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For: Corona E, Dudley JT, Butte AJ. Extreme evolutionary disparities seen in positive selection across seven complex diseases. PLoS One 2010;5:e12236. [PMID: 20808933 DOI: 10.1371/journal.pone.0012236] [Cited by in Crossref: 38] [Cited by in F6Publishing: 37] [Article Influence: 3.2] [Reference Citation Analysis]
Number Citing Articles
1 Goris A, Liston A. The immunogenetic architecture of autoimmune disease. Cold Spring Harb Perspect Biol. 2012;4:a007260. [PMID: 22383754 DOI: 10.1101/cshperspect.a007260] [Cited by in Crossref: 52] [Cited by in F6Publishing: 45] [Article Influence: 5.2] [Reference Citation Analysis]
2 Prasad RB, Groop L. Genetics of type 2 diabetes-pitfalls and possibilities. Genes (Basel) 2015;6:87-123. [PMID: 25774817 DOI: 10.3390/genes6010087] [Cited by in Crossref: 219] [Cited by in F6Publishing: 182] [Article Influence: 31.3] [Reference Citation Analysis]
3 Ktsoyan ZA, Beloborodova NV, Sedrakyan AM, Osipov GA, Khachatryan ZA, Manukyan GP, Arakelova KA, Hovhannisyan AI, Arakelyan AA, Ghazaryan KA, Zakaryan MK, Aminov RI. Management of familial Mediterranean fever by colchicine does not normalize the altered profile of microbial long chain fatty acids in the human metabolome. Front Cell Infect Microbiol 2013;3:2. [PMID: 23373011 DOI: 10.3389/fcimb.2013.00002] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
4 Gall BJ, Wilson A, Schroer AB, Gross JD, Stoilov P, Setola V, Watkins CM, Siderovski DP. Genetic variations in GPSM3 associated with protection from rheumatoid arthritis affect its transcript abundance. Genes Immun 2016;17:139-47. [PMID: 26821282 DOI: 10.1038/gene.2016.3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
5 Bitarello BD, de Filippo C, Teixeira JC, Schmidt JM, Kleinert P, Meyer D, Andrés AM. Signatures of Long-Term Balancing Selection in Human Genomes. Genome Biol Evol 2018;10:939-55. [PMID: 29608730 DOI: 10.1093/gbe/evy054] [Cited by in Crossref: 62] [Cited by in F6Publishing: 37] [Article Influence: 15.5] [Reference Citation Analysis]
6 Goris A, van Setten J, Diekstra F, Ripke S, Patsopoulos NA, Sawcer SJ, van Es M, Andersen PM, Melki J, Meininger V, Hardiman O, Landers JE, Brown RH Jr, Shatunov A, Leigh N, Al-Chalabi A, Shaw CE, Traynor BJ, Chiò A, Restagno G, Mora G, Ophoff RA, Oksenberg JR, Van Damme P, Compston A, Robberecht W, Dubois B, van den Berg LH, De Jager PL, Veldink JH, de Bakker PI; International Multiple Sclerosis Genetics Consortium., Australia and New Zealand MS Genetics Consortium. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Hum Mol Genet 2014;23:1916-22. [PMID: 24234648 DOI: 10.1093/hmg/ddt574] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 1.6] [Reference Citation Analysis]
7 Cagliani R, Pozzoli U, Forni D, Cassinotti A, Fumagalli M, Giani M, Fichera M, Lombardini M, Ardizzone S, Asselta R, de Franchis R, Riva S, Biasin M, Comi GP, Bresolin N, Clerici M, Sironi M. Crohn's disease loci are common targets of protozoa-driven selection. Mol Biol Evol 2013;30:1077-87. [PMID: 23389767 DOI: 10.1093/molbev/mst020] [Cited by in Crossref: 18] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
8 Vatsiou AI, Bazin E, Gaggiotti OE. Changes in selective pressures associated with human population expansion may explain metabolic and immune related pathways enriched for signatures of positive selection. BMC Genomics 2016;17:504. [PMID: 27444955 DOI: 10.1186/s12864-016-2783-2] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
9 Blanco I, Kuchenbaecker K, Cuadras D, Wang X, Barrowdale D, de Garibay GR, Librado P, Sánchez-Gracia A, Rozas J, Bonifaci N, McGuffog L, Pankratz VS, Islam A, Mateo F, Berenguer A, Petit A, Català I, Brunet J, Feliubadaló L, Tornero E, Benítez J, Osorio A, Ramón y Cajal T, Nevanlinna H, Aittomäki K, Arun BK, Toland AE, Karlan BY, Walsh C, Lester J, Greene MH, Mai PL, Nussbaum RL, Andrulis IL, Domchek SM, Nathanson KL, Rebbeck TR, Barkardottir RB, Jakubowska A, Lubinski J, Durda K, Jaworska-Bieniek K, Claes K, Van Maerken T, Díez O, Hansen TV, Jønson L, Gerdes AM, Ejlertsen B, de la Hoya M, Caldés T, Dunning AM, Oliver C, Fineberg E, Cook M, Peock S, McCann E, Murray A, Jacobs C, Pichert G, Lalloo F, Chu C, Dorkins H, Paterson J, Ong KR, Teixeira MR, Hogervorst FB, van der Hout AH, Seynaeve C, van der Luijt RB, Ligtenberg MJ, Devilee P, Wijnen JT, Rookus MA, Meijers-Heijboer HE, Blok MJ, van den Ouweland AM, Aalfs CM, Rodriguez GC, Phillips KA, Piedmonte M, Nerenstone SR, Bae-Jump VL, O'Malley DM, Ratner ES, Schmutzler RK, Wappenschmidt B, Rhiem K, Engel C, Meindl A, Ditsch N, Arnold N, Plendl HJ, Niederacher D, Sutter C, Wang-Gohrke S, Steinemann D, Preisler-Adams S, Kast K, Varon-Mateeva R, Gehrig A, Bojesen A, Pedersen IS, Sunde L, Jensen UB, Thomassen M, Kruse TA, Foretova L, Peterlongo P, Bernard L, Peissel B, Scuvera G, Manoukian S, Radice P, Ottini L, Montagna M, Agata S, Maugard C, Simard J, Soucy P, Berger A, Fink-Retter A, Singer CF, Rappaport C, Geschwantler-Kaulich D, Tea MK, Pfeiler G, John EM, Miron A, Neuhausen SL, Terry MB, Chung WK, Daly MB, Goldgar DE, Janavicius R, Dorfling CM, van Rensburg EJ, Fostira F, Konstantopoulou I, Garber J, Godwin AK, Olah E, Narod SA, Rennert G, Paluch SS, Laitman Y, Friedman E, Liljegren A, Rantala J, Stenmark-Askmalm M, Loman N, Imyanitov EN, Hamann U, Spurdle AB, Healey S, Weitzel JN, Herzog J, Margileth D, Gorrini C, Esteller M, Gómez A, Sayols S, Vidal E, Heyn H, Stoppa-Lyonnet D, Léoné M, Barjhoux L, Fassy-Colcombet M, de Pauw A, Lasset C, Ferrer SF, Castera L, Berthet P, Cornelis F, Bignon YJ, Damiola F, Mazoyer S, Sinilnikova OM, Maxwell CA, Vijai J, Robson M, Kauff N, Corines MJ, Villano D, Cunningham J, Lee A, Lindor N, Lázaro C, Easton DF, Offit K, Chenevix-Trench G, Couch FJ, Antoniou AC, Pujana MA; Teixeira., BCFR., SWE-BRCA., kConFab Investigators., GEMO. Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers. PLoS One 2015;10:e0120020. [PMID: 25830658 DOI: 10.1371/journal.pone.0120020] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 2.6] [Reference Citation Analysis]
10 Gall BJ, Schroer AB, Gross JD, Setola V, Siderovski DP. Reduction of GPSM3 expression akin to the arthritis-protective SNP rs204989 differentially affects migration in a neutrophil model. Genes Immun 2016;17:321-7. [PMID: 27307211 DOI: 10.1038/gene.2016.26] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
11 Carreras-Torres R, Ferran A, Zanetti D, Esteban E, Varesi L, Pojskic N, Coia V, Chaabani H, Via M, Moral P. Population structure from NOS genes correlates with geographical differences in coronary incidence across Europe. Am J Phys Anthropol 2016;161:634-45. [PMID: 27500977 DOI: 10.1002/ajpa.23063] [Reference Citation Analysis]
12 Zhang G, Pei Z, Krawczak M, Ball EV, Mort M, Kehrer-sawatzki H, Cooper DN. Triangulation of the human, chimpanzee, and Neanderthal genome sequences identifies potentially compensated mutations. Hum Mutat 2010;31:1286-93. [DOI: 10.1002/humu.21389] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
13 Hemani G, Knott S, Haley C. An evolutionary perspective on epistasis and the missing heritability. PLoS Genet 2013;9:e1003295. [PMID: 23509438 DOI: 10.1371/journal.pgen.1003295] [Cited by in Crossref: 80] [Cited by in F6Publishing: 65] [Article Influence: 8.9] [Reference Citation Analysis]
14 Xu J, Ji P, Wang B, Zhao L, Wang J, Zhao Z, Zhang Y, Li J, Xu P, Sun X. Transcriptome sequencing and analysis of wild Amur Ide (Leuciscus waleckii) inhabiting an extreme alkaline-saline lake reveals insights into stress adaptation. PLoS One 2013;8:e59703. [PMID: 23573207 DOI: 10.1371/journal.pone.0059703] [Cited by in Crossref: 33] [Cited by in F6Publishing: 31] [Article Influence: 3.7] [Reference Citation Analysis]
15 Hu X, Daly M. What have we learned from six years of GWAS in autoimmune diseases, and what is next? Curr Opin Immunol 2012;24:571-5. [PMID: 23017373 DOI: 10.1016/j.coi.2012.09.001] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 2.1] [Reference Citation Analysis]
16 Dudley JT, Kim Y, Liu L, Markov GJ, Gerold K, Chen R, Butte AJ, Kumar S. Human genomic disease variants: a neutral evolutionary explanation. Genome Res 2012;22:1383-94. [PMID: 22665443 DOI: 10.1101/gr.133702.111] [Cited by in Crossref: 31] [Cited by in F6Publishing: 24] [Article Influence: 3.1] [Reference Citation Analysis]
17 Botigué LR, Henn BM, Gravel S, Maples BK, Gignoux CR, Corona E, Atzmon G, Burns E, Ostrer H, Flores C, Bertranpetit J, Comas D, Bustamante CD. Gene flow from North Africa contributes to differential human genetic diversity in southern Europe. Proc Natl Acad Sci U S A 2013;110:11791-6. [PMID: 23733930 DOI: 10.1073/pnas.1306223110] [Cited by in Crossref: 123] [Cited by in F6Publishing: 101] [Article Influence: 13.7] [Reference Citation Analysis]
18 Zhang G, Pei Z, Ball EV, Mort M, Kehrer-Sawatzki H, Cooper DN. Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations. Hum Genomics 2011;5:453-84. [PMID: 21807602 DOI: 10.1186/1479-7364-5-5-453] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
19 Zanetti D, Carreras-Torres R, Esteban E, Via M, Moral P. Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11. PLoS One 2015;10:e0134840. [PMID: 26252781 DOI: 10.1371/journal.pone.0134840] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 0.9] [Reference Citation Analysis]
20 Pedersen NC, Liu H, Leonard A, Griffioen L. A search for genetic diversity among Italian Greyhounds from Continental Europe and the USA and the effect of inbreeding on susceptibility to autoimmune disease. Canine Genet Epidemiol 2015;2:17. [PMID: 26526059 DOI: 10.1186/s40575-015-0030-9] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
21 Little BB, Peña Reyes ME, Malina RM. Natural selection and type 2 diabetes‐associated mortality in an isolated indigenous community in the valley of Oaxaca, southern Mexico. Am J Phys Anthropol 2017;162:561-72. [DOI: 10.1002/ajpa.23139] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
22 Raj T, Kuchroo M, Replogle JM, Raychaudhuri S, Stranger BE, De Jager PL. Common risk alleles for inflammatory diseases are targets of recent positive selection. Am J Hum Genet 2013;92:517-29. [PMID: 23522783 DOI: 10.1016/j.ajhg.2013.03.001] [Cited by in Crossref: 83] [Cited by in F6Publishing: 65] [Article Influence: 9.2] [Reference Citation Analysis]
23 Devarajan P, Chen Z. Autoimmune effector memory T cells: the bad and the good. Immunol Res 2013;57:12-22. [PMID: 24203440 DOI: 10.1007/s12026-013-8448-1] [Cited by in Crossref: 59] [Cited by in F6Publishing: 52] [Article Influence: 7.4] [Reference Citation Analysis]
24 Pahikkala T, Okser S, Airola A, Salakoski T, Aittokallio T. Wrapper-based selection of genetic features in genome-wide association studies through fast matrix operations. Algorithms Mol Biol 2012;7:11. [PMID: 22551170 DOI: 10.1186/1748-7188-7-11] [Cited by in Crossref: 23] [Cited by in F6Publishing: 14] [Article Influence: 2.3] [Reference Citation Analysis]
25 Chevalier RL. Evolutionary Nephrology. Kidney Int Rep 2017;2:302-17. [PMID: 28845468 DOI: 10.1016/j.ekir.2017.01.012] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 3.2] [Reference Citation Analysis]
26 Hayden EJ, Weikert C, Wagner A. Directional selection causes decanalization in a group I ribozyme. PLoS One 2012;7:e45351. [PMID: 23028955 DOI: 10.1371/journal.pone.0045351] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
27 Álvarez-Álvarez MM, Zanetti D, Carreras-Torres R, Moral P, Athanasiadis G. A survey of sub-Saharan gene flow into the Mediterranean at risk loci for coronary artery disease. Eur J Hum Genet 2017;25:472-6. [PMID: 28098150 DOI: 10.1038/ejhg.2016.200] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
28 Byars SG, Voskarides K. Antagonistic Pleiotropy in Human Disease. J Mol Evol 2020;88:12-25. [PMID: 31863128 DOI: 10.1007/s00239-019-09923-2] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
29 Corona E, Chen R, Sikora M, Morgan AA, Patel CJ, Ramesh A, Bustamante CD, Butte AJ. Analysis of the genetic basis of disease in the context of worldwide human relationships and migration. PLoS Genet 2013;9:e1003447. [PMID: 23717210 DOI: 10.1371/journal.pgen.1003447] [Cited by in Crossref: 58] [Cited by in F6Publishing: 48] [Article Influence: 6.4] [Reference Citation Analysis]
30 Liu L, Sanderford MD, Patel R, Chandrashekar P, Gibson G, Kumar S. Biological relevance of computationally predicted pathogenicity of noncoding variants. Nat Commun 2019;10:330. [PMID: 30659175 DOI: 10.1038/s41467-018-08270-y] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 7.0] [Reference Citation Analysis]
31 Doran AG, Creevey CJ. Snpdat: easy and rapid annotation of results from de novo snp discovery projects for model and non-model organisms. BMC Bioinformatics 2013;14:45. [PMID: 23390980 DOI: 10.1186/1471-2105-14-45] [Cited by in Crossref: 27] [Cited by in F6Publishing: 24] [Article Influence: 3.0] [Reference Citation Analysis]
32 Giguère PM, Billard MJ, Laroche G, Buckley BK, Timoshchenko RG, McGinnis MW, Esserman D, Foreman O, Liu P, Siderovski DP, Tarrant TK. G-protein signaling modulator-3, a gene linked to autoimmune diseases, regulates monocyte function and its deficiency protects from inflammatory arthritis. Mol Immunol 2013;54:193-8. [PMID: 23280397 DOI: 10.1016/j.molimm.2012.12.001] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 1.8] [Reference Citation Analysis]
33 Meyer D, C Aguiar VR, Bitarello BD, C Brandt DY, Nunes K. A genomic perspective on HLA evolution. Immunogenetics 2018;70:5-27. [PMID: 28687858 DOI: 10.1007/s00251-017-1017-3] [Cited by in Crossref: 69] [Cited by in F6Publishing: 64] [Article Influence: 13.8] [Reference Citation Analysis]
34 Kachuri L, Amos CI, McKay JD, Johansson M, Vineis P, Bueno-de-Mesquita HB, Boutron-Ruault MC, Johansson M, Quirós JR, Sieri S, Travis RC, Weiderpass E, Le Marchand L, Henderson BE, Wilkens L, Goodman GE, Chen C, Doherty JA, Christiani DC, Wei Y, Su L, Tworoger S, Zhang X, Kraft P, Zaridze D, Field JK, Marcus MW, Davies MPA, Hyde R, Caporaso NE, Landi MT, Severi G, Giles GG, Liu G, McLaughlin JR, Li Y, Xiao X, Fehringer G, Zong X, Denroche RE, Zuzarte PC, McPherson JD, Brennan P, Hung RJ. Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci. Carcinogenesis 2016;37:96-105. [PMID: 26590902 DOI: 10.1093/carcin/bgv165] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 3.6] [Reference Citation Analysis]
35 Fay JC. Disease consequences of human adaptation. Appl Transl Genom 2013;2:42-7. [PMID: 27896054 DOI: 10.1016/j.atg.2013.08.001] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
36 Morrow EH, Connallon T. Implications of sex-specific selection for the genetic basis of disease. Evol Appl 2013;6:1208-17. [PMID: 24478802 DOI: 10.1111/eva.12097] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 2.3] [Reference Citation Analysis]
37 Kumar S, Dudley JT, Filipski A, Liu L. Phylomedicine: an evolutionary telescope to explore and diagnose the universe of disease mutations. Trends Genet 2011;27:377-86. [PMID: 21764165 DOI: 10.1016/j.tig.2011.06.004] [Cited by in Crossref: 59] [Cited by in F6Publishing: 49] [Article Influence: 5.4] [Reference Citation Analysis]
38 Malakar AK, Choudhury D, Halder B, Paul P, Uddin A, Chakraborty S. A review on coronary artery disease, its risk factors, and therapeutics. J Cell Physiol 2019;234:16812-23. [PMID: 30790284 DOI: 10.1002/jcp.28350] [Cited by in Crossref: 83] [Cited by in F6Publishing: 69] [Article Influence: 27.7] [Reference Citation Analysis]
39 Goris A, Pauwels I, Dubois B. Progress in multiple sclerosis genetics. Curr Genomics 2012;13:646-63. [PMID: 23730204 DOI: 10.2174/138920212803759695] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 1.7] [Reference Citation Analysis]