204 related articles for article (PubMed ID: 33418499)
1. Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Lin BM; Grinde KE; Brody JA; Breeze CE; Raffield LM; Mychaleckyj JC; Thornton TA; Perry JA; Baier LJ; de Las Fuentes L; Guo X; Heavner BD; Hanson RL; Hung YJ; Qian H; Hsiung CA; Hwang SJ; Irvin MR; Jain D; Kelly TN; Kobes S; Lange L; Lash JP; Li Y; Liu X; Mi X; Musani SK; Papanicolaou GJ; Parsa A; Reiner AP; Salimi S; Sheu WH; Shuldiner AR; Taylor KD; Smith AV; Smith JA; Tin A; Vaidya D; Wallace RB; Yamamoto K; Sakaue S; Matsuda K; Kamatani Y; Momozawa Y; Yanek LR; Young BA; Zhao W; Okada Y; Abecasis G; Psaty BM; Arnett DK; Boerwinkle E; Cai J; Yii-Der Chen I; Correa A; Cupples LA; He J; Kardia SL; Kooperberg C; Mathias RA; Mitchell BD; Nickerson DA; Turner ST; Vasan RS; Rotter JI; Levy D; Kramer HJ; Köttgen A; Nhlbi Trans-Omics For Precision Medicine TOPMed Consortium ; TOPMed Kidney Working Group ; Rich SS; Lin DY; Browning SR; Franceschini N
EBioMedicine; 2021 Jan; 63():103157. PubMed ID: 33418499
[TBL] [Abstract][Full Text] [Related]
2. Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
Kowalski MH; Qian H; Hou Z; Rosen JD; Tapia AL; Shan Y; Jain D; Argos M; Arnett DK; Avery C; Barnes KC; Becker LC; Bien SA; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Buyske S; Cai J; Cho MH; Choi SH; Choquet H; Cupples LA; Cushman M; Daya M; de Vries PS; Ellinor PT; Faraday N; Fornage M; Gabriel S; Ganesh SK; Graff M; Gupta N; He J; Heckbert SR; Hidalgo B; Hodonsky CJ; Irvin MR; Johnson AD; Jorgenson E; Kaplan R; Kardia SLR; Kelly TN; Kooperberg C; Lasky-Su JA; Loos RJF; Lubitz SA; Mathias RA; McHugh CP; Montgomery C; Moon JY; Morrison AC; Palmer ND; Pankratz N; Papanicolaou GJ; Peralta JM; Peyser PA; Rich SS; Rotter JI; Silverman EK; Smith JA; Smith NL; Taylor KD; Thornton TA; Tiwari HK; Tracy RP; Wang T; Weiss ST; Weng LC; Wiggins KL; Wilson JG; Yanek LR; Zöllner S; North KE; Auer PL; ; ; Raffield LM; Reiner AP; Li Y
PLoS Genet; 2019 Dec; 15(12):e1008500. PubMed ID: 31869403
[TBL] [Abstract][Full Text] [Related]
3. Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.
Hu Y; Haessler JW; Manansala R; Wiggins KL; Moscati A; Beiser A; Heard-Costa NL; Sarnowski C; Raffield LM; Chung J; Marini S; Anderson CD; Rosand J; Xu H; Sun X; Kelly TN; Wong Q; Lange LA; Rotter JI; Correa A; Vasan RS; Seshadri S; Rich SS; Do R; Loos RJF; Longstreth WT; Bis JC; Psaty BM; Tirschwell DL; Assimes TL; Silver B; Liu S; Jackson R; Wassertheil-Smoller S; Mitchell BD; Fornage M; Auer PL; Reiner AP; Kooperberg C;
Stroke; 2022 Mar; 53(3):875-885. PubMed ID: 34727735
[TBL] [Abstract][Full Text] [Related]
4. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Hu Y; Stilp AM; McHugh CP; Rao S; Jain D; Zheng X; Lane J; Méric de Bellefon S; Raffield LM; Chen MH; Yanek LR; Wheeler M; Yao Y; Ren C; Broome J; Moon JY; de Vries PS; Hobbs BD; Sun Q; Surendran P; Brody JA; Blackwell TW; Choquet H; Ryan K; Duggirala R; Heard-Costa N; Wang Z; Chami N; Preuss MH; Min N; Ekunwe L; Lange LA; Cushman M; Faraday N; Curran JE; Almasy L; Kundu K; Smith AV; Gabriel S; Rotter JI; Fornage M; Lloyd-Jones DM; Vasan RS; Smith NL; North KE; Boerwinkle E; Becker LC; Lewis JP; Abecasis GR; Hou L; O'Connell JR; Morrison AC; Beaty TH; Kaplan R; Correa A; Blangero J; Jorgenson E; Psaty BM; Kooperberg C; Walton RT; Kleinstiver BP; Tang H; Loos RJF; Soranzo N; Butterworth AS; Nickerson D; Rich SS; Mitchell BD; Johnson AD; Auer PL; Li Y; Mathias RA; Lettre G; Pankratz N; Laurie CC; Laurie CA; Bauer DE; Conomos MP; Reiner AP;
Am J Hum Genet; 2021 May; 108(5):874-893. PubMed ID: 33887194
[TBL] [Abstract][Full Text] [Related]
5. Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Little A; Hu Y; Sun Q; Jain D; Broome J; Chen MH; Thibord F; McHugh C; Surendran P; Blackwell TW; Brody JA; Bhan A; Chami N; de Vries PS; Ekunwe L; Heard-Costa N; Hobbs BD; Manichaikul A; Moon JY; Preuss MH; Ryan K; Wang Z; Wheeler M; Yanek LR; Abecasis GR; Almasy L; Beaty TH; Becker LC; Blangero J; Boerwinkle E; Butterworth AS; Choquet H; Correa A; Curran JE; Faraday N; Fornage M; Glahn DC; Hou L; Jorgenson E; Kooperberg C; Lewis JP; Lloyd-Jones DM; Loos RJF; Min YI; Mitchell BD; Morrison AC; Nickerson DA; North KE; O'Connell JR; Pankratz N; Psaty BM; Vasan RS; Rich SS; Rotter JI; Smith AV; Smith NL; Tang H; Tracy RP; Conomos MP; Laurie CA; Mathias RA; Li Y; Auer PL; ; Thornton T; Reiner AP; Johnson AD; Raffield LM
Hum Mol Genet; 2022 Feb; 31(3):347-361. PubMed ID: 34553764
[TBL] [Abstract][Full Text] [Related]
6. Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
Sarnowski C; Leong A; Raffield LM; Wu P; de Vries PS; DiCorpo D; Guo X; Xu H; Liu Y; Zheng X; Hu Y; Brody JA; Goodarzi MO; Hidalgo BA; Highland HM; Jain D; Liu CT; Naik RP; O'Connell JR; Perry JA; Porneala BC; Selvin E; Wessel J; Psaty BM; Curran JE; Peralta JM; Blangero J; Kooperberg C; Mathias R; Johnson AD; Reiner AP; Mitchell BD; Cupples LA; Vasan RS; Correa A; Morrison AC; Boerwinkle E; Rotter JI; Rich SS; Manning AK; Dupuis J; Meigs JB; ; ; ;
Am J Hum Genet; 2019 Oct; 105(4):706-718. PubMed ID: 31564435
[TBL] [Abstract][Full Text] [Related]
7. Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program.
Cade BE; Lee J; Sofer T; Wang H; Zhang M; Chen H; Gharib SA; Gottlieb DJ; Guo X; Lane JM; Liang J; Lin X; Mei H; Patel SR; Purcell SM; Saxena R; Shah NA; Evans DS; Hanis CL; Hillman DR; Mukherjee S; Palmer LJ; Stone KL; Tranah GJ; ; Abecasis GR; Boerwinkle EA; Correa A; Cupples LA; Kaplan RC; Nickerson DA; North KE; Psaty BM; Rotter JI; Rich SS; Tracy RP; Vasan RS; Wilson JG; Zhu X; Redline S;
Genome Med; 2021 Aug; 13(1):136. PubMed ID: 34446064
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program.
Sarnowski C; Chen H; Biggs ML; Wassertheil-Smoller S; Bressler J; Irvin MR; Ryan KA; Karasik D; Arnett DK; Cupples LA; Fardo DW; Gogarten SM; Heavner BD; Jain D; Kang HM; Kooperberg C; Mainous AG; Mitchell BD; Morrison AC; O'Connell JR; Psaty BM; Rice K; Smith AV; Vasan RS; Windham BG; Kiel DP; Murabito JM; Lunetta KL; ;
PLoS One; 2021; 16(7):e0253611. PubMed ID: 34214102
[TBL] [Abstract][Full Text] [Related]
9. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
Dinardo CL; Oliveira TGM; Kelly S; Ashley-Koch A; Telen M; Schmidt LC; Castilho S; Melo K; Dezan MR; Wheeler MM; Johnsen JM; Nickerson DA; Jain D; Custer B; Pereira AC; Sabino EC;
Transfusion; 2021 Feb; 61(2):603-616. PubMed ID: 33231305
[TBL] [Abstract][Full Text] [Related]
10. Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos.
Qian H; Kowalski MH; Kramer HJ; Tao R; Lash JP; Stilp AM; Cai J; Li Y; Franceschini N
Circ Genom Precis Med; 2020 Aug; 13(4):e002891. PubMed ID: 32600054
[TBL] [Abstract][Full Text] [Related]
11. Multiethnic genome-wide and HLA association study of total serum IgE level.
Daya M; Cox C; Acevedo N; Boorgula MP; Campbell M; Chavan S; Cho MH; David GL; Kachroo P; Lasky-Su J; Li X; McHugh CP; Qiao D; Rafaels N; Beck LA; Bleecker ER; Caraballo L; Cupples AL; Figueiredo CA; Gallo RL; Hanifin J; Hansel NN; Hata TR; Hersh CP; Knight-Madden J; Leung DYM; Guttman-Yassky E; Meyers DA; O'Connor G; Ober C; Ong PY; Ortega VE; Paller AS; Putcha N; Reed RM; Schneider LC; Silverman EK; Slifka MK; Spergel JM; Vasan RS; Viaud-Martinez KA; Watson H; Weiss ST; ; Ruczinski I; Beaty TH; Mathias RA; Barnes KC
J Allergy Clin Immunol; 2021 Dec; 148(6):1589-1595. PubMed ID: 34536413
[TBL] [Abstract][Full Text] [Related]
12. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Mikhaylova AV; McHugh CP; Polfus LM; Raffield LM; Boorgula MP; Blackwell TW; Brody JA; Broome J; Chami N; Chen MH; Conomos MP; Cox C; Curran JE; Daya M; Ekunwe L; Glahn DC; Heard-Costa N; Highland HM; Hobbs BD; Ilboudo Y; Jain D; Lange LA; Miller-Fleming TW; Min N; Moon JY; Preuss MH; Rosen J; Ryan K; Smith AV; Sun Q; Surendran P; de Vries PS; Walter K; Wang Z; Wheeler M; Yanek LR; Zhong X; Abecasis GR; Almasy L; Barnes KC; Beaty TH; Becker LC; Blangero J; Boerwinkle E; Butterworth AS; Chavan S; Cho MH; Choquet H; Correa A; Cox N; DeMeo DL; Faraday N; Fornage M; Gerszten RE; Hou L; Johnson AD; Jorgenson E; Kaplan R; Kooperberg C; Kundu K; Laurie CA; Lettre G; Lewis JP; Li B; Li Y; Lloyd-Jones DM; Loos RJF; Manichaikul A; Meyers DA; Mitchell BD; Morrison AC; Ngo D; Nickerson DA; Nongmaithem S; North KE; O'Connell JR; Ortega VE; Pankratz N; Perry JA; Psaty BM; Rich SS; Soranzo N; Rotter JI; Silverman EK; Smith NL; Tang H; Tracy RP; Thornton TA; Vasan RS; Zein J; Mathias RA; ; Reiner AP; Auer PL
Am J Hum Genet; 2021 Oct; 108(10):1836-1851. PubMed ID: 34582791
[TBL] [Abstract][Full Text] [Related]
13. The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes.
Huerta-Chagoya A; Schroeder P; Mandla R; Deutsch AJ; Zhu W; Petty L; Yi X; Cole JB; Udler MS; Dornbos P; Porneala B; DiCorpo D; Liu CT; Li JH; Szczerbiński L; Kaur V; Kim J; Lu Y; Martin A; Eizirik DL; Marchetti P; Marselli L; Chen L; Srinivasan S; Todd J; Flannick J; Gubitosi-Klug R; Levitsky L; Shah R; Kelsey M; Burke B; Dabelea DM; Divers J; Marcovina S; Stalbow L; Loos RJF; Darst BF; Kooperberg C; Raffield LM; Haiman C; Sun Q; McCormick JB; Fisher-Hoch SP; Ordoñez ML; Meigs J; Baier LJ; González-Villalpando C; González-Villalpando ME; Orozco L; García-García L; Moreno-Estrada A; ; Aguilar-Salinas CA; Tusié T; Dupuis J; Ng MCY; Manning A; Highland HM; Cnop M; Hanson R; Below J; Florez JC; Leong A; Mercader JM
Diabetologia; 2023 Jul; 66(7):1273-1288. PubMed ID: 37148359
[TBL] [Abstract][Full Text] [Related]
14. Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
Raffield LM; Iyengar AK; Wang B; Gaynor SM; Spracklen CN; Zhong X; Kowalski MH; Salimi S; Polfus LM; Benjamin EJ; Bis JC; Bowler R; Cade BE; Choi WJ; Comellas AP; Correa A; Cruz P; Doddapaneni H; Durda P; Gogarten SM; Jain D; Kim RW; Kral BG; Lange LA; Larson MG; Laurie C; Lee J; Lee S; Lewis JP; Metcalf GA; Mitchell BD; Momin Z; Muzny DM; Pankratz N; Park CJ; Rich SS; Rotter JI; Ryan K; Seo D; Tracy RP; Viaud-Martinez KA; Yanek LR; Zhao LP; Lin X; Li B; Li Y; Dupuis J; Reiner AP; Mohlke KL; Auer PL; ;
Am J Hum Genet; 2020 Jan; 106(1):112-120. PubMed ID: 31883642
[TBL] [Abstract][Full Text] [Related]
15. Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.
Du M; Auer PL; Jiao S; Haessler J; Altshuler D; Boerwinkle E; Carlson CS; Carty CL; Chen YD; Curtis K; Franceschini N; Hsu L; Jackson R; Lange LA; Lettre G; Monda KL; ; Nickerson DA; Reiner AP; Rich SS; Rosse SA; Rotter JI; Willer CJ; Wilson JG; North K; Kooperberg C; Heard-Costa N; Peters U
Hum Mol Genet; 2014 Dec; 23(24):6607-15. PubMed ID: 25027330
[TBL] [Abstract][Full Text] [Related]
16. Rare coding variants in RCN3 are associated with blood pressure.
He KY; Kelly TN; Wang H; Liang J; Zhu L; Cade BE; Assimes TL; Becker LC; Beitelshees AL; Bielak LF; Bress AP; Brody JA; Chang YC; Chang YC; de Vries PS; Duggirala R; Fox ER; Franceschini N; Furniss AL; Gao Y; Guo X; Haessler J; Hung YJ; Hwang SJ; Irvin MR; Kalyani RR; Liu CT; Liu C; Martin LW; Montasser ME; Muntner PM; Mwasongwe S; Naseri T; Palmas W; Reupena MS; Rice KM; Sheu WH; Shimbo D; Smith JA; Snively BM; Yanek LR; Zhao W; Blangero J; Boerwinkle E; Chen YI; Correa A; Cupples LA; Curran JE; Fornage M; He J; Hou L; Kaplan RC; Kardia SLR; Kenny EE; Kooperberg C; Lloyd-Jones D; Loos RJF; Mathias RA; McGarvey ST; Mitchell BD; North KE; Peyser PA; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Rotter JI; Taylor KD; Tracy R; Vasan RS; ; Morrison AC; Levy D; Chakravarti A; Arnett DK; Zhu X
BMC Genomics; 2022 Feb; 23(1):148. PubMed ID: 35183128
[TBL] [Abstract][Full Text] [Related]
17. Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Wang Y; Selvaraj MS; Li X; Li Z; Holdcraft JA; Arnett DK; Bis JC; Blangero J; Boerwinkle E; Bowden DW; Cade BE; Carlson JC; Carson AP; Chen YI; Curran JE; de Vries PS; Dutcher SK; Ellinor PT; Floyd JS; Fornage M; Freedman BI; Gabriel S; Germer S; Gibbs RA; Guo X; He J; Heard-Costa N; Hildalgo B; Hou L; Irvin MR; Joehanes R; Kaplan RC; Kardia SL; Kelly TN; Kim R; Kooperberg C; Kral BG; Levy D; Li C; Liu C; Lloyd-Jone D; Loos RJ; Mahaney MC; Martin LW; Mathias RA; Minster RL; Mitchell BD; Montasser ME; Morrison AC; Murabito JM; Naseri T; O'Connell JR; Palmer ND; Preuss MH; Psaty BM; Raffield LM; Rao DC; Redline S; Reiner AP; Rich SS; Ruepena MS; Sheu WH; Smith JA; Smith A; Tiwari HK; Tsai MY; Viaud-Martinez KA; Wang Z; Yanek LR; Zhao W; ; Rotter JI; Lin X; Natarajan P; Peloso GM
Am J Hum Genet; 2023 Oct; 110(10):1704-1717. PubMed ID: 37802043
[TBL] [Abstract][Full Text] [Related]
18. Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche.
Sarnowski C; Cousminer DL; Franceschini N; Raffield LM; Jia G; Fernández-Rhodes L; Grant SFA; Hakonarson H; Lange LA; Long J; Sofer T; Tao R; Wallace RB; Wong Q; Zirpoli G; Boerwinkle E; Bradfield JP; Correa A; Kooperberg CL; North KE; Palmer JR; Zemel BS; Zheng W; Murabito JM; Lunetta KL
Hum Reprod; 2021 Jun; 36(7):1999-2010. PubMed ID: 34021356
[TBL] [Abstract][Full Text] [Related]
19. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Taliun D; Harris DN; Kessler MD; Carlson J; Szpiech ZA; Torres R; Taliun SAG; Corvelo A; Gogarten SM; Kang HM; Pitsillides AN; LeFaive J; Lee SB; Tian X; Browning BL; Das S; Emde AK; Clarke WE; Loesch DP; Shetty AC; Blackwell TW; Smith AV; Wong Q; Liu X; Conomos MP; Bobo DM; Aguet F; Albert C; Alonso A; Ardlie KG; Arking DE; Aslibekyan S; Auer PL; Barnard J; Barr RG; Barwick L; Becker LC; Beer RL; Benjamin EJ; Bielak LF; Blangero J; Boehnke M; Bowden DW; Brody JA; Burchard EG; Cade BE; Casella JF; Chalazan B; Chasman DI; Chen YI; Cho MH; Choi SH; Chung MK; Clish CB; Correa A; Curran JE; Custer B; Darbar D; Daya M; de Andrade M; DeMeo DL; Dutcher SK; Ellinor PT; Emery LS; Eng C; Fatkin D; Fingerlin T; Forer L; Fornage M; Franceschini N; Fuchsberger C; Fullerton SM; Germer S; Gladwin MT; Gottlieb DJ; Guo X; Hall ME; He J; Heard-Costa NL; Heckbert SR; Irvin MR; Johnsen JM; Johnson AD; Kaplan R; Kardia SLR; Kelly T; Kelly S; Kenny EE; Kiel DP; Klemmer R; Konkle BA; Kooperberg C; Köttgen A; Lange LA; Lasky-Su J; Levy D; Lin X; Lin KH; Liu C; Loos RJF; Garman L; Gerszten R; Lubitz SA; Lunetta KL; Mak ACY; Manichaikul A; Manning AK; Mathias RA; McManus DD; McGarvey ST; Meigs JB; Meyers DA; Mikulla JL; Minear MA; Mitchell BD; Mohanty S; Montasser ME; Montgomery C; Morrison AC; Murabito JM; Natale A; Natarajan P; Nelson SC; North KE; O'Connell JR; Palmer ND; Pankratz N; Peloso GM; Peyser PA; Pleiness J; Post WS; Psaty BM; Rao DC; Redline S; Reiner AP; Roden D; Rotter JI; Ruczinski I; Sarnowski C; Schoenherr S; Schwartz DA; Seo JS; Seshadri S; Sheehan VA; Sheu WH; Shoemaker MB; Smith NL; Smith JA; Sotoodehnia N; Stilp AM; Tang W; Taylor KD; Telen M; Thornton TA; Tracy RP; Van Den Berg DJ; Vasan RS; Viaud-Martinez KA; Vrieze S; Weeks DE; Weir BS; Weiss ST; Weng LC; Willer CJ; Zhang Y; Zhao X; Arnett DK; Ashley-Koch AE; Barnes KC; Boerwinkle E; Gabriel S; Gibbs R; Rice KM; Rich SS; Silverman EK; Qasba P; Gan W; ; Papanicolaou GJ; Nickerson DA; Browning SR; Zody MC; Zöllner S; Wilson JG; Cupples LA; Laurie CC; Jaquish CE; Hernandez RD; O'Connor TD; Abecasis GR
Nature; 2021 Feb; 590(7845):290-299. PubMed ID: 33568819
[TBL] [Abstract][Full Text] [Related]
20. Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank.
De Lillo A; D'Antona S; Pathak GA; Wendt FR; De Angelis F; Fuciarelli M; Polimanti R
Hum Mol Genet; 2021 Jul; 30(15):1457-1467. PubMed ID: 33890984
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
