Geneetiline assotsiatsiooniuuring (Estonian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Geneetiline assotsiatsiooniuuring" in Estonian language version.

refsWebsite

Global rank Estonian rank

27nih.gov

4^th place

14^th place

17doi.org

2^nd place

16^th place

1elnet.ee

low place

916^th place

1genome.gov

9,308^th place

5,569^th place

1nature.com

234^th place

88^th place

1archive.org

6^th place

41^st place

1omim.org

4,380^th place

low place

1web.archive.org

1^st place

1wtccc.org.uk

low place

archive.org

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

doi.org

Manolio TA; Guttmacher, Alan E.; Manolio, Teri A. (juuli 2010). "Genomewide association studies and assessment of the risk of disease". N. Engl. J. Med. 363 (2): 166–76. DOI:10.1056/NEJMra0905980. PMID 20647212.
Pearson TA, Manolio TA (märts 2008). "How to interpret a genome-wide association study". JAMA. 299 (11): 1335–44. DOI:10.1001/jama.299.11.1335. PMID 18349094.
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J (aprill 2005). "Complement Factor H Polymorphism in Age-Related Macular Degeneration". Science. 308 (5720): 385–9. DOI:10.1126/science.1109557. PMC 1512523. PMID 15761122.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Johnson AD, O'Donnell CJ (2009). "An Open Access Database of Genome-wide Association Results". BMC Med. Genet. 10: 6. DOI:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Ikram MK, Sim X, Xueling S; et al. (oktoober 2010). McCarthy, Mark I (toim). "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo". PLoS Genet. 6 (10): e1001184. DOI:10.1371/journal.pgen.1001184. PMC 2965750. PMID 21060863. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (november 2001). "Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to Find". Am. J. Hum. Genet. 69 (5): 936–50. DOI:10.1086/324069. PMC 1274370. PMID 11565063.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Risch N, Merikangas K (september 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. DOI:10.1126/science.273.5281.1516. PMID 8801636.
Greely HT (2007). "The uneasy ethical and legal underpinnings of large-scale genomic biobanks". Annu Rev Genomics Hum Genet. 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 L-Y, Huang W (detsember 2003). "The International HapMap Project". Nature. 426 (6968): 789–96. DOI:10.1038/nature02168. PMID 14685227.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Schena M, Shalon D, Davis RW, Brown PO (oktoober 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. DOI:10.1126/science.270.5235.467. PMID 7569999.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (veebruar 2011). "Basic statistical analysis in genetic case-control studies". Nat Protoc. 6 (2): 121–33. DOI:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (september 2007). "PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses". Am. J. Hum. Genet. 81 (3): 559–75. DOI:10.1086/519795. PMC 1950838. PMID 17701901.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
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. DOI:10.1038/nature07331. PMC 2735096. PMID 18758442.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (juuni 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proc. Natl. Acad. Sci. U.S.A. 106 (23): 9362–7. DOI:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (oktoober 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.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Wellcome Trust Case Control Consortium, Burton PR, Clayton DG, Cardon LR; et al. (juuni 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. DOI:10.1038/nature05911. PMC 2719288. PMID 17554300. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Couzin-Frankel J (juuni 2010). "Major heart disease genes prove elusive". Science. 328 (5983): 1220–1. DOI:10.1126/science.328.5983.1220. PMID 20522751.

elnet.ee

ems.elnet.ee

"EMS". Eesti märksõnastik. Vaadatud 13.04.2022.

genome.gov

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

nature.com

Loos, Ruth (19. november 2020). "15 years of genome-wide association studies and no signs of slowing down". Nature Communications. Vaadatud 13.04.2022.

nih.gov

pubmed.ncbi.nlm.nih.gov

Manolio TA; Guttmacher, Alan E.; Manolio, Teri A. (juuli 2010). "Genomewide association studies and assessment of the risk of disease". N. Engl. J. Med. 363 (2): 166–76. DOI:10.1056/NEJMra0905980. PMID 20647212.
Pearson TA, Manolio TA (märts 2008). "How to interpret a genome-wide association study". JAMA. 299 (11): 1335–44. DOI:10.1001/jama.299.11.1335. PMID 18349094.
Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J (aprill 2005). "Complement Factor H Polymorphism in Age-Related Macular Degeneration". Science. 308 (5720): 385–9. DOI:10.1126/science.1109557. PMC 1512523. PMID 15761122.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Johnson AD, O'Donnell CJ (2009). "An Open Access Database of Genome-wide Association Results". BMC Med. Genet. 10: 6. DOI:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Ikram MK, Sim X, Xueling S; et al. (oktoober 2010). McCarthy, Mark I (toim). "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo". PLoS Genet. 6 (10): e1001184. DOI:10.1371/journal.pgen.1001184. PMC 2965750. PMID 21060863. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (november 2001). "Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to Find". Am. J. Hum. Genet. 69 (5): 936–50. DOI:10.1086/324069. PMC 1274370. PMID 11565063.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Risch N, Merikangas K (september 1996). "The future of genetic studies of complex human diseases". Science. 273 (5281): 1516–7. DOI:10.1126/science.273.5281.1516. PMID 8801636.
Greely HT (2007). "The uneasy ethical and legal underpinnings of large-scale genomic biobanks". Annu Rev Genomics Hum Genet. 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 L-Y, Huang W (detsember 2003). "The International HapMap Project". Nature. 426 (6968): 789–96. DOI:10.1038/nature02168. PMID 14685227.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Schena M, Shalon D, Davis RW, Brown PO (oktoober 1995). "Quantitative monitoring of gene expression patterns with a complementary DNA microarray". Science. 270 (5235): 467–70. DOI:10.1126/science.270.5235.467. PMID 7569999.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (veebruar 2011). "Basic statistical analysis in genetic case-control studies". Nat Protoc. 6 (2): 121–33. DOI:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (september 2007). "PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses". Am. J. Hum. Genet. 81 (3): 559–75. DOI:10.1086/519795. PMC 1950838. PMID 17701901.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
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. DOI:10.1038/nature07331. PMC 2735096. PMID 18758442.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (juuni 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proc. Natl. Acad. Sci. U.S.A. 106 (23): 9362–7. DOI:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (oktoober 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.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Wellcome Trust Case Control Consortium, Burton PR, Clayton DG, Cardon LR; et al. (juuni 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. DOI:10.1038/nature05911. PMC 2719288. PMID 17554300. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Couzin-Frankel J (juuni 2010). "Major heart disease genes prove elusive". Science. 328 (5983): 1220–1. DOI:10.1126/science.328.5983.1220. PMID 20522751.

ncbi.nlm.nih.gov

Klein RJ, Zeiss C, Chew EY, Tsai JY, Sackler RS, Haynes C, Henning AK, SanGiovanni JP, Mane SM, Mayne ST, Bracken MB, Ferris FL, Ott J, Barnstable C, Hoh J (aprill 2005). "Complement Factor H Polymorphism in Age-Related Macular Degeneration". Science. 308 (5720): 385–9. DOI:10.1126/science.1109557. PMC 1512523. PMID 15761122.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Johnson AD, O'Donnell CJ (2009). "An Open Access Database of Genome-wide Association Results". BMC Med. Genet. 10: 6. DOI:10.1186/1471-2350-10-6. PMC 2639349. PMID 19161620.
Ikram MK, Sim X, Xueling S; et al. (oktoober 2010). McCarthy, Mark I (toim). "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo". PLoS Genet. 6 (10): e1001184. DOI:10.1371/journal.pgen.1001184. PMC 2965750. PMID 21060863. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M (november 2001). "Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to Find". Am. J. Hum. Genet. 69 (5): 936–50. DOI:10.1086/324069. PMC 1274370. PMID 11565063.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Clarke GM, Anderson CA, Pettersson FH, Cardon LR, Morris AP, Zondervan KT (veebruar 2011). "Basic statistical analysis in genetic case-control studies". Nat Protoc. 6 (2): 121–33. DOI:10.1038/nprot.2010.182. PMC 3154648. PMID 21293453.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC (september 2007). "PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses". Am. J. Hum. Genet. 81 (3): 559–75. DOI:10.1086/519795. PMC 1950838. PMID 17701901.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
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. DOI:10.1038/nature07331. PMC 2735096. PMID 18758442.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA (juuni 2009). "Potential etiologic and functional implications of genome-wide association loci for human diseases and traits". Proc. Natl. Acad. Sci. U.S.A. 106 (23): 9362–7. DOI:10.1073/pnas.0903103106. PMC 2687147. PMID 19474294.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Fridkis-Hareli M, Storek M, Mazsaroff I, Risitano AM, Lundberg AS, Horvath CJ, Holers VM (oktoober 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.{{cite journal}}: CS1 hooldus: mitu nime: autorite loend (link)
Wellcome Trust Case Control Consortium, Burton PR, Clayton DG, Cardon LR; et al. (juuni 2007). "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls". Nature. 447 (7145): 661–78. DOI:10.1038/nature05911. PMC 2719288. PMID 17554300. {{cite journal}}: et al.-i üleliigne kasutus kohas: |author= (juhend)CS1 hooldus: mitu nime: autorite loend (link)

omim.org

"Online Mendelian Inheritance in Man". Vaadatud 6.12.2011.

web.archive.org

"Largest ever study of genetics of common diseases published today". Wellcome Trust Case Control Consortium. 6. juuni 2007. Originaali arhiivikoopia seisuga 4.06.2008. Vaadatud 19.06.2008.

wtccc.org.uk

"Largest ever study of genetics of common diseases published today". Wellcome Trust Case Control Consortium. 6. juuni 2007. Originaali arhiivikoopia seisuga 4.06.2008. Vaadatud 19.06.2008.