Сложные признаки (Russian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Сложные признаки" in Russian language version.

refsWebsite

Global rank Russian rank

16nih.gov

4^th place

6^th place

11doi.org

2^nd place

3^rd place

3semanticscholar.org

11^th place

286^th place

2harvard.edu

18^th place

63^rd place

1zenodo.org

621^st place

3,286^th place

1web.archive.org

1^st place

doi.org

Fisher, R. A. (1919). XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance. Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163. S2CID 181213898. Архивировано 28 ноября 2022. Дата обращения: 21 апреля 2024.
Gibson G (January 2012). Rare and common variants: twenty arguments. Nature Reviews. Genetics. 13 (2): 135–45. doi:10.1038/nrg3118. PMC 4408201. PMID 22251874.
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (October 2009). Finding the missing heritability of complex diseases. Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. doi:10.1038/nature08494. PMC 2831613. PMID 19812666.
Shi H, Kichaev G, Pasaniuc B (July 2016). Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data. American Journal of Human Genetics. 99 (1): 139–53. doi:10.1016/j.ajhg.2016.05.013. PMC 5005444. PMID 27346688.
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (June 2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47 (6): 582–8. doi:10.1038/ng.3303. PMC 4449286. PMID 25961944.
Boyle EA, Li YI, Pritchard JK (June 2017). An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell. 169 (7): 1177–1186. doi:10.1016/j.cell.2017.05.038. PMC 5536862. PMID 28622505.
Frazer KA, Murray SS, Schork NJ, Topol EJ (April 2009). Human genetic variation and its contribution to complex traits. Nature Reviews. Genetics. 10 (4): 241–51. doi:10.1038/nrg2554. PMID 19293820. S2CID 19987352.
Li YI, van de Geijn B, Raj A, Knowles DA, Petti AA, Golan D, Gilad Y, Pritchard JK (April 2016). RNA splicing is a primary link between genetic variation and disease. Science. 352 (6285): 600–4. Bibcode:2016Sci...352..600L. doi:10.1126/science.aad9417. PMC 5182069. PMID 27126046.
Chakravarti A, Turner TN (June 2016). Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families. BioEssays. 38 (6): 578–86. doi:10.1002/bies.201500203. PMID 27062178. S2CID 3813041.
Preininger M, Arafat D, Kim J, Nath AP, Idaghdour Y, Brigham KL, Gibson G (14 марта 2013). Blood-informative transcripts define nine common axes of peripheral blood gene expression. PLOS Genetics. 9 (3): e1003362. doi:10.1371/journal.pgen.1003362. PMC 3597511. PMID 23516379.
He X (October 2017). Comment on: An Expanded View of Complex Traits: From Polygenic to Omnigenic. Journal of Psychiatry and Brain Science. 2 (5). doi:10.20900/jpbs.20170014s2.

harvard.edu

ui.adsabs.harvard.edu

Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (October 2009). Finding the missing heritability of complex diseases. Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. doi:10.1038/nature08494. PMC 2831613. PMID 19812666.
Li YI, van de Geijn B, Raj A, Knowles DA, Petti AA, Golan D, Gilad Y, Pritchard JK (April 2016). RNA splicing is a primary link between genetic variation and disease. Science. 352 (6285): 600–4. Bibcode:2016Sci...352..600L. doi:10.1126/science.aad9417. PMC 5182069. PMID 27126046.

nih.gov

pubmed.ncbi.nlm.nih.gov

Gibson G (January 2012). Rare and common variants: twenty arguments. Nature Reviews. Genetics. 13 (2): 135–45. doi:10.1038/nrg3118. PMC 4408201. PMID 22251874.
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (October 2009). Finding the missing heritability of complex diseases. Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. doi:10.1038/nature08494. PMC 2831613. PMID 19812666.
Shi H, Kichaev G, Pasaniuc B (July 2016). Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data. American Journal of Human Genetics. 99 (1): 139–53. doi:10.1016/j.ajhg.2016.05.013. PMC 5005444. PMID 27346688.
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (June 2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47 (6): 582–8. doi:10.1038/ng.3303. PMC 4449286. PMID 25961944.
Boyle EA, Li YI, Pritchard JK (June 2017). An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell. 169 (7): 1177–1186. doi:10.1016/j.cell.2017.05.038. PMC 5536862. PMID 28622505.
Frazer KA, Murray SS, Schork NJ, Topol EJ (April 2009). Human genetic variation and its contribution to complex traits. Nature Reviews. Genetics. 10 (4): 241–51. doi:10.1038/nrg2554. PMID 19293820. S2CID 19987352.
Li YI, van de Geijn B, Raj A, Knowles DA, Petti AA, Golan D, Gilad Y, Pritchard JK (April 2016). RNA splicing is a primary link between genetic variation and disease. Science. 352 (6285): 600–4. Bibcode:2016Sci...352..600L. doi:10.1126/science.aad9417. PMC 5182069. PMID 27126046.
Chakravarti A, Turner TN (June 2016). Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families. BioEssays. 38 (6): 578–86. doi:10.1002/bies.201500203. PMID 27062178. S2CID 3813041.
Preininger M, Arafat D, Kim J, Nath AP, Idaghdour Y, Brigham KL, Gibson G (14 марта 2013). Blood-informative transcripts define nine common axes of peripheral blood gene expression. PLOS Genetics. 9 (3): e1003362. doi:10.1371/journal.pgen.1003362. PMC 3597511. PMID 23516379.

ncbi.nlm.nih.gov

Gibson G (January 2012). Rare and common variants: twenty arguments. Nature Reviews. Genetics. 13 (2): 135–45. doi:10.1038/nrg3118. PMC 4408201. PMID 22251874.
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, et al. (October 2009). Finding the missing heritability of complex diseases. Nature. 461 (7265): 747–53. Bibcode:2009Natur.461..747M. doi:10.1038/nature08494. PMC 2831613. PMID 19812666.
Shi H, Kichaev G, Pasaniuc B (July 2016). Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data. American Journal of Human Genetics. 99 (1): 139–53. doi:10.1016/j.ajhg.2016.05.013. PMC 5005444. PMID 27346688.
Krumm N, Turner TN, Baker C, Vives L, Mohajeri K, Witherspoon K, Raja A, Coe BP, Stessman HA, He ZX, Leal SM, Bernier R, Eichler EE (June 2015). Excess of rare, inherited truncating mutations in autism. Nature Genetics. 47 (6): 582–8. doi:10.1038/ng.3303. PMC 4449286. PMID 25961944.
Boyle EA, Li YI, Pritchard JK (June 2017). An Expanded View of Complex Traits: From Polygenic to Omnigenic. Cell. 169 (7): 1177–1186. doi:10.1016/j.cell.2017.05.038. PMC 5536862. PMID 28622505.
Li YI, van de Geijn B, Raj A, Knowles DA, Petti AA, Golan D, Gilad Y, Pritchard JK (April 2016). RNA splicing is a primary link between genetic variation and disease. Science. 352 (6285): 600–4. Bibcode:2016Sci...352..600L. doi:10.1126/science.aad9417. PMC 5182069. PMID 27126046.
Preininger M, Arafat D, Kim J, Nath AP, Idaghdour Y, Brigham KL, Gibson G (14 марта 2013). Blood-informative transcripts define nine common axes of peripheral blood gene expression. PLOS Genetics. 9 (3): e1003362. doi:10.1371/journal.pgen.1003362. PMC 3597511. PMID 23516379.

semanticscholar.org

api.semanticscholar.org

Fisher, R. A. (1919). XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance. Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163. S2CID 181213898. Архивировано 28 ноября 2022. Дата обращения: 21 апреля 2024.
Frazer KA, Murray SS, Schork NJ, Topol EJ (April 2009). Human genetic variation and its contribution to complex traits. Nature Reviews. Genetics. 10 (4): 241–51. doi:10.1038/nrg2554. PMID 19293820. S2CID 19987352.
Chakravarti A, Turner TN (June 2016). Revealing rate-limiting steps in complex disease biology: The crucial importance of studying rare, extreme-phenotype families. BioEssays. 38 (6): 578–86. doi:10.1002/bies.201500203. PMID 27062178. S2CID 3813041.

web.archive.org

Fisher, R. A. (1919). XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance. Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163. S2CID 181213898. Архивировано 28 ноября 2022. Дата обращения: 21 апреля 2024.

zenodo.org

Fisher, R. A. (1919). XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance. Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 52 (2): 399–433. doi:10.1017/S0080456800012163. S2CID 181213898. Архивировано 28 ноября 2022. Дата обращения: 21 апреля 2024.