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Items: 1 to 20 of 100

1.

Are minor alleles more likely to be risk alleles?

Kido T, Sikora-Wohlfeld W, Kawashima M, Kikuchi S, Kamatani N, Patwardhan A, Chen R, Sirota M, Kodama K, Hadley D, Butte AJ.

BMC Med Genomics. 2018 Jan 19;11(1):3. doi: 10.1186/s12920-018-0322-5.

2.

Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases.

Gorlov IP, Gorlova OY, Amos CI.

PLoS Genet. 2015 Jul 22;11(7):e1005371. doi: 10.1371/journal.pgen.1005371. eCollection 2015 Jul.

3.

Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies.

Siontis KC, Patsopoulos NA, Ioannidis JP.

Eur J Hum Genet. 2010 Jul;18(7):832-7. doi: 10.1038/ejhg.2010.26. Epub 2010 Mar 17.

4.

Population genetics of rare variants and complex diseases.

Maher MC, Uricchio LH, Torgerson DG, Hernandez RD.

Hum Hered. 2012;74(3-4):118-28. doi: 10.1159/000346826. Epub 2013 Apr 11.

5.

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Rivas MA, Avila BE, Koskela J, Huang H, Stevens C, Pirinen M, Haritunians T, Neale BM, Kurki M, Ganna A, Graham D, Glaser B, Peter I, Atzmon G, Barzilai N, Levine AP, Schiff E, Pontikos N, Weisburd B, Lek M, Karczewski KJ, Bloom J, Minikel EV, Petersen BS, Beaugerie L, Seksik P, Cosnes J, Schreiber S, Bokemeyer B, Bethge J; International IBD Genetics Consortium; NIDDK IBD Genetics Consortium; T2D-GENES Consortium, Heap G, Ahmad T, Plagnol V, Segal AW, Targan S, Turner D, Saavalainen P, Farkkila M, Kontula K, Palotie A, Brant SR, Duerr RH, Silverberg MS, Rioux JD, Weersma RK, Franke A, Jostins L, Anderson CA, Barrett JC, MacArthur DG, Jalas C, Sokol H, Xavier RJ, Pulver A, Cho JH, McGovern DPB, Daly MJ.

PLoS Genet. 2018 May 24;14(5):e1007329. doi: 10.1371/journal.pgen.1007329. eCollection 2018 May. Erratum in: PLoS Genet. 2019 May 30;15(5):e1008190.

6.
7.

Widespread Allelic Heterogeneity in Complex Traits.

Hormozdiari F, Zhu A, Kichaev G, Ju CJ, Segrè AV, Joo JWJ, Won H, Sankararaman S, Pasaniuc B, Shifman S, Eskin E.

Am J Hum Genet. 2017 May 4;100(5):789-802. doi: 10.1016/j.ajhg.2017.04.005.

8.

Functional and Structural Consequence of Rare Exonic Single Nucleotide Polymorphisms: One Story, Two Tales.

Gu W, Gurguis CI, Zhou JJ, Zhu Y, Ko EA, Ko JH, Wang T, Zhou T.

Genome Biol Evol. 2015 Oct 9;7(10):2929-40. doi: 10.1093/gbe/evv191.

9.

Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.

Thornton KR, Foran AJ, Long AD.

PLoS Genet. 2013;9(2):e1003258. doi: 10.1371/journal.pgen.1003258. Epub 2013 Feb 21.

10.

Derived SNP alleles are used more frequently than ancestral alleles as risk-associated variants in common human diseases.

Gorlova OY, Ying J, Amos CI, Spitz MR, Peng B, Gorlov IP.

J Bioinform Comput Biol. 2012 Apr;10(2):1241008. doi: 10.1142/S0219720012410089.

11.

Gene-based rare allele analysis identified a risk gene of Alzheimer's disease.

Kim JH, Song P, Lim H, Lee JH, Lee JH, Park SA; Alzheimer’s Disease Neuroimaging Initiative.

PLoS One. 2014 Oct 20;9(10):e107983. doi: 10.1371/journal.pone.0107983. eCollection 2014.

12.

Detecting association of rare and common variants by adaptive combination of P-values.

Zhou Y, Wang Y.

Genet Res (Camb). 2015 Oct 6;97:e20. doi: 10.1017/S0016672315000208.

PMID:
26440553
13.

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans.

Carlson CS, Eberle MA, Rieder MJ, Smith JD, Kruglyak L, Nickerson DA.

Nat Genet. 2003 Apr;33(4):518-21. Epub 2003 Mar 24.

PMID:
12652300
14.
15.

Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis.

International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC) and OCD Collaborative Genetics Association Studies (OCGAS).

Mol Psychiatry. 2018 May;23(5):1181-1188. doi: 10.1038/mp.2017.154. Epub 2017 Aug 1.

PMID:
28761083
16.

Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs.

Watson CT, Disanto G, Breden F, Giovannoni G, Ramagopalan SV.

Sci Rep. 2012;2:770. doi: 10.1038/srep00770. Epub 2012 Oct 25.

17.

Use of a multiethnic approach to identify rheumatoid- arthritis-susceptibility loci, 1p36 and 17q12.

Kurreeman FA, Stahl EA, Okada Y, Liao K, Diogo D, Raychaudhuri S, Freudenberg J, Kochi Y, Patsopoulos NA, Gupta N; CLEAR investigators, Sandor C, Bang SY, Lee HS, Padyukov L, Suzuki A, Siminovitch K, Worthington J, Gregersen PK, Hughes LB, Reynolds RJ, Bridges SL Jr, Bae SC, Yamamoto K, Plenge RM.

Am J Hum Genet. 2012 Mar 9;90(3):524-32. doi: 10.1016/j.ajhg.2012.01.010. Epub 2012 Feb 23.

19.

Efficient strategy for detecting gene × gene joint action and its application in schizophrenia.

Won S, Kwon MS, Mattheisen M, Park S, Park C, Kihara D, Cichon S, Ophoff R, Nöthen MM, Rietschel M, Baur M, Uitterlinden AG, Hofmann A; GROUP Investigators, Lange C.

Genet Epidemiol. 2014 Jan;38(1):60-71. doi: 10.1002/gepi.21779. Epub 2013 Nov 23.

PMID:
24272960
20.

Genetic variation in the progesterone receptor gene and susceptibility to recurrent pregnancy loss: a case-control study.

Bahia W, Finan RR, Al-Mutawa M, Haddad A, Soua A, Janhani F, Mahjoub T, Almawi WY.

BJOG. 2018 May;125(6):729-735. doi: 10.1111/1471-0528.14949. Epub 2017 Nov 13.

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