". Proceedings of the 6th ACM Conference on Bioinformatics, Computational Biology and Health Informatics. BCB '15. New York, NY, USA: ACM. pp. 376–385. doi:10.1145/2808719.2808758. ISBN 978-1-4503-3853-0. S2CID 5942777.
Carré C, Carluer JB, Chaux C, Estoup-Streiff C, Roche N, Hosy E, Mas A, Krouk G (25 March 2024). "Next-Gen GWAS: full 2D epistatic interaction maps retrieve part of missing heritability and improve phenotypic prediction". Genome Biology. 25 (1): 76. doi:10.1186/s13059-024-03202-0. ISSN 1474-760X. PMC 10962106. PMID 38523316.
Marchini J, Howie B (July 2010). "Genotype imputation for genome-wide association studies". Nature Reviews Genetics. 11 (7): 499–511. doi:10.1038/nrg2796. PMID 20517342. S2CID 1465707.
Howie B, Marchini J, Stephens M (November 2011). "Genotype imputation with thousands of genomes". G3. 1 (6): 457–70. doi:10.1534/g3.111.001198. PMC 3276165. PMID 22384356.
Browning BL, Browning SR (February 2009). "A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals". American Journal of Human Genetics. 84 (2): 210–23. doi:10.1016/j.ajhg.2009.01.005. PMC 2668004. PMID 19200528.
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (December 2010). "MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes". Genetic Epidemiology. 34 (8): 816–34. doi:10.1002/gepi.20533. PMC 3175618. PMID 21058334.
Novembre J, Johnson T, Bryc K, Kutalik Z, Boyko AR, Auton A, Indap A, King KS, Bergmann S, Nelson MR, Stephens M, Bustamante CD (November 2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
Charney E (January 2017). "Genes, behavior, and behavior genetics". Wiley Interdisciplinary Reviews. Cognitive Science. 8 (1–2): e1405. doi:10.1002/wcs.1405. hdl:10161/13337. PMID 27906529.
Wittkowski KM, Sonakya V, Bigio B, Tonn MK, Shic F, Ascano M, Nasca C, Gold-Von Simson G (January 2014). "A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism". Translational Psychiatry. 4 (1): e354. doi:10.1038/tp.2013.124. PMC 3905234. PMID 24473445.
Barsh GS, Copenhaver GP, Gibson G, Williams SM (July 2012). "Guidelines for genome-wide association studies". PLOS Genetics. 8 (7): e1002812. doi:10.1371/journal.pgen.1002812. PMC 3390399. PMID 22792080.
Smith SM, Douaud G, Chen W, Hanayik T, Alfaro-Almagro F, Sharp K, Elliott LT (2021). "An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank". Nat Neurosci. 24 (5): 737–745. doi:10.1038/s41593-021-00826-4. PMC 7610742. PMID 33875891.
Sanna S, Li B, Mulas A, Sidore C, Kang HM, Jackson AU, et al. (July 2011). Gibson G (ed.). "Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability". PLOS Genetics. 7 (7): e1002198. doi:10.1371/journal.pgen.1002198. PMC 3145627. PMID 21829380.
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (June 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proceedings of the National Academy of Sciences of the United States of America. 106 (23): 9362–7. Bibcode:2009PNAS..106.9362H. doi:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.
Johnson AD, O'Donnell CJ (January 2009). "An open access database of genome-wide association results". BMC Medical Genetics. 10: 6. doi:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA (April 2005). "Complement factor H variant increases the risk of age-related macular degeneration". Science. 308 (5720): 419–21. Bibcode:2005Sci...308..419H. doi:10.1126/science.1110359. PMID 15761120. S2CID 32716116.
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (October 2011). "Design and development of TT30, a novel C3d-targeted C3/C5 convertase inhibitor for treatment of human complement alternative pathway-mediated diseases". Blood. 118 (17): 4705–13. doi:10.1182/blood-2011-06-359646. PMC 3208285. PMID 21860027.
Ioannidis JP, Thomas G, Daly MJ (May 2009). "Validating, augmenting and refining genome-wide association signals". Nature Reviews Genetics. 10 (5): 318–29. doi:10.1038/nrg2544. PMC 7877552. PMID 19373277. S2CID 6463743.
Lee JJ, Wedow R, Okbay A, Kong E, Maghzian O, Zacher M, Nguyen-Viet TA, Bowers P, Sidorenko J, Karlsson Linnér R, et al. (July 2018). "Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals". Nature Genetics. 50 (8): 1112–1121. doi:10.1038/s41588-018-0147-3. PMC 6393768. PMID 30038396.
Okbay A, Wu Y, Wang N, Jayashankar H, Bennett M, Nehzati SM, et al. (April 2022). "Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals". Nature Genetics. 54 (4): 437–449. doi:10.1038/s41588-022-01016-z. hdl:11368/3026010. PMC 9005349. PMID 35361970.
Jansen PR, Watanabe K, Stringer S, Skene N, Bryois J, Hammerschlag AR, et al. (March 2019). "Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways". Nature Genetics. 51 (3): 394–403. bioRxiv 10.1101/214973. doi:10.1038/s41588-018-0333-3. hdl:1871.1/08af5d9e-8621-41f1-97c5-e77a1063495f. PMID 30804565.
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, et al. (January 2009). "Common variants at 30 loci contribute to polygenic dyslipidemia". Nature Genetics. 41 (1): 56–65. doi:10.1038/ng.291. PMC 2881676. PMID 19060906.
Strawbridge RJ, Dupuis J, Prokopenko I, Barker A, Ahlqvist E, Rybin D, et al. (October 2011). "Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes". Diabetes. 60 (10): 2624–34. doi:10.2337/db11-0415. PMC 3178302. PMID 21873549.
Danesh J, Pepys MB (November 2009). "C-reactive protein and coronary disease: is there a causal link?". Circulation. 120 (21): 2036–9. doi:10.1161/CIRCULATIONAHA.109.907212. PMID 19901186.
Liu JZ, Erlich Y, Pickrell JK (March 2017). "Case-control association mapping by proxy using family history of disease". Nature Genetics. 49 (3): 325–331. doi:10.1038/ng.3766. PMID 28092683. S2CID 5598845.
Ku CS, Loy EY, Pawitan Y, Chia KS (April 2010). "The pursuit of genome-wide association studies: where are we now?". Journal of Human Genetics. 55 (4): 195–206. doi:10.1038/jhg.2010.19. PMID 20300123.
Maher B (November 2008). "Personal genomes: The case of the missing heritability". Nature. 456 (7218): 18–21. doi:10.1038/456018a. PMID 18987709.
Iadonato SP, Katze MG (September 2009). "Genomics: Hepatitis C virus gets personal". Nature. 461 (7262): 357–8. Bibcode:2009Natur.461..357I. doi:10.1038/461357a. PMID 19759611. S2CID 7602652.
Muehlschlegel JD, Liu KY, Perry TE, Fox AA, Collard CD, Shernan SK, Body SC (September 2010). "Chromosome 9p21 variant predicts mortality after coronary artery bypass graft surgery". Circulation. 122 (11 Suppl): S60–5. doi:10.1161/CIRCULATIONAHA.109.924233. PMC 2943860. PMID 20837927.
Paynter NP, Chasman DI, Paré G, Buring JE, Cook NR, Miletich JP, Ridker PM (February 2010). "Association between a literature-based genetic risk score and cardiovascular events in women". JAMA. 303 (7): 631–7. doi:10.1001/jama.2010.119. PMC 2845522. PMID 20159871.
Couzin-Frankel J (June 2010). "Major heart disease genes prove elusive". Science. 328 (5983): 1220–1. Bibcode:2010Sci...328.1220C. doi:10.1126/science.328.5983.1220. PMID 20522751.
Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sulkowski M, McHutchison JG, Goldstein DB (September 2009). "Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance". Nature. 461 (7262): 399–401. Bibcode:2009Natur.461..399G. doi:10.1038/nature08309. PMID 19684573. S2CID 1707096.
Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O'Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M (October 2009). "Genetic variation in IL28B and spontaneous clearance of hepatitis C virus". Nature. 461 (7265): 798–801. Bibcode:2009Natur.461..798T. doi:10.1038/nature08463. PMC 3172006. PMID 19759533.
Lu YF, Goldstein DB, Angrist M, Cavalleri G (July 2014). "Personalized medicine and human genetic diversity". Cold Spring Harbor Perspectives in Medicine. 4 (9): a008581. doi:10.1101/cshperspect.a008581. PMC 4143101. PMID 25059740.
Folkersen L, van't Hooft F, Chernogubova E, Agardh HE, Hansson GK, Hedin U, Liska J, Syvänen AC, Paulsson-Berne G, Paulssson-Berne G, Franco-Cereceda A, Hamsten A, Gabrielsen A, Eriksson P (August 2010). "Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease". Circulation: Cardiovascular Genetics. 3 (4): 365–73. doi:10.1161/CIRCGENETICS.110.948935. PMID 20562444.
Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, et al. (November 2011). "Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1". American Journal of Human Genetics. 89 (5): 619–27. doi:10.1016/j.ajhg.2011.10.002. PMC 3213391. PMID 22055160.
Coronary Artery Disease (C4D) Genetics Consortium (March 2011). "A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease". Nature Genetics. 43 (4): 339–44. doi:10.1038/ng.782. PMID 21378988. S2CID 39712343.{{cite journal}}: CS1 maint: numeric names: authors list (link)^{[permanent dead link]}
Johnson T, Gaunt TR, Newhouse SJ, Padmanabhan S, Tomaszewski M, Kumari M, et al. (December 2011). "Blood pressure loci identified with a gene-centric array". American Journal of Human Genetics. 89 (6): 688–700. doi:10.1016/j.ajhg.2011.10.013. PMC 3234370. PMID 22100073.
Dubé JB, Johansen CT, Hegele RA (June 2011). "Sortilin: an unusual suspect in cholesterol metabolism: from GWAS identification to in vivo biochemical analyses, sortilin has been identified as a novel mediator of human lipoprotein metabolism". BioEssays. 33 (6): 430–7. doi:10.1002/bies.201100003. PMID 21462369.
Bauer RC, Stylianou IM, Rader DJ (April 2011). "Functional validation of new pathways in lipoprotein metabolism identified by human genetics". Current Opinion in Lipidology. 22 (2): 123–8. doi:10.1097/MOL.0b013e32834469b3. PMID 21311327. S2CID 24020035.
Roselli C, Chafin M, Weng L (2018). "Multi-ethnic genome-wide association study for atrial fibrillation". Nature Genetics. 50 (9): 1225–1233. doi:10.1038/s41588-018-0133-9. PMC 6136836. PMID 29892015.
Ganapathiraju MK, Thahir M, Handen A, Sarkar SN, Sweet RA, Nimgaonkar VL, Loscher CE, Bauer EM, Chaparala S (27 April 2016). "Schizophrenia interactome with 504 novel protein-protein interactions". npj Schizophrenia. 2: 16012. doi:10.1038/npjschz.2016.12. PMC 4898894. PMID 27336055.
Ganapathiraju M, Chaparala S, Lo C (April 2018). "F200. Elucidating The Role of Cilia in Neuropsychiatric Diseases Through Interactome Analysis". Schizophrenia Bulletin. 44 (suppl_1): S298-9. doi:10.1093/schbul/sby017.731. PMC 5887623.
Johnson EC, Border R, Melroy-Greif WE, de Leeuw CA, Ehringer MA, Keller MC (November 2017). "No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes". Biological Psychiatry. 82 (10): 702–708. doi:10.1016/j.biopsych.2017.06.033. PMC 5643230. PMID 28823710.
Mocci E, Ward K, Perry JA, Starkweather A, Stone LS, Schabrun SM, Renn C, Dorsey SG, Ament SA (2023). "Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits". PLOS Genetics. 19 (10): e1010977. doi:10.1371/journal.pgen.1010977. ISSN 1553-7404. PMC 10602383. PMID 37844115.
Willi Y, Kristensen TN, Sgrò CM, Weeks AR, Ørsted M, Hoffmann AA (January 2022). "Conservation genetics as a management tool: The five best-supported paradigms to assist the management of threatened species". Proceedings of the National Academy of Sciences of the United States of America. 119 (1): e2105076119. Bibcode:2022PNAS..11905076W. doi:10.1073/pnas.2105076119. PMC 8740573. PMID 34930821.
Turuspekov Y, Baibulatova A, Yermekbayev K, Tokhetova L, Chudinov V, Sereda G, et al. (November 2017). "GWAS for plant growth stages and yield components in spring wheat (Triticum aestivum L.) harvested in three regions of Kazakhstan". BMC Plant Biology. 17 (Suppl 1): 190. Bibcode:2017BMCPB..17S.190T. doi:10.1186/s12870-017-1131-2. PMC 5688510. PMID 29143598.
Zhao K, Tung CW, Eizenga GC, Wright MH, Ali ML, Price AH, et al. (September 2011). "Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa". Nature Communications. 2 (1): 467. Bibcode:2011NatCo...2..467Z. doi:10.1038/ncomms1467. PMC 3195253. PMID 21915109.
Bartoli C, Roux F (2017). "Genome-Wide Association Studies In Plant Pathosystems: Toward an Ecological Genomics Approach". Frontiers in Plant Science. 8: 763. Bibcode:2017FrPS....8..763B. doi:10.3389/fpls.2017.00763. PMC 5441063. PMID 28588588.
Abasht B, Lamont SJ (October 2007). "Genome-wide association analysis reveals cryptic alleles as an important factor in heterosis for fatness in chicken F2 population". Animal Genetics. 38 (5): 491–498. doi:10.1111/j.1365-2052.2007.01642.x. PMID 17894563.
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2010). "Genetic signatures of exceptional longevity in humans". Science. 2010 (5987). doi:10.1126/science.1190532. PMID 20595579. (Retracted, see doi:10.1126/science.333.6041.404-a, PMID 21778381, Retraction Watch)
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2011). "Retraction". Science. 333 (6041): 404. doi:10.1126/science.333.6041.404-a. PMID 21778381.
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT (18 January 2012). "Genetic signatures of exceptional longevity in humans". PLOS ONE. 7 (1): e29848. Bibcode:2012PLoSO...729848S. doi:10.1371/journal.pone.0029848. PMC 3261167. PMID 22279548.
Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D (May 2019). "Benefits and limitations of genome-wide association studies". Nature Reviews Genetics. 20 (8): 467–484. doi:10.1038/s41576-019-0127-1. ISSN 1471-0056. PMID 31068683. S2CID 148570302.
Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, Boehnke M (May 2010). "Genome-wide association studies in diverse populations". Nature Reviews Genetics. 11 (5): 356–66. doi:10.1038/nrg2760. PMC 3079573. PMID 20395969.
Sham PC, Cherny SS, Purcell S, Hewitt JK (May 2000). "Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data". American Journal of Human Genetics. 66 (5): 1616–30. doi:10.1086/302891. PMC 1378020. PMID 10762547.
Wiley (9 September 2005). Encyclopedia of Life Sciences (1 ed.). Wiley. doi:10.1038/npg.els.0005483. ISBN 978-0-470-01617-6.
Visscher PM, Goddard ME, Derks EM, Wray NR (May 2012). "Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses". Molecular Psychiatry. 17 (5): 474–85. doi:10.1038/mp.2011.65. PMID 21670730.
Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA (2022). "Cross-trait assortative mating is widespread and inflates genetic correlation estimates". Science. 378 (6621): 754–761. Bibcode:2022Sci...378..754B. doi:10.1126/science.abo2059. ISSN 0036-8075. PMC 9901291. PMID 36395242.

ebi.ac.uk

"GWAS Catalog: The NHGRI-EBI Catalog of published genome-wide association studies". European Molecular Biology Laboratory. Retrieved 18 April 2017.

escholarship.org

Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2010). "Genetic signatures of exceptional longevity in humans". Science. 2010 (5987). doi:10.1126/science.1190532. PMID 20595579. (Retracted, see doi:10.1126/science.333.6041.404-a, PMID 21778381, Retraction Watch)

genome.gov

"Genome-Wide Association Studies". National Human Genome Research Institute.

handle.net

hdl.handle.net

The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.
Charney E (January 2017). "Genes, behavior, and behavior genetics". Wiley Interdisciplinary Reviews. Cognitive Science. 8 (1–2): e1405. doi:10.1002/wcs.1405. hdl:10161/13337. PMID 27906529.
Okbay A, Wu Y, Wang N, Jayashankar H, Bennett M, Nehzati SM, et al. (April 2022). "Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals". Nature Genetics. 54 (4): 437–449. doi:10.1038/s41588-022-01016-z. hdl:11368/3026010. PMC 9005349. PMID 35361970.
Jansen PR, Watanabe K, Stringer S, Skene N, Bryois J, Hammerschlag AR, et al. (March 2019). "Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways". Nature Genetics. 51 (3): 394–403. bioRxiv 10.1101/214973. doi:10.1038/s41588-018-0333-3. hdl:1871.1/08af5d9e-8621-41f1-97c5-e77a1063495f. PMID 30804565.

harvard.edu

ui.adsabs.harvard.edu

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, et al. (April 2005). "Complement factor H polymorphism in age-related macular degeneration". Science. 308 (5720): 385–9. Bibcode:2005Sci...308..385K. doi:10.1126/science.1109557. PMC 1512523. PMID 15761122.
Bush WS, Moore JH (2012). Lewitter F, Kann M (eds.). "Chapter 11: Genome-wide association studies". PLOS Computational Biology. 8 (12): e1002822. Bibcode:2012PLSCB...8E2822B. doi:10.1371/journal.pcbi.1002822. PMC 3531285. PMID 23300413.
Risch N, Merikangas K (September 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. Bibcode:1996Sci...273.1516R. doi:10.1126/science.273.5281.1516. PMID 8801636. S2CID 5228523.
The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.
Schena M, Shalon D, Davis RW, Brown PO (October 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. Bibcode:1995Sci...270..467S. doi:10.1126/science.270.5235.467. PMID 7569999. S2CID 6720459.
Wellcome Trust Case Control Consortium, Burton PR (June 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. Bibcode:2007Natur.447..661B. doi:10.1038/nature05911. PMC 2719288. PMID 17554300.
Novembre J, Johnson T, Bryc K, Kutalik Z, Boyko AR, Auton A, Indap A, King KS, Bergmann S, Nelson MR, Stephens M, Bustamante CD (November 2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (June 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proceedings of the National Academy of Sciences of the United States of America. 106 (23): 9362–7. Bibcode:2009PNAS..106.9362H. doi:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA (April 2005). "Complement factor H variant increases the risk of age-related macular degeneration". Science. 308 (5720): 419–21. Bibcode:2005Sci...308..419H. doi:10.1126/science.1110359. PMID 15761120. S2CID 32716116.
Iadonato SP, Katze MG (September 2009). "Genomics: Hepatitis C virus gets personal". Nature. 461 (7262): 357–8. Bibcode:2009Natur.461..357I. doi:10.1038/461357a. PMID 19759611. S2CID 7602652.
Couzin-Frankel J (June 2010). "Major heart disease genes prove elusive". Science. 328 (5983): 1220–1. Bibcode:2010Sci...328.1220C. doi:10.1126/science.328.5983.1220. PMID 20522751.
Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sulkowski M, McHutchison JG, Goldstein DB (September 2009). "Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance". Nature. 461 (7262): 399–401. Bibcode:2009Natur.461..399G. doi:10.1038/nature08309. PMID 19684573. S2CID 1707096.
Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O'Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M (October 2009). "Genetic variation in IL28B and spontaneous clearance of hepatitis C virus". Nature. 461 (7265): 798–801. Bibcode:2009Natur.461..798T. doi:10.1038/nature08463. PMC 3172006. PMID 19759533.
Willi Y, Kristensen TN, Sgrò CM, Weeks AR, Ørsted M, Hoffmann AA (January 2022). "Conservation genetics as a management tool: The five best-supported paradigms to assist the management of threatened species". Proceedings of the National Academy of Sciences of the United States of America. 119 (1): e2105076119. Bibcode:2022PNAS..11905076W. doi:10.1073/pnas.2105076119. PMC 8740573. PMID 34930821.
Turuspekov Y, Baibulatova A, Yermekbayev K, Tokhetova L, Chudinov V, Sereda G, et al. (November 2017). "GWAS for plant growth stages and yield components in spring wheat (Triticum aestivum L.) harvested in three regions of Kazakhstan". BMC Plant Biology. 17 (Suppl 1): 190. Bibcode:2017BMCPB..17S.190T. doi:10.1186/s12870-017-1131-2. PMC 5688510. PMID 29143598.
Zhao K, Tung CW, Eizenga GC, Wright MH, Ali ML, Price AH, et al. (September 2011). "Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa". Nature Communications. 2 (1): 467. Bibcode:2011NatCo...2..467Z. doi:10.1038/ncomms1467. PMC 3195253. PMID 21915109.
Bartoli C, Roux F (2017). "Genome-Wide Association Studies In Plant Pathosystems: Toward an Ecological Genomics Approach". Frontiers in Plant Science. 8: 763. Bibcode:2017FrPS....8..763B. doi:10.3389/fpls.2017.00763. PMC 5441063. PMID 28588588.
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT (18 January 2012). "Genetic signatures of exceptional longevity in humans". PLOS ONE. 7 (1): e29848. Bibcode:2012PLoSO...729848S. doi:10.1371/journal.pone.0029848. PMC 3261167. PMID 22279548.
Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA (2022). "Cross-trait assortative mating is widespread and inflates genetic correlation estimates". Science. 378 (6621): 754–761. Bibcode:2022Sci...378..754B. doi:10.1126/science.abo2059. ISSN 0036-8075. PMC 9901291. PMID 36395242.

man.ac.uk

Lee JJ, Wedow R, Okbay A, Kong E, Maghzian O, Zacher M, Nguyen-Viet TA, Bowers P, Sidorenko J, Karlsson Linnér R, et al. (July 2018). "Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals". Nature Genetics. 50 (8): 1112–1121. doi:10.1038/s41588-018-0147-3. PMC 6393768. PMID 30038396.

nature.com

Uffelmann E, Huang QQ, Munung NS, de Vries J, Okada Y, Martin AR, Martin HC, Lappalainen T, Posthuma D (26 August 2021). "Genome-wide association studies". Nature Reviews Methods Primers. 1 (1): 1–21. doi:10.1038/s43586-021-00056-9. ISSN 2662-8449.
Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, et al. (December 2002). "Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction". Nature Genetics. 32 (4): 650–4. doi:10.1038/ng1047. PMID 12426569. S2CID 21414260.
Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D (May 2019). "Benefits and limitations of genome-wide association studies". Nature Reviews Genetics. 20 (8): 467–484. doi:10.1038/s41576-019-0127-1. ISSN 1471-0056. PMID 31068683. S2CID 148570302.

nih.gov

pubmed.ncbi.nlm.nih.gov

Manolio TA (July 2010). "Genomewide association studies and assessment of the risk of disease". The New England Journal of Medicine. 363 (2): 166–76. doi:10.1056/NEJMra0905980. PMID 20647212.
Pearson TA, Manolio TA (March 2008). "How to interpret a genome-wide association study". JAMA. 299 (11): 1335–44. doi:10.1001/jama.299.11.1335. PMID 18349094.
Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, et al. (December 2002). "Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction". Nature Genetics. 32 (4): 650–4. doi:10.1038/ng1047. PMID 12426569. S2CID 21414260.
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, et al. (April 2005). "Complement factor H polymorphism in age-related macular degeneration". Science. 308 (5720): 385–9. Bibcode:2005Sci...308..385K. doi:10.1126/science.1109557. PMC 1512523. PMID 15761122.
Bush WS, Moore JH (2012). Lewitter F, Kann M (eds.). "Chapter 11: Genome-wide association studies". PLOS Computational Biology. 8 (12): e1002822. Bibcode:2012PLSCB...8E2822B. doi:10.1371/journal.pcbi.1002822. PMC 3531285. PMID 23300413.
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (November 2001). "Genomewide scans of complex human diseases: true linkage is hard to find". American Journal of Human Genetics. 69 (5): 936–50. doi:10.1086/324069. PMC 1274370. PMID 11565063.
Risch N, Merikangas K (September 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. Bibcode:1996Sci...273.1516R. doi:10.1126/science.273.5281.1516. PMID 8801636. S2CID 5228523.
Greely HT (2007). "The uneasy ethical and legal underpinnings of large-scale genomic biobanks". Annual Review of Genomics and Human Genetics. 8: 343–64. doi:10.1146/annurev.genom.7.080505.115721. PMID 17550341.
The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.
Schena M, Shalon D, Davis RW, Brown PO (October 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. Bibcode:1995Sci...270..467S. doi:10.1126/science.270.5235.467. PMID 7569999. S2CID 6720459.
Wellcome Trust Case Control Consortium, Burton PR (June 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. Bibcode:2007Natur.447..661B. doi:10.1038/nature05911. PMC 2719288. PMID 17554300.
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (February 2011). "Basic statistical analysis in genetic case-control studies". Nature Protocols. 6 (2): 121–33. doi:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. (September 2007). "PLINK: a tool set for whole-genome association and population-based linkage analyses". American Journal of Human Genetics. 81 (3): 559–75. doi:10.1086/519795. PMC 1950838. PMID 17701901.
Llinares-López F, Grimm DG, Bodenham DA, Gieraths U, Sugiyama M, Rowan B, Borgwardt K (June 2015). "Genome-wide detection of intervals of genetic heterogeneity associated with complex traits". Bioinformatics. 31 (12): i240-9. doi:10.1093/bioinformatics/btv263. PMC 4559912. PMID 26072488.
Ayati M, Erten S, Chance MR, Koyutürk M (December 2015). "MOBAS: identification of disease-associated protein subnetworks using modularity-based scoring". EURASIP Journal on Bioinformatics & Systems Biology. 2015 (1): 7. doi:10.1186/s13637-015-0025-6. PMC 5270451. PMID 28194175.
Carré C, Carluer JB, Chaux C, Estoup-Streiff C, Roche N, Hosy E, Mas A, Krouk G (25 March 2024). "Next-Gen GWAS: full 2D epistatic interaction maps retrieve part of missing heritability and improve phenotypic prediction". Genome Biology. 25 (1): 76. doi:10.1186/s13059-024-03202-0. ISSN 1474-760X. PMC 10962106. PMID 38523316.
Marchini J, Howie B (July 2010). "Genotype imputation for genome-wide association studies". Nature Reviews Genetics. 11 (7): 499–511. doi:10.1038/nrg2796. PMID 20517342. S2CID 1465707.
Howie B, Marchini J, Stephens M (November 2011). "Genotype imputation with thousands of genomes". G3. 1 (6): 457–70. doi:10.1534/g3.111.001198. PMC 3276165. PMID 22384356.
Browning BL, Browning SR (February 2009). "A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals". American Journal of Human Genetics. 84 (2): 210–23. doi:10.1016/j.ajhg.2009.01.005. PMC 2668004. PMID 19200528.
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (December 2010). "MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes". Genetic Epidemiology. 34 (8): 816–34. doi:10.1002/gepi.20533. PMC 3175618. PMID 21058334.
Novembre J, Johnson T, Bryc K, Kutalik Z, Boyko AR, Auton A, Indap A, King KS, Bergmann S, Nelson MR, Stephens M, Bustamante CD (November 2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
Charney E (January 2017). "Genes, behavior, and behavior genetics". Wiley Interdisciplinary Reviews. Cognitive Science. 8 (1–2): e1405. doi:10.1002/wcs.1405. hdl:10161/13337. PMID 27906529.
Wittkowski KM, Sonakya V, Bigio B, Tonn MK, Shic F, Ascano M, Nasca C, Gold-Von Simson G (January 2014). "A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism". Translational Psychiatry. 4 (1): e354. doi:10.1038/tp.2013.124. PMC 3905234. PMID 24473445.
Barsh GS, Copenhaver GP, Gibson G, Williams SM (July 2012). "Guidelines for genome-wide association studies". PLOS Genetics. 8 (7): e1002812. doi:10.1371/journal.pgen.1002812. PMC 3390399. PMID 22792080.
Smith SM, Douaud G, Chen W, Hanayik T, Alfaro-Almagro F, Sharp K, Elliott LT (2021). "An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank". Nat Neurosci. 24 (5): 737–745. doi:10.1038/s41593-021-00826-4. PMC 7610742. PMID 33875891.
Sanna S, Li B, Mulas A, Sidore C, Kang HM, Jackson AU, et al. (July 2011). Gibson G (ed.). "Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability". PLOS Genetics. 7 (7): e1002198. doi:10.1371/journal.pgen.1002198. PMC 3145627. PMID 21829380.
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (June 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proceedings of the National Academy of Sciences of the United States of America. 106 (23): 9362–7. Bibcode:2009PNAS..106.9362H. doi:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.
Johnson AD, O'Donnell CJ (January 2009). "An open access database of genome-wide association results". BMC Medical Genetics. 10: 6. doi:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA (April 2005). "Complement factor H variant increases the risk of age-related macular degeneration". Science. 308 (5720): 419–21. Bibcode:2005Sci...308..419H. doi:10.1126/science.1110359. PMID 15761120. S2CID 32716116.
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (October 2011). "Design and development of TT30, a novel C3d-targeted C3/C5 convertase inhibitor for treatment of human complement alternative pathway-mediated diseases". Blood. 118 (17): 4705–13. doi:10.1182/blood-2011-06-359646. PMC 3208285. PMID 21860027.
Ioannidis JP, Thomas G, Daly MJ (May 2009). "Validating, augmenting and refining genome-wide association signals". Nature Reviews Genetics. 10 (5): 318–29. doi:10.1038/nrg2544. PMC 7877552. PMID 19373277. S2CID 6463743.
Lee JJ, Wedow R, Okbay A, Kong E, Maghzian O, Zacher M, Nguyen-Viet TA, Bowers P, Sidorenko J, Karlsson Linnér R, et al. (July 2018). "Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals". Nature Genetics. 50 (8): 1112–1121. doi:10.1038/s41588-018-0147-3. PMC 6393768. PMID 30038396.
Okbay A, Wu Y, Wang N, Jayashankar H, Bennett M, Nehzati SM, et al. (April 2022). "Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals". Nature Genetics. 54 (4): 437–449. doi:10.1038/s41588-022-01016-z. hdl:11368/3026010. PMC 9005349. PMID 35361970.
Jansen PR, Watanabe K, Stringer S, Skene N, Bryois J, Hammerschlag AR, et al. (March 2019). "Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways". Nature Genetics. 51 (3): 394–403. bioRxiv 10.1101/214973. doi:10.1038/s41588-018-0333-3. hdl:1871.1/08af5d9e-8621-41f1-97c5-e77a1063495f. PMID 30804565.
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, et al. (January 2009). "Common variants at 30 loci contribute to polygenic dyslipidemia". Nature Genetics. 41 (1): 56–65. doi:10.1038/ng.291. PMC 2881676. PMID 19060906.
Strawbridge RJ, Dupuis J, Prokopenko I, Barker A, Ahlqvist E, Rybin D, et al. (October 2011). "Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes". Diabetes. 60 (10): 2624–34. doi:10.2337/db11-0415. PMC 3178302. PMID 21873549.
Danesh J, Pepys MB (November 2009). "C-reactive protein and coronary disease: is there a causal link?". Circulation. 120 (21): 2036–9. doi:10.1161/CIRCULATIONAHA.109.907212. PMID 19901186.
Liu JZ, Erlich Y, Pickrell JK (March 2017). "Case-control association mapping by proxy using family history of disease". Nature Genetics. 49 (3): 325–331. doi:10.1038/ng.3766. PMID 28092683. S2CID 5598845.
Ku CS, Loy EY, Pawitan Y, Chia KS (April 2010). "The pursuit of genome-wide association studies: where are we now?". Journal of Human Genetics. 55 (4): 195–206. doi:10.1038/jhg.2010.19. PMID 20300123.
Maher B (November 2008). "Personal genomes: The case of the missing heritability". Nature. 456 (7218): 18–21. doi:10.1038/456018a. PMID 18987709.
Iadonato SP, Katze MG (September 2009). "Genomics: Hepatitis C virus gets personal". Nature. 461 (7262): 357–8. Bibcode:2009Natur.461..357I. doi:10.1038/461357a. PMID 19759611. S2CID 7602652.
Muehlschlegel JD, Liu KY, Perry TE, Fox AA, Collard CD, Shernan SK, Body SC (September 2010). "Chromosome 9p21 variant predicts mortality after coronary artery bypass graft surgery". Circulation. 122 (11 Suppl): S60–5. doi:10.1161/CIRCULATIONAHA.109.924233. PMC 2943860. PMID 20837927.
Paynter NP, Chasman DI, Paré G, Buring JE, Cook NR, Miletich JP, Ridker PM (February 2010). "Association between a literature-based genetic risk score and cardiovascular events in women". JAMA. 303 (7): 631–7. doi:10.1001/jama.2010.119. PMC 2845522. PMID 20159871.
Couzin-Frankel J (June 2010). "Major heart disease genes prove elusive". Science. 328 (5983): 1220–1. Bibcode:2010Sci...328.1220C. doi:10.1126/science.328.5983.1220. PMID 20522751.
Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sulkowski M, McHutchison JG, Goldstein DB (September 2009). "Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance". Nature. 461 (7262): 399–401. Bibcode:2009Natur.461..399G. doi:10.1038/nature08309. PMID 19684573. S2CID 1707096.
Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O'Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M (October 2009). "Genetic variation in IL28B and spontaneous clearance of hepatitis C virus". Nature. 461 (7265): 798–801. Bibcode:2009Natur.461..798T. doi:10.1038/nature08463. PMC 3172006. PMID 19759533.
Lu YF, Goldstein DB, Angrist M, Cavalleri G (July 2014). "Personalized medicine and human genetic diversity". Cold Spring Harbor Perspectives in Medicine. 4 (9): a008581. doi:10.1101/cshperspect.a008581. PMC 4143101. PMID 25059740.
Folkersen L, van't Hooft F, Chernogubova E, Agardh HE, Hansson GK, Hedin U, Liska J, Syvänen AC, Paulsson-Berne G, Paulssson-Berne G, Franco-Cereceda A, Hamsten A, Gabrielsen A, Eriksson P (August 2010). "Association of genetic risk variants with expression of proximal genes identifies novel susceptibility genes for cardiovascular disease". Circulation: Cardiovascular Genetics. 3 (4): 365–73. doi:10.1161/CIRCGENETICS.110.948935. PMID 20562444.
Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, et al. (November 2011). "Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1". American Journal of Human Genetics. 89 (5): 619–27. doi:10.1016/j.ajhg.2011.10.002. PMC 3213391. PMID 22055160.
Coronary Artery Disease (C4D) Genetics Consortium (March 2011). "A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease". Nature Genetics. 43 (4): 339–44. doi:10.1038/ng.782. PMID 21378988. S2CID 39712343.{{cite journal}}: CS1 maint: numeric names: authors list (link)^{[permanent dead link]}
Johnson T, Gaunt TR, Newhouse SJ, Padmanabhan S, Tomaszewski M, Kumari M, et al. (December 2011). "Blood pressure loci identified with a gene-centric array". American Journal of Human Genetics. 89 (6): 688–700. doi:10.1016/j.ajhg.2011.10.013. PMC 3234370. PMID 22100073.
Dubé JB, Johansen CT, Hegele RA (June 2011). "Sortilin: an unusual suspect in cholesterol metabolism: from GWAS identification to in vivo biochemical analyses, sortilin has been identified as a novel mediator of human lipoprotein metabolism". BioEssays. 33 (6): 430–7. doi:10.1002/bies.201100003. PMID 21462369.
Bauer RC, Stylianou IM, Rader DJ (April 2011). "Functional validation of new pathways in lipoprotein metabolism identified by human genetics". Current Opinion in Lipidology. 22 (2): 123–8. doi:10.1097/MOL.0b013e32834469b3. PMID 21311327. S2CID 24020035.
Roselli C, Chafin M, Weng L (2018). "Multi-ethnic genome-wide association study for atrial fibrillation". Nature Genetics. 50 (9): 1225–1233. doi:10.1038/s41588-018-0133-9. PMC 6136836. PMID 29892015.
Ganapathiraju MK, Thahir M, Handen A, Sarkar SN, Sweet RA, Nimgaonkar VL, Loscher CE, Bauer EM, Chaparala S (27 April 2016). "Schizophrenia interactome with 504 novel protein-protein interactions". npj Schizophrenia. 2: 16012. doi:10.1038/npjschz.2016.12. PMC 4898894. PMID 27336055.
Johnson EC, Border R, Melroy-Greif WE, de Leeuw CA, Ehringer MA, Keller MC (November 2017). "No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes". Biological Psychiatry. 82 (10): 702–708. doi:10.1016/j.biopsych.2017.06.033. PMC 5643230. PMID 28823710.
Mocci E, Ward K, Perry JA, Starkweather A, Stone LS, Schabrun SM, Renn C, Dorsey SG, Ament SA (2023). "Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits". PLOS Genetics. 19 (10): e1010977. doi:10.1371/journal.pgen.1010977. ISSN 1553-7404. PMC 10602383. PMID 37844115.
Willi Y, Kristensen TN, Sgrò CM, Weeks AR, Ørsted M, Hoffmann AA (January 2022). "Conservation genetics as a management tool: The five best-supported paradigms to assist the management of threatened species". Proceedings of the National Academy of Sciences of the United States of America. 119 (1): e2105076119. Bibcode:2022PNAS..11905076W. doi:10.1073/pnas.2105076119. PMC 8740573. PMID 34930821.
Turuspekov Y, Baibulatova A, Yermekbayev K, Tokhetova L, Chudinov V, Sereda G, et al. (November 2017). "GWAS for plant growth stages and yield components in spring wheat (Triticum aestivum L.) harvested in three regions of Kazakhstan". BMC Plant Biology. 17 (Suppl 1): 190. Bibcode:2017BMCPB..17S.190T. doi:10.1186/s12870-017-1131-2. PMC 5688510. PMID 29143598.
Zhao K, Tung CW, Eizenga GC, Wright MH, Ali ML, Price AH, et al. (September 2011). "Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa". Nature Communications. 2 (1): 467. Bibcode:2011NatCo...2..467Z. doi:10.1038/ncomms1467. PMC 3195253. PMID 21915109.
Bartoli C, Roux F (2017). "Genome-Wide Association Studies In Plant Pathosystems: Toward an Ecological Genomics Approach". Frontiers in Plant Science. 8: 763. Bibcode:2017FrPS....8..763B. doi:10.3389/fpls.2017.00763. PMC 5441063. PMID 28588588.
Abasht B, Lamont SJ (October 2007). "Genome-wide association analysis reveals cryptic alleles as an important factor in heterosis for fatness in chicken F2 population". Animal Genetics. 38 (5): 491–498. doi:10.1111/j.1365-2052.2007.01642.x. PMID 17894563.
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2010). "Genetic signatures of exceptional longevity in humans". Science. 2010 (5987). doi:10.1126/science.1190532. PMID 20595579. (Retracted, see doi:10.1126/science.333.6041.404-a, PMID 21778381, Retraction Watch)
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2011). "Retraction". Science. 333 (6041): 404. doi:10.1126/science.333.6041.404-a. PMID 21778381.
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT (18 January 2012). "Genetic signatures of exceptional longevity in humans". PLOS ONE. 7 (1): e29848. Bibcode:2012PLoSO...729848S. doi:10.1371/journal.pone.0029848. PMC 3261167. PMID 22279548.
Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D (May 2019). "Benefits and limitations of genome-wide association studies". Nature Reviews Genetics. 20 (8): 467–484. doi:10.1038/s41576-019-0127-1. ISSN 1471-0056. PMID 31068683. S2CID 148570302.
Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, Boehnke M (May 2010). "Genome-wide association studies in diverse populations". Nature Reviews Genetics. 11 (5): 356–66. doi:10.1038/nrg2760. PMC 3079573. PMID 20395969.
Sham PC, Cherny SS, Purcell S, Hewitt JK (May 2000). "Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data". American Journal of Human Genetics. 66 (5): 1616–30. doi:10.1086/302891. PMC 1378020. PMID 10762547.
Visscher PM, Goddard ME, Derks EM, Wray NR (May 2012). "Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses". Molecular Psychiatry. 17 (5): 474–85. doi:10.1038/mp.2011.65. PMID 21670730.
Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA (2022). "Cross-trait assortative mating is widespread and inflates genetic correlation estimates". Science. 378 (6621): 754–761. Bibcode:2022Sci...378..754B. doi:10.1126/science.abo2059. ISSN 0036-8075. PMC 9901291. PMID 36395242.

ncbi.nlm.nih.gov

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, et al. (April 2005). "Complement factor H polymorphism in age-related macular degeneration". Science. 308 (5720): 385–9. Bibcode:2005Sci...308..385K. doi:10.1126/science.1109557. PMC 1512523. PMID 15761122.
Bush WS, Moore JH (2012). Lewitter F, Kann M (eds.). "Chapter 11: Genome-wide association studies". PLOS Computational Biology. 8 (12): e1002822. Bibcode:2012PLSCB...8E2822B. doi:10.1371/journal.pcbi.1002822. PMC 3531285. PMID 23300413.
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (November 2001). "Genomewide scans of complex human diseases: true linkage is hard to find". American Journal of Human Genetics. 69 (5): 936–50. doi:10.1086/324069. PMC 1274370. PMID 11565063.
Wellcome Trust Case Control Consortium, Burton PR (June 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. Bibcode:2007Natur.447..661B. doi:10.1038/nature05911. PMC 2719288. PMID 17554300.
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (February 2011). "Basic statistical analysis in genetic case-control studies". Nature Protocols. 6 (2): 121–33. doi:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al. (September 2007). "PLINK: a tool set for whole-genome association and population-based linkage analyses". American Journal of Human Genetics. 81 (3): 559–75. doi:10.1086/519795. PMC 1950838. PMID 17701901.
Llinares-López F, Grimm DG, Bodenham DA, Gieraths U, Sugiyama M, Rowan B, Borgwardt K (June 2015). "Genome-wide detection of intervals of genetic heterogeneity associated with complex traits". Bioinformatics. 31 (12): i240-9. doi:10.1093/bioinformatics/btv263. PMC 4559912. PMID 26072488.
Ayati M, Erten S, Chance MR, Koyutürk M (December 2015). "MOBAS: identification of disease-associated protein subnetworks using modularity-based scoring". EURASIP Journal on Bioinformatics & Systems Biology. 2015 (1): 7. doi:10.1186/s13637-015-0025-6. PMC 5270451. PMID 28194175.
Carré C, Carluer JB, Chaux C, Estoup-Streiff C, Roche N, Hosy E, Mas A, Krouk G (25 March 2024). "Next-Gen GWAS: full 2D epistatic interaction maps retrieve part of missing heritability and improve phenotypic prediction". Genome Biology. 25 (1): 76. doi:10.1186/s13059-024-03202-0. ISSN 1474-760X. PMC 10962106. PMID 38523316.
Howie B, Marchini J, Stephens M (November 2011). "Genotype imputation with thousands of genomes". G3. 1 (6): 457–70. doi:10.1534/g3.111.001198. PMC 3276165. PMID 22384356.
Browning BL, Browning SR (February 2009). "A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals". American Journal of Human Genetics. 84 (2): 210–23. doi:10.1016/j.ajhg.2009.01.005. PMC 2668004. PMID 19200528.
Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (December 2010). "MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes". Genetic Epidemiology. 34 (8): 816–34. doi:10.1002/gepi.20533. PMC 3175618. PMID 21058334.
Novembre J, Johnson T, Bryc K, Kutalik Z, Boyko AR, Auton A, Indap A, King KS, Bergmann S, Nelson MR, Stephens M, Bustamante CD (November 2008). "Genes mirror geography within Europe". Nature. 456 (7218): 98–101. Bibcode:2008Natur.456...98N. doi:10.1038/nature07331. PMC 2735096. PMID 18758442.
Wittkowski KM, Sonakya V, Bigio B, Tonn MK, Shic F, Ascano M, Nasca C, Gold-Von Simson G (January 2014). "A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism". Translational Psychiatry. 4 (1): e354. doi:10.1038/tp.2013.124. PMC 3905234. PMID 24473445.
Barsh GS, Copenhaver GP, Gibson G, Williams SM (July 2012). "Guidelines for genome-wide association studies". PLOS Genetics. 8 (7): e1002812. doi:10.1371/journal.pgen.1002812. PMC 3390399. PMID 22792080.
Smith SM, Douaud G, Chen W, Hanayik T, Alfaro-Almagro F, Sharp K, Elliott LT (2021). "An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank". Nat Neurosci. 24 (5): 737–745. doi:10.1038/s41593-021-00826-4. PMC 7610742. PMID 33875891.
Sanna S, Li B, Mulas A, Sidore C, Kang HM, Jackson AU, et al. (July 2011). Gibson G (ed.). "Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability". PLOS Genetics. 7 (7): e1002198. doi:10.1371/journal.pgen.1002198. PMC 3145627. PMID 21829380.
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (June 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proceedings of the National Academy of Sciences of the United States of America. 106 (23): 9362–7. Bibcode:2009PNAS..106.9362H. doi:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.
Johnson AD, O'Donnell CJ (January 2009). "An open access database of genome-wide association results". BMC Medical Genetics. 10: 6. doi:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (October 2011). "Design and development of TT30, a novel C3d-targeted C3/C5 convertase inhibitor for treatment of human complement alternative pathway-mediated diseases". Blood. 118 (17): 4705–13. doi:10.1182/blood-2011-06-359646. PMC 3208285. PMID 21860027.
Ioannidis JP, Thomas G, Daly MJ (May 2009). "Validating, augmenting and refining genome-wide association signals". Nature Reviews Genetics. 10 (5): 318–29. doi:10.1038/nrg2544. PMC 7877552. PMID 19373277. S2CID 6463743.
Lee JJ, Wedow R, Okbay A, Kong E, Maghzian O, Zacher M, Nguyen-Viet TA, Bowers P, Sidorenko J, Karlsson Linnér R, et al. (July 2018). "Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals". Nature Genetics. 50 (8): 1112–1121. doi:10.1038/s41588-018-0147-3. PMC 6393768. PMID 30038396.
Okbay A, Wu Y, Wang N, Jayashankar H, Bennett M, Nehzati SM, et al. (April 2022). "Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals". Nature Genetics. 54 (4): 437–449. doi:10.1038/s41588-022-01016-z. hdl:11368/3026010. PMC 9005349. PMID 35361970.
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, et al. (January 2009). "Common variants at 30 loci contribute to polygenic dyslipidemia". Nature Genetics. 41 (1): 56–65. doi:10.1038/ng.291. PMC 2881676. PMID 19060906.
Strawbridge RJ, Dupuis J, Prokopenko I, Barker A, Ahlqvist E, Rybin D, et al. (October 2011). "Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes". Diabetes. 60 (10): 2624–34. doi:10.2337/db11-0415. PMC 3178302. PMID 21873549.
Muehlschlegel JD, Liu KY, Perry TE, Fox AA, Collard CD, Shernan SK, Body SC (September 2010). "Chromosome 9p21 variant predicts mortality after coronary artery bypass graft surgery". Circulation. 122 (11 Suppl): S60–5. doi:10.1161/CIRCULATIONAHA.109.924233. PMC 2943860. PMID 20837927.
Paynter NP, Chasman DI, Paré G, Buring JE, Cook NR, Miletich JP, Ridker PM (February 2010). "Association between a literature-based genetic risk score and cardiovascular events in women". JAMA. 303 (7): 631–7. doi:10.1001/jama.2010.119. PMC 2845522. PMID 20159871.
Thomas DL, Thio CL, Martin MP, Qi Y, Ge D, O'Huigin C, Kidd J, Kidd K, Khakoo SI, Alexander G, Goedert JJ, Kirk GD, Donfield SM, Rosen HR, Tobler LH, Busch MP, McHutchison JG, Goldstein DB, Carrington M (October 2009). "Genetic variation in IL28B and spontaneous clearance of hepatitis C virus". Nature. 461 (7265): 798–801. Bibcode:2009Natur.461..798T. doi:10.1038/nature08463. PMC 3172006. PMID 19759533.
Lu YF, Goldstein DB, Angrist M, Cavalleri G (July 2014). "Personalized medicine and human genetic diversity". Cold Spring Harbor Perspectives in Medicine. 4 (9): a008581. doi:10.1101/cshperspect.a008581. PMC 4143101. PMID 25059740.
Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, et al. (November 2011). "Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1". American Journal of Human Genetics. 89 (5): 619–27. doi:10.1016/j.ajhg.2011.10.002. PMC 3213391. PMID 22055160.
Johnson T, Gaunt TR, Newhouse SJ, Padmanabhan S, Tomaszewski M, Kumari M, et al. (December 2011). "Blood pressure loci identified with a gene-centric array". American Journal of Human Genetics. 89 (6): 688–700. doi:10.1016/j.ajhg.2011.10.013. PMC 3234370. PMID 22100073.
Roselli C, Chafin M, Weng L (2018). "Multi-ethnic genome-wide association study for atrial fibrillation". Nature Genetics. 50 (9): 1225–1233. doi:10.1038/s41588-018-0133-9. PMC 6136836. PMID 29892015.
Ganapathiraju MK, Thahir M, Handen A, Sarkar SN, Sweet RA, Nimgaonkar VL, Loscher CE, Bauer EM, Chaparala S (27 April 2016). "Schizophrenia interactome with 504 novel protein-protein interactions". npj Schizophrenia. 2: 16012. doi:10.1038/npjschz.2016.12. PMC 4898894. PMID 27336055.
Ganapathiraju M, Chaparala S, Lo C (April 2018). "F200. Elucidating The Role of Cilia in Neuropsychiatric Diseases Through Interactome Analysis". Schizophrenia Bulletin. 44 (suppl_1): S298-9. doi:10.1093/schbul/sby017.731. PMC 5887623.
Johnson EC, Border R, Melroy-Greif WE, de Leeuw CA, Ehringer MA, Keller MC (November 2017). "No Evidence That Schizophrenia Candidate Genes Are More Associated With Schizophrenia Than Noncandidate Genes". Biological Psychiatry. 82 (10): 702–708. doi:10.1016/j.biopsych.2017.06.033. PMC 5643230. PMID 28823710.
Mocci E, Ward K, Perry JA, Starkweather A, Stone LS, Schabrun SM, Renn C, Dorsey SG, Ament SA (2023). "Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits". PLOS Genetics. 19 (10): e1010977. doi:10.1371/journal.pgen.1010977. ISSN 1553-7404. PMC 10602383. PMID 37844115.
Willi Y, Kristensen TN, Sgrò CM, Weeks AR, Ørsted M, Hoffmann AA (January 2022). "Conservation genetics as a management tool: The five best-supported paradigms to assist the management of threatened species". Proceedings of the National Academy of Sciences of the United States of America. 119 (1): e2105076119. Bibcode:2022PNAS..11905076W. doi:10.1073/pnas.2105076119. PMC 8740573. PMID 34930821.
Turuspekov Y, Baibulatova A, Yermekbayev K, Tokhetova L, Chudinov V, Sereda G, et al. (November 2017). "GWAS for plant growth stages and yield components in spring wheat (Triticum aestivum L.) harvested in three regions of Kazakhstan". BMC Plant Biology. 17 (Suppl 1): 190. Bibcode:2017BMCPB..17S.190T. doi:10.1186/s12870-017-1131-2. PMC 5688510. PMID 29143598.
Zhao K, Tung CW, Eizenga GC, Wright MH, Ali ML, Price AH, et al. (September 2011). "Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa". Nature Communications. 2 (1): 467. Bibcode:2011NatCo...2..467Z. doi:10.1038/ncomms1467. PMC 3195253. PMID 21915109.
Bartoli C, Roux F (2017). "Genome-Wide Association Studies In Plant Pathosystems: Toward an Ecological Genomics Approach". Frontiers in Plant Science. 8: 763. Bibcode:2017FrPS....8..763B. doi:10.3389/fpls.2017.00763. PMC 5441063. PMID 28588588.
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT (18 January 2012). "Genetic signatures of exceptional longevity in humans". PLOS ONE. 7 (1): e29848. Bibcode:2012PLoSO...729848S. doi:10.1371/journal.pone.0029848. PMC 3261167. PMID 22279548.
Rosenberg NA, Huang L, Jewett EM, Szpiech ZA, Jankovic I, Boehnke M (May 2010). "Genome-wide association studies in diverse populations". Nature Reviews Genetics. 11 (5): 356–66. doi:10.1038/nrg2760. PMC 3079573. PMID 20395969.
Sham PC, Cherny SS, Purcell S, Hewitt JK (May 2000). "Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data". American Journal of Human Genetics. 66 (5): 1616–30. doi:10.1086/302891. PMC 1378020. PMID 10762547.
Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA (2022). "Cross-trait assortative mating is widespread and inflates genetic correlation estimates". Science. 378 (6621): 754–761. Bibcode:2022Sci...378..754B. doi:10.1126/science.abo2059. ISSN 0036-8075. PMC 9901291. PMID 36395242.

omim.org

"Online Mendelian Inheritance in Man". Archived from the original on 5 December 2011. Retrieved 6 December 2011.

psychcentral.com

"New Schizophrenia Study Focuses on Protein-Protein Interactions". psychcentral.com. 3 May 2016. Archived from the original on 11 January 2020. Retrieved 22 April 2023.

retractionwatch.com

Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT (July 2010). "Genetic signatures of exceptional longevity in humans". Science. 2010 (5987). doi:10.1126/science.1190532. PMID 20595579. (Retracted, see doi:10.1126/science.333.6041.404-a, PMID 21778381, Retraction Watch)

semanticscholar.org

api.semanticscholar.org

Ozaki K, Ohnishi Y, Iida A, Sekine A, Yamada R, Tsunoda T, et al. (December 2002). "Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction". Nature Genetics. 32 (4): 650–4. doi:10.1038/ng1047. PMID 12426569. S2CID 21414260.
Risch N, Merikangas K (September 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. Bibcode:1996Sci...273.1516R. doi:10.1126/science.273.5281.1516. PMID 8801636. S2CID 5228523.
The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.
Schena M, Shalon D, Davis RW, Brown PO (October 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. Bibcode:1995Sci...270..467S. doi:10.1126/science.270.5235.467. PMID 7569999. S2CID 6720459.
Ayati M, Koyutürk M (1 January 2015). "Assessing the Collective Disease Association of Multiple Genomic Loci". Proceedings of the 6th ACM Conference on Bioinformatics, Computational Biology and Health Informatics. BCB '15. New York, NY, USA: ACM. pp. 376–385. doi:10.1145/2808719.2808758. ISBN 978-1-4503-3853-0. S2CID 5942777.
Marchini J, Howie B (July 2010). "Genotype imputation for genome-wide association studies". Nature Reviews Genetics. 11 (7): 499–511. doi:10.1038/nrg2796. PMID 20517342. S2CID 1465707.
Haines JL, Hauser MA, Schmidt S, Scott WK, Olson LM, Gallins P, Spencer KL, Kwan SY, Noureddine M, Gilbert JR, Schnetz-Boutaud N, Agarwal A, Postel EA, Pericak-Vance MA (April 2005). "Complement factor H variant increases the risk of age-related macular degeneration". Science. 308 (5720): 419–21. Bibcode:2005Sci...308..419H. doi:10.1126/science.1110359. PMID 15761120. S2CID 32716116.
Ioannidis JP, Thomas G, Daly MJ (May 2009). "Validating, augmenting and refining genome-wide association signals". Nature Reviews Genetics. 10 (5): 318–29. doi:10.1038/nrg2544. PMC 7877552. PMID 19373277. S2CID 6463743.
Liu JZ, Erlich Y, Pickrell JK (March 2017). "Case-control association mapping by proxy using family history of disease". Nature Genetics. 49 (3): 325–331. doi:10.1038/ng.3766. PMID 28092683. S2CID 5598845.
Iadonato SP, Katze MG (September 2009). "Genomics: Hepatitis C virus gets personal". Nature. 461 (7262): 357–8. Bibcode:2009Natur.461..357I. doi:10.1038/461357a. PMID 19759611. S2CID 7602652.
Ge D, Fellay J, Thompson AJ, Simon JS, Shianna KV, Urban TJ, Heinzen EL, Qiu P, Bertelsen AH, Muir AJ, Sulkowski M, McHutchison JG, Goldstein DB (September 2009). "Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance". Nature. 461 (7262): 399–401. Bibcode:2009Natur.461..399G. doi:10.1038/nature08309. PMID 19684573. S2CID 1707096.
Coronary Artery Disease (C4D) Genetics Consortium (March 2011). "A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease". Nature Genetics. 43 (4): 339–44. doi:10.1038/ng.782. PMID 21378988. S2CID 39712343.{{cite journal}}: CS1 maint: numeric names: authors list (link)^{[permanent dead link]}
Bauer RC, Stylianou IM, Rader DJ (April 2011). "Functional validation of new pathways in lipoprotein metabolism identified by human genetics". Current Opinion in Lipidology. 22 (2): 123–8. doi:10.1097/MOL.0b013e32834469b3. PMID 21311327. S2CID 24020035.
Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D (May 2019). "Benefits and limitations of genome-wide association studies". Nature Reviews Genetics. 20 (8): 467–484. doi:10.1038/s41576-019-0127-1. ISSN 1471-0056. PMID 31068683. S2CID 148570302.

umich.edu

deepblue.lib.umich.edu

The International HapMap Project, Gibbs RA, Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W (December 2003). "The International HapMap Project" (PDF). Nature. 426 (6968): 789–96. Bibcode:2003Natur.426..789G. doi:10.1038/nature02168. hdl:2027.42/62838. PMID 14685227. S2CID 4387110.

web.archive.org

"Online Mendelian Inheritance in Man". Archived from the original on 5 December 2011. Retrieved 6 December 2011.
"Largest ever study of genetics of common diseases published today" (Press release). Wellcome Trust Case Control Consortium. 6 June 2007. Archived from the original on 4 June 2008. Retrieved 19 June 2008.
"New Schizophrenia Study Focuses on Protein-Protein Interactions". psychcentral.com. 3 May 2016. Archived from the original on 11 January 2020. Retrieved 22 April 2023.

wiley.com

onlinelibrary.wiley.com

Wiley (9 September 2005). Encyclopedia of Life Sciences (1 ed.). Wiley. doi:10.1038/npg.els.0005483. ISBN 978-0-470-01617-6.

wired.com

MacArthur D (8 July 2010). "Serious flaws revealed in "longevity genes" study". Wired. Retrieved 7 December 2011.

worldcat.org

search.worldcat.org

Uffelmann E, Huang QQ, Munung NS, de Vries J, Okada Y, Martin AR, Martin HC, Lappalainen T, Posthuma D (26 August 2021). "Genome-wide association studies". Nature Reviews Methods Primers. 1 (1): 1–21. doi:10.1038/s43586-021-00056-9. ISSN 2662-8449.
Carré C, Carluer JB, Chaux C, Estoup-Streiff C, Roche N, Hosy E, Mas A, Krouk G (25 March 2024). "Next-Gen GWAS: full 2D epistatic interaction maps retrieve part of missing heritability and improve phenotypic prediction". Genome Biology. 25 (1): 76. doi:10.1186/s13059-024-03202-0. ISSN 1474-760X. PMC 10962106. PMID 38523316.
Mocci E, Ward K, Perry JA, Starkweather A, Stone LS, Schabrun SM, Renn C, Dorsey SG, Ament SA (2023). "Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits". PLOS Genetics. 19 (10): e1010977. doi:10.1371/journal.pgen.1010977. ISSN 1553-7404. PMC 10602383. PMID 37844115.
Tam V, Patel N, Turcotte M, Bossé Y, Paré G, Meyre D (May 2019). "Benefits and limitations of genome-wide association studies". Nature Reviews Genetics. 20 (8): 467–484. doi:10.1038/s41576-019-0127-1. ISSN 1471-0056. PMID 31068683. S2CID 148570302.
Border R, Athanasiadis G, Buil A, Schork AJ, Cai N, Young AI, Werge T, Flint J, Kendler KS, Sankararaman S, Dahl AW, Zaitlen NA (2022). "Cross-trait assortative mating is widespread and inflates genetic correlation estimates". Science. 378 (6621): 754–761. Bibcode:2022Sci...378..754B. doi:10.1126/science.abo2059. ISSN 0036-8075. PMC 9901291. PMID 36395242.

wtccc.org.uk

"Largest ever study of genetics of common diseases published today" (Press release). Wellcome Trust Case Control Consortium. 6 June 2007. Archived from the original on 4 June 2008. Retrieved 19 June 2008.

zenodo.org

Coronary Artery Disease (C4D) Genetics Consortium (March 2011). "A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease". Nature Genetics. 43 (4): 339–44. doi:10.1038/ng.782. PMID 21378988. S2CID 39712343.{{cite journal}}: CS1 maint: numeric names: authors list (link)^{[permanent dead link]}