199 related articles for article (PubMed ID: 31891604)
1. A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans.
Pendergrass SA; Buyske S; Jeff JM; Frase A; Dudek S; Bradford Y; Ambite JL; Avery CL; Buzkova P; Deelman E; Fesinmeyer MD; Haiman C; Heiss G; Hindorff LA; Hsu CN; Jackson RD; Lin Y; Le Marchand L; Matise TC; Monroe KR; Moreland L; North KE; Park SL; Reiner A; Wallace R; Wilkens LR; Kooperberg C; Ritchie MD; Crawford DC
PLoS One; 2019; 14(12):e0226771. PubMed ID: 31891604
[TBL] [Abstract][Full Text] [Related]
2. Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study.
Carty CL; Bhattacharjee S; Haessler J; Cheng I; Hindorff LA; Aroda V; Carlson CS; Hsu CN; Wilkens L; Liu S; Selvin E; Jackson R; North KE; Peters U; Pankow JS; Chatterjee N; Kooperberg C
Circ Cardiovasc Genet; 2014 Aug; 7(4):505-13. PubMed ID: 25023634
[TBL] [Abstract][Full Text] [Related]
3. A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals.
Jennings MV; Martínez-Magaña JJ; Courchesne-Krak NS; Cupertino RB; Vilar-Ribó L; Bianchi SB; Hatoum AS; Atkinson EG; Giusti-Rodriguez P; Montalvo-Ortiz JL; Gelernter J; Artigas MS; ; Elson SL; Edenberg HJ; Fontanillas P; Palmer AA; Sanchez-Roige S
EBioMedicine; 2024 May; 103():105086. PubMed ID: 38580523
[TBL] [Abstract][Full Text] [Related]
4. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.
Zhao J; Cheng F; Jia P; Cox N; Denny JC; Zhao Z
Genome Med; 2018 Jan; 10(1):7. PubMed ID: 29378629
[TBL] [Abstract][Full Text] [Related]
5. Genetic variation and reproductive timing: African American women from the Population Architecture using Genomics and Epidemiology (PAGE) Study.
Spencer KL; Malinowski J; Carty CL; Franceschini N; Fernández-Rhodes L; Young A; Cheng I; Ritchie MD; Haiman CA; Wilkens L; Chunyuanwu ; Matise TC; Carlson CS; Brennan K; Park A; Rajkovic A; Hindorff LA; Buyske S; Crawford DC
PLoS One; 2013; 8(2):e55258. PubMed ID: 23424626
[TBL] [Abstract][Full Text] [Related]
6. A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Shameer K; Denny JC; Ding K; Jouni H; Crosslin DR; de Andrade M; Chute CG; Peissig P; Pacheco JA; Li R; Bastarache L; Kho AN; Ritchie MD; Masys DR; Chisholm RL; Larson EB; McCarty CA; Roden DM; Jarvik GP; Kullo IJ
Hum Genet; 2014 Jan; 133(1):95-109. PubMed ID: 24026423
[TBL] [Abstract][Full Text] [Related]
7. Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery.
Pendergrass SA; Ritchie MD
Curr Genet Med Rep; 2015 Jun; 3(2):92-100. PubMed ID: 26146598
[TBL] [Abstract][Full Text] [Related]
8. Abdominal CT metrics in 17,646 patients reveal associations between myopenia, myosteatosis, and medical phenotypes: a phenome-wide association study.
Zambrano Chaves JM; Lenchik L; Gallegos IO; Blankemeier L; Liang T; Rubin DL; Willis MH; Chaudhari AS; Boutin RD
EBioMedicine; 2024 May; 103():105116. PubMed ID: 38636199
[TBL] [Abstract][Full Text] [Related]
9. INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.
Verma A; Leader JB; Verma SS; Frase A; Wallace J; Dudek S; Lavage DR; Van Hout CV; Dewey FE; Penn J; Lopez A; Overton JD; Carey DJ; Ledbetter DH; Kirchner HL; Ritchie MD; Pendergrass SA
Pac Symp Biocomput; 2016; 21():168-79. PubMed ID: 26776183
[TBL] [Abstract][Full Text] [Related]
10. Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Kocarnik JM; Richard M; Graff M; Haessler J; Bien S; Carlson C; Carty CL; Reiner AP; Avery CL; Ballantyne CM; LaCroix AZ; Assimes TL; Barbalic M; Pankratz N; Tang W; Tao R; Chen D; Talavera GA; Daviglus ML; Chirinos-Medina DA; Pereira R; Nishimura K; Bužková P; Best LG; Ambite JL; Cheng I; Crawford DC; Hindorff LA; Fornage M; Heiss G; North KE; Haiman CA; Peters U; Le Marchand L; Kooperberg C
Hum Mol Genet; 2018 Aug; 27(16):2940-2953. PubMed ID: 29878111
[TBL] [Abstract][Full Text] [Related]
11. Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study.
Buyske S; Wu Y; Carty CL; Cheng I; Assimes TL; Dumitrescu L; Hindorff LA; Mitchell S; Ambite JL; Boerwinkle E; Buzkova P; Carlson CS; Cochran B; Duggan D; Eaton CB; Fesinmeyer MD; Franceschini N; Haessler J; Jenny N; Kang HM; Kooperberg C; Lin Y; Le Marchand L; Matise TC; Robinson JG; Rodriguez C; Schumacher FR; Voight BF; Young A; Manolio TA; Mohlke KL; Haiman CA; Peters U; Crawford DC; North KE
PLoS One; 2012; 7(4):e35651. PubMed ID: 22539988
[TBL] [Abstract][Full Text] [Related]
12. Phenome-wide association studies: a new method for functional genomics in humans.
Roden DM
J Physiol; 2017 Jun; 595(12):4109-4115. PubMed ID: 28229460
[TBL] [Abstract][Full Text] [Related]
13. Phenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits.
Shikov AE; Skitchenko RK; Predeus AV; Barbitoff YA
Sci Rep; 2020 Jan; 10(1):1037. PubMed ID: 31974475
[TBL] [Abstract][Full Text] [Related]
14. Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Denny JC; Crawford DC; Ritchie MD; Bielinski SJ; Basford MA; Bradford Y; Chai HS; Bastarache L; Zuvich R; Peissig P; Carrell D; Ramirez AH; Pathak J; Wilke RA; Rasmussen L; Wang X; Pacheco JA; Kho AN; Hayes MG; Weston N; Matsumoto M; Kopp PA; Newton KM; Jarvik GP; Li R; Manolio TA; Kullo IJ; Chute CG; Chisholm RL; Larson EB; McCarty CA; Masys DR; Roden DM; de Andrade M
Am J Hum Genet; 2011 Oct; 89(4):529-42. PubMed ID: 21981779
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans.
Wheeler HE; Gorsic LK; Welsh M; Stark AL; Gamazon ER; Cox NJ; Dolan ME
PLoS One; 2011; 6(7):e21920. PubMed ID: 21755009
[TBL] [Abstract][Full Text] [Related]
16. Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Hu Y; Bien SA; Nishimura KK; Haessler J; Hodonsky CJ; Baldassari AR; Highland HM; Wang Z; Preuss M; Sitlani CM; Wojcik GL; Tao R; Graff M; Huckins LM; Sun Q; Chen MH; Mousas A; Auer PL; Lettre G; ; Tang W; Qi L; Thyagarajan B; Buyske S; Fornage M; Hindorff LA; Li Y; Lin D; Reiner AP; North KE; Loos RJF; Raffield LM; Peters U; Avery CL; Kooperberg C
BMC Genomics; 2021 Jun; 22(1):432. PubMed ID: 34107879
[TBL] [Abstract][Full Text] [Related]
17. CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice.
Sanchez-Roige S; Jennings MV; Thorpe HHA; Mallari JE; van der Werf LC; Bianchi SB; Huang Y; Lee C; Mallard TT; Barnes SA; Wu JY; Barkley-Levenson AM; Boussaty EC; Snethlage CE; Schafer D; Babic Z; Winters BD; Watters KE; Biederer T; ; Mackillop J; Stephens DN; Elson SL; Fontanillas P; Khokhar JY; Young JW; Palmer AA
Transl Psychiatry; 2023 May; 13(1):167. PubMed ID: 37173343
[TBL] [Abstract][Full Text] [Related]
18. Korea4K: whole genome sequences of 4,157 Koreans with 107 phenotypes derived from extensive health check-ups.
Jeon S; Choi H; Jeon Y; Choi WH; Choi H; An K; Ryu H; Bhak J; Lee H; Kwon Y; Ha S; Kim YJ; Blazyte A; Kim C; Kim Y; Kang Y; Woo YJ; Lee C; Seo J; Yoon C; Bolser D; Biro O; Shin ES; Kim BC; Kim SY; Park JH; Jeon J; Jung D; Lee S; Bhak J
Gigascience; 2024 Jan; 13():. PubMed ID: 38626723
[TBL] [Abstract][Full Text] [Related]
19. PHENOME-WIDE INTERACTION STUDY (PheWIS) IN AIDS CLINICAL TRIALS GROUP DATA (ACTG).
Verma SS; Frase AT; Verma A; Pendergrass SA; Mahony S; Haas DW; Ritchie MD
Pac Symp Biocomput; 2016; 21():57-68. PubMed ID: 26776173
[TBL] [Abstract][Full Text] [Related]
20. Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.
Denny JC; Bastarache L; Roden DM
Annu Rev Genomics Hum Genet; 2016 Aug; 17():353-73. PubMed ID: 27147087
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]