110 related articles for article (PubMed ID: 24810602)
1. Exome-wide association study of endometrial cancer in a multiethnic population.
Chen MM; Crous-Bou M; Setiawan VW; Prescott J; Olson SH; Wentzensen N; Black A; Brinton L; Chen C; Chen C; Cook LS; Doherty J; Friedenreich CM; Hankinson SE; Hartge P; Henderson BE; Hunter DJ; Le Marchand L; Liang X; Lissowska J; Lu L; Orlow I; Petruzella S; Polidoro S; Pooler L; Rebbeck TR; Risch H; Sacerdote C; Schumacher F; Sheng X; Shu XO; Weiss NS; Xia L; Van Den Berg D; Yang HP; Yu H; Chanock S; Haiman C; Kraft P; De Vivo I
PLoS One; 2014; 9(5):e97045. PubMed ID: 24810602
[TBL] [Abstract][Full Text] [Related]
2. Genome-wide association study of endometrial cancer in E2C2.
De Vivo I; Prescott J; Setiawan VW; Olson SH; Wentzensen N; ; Attia J; Black A; Brinton L; Chen C; Chen C; Cook LS; Crous-Bou M; Doherty J; Dunning AM; Easton DF; Friedenreich CM; Garcia-Closas M; Gaudet MM; Haiman C; Hankinson SE; Hartge P; Henderson BE; Holliday E; Horn-Ross PL; Hunter DJ; Le Marchand L; Liang X; Lissowska J; Long J; Lu L; Magliocco AM; McEvoy M; O'Mara TA; Orlow I; Painter JN; Pooler L; Rastogi R; Rebbeck TR; Risch H; Sacerdote C; Schumacher F; Scott RJ; Sheng X; Shu XO; Spurdle AB; Thompson D; Vanden Berg D; Weiss NS; Xia L; Xiang YB; Yang HP; Yu H; Zheng W; Chanock S; Kraft P
Hum Genet; 2014 Feb; 133(2):211-24. PubMed ID: 24096698
[TBL] [Abstract][Full Text] [Related]
3. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
[TBL] [Abstract][Full Text] [Related]
4. Meta-dimensional data integration identifies critical pathways for susceptibility, tumorigenesis and progression of endometrial cancer.
Wei R; De Vivo I; Huang S; Zhu X; Risch H; Moore JH; Yu H; Garmire LX
Oncotarget; 2016 Aug; 7(34):55249-55263. PubMed ID: 27409342
[TBL] [Abstract][Full Text] [Related]
5. Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
Spurdle AB; Thompson DJ; Ahmed S; Ferguson K; Healey CS; O'Mara T; Walker LC; Montgomery SB; Dermitzakis ET; ; Fahey P; Montgomery GW; Webb PM; Fasching PA; Beckmann MW; Ekici AB; Hein A; Lambrechts D; Coenegrachts L; Vergote I; Amant F; Salvesen HB; Trovik J; Njolstad TS; Helland H; Scott RJ; Ashton K; Proietto T; Otton G; ; Tomlinson I; Gorman M; Howarth K; Hodgson S; Garcia-Closas M; Wentzensen N; Yang H; Chanock S; Hall P; Czene K; Liu J; Li J; Shu XO; Zheng W; Long J; Xiang YB; Shah M; Morrison J; Michailidou K; Pharoah PD; Dunning AM; Easton DF
Nat Genet; 2011 May; 43(5):451-4. PubMed ID: 21499250
[TBL] [Abstract][Full Text] [Related]
6. Assessing the Power of Exome Chips.
Page CM; Baranzini SE; Mevik BH; Bos SD; Harbo HF; Andreassen BK
PLoS One; 2015; 10(10):e0139642. PubMed ID: 26437075
[TBL] [Abstract][Full Text] [Related]
7. A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
Wang H; St Julien KR; Stevenson DK; Hoffmann TJ; Witte JS; Lazzeroni LC; Krasnow MA; Quaintance CC; Oehlert JW; Jelliffe-Pawlowski LL; Gould JB; Shaw GM; O'Brodovich HM
Pediatrics; 2013 Aug; 132(2):290-7. PubMed ID: 23897914
[TBL] [Abstract][Full Text] [Related]
8. No large-effect low-frequency coding variation found for myocardial infarction.
Holmen OL; Zhang H; Zhou W; Schmidt E; Hovelson DH; Langhammer A; Løchen ML; Ganesh SK; Mathiesen EB; Vatten L; Platou C; Wilsgaard T; Chen J; Skorpen F; Dalen H; Boehnke M; Abecasis GR; Njølstad I; Hveem K; Willer CJ
Hum Mol Genet; 2014 Sep; 23(17):4721-8. PubMed ID: 24728188
[TBL] [Abstract][Full Text] [Related]
9. Exome array analysis suggests an increased variant burden in families with schizophrenia.
McCarthy NS; Melton PE; Ward SV; Allan SM; Dragovic M; Clark ML; Morar B; Rubio JP; Blangero J; Badcock JC; Morgan VA; Moses EK; Jablensky A
Schizophr Res; 2017 Jul; 185():9-16. PubMed ID: 27939555
[TBL] [Abstract][Full Text] [Related]
10. A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy.
Chen JA; Wang Q; Davis-Turak J; Li Y; Karydas AM; Hsu SC; Sears RL; Chatzopoulou D; Huang AY; Wojta KJ; Klein E; Lee J; Beekly DL; Boxer A; Faber KM; Haase CM; Miller J; Poon WW; Rosen A; Rosen H; Sapozhnikova A; Shapira J; Varpetian A; Foroud TM; Levenson RW; Levey AI; Kukull WA; Mendez MF; Ringman J; Chui H; Cotman C; DeCarli C; Miller BL; Geschwind DH; Coppola G
JAMA Neurol; 2015 Apr; 72(4):414-22. PubMed ID: 25706306
[TBL] [Abstract][Full Text] [Related]
11. Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.
Archer NP; Perez-Andreu V; Scheurer ME; Rabin KR; Peckham-Gregory EC; Plon SE; Zabriskie RC; De Alarcon PA; Fernandez KS; Najera CR; Yang JJ; Antillon-Klussmann F; Lupo PJ
Cancer; 2016 Dec; 122(23):3697-3704. PubMed ID: 27529658
[TBL] [Abstract][Full Text] [Related]
12. Association of obesity-related genetic variants with endometrial cancer risk: a report from the Shanghai Endometrial Cancer Genetics Study.
Delahanty RJ; Beeghly-Fadiel A; Xiang YB; Long J; Cai Q; Wen W; Xu WH; Cai H; He J; Gao YT; Zheng W; Shu XO
Am J Epidemiol; 2011 Nov; 174(10):1115-26. PubMed ID: 21976109
[TBL] [Abstract][Full Text] [Related]
13. Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.
Huckins LM; Hatzikotoulas K; Southam L; Thornton LM; Steinberg J; Aguilera-McKay F; Treasure J; Schmidt U; Gunasinghe C; Romero A; Curtis C; Rhodes D; Moens J; Kalsi G; Dempster D; Leung R; Keohane A; Burghardt R; Ehrlich S; Hebebrand J; Hinney A; Ludolph A; Walton E; Deloukas P; Hofman A; Palotie A; Palta P; van Rooij FJA; Stirrups K; Adan R; Boni C; Cone R; Dedoussis G; van Furth E; Gonidakis F; Gorwood P; Hudson J; Kaprio J; Kas M; Keski-Rahkonen A; Kiezebrink K; Knudsen GP; Slof-Op 't Landt MCT; Maj M; Monteleone AM; Monteleone P; Raevuori AH; Reichborn-Kjennerud T; Tozzi F; Tsitsika A; van Elburg A; ; Collier DA; Sullivan PF; Breen G; Bulik CM; Zeggini E
Mol Psychiatry; 2018 May; 23(5):1169-1180. PubMed ID: 29155802
[TBL] [Abstract][Full Text] [Related]
14. Common and Rare Variants Genetic Association Analysis of Cigarettes per Day Among Ever-Smokers in Chronic Obstructive Pulmonary Disease Cases and Controls.
Lutz SM; Frederiksen B; Begum F; McDonald MN; Cho MH; Hobbs BD; Parker MM; DeMeo DL; Hersh CP; Ehringer MA; Young K; Jiang L; Foreman MG; Kinney GL; Make BJ; Lomas DA; Bakke P; Gulsvik A; Crapo JD; Silverman EK; Beaty TH; Hokanson JE;
Nicotine Tob Res; 2019 May; 21(6):714-722. PubMed ID: 29767774
[TBL] [Abstract][Full Text] [Related]
15. Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.
Setiawan VW; Schumacher F; Prescott J; Haessler J; Malinowski J; Wentzensen N; Yang H; Chanock S; Brinton L; Hartge P; Lissowska J; Park SL; Cheng I; Bush WS; Crawford DC; Ursin G; Horn-Ross P; Bernstein L; Lu L; Risch H; Yu H; Sakoda LC; Doherty J; Chen C; Jackson R; Yasmeen S; Cote M; Kocarnik JM; Peters U; Kraft P; De Vivo I; Haiman CA; Kooperberg C; Le Marchand L
Carcinogenesis; 2014 Sep; 35(9):2068-73. PubMed ID: 24832084
[TBL] [Abstract][Full Text] [Related]
16. Imputation-based assessment of next generation rare exome variant arrays.
Martin AR; Tse G; Bustamante CD; Kenny EE
Pac Symp Biocomput; 2014; ():241-52. PubMed ID: 24297551
[TBL] [Abstract][Full Text] [Related]
17. Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Jian X; Satizabal CL; Smith AV; Wittfeld K; Bis JC; Smith JA; Hsu FC; Nho K; Hofer E; Hagenaars SP; Nyquist PA; Mishra A; Adams HHH; Li S; Teumer A; Zhao W; Freedman BI; Saba Y; Yanek LR; Chauhan G; van Buchem MA; Cushman M; Royle NA; Bryan RN; Niessen WJ; Windham BG; DeStefano AL; Habes M; Heckbert SR; Palmer ND; Lewis CE; Eiriksdottir G; Maillard P; Mathias RA; Homuth G; Valdés-Hernández MDC; Divers J; Beiser AS; Langner S; Rice KM; Bastin ME; Yang Q; Maldjian JA; Starr JM; Sidney S; Risacher SL; Uitterlinden AG; Gudnason VG; Nauck M; Rotter JI; Schreiner PJ; Boerwinkle E; van Duijn CM; Mazoyer B; von Sarnowski B; Gottesman RF; Levy D; Sigurdsson S; Vernooij MW; Turner ST; Schmidt R; Wardlaw JM; Psaty BM; Mosley TH; DeCarli CS; Saykin AJ; Bowden DW; Becker DM; Deary IJ; Schmidt H; Kardia SLR; Ikram MA; Debette S; Grabe HJ; Longstreth WT; Seshadri S; Launer LJ; Fornage M;
Stroke; 2018 Aug; 49(8):1812-1819. PubMed ID: 30002152
[TBL] [Abstract][Full Text] [Related]
18. Exome Sequencing of Familial Bipolar Disorder.
Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
[TBL] [Abstract][Full Text] [Related]
19. Exome-Wide Pan-Cancer Analysis of Germline Variants in 8,719 Individuals Finds Little Evidence of Rare Variant Associations.
Guan Z; Shen R; Begg CB
Hum Hered; 2021; 86(1-4):34-44. PubMed ID: 34718237
[TBL] [Abstract][Full Text] [Related]
20. Characterization of Exome Variants and Their Metabolic Impact in 6,716 American Indians from the Southwest US.
Kim HI; Ye B; Gosalia N; ; Köroğlu Ç; Hanson RL; Hsueh WC; Knowler WC; Baier LJ; Bogardus C; Shuldiner AR; Van Hout CV
Am J Hum Genet; 2020 Aug; 107(2):251-264. PubMed ID: 32640185
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
