138 related articles for article (PubMed ID: 37451613)
1. Association Analyses of Predicted Loss-of-Function Variants Prioritized 15 Genes as Blood Pressure Regulators.
Lecluze E; Lettre G
Can J Cardiol; 2023 Dec; 39(12):1888-1897. PubMed ID: 37451613
[TBL] [Abstract][Full Text] [Related]
2. Metabolites downstream of predicted loss-of-function variants inform relationship to disease.
Li M; Wang A; Quek LE; Vernon S; Figtree GA; Yang J; O'Sullivan JF
Mol Genet Metab; 2019 Dec; 128(4):476-482. PubMed ID: 31679996
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals.
Kraja AT; Cook JP; Warren HR; Surendran P; Liu C; Evangelou E; Manning AK; Grarup N; Drenos F; Sim X; Smith AV; Amin N; Blakemore AIF; Bork-Jensen J; Brandslund I; Farmaki AE; Fava C; Ferreira T; Herzig KH; Giri A; Giulianini F; Grove ML; Guo X; Harris SE; Have CT; Havulinna AS; Zhang H; Jørgensen ME; Käräjämäki A; Kooperberg C; Linneberg A; Little L; Liu Y; Bonnycastle LL; Lu Y; Mägi R; Mahajan A; Malerba G; Marioni RE; Mei H; Menni C; Morrison AC; Padmanabhan S; Palmas W; Poveda A; Rauramaa R; Rayner NW; Riaz M; Rice K; Richard MA; Smith JA; Southam L; Stančáková A; Stirrups KE; Tragante V; Tuomi T; Tzoulaki I; Varga TV; Weiss S; Yiorkas AM; Young R; Zhang W; Barnes MR; Cabrera CP; Gao H; Boehnke M; Boerwinkle E; Chambers JC; Connell JM; Christensen CK; de Boer RA; Deary IJ; Dedoussis G; Deloukas P; Dominiczak AF; Dörr M; Joehanes R; Edwards TL; Esko T; Fornage M; Franceschini N; Franks PW; Gambaro G; Groop L; Hallmans G; Hansen T; Hayward C; Heikki O; Ingelsson E; Tuomilehto J; Jarvelin MR; Kardia SLR; Karpe F; Kooner JS; Lakka TA; Langenberg C; Lind L; Loos RJF; Laakso M; McCarthy MI; Melander O; Mohlke KL; Morris AP; Palmer CNA; Pedersen O; Polasek O; Poulter NR; Province MA; Psaty BM; Ridker PM; Rotter JI; Rudan I; Salomaa V; Samani NJ; Sever PJ; Skaaby T; Stafford JM; Starr JM; van der Harst P; van der Meer P; ; van Duijn CM; Vergnaud AC; Gudnason V; Wareham NJ; Wilson JG; Willer CJ; Witte DR; Zeggini E; Saleheen D; Butterworth AS; Danesh J; Asselbergs FW; Wain LV; Ehret GB; Chasman DI; Caulfield MJ; Elliott P; Lindgren CM; Levy D; Newton-Cheh C; Munroe PB; Howson JMM;
Circ Cardiovasc Genet; 2017 Oct; 10(5):. PubMed ID: 29030403
[TBL] [Abstract][Full Text] [Related]
5. Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.
Yu B; Pulit SL; Hwang SJ; Brody JA; Amin N; Auer PL; Bis JC; Boerwinkle E; Burke GL; Chakravarti A; Correa A; Dreisbach AW; Franco OH; Ehret GB; Franceschini N; Hofman A; Lin DY; Metcalf GA; Musani SK; Muzny D; Palmas W; Raffel L; Reiner A; Rice K; Rotter JI; Veeraraghavan N; Fox E; Guo X; North KE; Gibbs RA; van Duijn CM; Psaty BM; Levy D; Newton-Cheh C; Morrison AC;
Circ Cardiovasc Genet; 2016 Feb; 9(1):64-70. PubMed ID: 26658788
[TBL] [Abstract][Full Text] [Related]
6. Association of Rare Predicted Loss-of-Function Variants in Cellular Pathways with Sub-Phenotypes in Age-Related Macular Degeneration.
Pietraszkiewicz A; van Asten F; Kwong A; Ratnapriya R; Abecasis G; Swaroop A; Chew EY
Ophthalmology; 2018 Mar; 125(3):398-406. PubMed ID: 29224928
[TBL] [Abstract][Full Text] [Related]
7. Reevaluation of the association of seven candidate genes with blood pressure and hypertension: a replication study and meta-analysis with a larger sample size.
Takeuchi F; Yamamoto K; Katsuya T; Sugiyama T; Nabika T; Ohnaka K; Yamaguchi S; Takayanagi R; Ogihara T; Kato N
Hypertens Res; 2012 Aug; 35(8):825-31. PubMed ID: 22456346
[TBL] [Abstract][Full Text] [Related]
8. Meta-Analysis and Multivariate GWAS Analyses in 80,950 Individuals of African Ancestry Identify Novel Variants Associated with Blood Pressure Traits.
Udosen B; Soremekun O; Kamiza A; Machipisa T; Cheickna C; Omotuyi O; Soliman M; Wélé M; Nashiru O; Chikowore T; Fatumo S
Int J Mol Sci; 2023 Jan; 24(3):. PubMed ID: 36768488
[TBL] [Abstract][Full Text] [Related]
9. The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study.
Lin C; Sun Z; Mei Z; Zeng H; Zhao M; Hu J; Xia M; Huang T; Wang C; Gao X; Zheng Y
BMC Med; 2022 Oct; 20(1):414. PubMed ID: 36307799
[TBL] [Abstract][Full Text] [Related]
10. Sequence analysis of six blood pressure candidate regions in 4,178 individuals: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.
Morrison AC; Bis JC; Hwang SJ; Ehret GB; Lumley T; Rice K; Muzny D; Gibbs RA; Boerwinkle E; Psaty BM; Chakravarti A; Levy D
PLoS One; 2014; 9(10):e109155. PubMed ID: 25275628
[TBL] [Abstract][Full Text] [Related]
11. Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Surendran P; Feofanova EV; Lahrouchi N; Ntalla I; Karthikeyan S; Cook J; Chen L; Mifsud B; Yao C; Kraja AT; Cartwright JH; Hellwege JN; Giri A; Tragante V; Thorleifsson G; Liu DJ; Prins BP; Stewart ID; Cabrera CP; Eales JM; Akbarov A; Auer PL; Bielak LF; Bis JC; Braithwaite VS; Brody JA; Daw EW; Warren HR; Drenos F; Nielsen SF; Faul JD; Fauman EB; Fava C; Ferreira T; Foley CN; Franceschini N; Gao H; Giannakopoulou O; Giulianini F; Gudbjartsson DF; Guo X; Harris SE; Havulinna AS; Helgadottir A; Huffman JE; Hwang SJ; Kanoni S; Kontto J; Larson MG; Li-Gao R; Lindström J; Lotta LA; Lu Y; Luan J; Mahajan A; Malerba G; Masca NGD; Mei H; Menni C; Mook-Kanamori DO; Mosen-Ansorena D; Müller-Nurasyid M; Paré G; Paul DS; Perola M; Poveda A; Rauramaa R; Richard M; Richardson TG; Sepúlveda N; Sim X; Smith AV; Smith JA; Staley JR; Stanáková A; Sulem P; Thériault S; Thorsteinsdottir U; Trompet S; Varga TV; Velez Edwards DR; Veronesi G; Weiss S; Willems SM; Yao J; Young R; Yu B; Zhang W; Zhao JH; Zhao W; Zhao W; Evangelou E; Aeschbacher S; Asllanaj E; Blankenberg S; Bonnycastle LL; Bork-Jensen J; Brandslund I; Braund PS; Burgess S; Cho K; Christensen C; Connell J; Mutsert R; Dominiczak AF; Dörr M; Eiriksdottir G; Farmaki AE; Gaziano JM; Grarup N; Grove ML; Hallmans G; Hansen T; Have CT; Heiss G; Jørgensen ME; Jousilahti P; Kajantie E; Kamat M; Käräjämäki A; Karpe F; Koistinen HA; Kovesdy CP; Kuulasmaa K; Laatikainen T; Lannfelt L; Lee IT; Lee WJ; ; Linneberg A; Martin LW; Moitry M; Nadkarni G; Neville MJ; Palmer CNA; Papanicolaou GJ; Pedersen O; Peters J; Poulter N; Rasheed A; Rasmussen KL; Rayner NW; Mägi R; Renström F; Rettig R; Rossouw J; Schreiner PJ; Sever PS; Sigurdsson EL; Skaaby T; Sun YV; Sundstrom J; Thorgeirsson G; Esko T; Trabetti E; Tsao PS; Tuomi T; Turner ST; Tzoulaki I; Vaartjes I; Vergnaud AC; Willer CJ; Wilson PWF; Witte DR; Yonova-Doing E; Zhang H; Aliya N; Almgren P; Amouyel P; Asselbergs FW; Barnes MR; Blakemore AI; Boehnke M; Bots ML; Bottinger EP; Buring JE; Chambers JC; Chen YI; Chowdhury R; Conen D; Correa A; Davey Smith G; Boer RA; Deary IJ; Dedoussis G; Deloukas P; Di Angelantonio E; Elliott P; ; ; Felix SB; Ferrières J; Ford I; Fornage M; Franks PW; Franks S; Frossard P; Gambaro G; Gaunt TR; Groop L; Gudnason V; Harris TB; Hayward C; Hennig BJ; Herzig KH; Ingelsson E; Tuomilehto J; Järvelin MR; Jukema JW; Kardia SLR; Kee F; Kooner JS; Kooperberg C; Launer LJ; Lind L; Loos RJF; Majumder AAS; Laakso M; McCarthy MI; Melander O; Mohlke KL; Murray AD; Nordestgaard BG; Orho-Melander M; Packard CJ; Padmanabhan S; Palmas W; Polasek O; Porteous DJ; Prentice AM; Province MA; Relton CL; Rice K; Ridker PM; Rolandsson O; Rosendaal FR; Rotter JI; Rudan I; Salomaa V; Samani NJ; Sattar N; Sheu WH; Smith BH; Soranzo N; Spector TD; Starr JM; Sebert S; Taylor KD; Lakka TA; Timpson NJ; Tobin MD; ; van der Harst P; van der Meer P; Ramachandran VS; Verweij N; Virtamo J; Völker U; Weir DR; Zeggini E; Charchar FJ; ; Wareham NJ; Langenberg C; Tomaszewski M; Butterworth AS; Caulfield MJ; Danesh J; Edwards TL; Holm H; Hung AM; Lindgren CM; Liu C; Manning AK; Morris AP; Morrison AC; O'Donnell CJ; Psaty BM; Saleheen D; Stefansson K; Boerwinkle E; Chasman DI; Levy D; Newton-Cheh C; Munroe PB; Howson JMM
Nat Genet; 2020 Dec; 52(12):1314-1332. PubMed ID: 33230300
[TBL] [Abstract][Full Text] [Related]
12. Adult derived genetic blood pressure scores and blood pressure measured in different body postures in young children.
Jansen MA; Dalmeijer GW; Visseren FL; van der Ent CK; Leusink M; Onland-Moret NC; Maitland-van der Zee AH; Grobbee DE; Uiterwaal CS
Eur J Prev Cardiol; 2017 Feb; 24(3):320-327. PubMed ID: 27856808
[TBL] [Abstract][Full Text] [Related]
13. Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes.
Deaton AM; Parker MM; Ward LD; Flynn-Carroll AO; BonDurant L; Hinkle G; Akbari P; Lotta LA; ; ; Baras A; Nioi P
Sci Rep; 2021 Nov; 11(1):21565. PubMed ID: 34732801
[TBL] [Abstract][Full Text] [Related]
14. A genome-wide association and replication study of blood pressure in Ugandan early adolescents.
Lule SA; Mentzer AJ; Namara B; Muwenzi AG; Nassanga B; Kizito D; Akurut H; Lubyayi L; Tumusiime J; Zziwa C; Akello F; Gurdasani D; Sandhu M; Smeeth L; Elliott AM; Webb EL
Mol Genet Genomic Med; 2019 Oct; 7(10):e00950. PubMed ID: 31469255
[TBL] [Abstract][Full Text] [Related]
15. Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease.
Emdin CA; Khera AV; Chaffin M; Klarin D; Natarajan P; Aragam K; Haas M; Bick A; Zekavat SM; Nomura A; Ardissino D; Wilson JG; Schunkert H; McPherson R; Watkins H; Elosua R; Bown MJ; Samani NJ; Baber U; Erdmann J; Gupta N; Danesh J; Chasman D; Ridker P; Denny J; Bastarache L; Lichtman JH; D'Onofrio G; Mattera J; Spertus JA; Sheu WH; Taylor KD; Psaty BM; Rich SS; Post W; Rotter JI; Chen YI; Krumholz H; Saleheen D; Gabriel S; Kathiresan S
Nat Commun; 2018 Apr; 9(1):1613. PubMed ID: 29691411
[TBL] [Abstract][Full Text] [Related]
16. Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31.
Wang H; Nandakumar P; Tekola-Ayele F; Tayo BO; Ware EB; Gu CC; Lu Y; Yao J; Zhao W; Smith JA; Hellwege JN; Guo X; Edwards TL; Loos RJF; Arnett DK; Fornage M; Rotimi C; Kardia SLR; Cooper RS; Rao DC; Ehret G; Chakravarti A; Zhu X
Eur J Hum Genet; 2019 Feb; 27(2):269-277. PubMed ID: 30262922
[TBL] [Abstract][Full Text] [Related]
17. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study.
Fox ER; Young JH; Li Y; Dreisbach AW; Keating BJ; Musani SK; Liu K; Morrison AC; Ganesh S; Kutlar A; Ramachandran VS; Polak JF; Fabsitz RR; Dries DL; Farlow DN; Redline S; Adeyemo A; Hirschorn JN; Sun YV; Wyatt SB; Penman AD; Palmas W; Rotter JI; Townsend RR; Doumatey AP; Tayo BO; Mosley TH; Lyon HN; Kang SJ; Rotimi CN; Cooper RS; Franceschini N; Curb JD; Martin LW; Eaton CB; Kardia SL; Taylor HA; Caulfield MJ; Ehret GB; Johnson T; ; Chakravarti A; Zhu X; Levy D
Hum Mol Genet; 2011 Jun; 20(11):2273-84. PubMed ID: 21378095
[TBL] [Abstract][Full Text] [Related]
18. Gene-education interactions identify novel blood pressure loci in the Framingham Heart Study.
Basson J; Sung YJ; Schwander K; Kume R; Simino J; de las Fuentes L; Rao D
Am J Hypertens; 2014 Mar; 27(3):431-44. PubMed ID: 24473254
[TBL] [Abstract][Full Text] [Related]
19. Replication of European hypertension associations in a case-control study of 9,534 African Americans.
Kaur H; Crawford DC; Liang J; Benchek P; ; Zhu X; Kallianpur AR; Bush WS
PLoS One; 2021; 16(11):e0259962. PubMed ID: 34793544
[TBL] [Abstract][Full Text] [Related]
20. Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She ethnic minority of China.
Lin Y; Lai X; Chen B; Xu Y; Huang B; Chen Z; Zhu S; Yao J; Jiang Q; Huang H; Wen J; Chen G
Atherosclerosis; 2011 Dec; 219(2):709-14. PubMed ID: 21963141
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
