207 related articles for article (PubMed ID: 37802043)
41. Rare non-coding variants are associated with plasma lipid traits in a founder population.
Igartua C; Mozaffari SV; Nicolae DL; Ober C
Sci Rep; 2017 Nov; 7(1):16415. PubMed ID: 29180722
[TBL] [Abstract][Full Text] [Related]
42. GWAS of lipids in Greenlanders finds association signals shared with Europeans and reveals an independent PCSK9 association signal.
Senftleber NK; Andersen MK; Jørsboe E; Stæger FF; Nøhr AK; Garcia-Erill G; Meisner J; Santander CG; Balboa RF; Gilly A; Bjerregaard P; Larsen CVL; Grarup N; Jørgensen ME; Zeggini E; Moltke I; Hansen T; Albrechtsen A
Eur J Hum Genet; 2024 Feb; 32(2):215-223. PubMed ID: 37903942
[TBL] [Abstract][Full Text] [Related]
43. Identification of Key Long Non-Coding RNAs in the Pathology of Alzheimer's Disease and their Functions Based on Genome-Wide Associations Study, Microarray, and RNA-seq Data.
Han Z; Xue W; Tao L; Zhu F
J Alzheimers Dis; 2019; 68(1):339-355. PubMed ID: 30776002
[TBL] [Abstract][Full Text] [Related]
44. The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.
Wang Z; Choi SW; Chami N; Boerwinkle E; Fornage M; Redline S; Bis JC; Brody JA; Psaty BM; Kim W; McDonald MN; Regan EA; Silverman EK; Liu CT; Vasan RS; Kalyani RR; Mathias RA; Yanek LR; Arnett DK; Justice AE; North KE; Kaplan R; Heckbert SR; de Andrade M; Guo X; Lange LA; Rich SS; Rotter JI; Ellinor PT; Lubitz SA; Blangero J; Shoemaker MB; Darbar D; Gladwin MT; Albert CM; Chasman DI; Jackson RD; Kooperberg C; Reiner AP; O'Reilly PF; Loos RJF
Front Endocrinol (Lausanne); 2022; 13():863893. PubMed ID: 35592775
[TBL] [Abstract][Full Text] [Related]
45. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.
Spracklen CN; Chen P; Kim YJ; Wang X; Cai H; Li S; Long J; Wu Y; Wang YX; Takeuchi F; Wu JY; Jung KJ; Hu C; Akiyama K; Zhang Y; Moon S; Johnson TA; Li H; Dorajoo R; He M; Cannon ME; Roman TS; Salfati E; Lin KH; Guo X; Sheu WHH; Absher D; Adair LS; Assimes TL; Aung T; Cai Q; Chang LC; Chen CH; Chien LH; Chuang LM; Chuang SC; Du S; Fan Q; Fann CSJ; Feranil AB; Friedlander Y; Gordon-Larsen P; Gu D; Gui L; Guo Z; Heng CK; Hixson J; Hou X; Hsiung CA; Hu Y; Hwang MY; Hwu CM; Isono M; Juang JJ; Khor CC; Kim YK; Koh WP; Kubo M; Lee IT; Lee SJ; Lee WJ; Liang KW; Lim B; Lim SH; Liu J; Nabika T; Pan WH; Peng H; Quertermous T; Sabanayagam C; Sandow K; Shi J; Sun L; Tan PC; Tan SP; Taylor KD; Teo YY; Toh SA; Tsunoda T; van Dam RM; Wang A; Wang F; Wang J; Wei WB; Xiang YB; Yao J; Yuan JM; Zhang R; Zhao W; Chen YI; Rich SS; Rotter JI; Wang TD; Wu T; Lin X; Han BG; Tanaka T; Cho YS; Katsuya T; Jia W; Jee SH; Chen YT; Kato N; Jonas JB; Cheng CY; Shu XO; He J; Zheng W; Wong TY; Huang W; Kim BJ; Tai ES; Mohlke KL; Sim X
Hum Mol Genet; 2017 May; 26(9):1770-1784. PubMed ID: 28334899
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.
Natarajan P; Peloso GM; Zekavat SM; Montasser M; Ganna A; Chaffin M; Khera AV; Zhou W; Bloom JM; Engreitz JM; Ernst J; O'Connell JR; Ruotsalainen SE; Alver M; Manichaikul A; Johnson WC; Perry JA; Poterba T; Seed C; Surakka IL; Esko T; Ripatti S; Salomaa V; Correa A; Vasan RS; Kellis M; Neale BM; Lander ES; Abecasis G; Mitchell B; Rich SS; Wilson JG; Cupples LA; Rotter JI; Willer CJ; Kathiresan S;
Nat Commun; 2018 Aug; 9(1):3391. PubMed ID: 30140000
[TBL] [Abstract][Full Text] [Related]
48. Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.
Seyerle AA; Laurie CA; Coombes BJ; Jain D; Conomos MP; Brody J; Chen MH; Gogarten SM; Beutel KM; Gupta N; Heckbert SR; Jackson RD; Johnson AD; Ko D; Manson JE; McKnight B; Metcalf GA; Morrison AC; Reiner AP; Sofer T; Tang W; Wiggins KL; ; Boerwinkle E; de Andrade M; Gabriel SB; Gibbs RA; Laurie CC; Psaty BM; Vasan RS; Rice K; Kooperberg C; Pankow JS; Smith NL; Pankratz N
Circ Genom Precis Med; 2023 Apr; 16(2):e003532. PubMed ID: 36960714
[TBL] [Abstract][Full Text] [Related]
49. Pleiotropy informed adaptive association test of multiple traits using genome-wide association study summary data.
Masotti M; Guo B; Wu B
Biometrics; 2019 Dec; 75(4):1076-1085. PubMed ID: 31021400
[TBL] [Abstract][Full Text] [Related]
50. A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders.
Ghanbari M; Peters MJ; de Vries PS; Boer CG; van Rooij JGJ; Lee YC; Kumar V; Uitterlinden AG; Ikram MA; Wijmenga C; Ordovas JM; Smith CE; van Meurs JBJ; Erkeland SJ; Franco OH; Dehghan A
J Hum Genet; 2018 Apr; 63(4):431-446. PubMed ID: 29382920
[TBL] [Abstract][Full Text] [Related]
51. Coding-sequence variants are associated with blood lipid levels in 14,473 Chinese.
Lu X; Li J; Li H; Chen Y; Wang L; He M; Wang Y; Sun L; Hu Y; Huang J; Wang F; Liu X; Chen S; Yu K; Yang X; Mo Z; Lin X; Wu T; Gu D
Hum Mol Genet; 2016 Sep; 25(18):4107-4116. PubMed ID: 27516387
[TBL] [Abstract][Full Text] [Related]
52. Identification of novel rare variants for anxiety: an exome-wide association study in the UK Biobank.
Pan C; Cheng S; Liu L; Chen Y; Meng P; Yang X; Li C; Zhang J; Zhang Z; Zhang H; Cheng B; Wen Y; Jia Y; Zhang F
Prog Neuropsychopharmacol Biol Psychiatry; 2024 Mar; 130():110928. PubMed ID: 38154517
[TBL] [Abstract][Full Text] [Related]
53. Multiplexed Targeted Resequencing Identifies Coding and Regulatory Variation Underlying Phenotypic Extremes of High-Density Lipoprotein Cholesterol in Humans.
Khetarpal SA; Babb PL; Zhao W; Hancock-Cerutti WF; Brown CD; Rader DJ; Voight BF
Circ Genom Precis Med; 2018 Jul; 11(7):e002070. PubMed ID: 29987113
[TBL] [Abstract][Full Text] [Related]
54. Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels.
Wang Z; Chen H; Bartz TM; Bielak LF; Chasman DI; Feitosa MF; Franceschini N; Guo X; Lim E; Noordam R; Richard MA; Wang H; Cade B; Cupples LA; de Vries PS; Giulanini F; Lee J; Lemaitre RN; Martin LW; Reiner AP; Rich SS; Schreiner PJ; Sidney S; Sitlani CM; Smith JA; Willems van Dijk K; Yao J; Zhao W; Fornage M; Kardia SLR; Kooperberg C; Liu CT; Mook-Kanamori DO; Province MA; Psaty BM; Redline S; Ridker PM; Rotter JI; Boerwinkle E; Morrison AC;
Circ Genom Precis Med; 2020 Aug; 13(4):e002772. PubMed ID: 32510982
[TBL] [Abstract][Full Text] [Related]
55. Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants.
Zhao X; Qiao D; Yang C; Kasela S; Kim W; Ma Y; Shrine N; Batini C; Sofer T; Taliun SAG; Sakornsakolpat P; Balte PP; Prokopenko D; Yu B; Lange LA; Dupuis J; Cade BE; Lee J; Gharib SA; Daya M; Laurie CA; Ruczinski I; Cupples LA; Loehr LR; Bartz TM; Morrison AC; Psaty BM; Vasan RS; Wilson JG; Taylor KD; Durda P; Johnson WC; Cornell E; Guo X; Liu Y; Tracy RP; Ardlie KG; Aguet F; VanDenBerg DJ; Papanicolaou GJ; Rotter JI; Barnes KC; Jain D; Nickerson DA; Muzny DM; Metcalf GA; Doddapaneni H; Dugan-Perez S; Gupta N; Gabriel S; Rich SS; O'Connor GT; Redline S; Reed RM; Laurie CC; Daviglus ML; Preudhomme LK; Burkart KM; Kaplan RC; Wain LV; Tobin MD; London SJ; Lappalainen T; Oelsner EC; Abecasis GR; Silverman EK; Barr RG; ; ; Cho MH; Manichaikul A
Nat Commun; 2020 Oct; 11(1):5182. PubMed ID: 33057025
[TBL] [Abstract][Full Text] [Related]
56. Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
Prokopenko D; Sakornsakolpat P; Fier HL; Qiao D; Parker MM; McDonald MN; Manichaikul A; Rich SS; Barr RG; Williams CJ; Brantly ML; Lange C; Beaty TH; Crapo JD; Silverman EK; Cho MH
Am J Respir Cell Mol Biol; 2018 Nov; 59(5):614-622. PubMed ID: 29949718
[TBL] [Abstract][Full Text] [Related]
57. Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank.
Nag A; Dhindsa RS; Middleton L; Jiang X; Vitsios D; Wigmore E; Allman EL; Reznichenko A; Carss K; Smith KR; Wang Q; Challis B; Paul DS; Harper AR; Petrovski S
Am J Hum Genet; 2023 Mar; 110(3):487-498. PubMed ID: 36809768
[TBL] [Abstract][Full Text] [Related]
58. Effects of GWAS-associated genetic variants on lncRNAs within IBD and T1D candidate loci.
Mirza AH; Kaur S; Brorsson CA; Pociot F
PLoS One; 2014; 9(8):e105723. PubMed ID: 25144376
[TBL] [Abstract][Full Text] [Related]
59. Methods for the Analysis and Interpretation for Rare Variants Associated with Complex Traits.
Weissenkampen JD; Jiang Y; Eckert S; Jiang B; Li B; Liu DJ
Curr Protoc Hum Genet; 2019 Apr; 101(1):e83. PubMed ID: 30849219
[TBL] [Abstract][Full Text] [Related]
60. Distinct patterns of genetic variations in potential functional elements in long noncoding RNAs.
Bhartiya D; Jalali S; Ghosh S; Scaria V
Hum Mutat; 2014 Feb; 35(2):192-201. PubMed ID: 24178912
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
