192 related articles for article (PubMed ID: 25326100)
21. ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
Wang Z; McPeek MS
Am J Hum Genet; 2009 Nov; 85(5):667-78. PubMed ID: 19913122
[TBL] [Abstract][Full Text] [Related]
22. Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
Zheng Y; Ogundiran TO; Falusi AG; Nathanson KL; John EM; Hennis AJ; Ambs S; Domchek SM; Rebbeck TR; Simon MS; Nemesure B; Wu SY; Leske MC; Odetunde A; Niu Q; Zhang J; Afolabi C; Gamazon ER; Cox NJ; Olopade CO; Olopade OI; Huo D
Carcinogenesis; 2013 Jul; 34(7):1520-8. PubMed ID: 23475944
[TBL] [Abstract][Full Text] [Related]
23. Endometrial vezatin and its association with endometriosis risk.
Holdsworth-Carson SJ; Fung JN; Luong HT; Sapkota Y; Bowdler LM; Wallace L; Teh WT; Powell JE; Girling JE; Healey M; Montgomery GW; Rogers PA
Hum Reprod; 2016 May; 31(5):999-1013. PubMed ID: 27005890
[TBL] [Abstract][Full Text] [Related]
24. Methods for fine-mapping with chromatin and expression data.
Roytman M; Kichaev G; Gusev A; Pasaniuc B
PLoS Genet; 2018 Feb; 14(2):e1007240. PubMed ID: 29481575
[TBL] [Abstract][Full Text] [Related]
25. Genetic and epigenetic variants contributing to clofarabine cytotoxicity.
Eadon MT; Wheeler HE; Stark AL; Zhang X; Moen EL; Delaney SM; Im HK; Cunningham PN; Zhang W; Dolan ME
Hum Mol Genet; 2013 Oct; 22(19):4007-20. PubMed ID: 23720496
[TBL] [Abstract][Full Text] [Related]
26. Rare and common regulatory variation in population-scale sequenced human genomes.
Montgomery SB; Lappalainen T; Gutierrez-Arcelus M; Dermitzakis ET
PLoS Genet; 2011 Jul; 7(7):e1002144. PubMed ID: 21811411
[TBL] [Abstract][Full Text] [Related]
27. PExFInS: An Integrative Post-GWAS Explorer for Functional Indels and SNPs.
Cheng Z; Chu H; Fan Y; Li C; Song YQ; Zhou J; Yuen KY
Sci Rep; 2015 Nov; 5():17302. PubMed ID: 26612672
[TBL] [Abstract][Full Text] [Related]
28.
Cannon ME; Duan Q; Wu Y; Zeynalzadeh M; Xu Z; Kangas AJ; Soininen P; Ala-Korpela M; Civelek M; Lusis AJ; Kuusisto J; Collins FS; Boehnke M; Tang H; Laakso M; Li Y; Mohlke KL
G3 (Bethesda); 2017 Sep; 7(9):3217-3227. PubMed ID: 28754724
[TBL] [Abstract][Full Text] [Related]
29. Genome-wide comparison of allele-specific gene expression between African and European populations.
Tian L; Khan A; Ning Z; Yuan K; Zhang C; Lou H; Yuan Y; Xu S
Hum Mol Genet; 2018 Mar; 27(6):1067-1077. PubMed ID: 29346564
[TBL] [Abstract][Full Text] [Related]
30. Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.
Varshney A; Scott LJ; Welch RP; Erdos MR; Chines PS; Narisu N; Albanus RD; Orchard P; Wolford BN; Kursawe R; Vadlamudi S; Cannon ME; Didion JP; Hensley J; Kirilusha A; ; Bonnycastle LL; Taylor DL; Watanabe R; Mohlke KL; Boehnke M; Collins FS; Parker SC; Stitzel ML
Proc Natl Acad Sci U S A; 2017 Feb; 114(9):2301-2306. PubMed ID: 28193859
[TBL] [Abstract][Full Text] [Related]
31. Functional evaluation of genetic variants associated with endometriosis near GREB1.
Fung JN; Holdsworth-Carson SJ; Sapkota Y; Zhao ZZ; Jones L; Girling JE; Paiva P; Healey M; Nyholt DR; Rogers PA; Montgomery GW
Hum Reprod; 2015 May; 30(5):1263-75. PubMed ID: 25788566
[TBL] [Abstract][Full Text] [Related]
32. Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.
Martin RI; Babaei MS; Choy MK; Owens WA; Chico TJ; Keenan D; Yonan N; Koref MS; Keavney BD
J Mol Cell Cardiol; 2015 Aug; 85():207-14. PubMed ID: 26073630
[TBL] [Abstract][Full Text] [Related]
33. Genome-wide variation of cytosine modifications between European and African populations and the implications for complex traits.
Moen EL; Zhang X; Mu W; Delaney SM; Wing C; McQuade J; Myers J; Godley LA; Dolan ME; Zhang W
Genetics; 2013 Aug; 194(4):987-96. PubMed ID: 23792949
[TBL] [Abstract][Full Text] [Related]
34. Evidence of Recent Intricate Adaptation in Human Populations.
Park L
PLoS One; 2016; 11(12):e0165870. PubMed ID: 27992444
[TBL] [Abstract][Full Text] [Related]
35. Fine-mapping
Tehranchi A; Hie B; Dacre M; Kaplow I; Pettie K; Combs P; Fraser HB
Elife; 2019 Jan; 8():. PubMed ID: 30650056
[TBL] [Abstract][Full Text] [Related]
36. Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.
Verlaan DJ; Berlivet S; Hunninghake GM; Madore AM; Larivière M; Moussette S; Grundberg E; Kwan T; Ouimet M; Ge B; Hoberman R; Swiatek M; Dias J; Lam KC; Koka V; Harmsen E; Soto-Quiros M; Avila L; Celedón JC; Weiss ST; Dewar K; Sinnett D; Laprise C; Raby BA; Pastinen T; Naumova AK
Am J Hum Genet; 2009 Sep; 85(3):377-93. PubMed ID: 19732864
[TBL] [Abstract][Full Text] [Related]
37. Discovering Single Nucleotide Polymorphisms Regulating Human Gene Expression Using Allele Specific Expression from RNA-seq Data.
Kang EY; Martin LJ; Mangul S; Isvilanonda W; Zou J; Ben-David E; Han B; Lusis AJ; Shifman S; Eskin E
Genetics; 2016 Nov; 204(3):1057-1064. PubMed ID: 27765809
[TBL] [Abstract][Full Text] [Related]
38. Variants on chromosome 6p22.3 associated with blood pressure in the HyperGEN study: follow-up of FBPP quantitative trait loci.
Simino J; Shi G; Arnett D; Broeckel U; Hunt SC; Rao DC
Am J Hypertens; 2011 Nov; 24(11):1227-33. PubMed ID: 21850057
[TBL] [Abstract][Full Text] [Related]
39. Genome scan study of prostate cancer in Arabs: identification of three genomic regions with multiple prostate cancer susceptibility loci in Tunisians.
Shan J; Al-Rumaihi K; Rabah D; Al-Bozom I; Kizhakayil D; Farhat K; Al-Said S; Kfoury H; Dsouza SP; Rowe J; Khalak HG; Jafri S; Aigha II; Chouchane L
J Transl Med; 2013 May; 11():121. PubMed ID: 23668334
[TBL] [Abstract][Full Text] [Related]
40. Fine-mapping of a novel premenopausal breast cancer susceptibility locus at Chr4q31.22 in Caucasian women and validation in African and Chinese women.
Kumaran M; Ghosh S; Joy AA; Mackey JR; Cass CE; Zheng W; Yasui Y; Damaraju S
Int J Cancer; 2020 Mar; 146(5):1219-1229. PubMed ID: 31087647
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]