110 related articles for article (PubMed ID: 38561338)
1. Genetic factors in pediatric venous thromboembolism.
Rühle F; Stoll M
Thromb Res; 2017 Mar; 151 Suppl 1():S97-S99. PubMed ID: 28262245
[TBL] [Abstract][Full Text] [Related]
2. Ethnic diversity in the genetics of venous thromboembolism.
Tang L; Hu Y
Thromb Haemost; 2015 Nov; 114(5):901-9. PubMed ID: 26156046
[TBL] [Abstract][Full Text] [Related]
3. Genetic associations of protein-coding variants in venous thromboembolism.
He XY; Wu BS; Yang L; Guo Y; Deng YT; Li ZY; Fei CJ; Liu WS; Ge YJ; Kang J; Feng J; Cheng W; Dong Q; Yu JT
Nat Commun; 2024 Apr; 15(1):2819. PubMed ID: 38561338
[TBL] [Abstract][Full Text] [Related]
4. Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study.
Tang W; Stimson MR; Basu S; Heckbert SR; Cushman M; Pankow JS; Folsom AR; Pankratz N
J Thromb Haemost; 2020 Feb; 18(2):445-453. PubMed ID: 31680443
[TBL] [Abstract][Full Text] [Related]
5. Whole exome sequencing identifies genetic variants in Chinese Han pregnant women with venous thromboembolism.
Shen Y; Zhang Y; Xiong Y; Zhang Z; Zhang B; Li A; Zhang Z; Ding J; Du J; Che Y
Thromb Res; 2022 Mar; 211():49-55. PubMed ID: 35074609
[TBL] [Abstract][Full Text] [Related]
6. Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.
Thibord F; Klarin D; Brody JA; Chen MH; Levin MG; Chasman DI; Goode EL; Hveem K; Teder-Laving M; Martinez-Perez A; Aïssi D; Daian-Bacq D; Ito K; Natarajan P; Lutsey PL; Nadkarni GN; de Vries PS; Cuellar-Partida G; Wolford BN; Pattee JW; Kooperberg C; Braekkan SK; Li-Gao R; Saut N; Sept C; Germain M; Judy RL; Wiggins KL; Ko D; O'Donnell CJ; Taylor KD; Giulianini F; De Andrade M; Nøst TH; Boland A; Empana JP; Koyama S; Gilliland T; Do R; Huffman JE; Wang X; Zhou W; Manuel Soria J; Carlos Souto J; Pankratz N; Haessler J; Hindberg K; Rosendaal FR; Turman C; Olaso R; Kember RL; Bartz TM; Lynch JA; Heckbert SR; Armasu SM; Brumpton B; Smadja DM; Jouven X; Komuro I; Clapham KR; Loos RJF; Willer CJ; Sabater-Lleal M; Pankow JS; Reiner AP; Morelli VM; Ridker PM; Vlieg AVH; Deleuze JF; Kraft P; Rader DJ; ; Min Lee K; Psaty BM; Heidi Skogholt A; Emmerich J; Suchon P; Rich SS; Vy HMT; Tang W; Jackson RD; Hansen JB; Morange PE; Kabrhel C; Trégouët DA; Damrauer SM; Johnson AD; Smith NL
Circulation; 2022 Oct; 146(16):1225-1242. PubMed ID: 36154123
[TBL] [Abstract][Full Text] [Related]
7. A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Tang W; Teichert M; Chasman DI; Heit JA; Morange PE; Li G; Pankratz N; Leebeek FW; Paré G; de Andrade M; Tzourio C; Psaty BM; Basu S; Ruiter R; Rose L; Armasu SM; Lumley T; Heckbert SR; Uitterlinden AG; Lathrop M; Rice KM; Cushman M; Hofman A; Lambert JC; Glazer NL; Pankow JS; Witteman JC; Amouyel P; Bis JC; Bovill EG; Kong X; Tracy RP; Boerwinkle E; Rotter JI; Trégouët DA; Loth DW; Stricker BHC; Ridker PM; Folsom AR; Smith NL
Genet Epidemiol; 2013 Jul; 37(5):512-521. PubMed ID: 23650146
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease.
Desch KC; Ozel AB; Halvorsen M; Jacobi PM; Golden K; Underwood M; Germain M; Tregouet DA; Reitsma PH; Kearon C; Mokry L; Richards JB; Williams F; Li JZ; Goldstein D; Ginsburg D
Blood; 2020 Jul; 136(5):533-541. PubMed ID: 32457982
[TBL] [Abstract][Full Text] [Related]
9. Rare coding variants in CHRNB2 reduce the likelihood of smoking.
Rajagopal VM; Watanabe K; Mbatchou J; Ayer A; Quon P; Sharma D; Kessler MD; Praveen K; Gelfman S; Parikshak N; Otto JM; Bao S; Chim SM; Pavlopoulos E; Avbersek A; Kapoor M; Chen E; Jones MB; Leblanc M; Emberson J; Collins R; Torres J; Morales PK; Tapia-Conyer R; Alegre J; Berumen J; ; ; Shuldiner AR; Balasubramanian S; Abecasis GR; Kang HM; Marchini J; Stahl EA; Jorgenson E; Sanchez R; Liedtke W; Anderson M; Cantor M; Lederer D; Baras A; Coppola G
Nat Genet; 2023 Jul; 55(7):1138-1148. PubMed ID: 37308787
[TBL] [Abstract][Full Text] [Related]
10. Rare penetrant mutations confer severe risk of common diseases.
Fiziev PP; McRae J; Ulirsch JC; Dron JS; Hamp T; Yang Y; Wainschtein P; Ni Z; Schraiber JG; Gao H; Cable D; Field Y; Aguet F; Fasnacht M; Metwally A; Rogers J; Marques-Bonet T; Rehm HL; O'Donnell-Luria A; Khera AV; Farh KK
Science; 2023 Jun; 380(6648):eabo1131. PubMed ID: 37262146
[TBL] [Abstract][Full Text] [Related]
11. The impact of rare protein coding genetic variation on adult cognitive function.
Chen CY; Tian R; Ge T; Lam M; Sanchez-Andrade G; Singh T; Urpa L; Liu JZ; Sanderson M; Rowley C; Ironfield H; Fang T; ; ; ; Daly M; Palotie A; Tsai EA; Huang H; Hurles ME; Gerety SS; Lencz T; Runz H
Nat Genet; 2023 Jun; 55(6):927-938. PubMed ID: 37231097
[TBL] [Abstract][Full Text] [Related]
12.
Usui Y; Taniyama Y; Endo M; Koyanagi YN; Kasugai Y; Oze I; Ito H; Imoto I; Tanaka T; Tajika M; Niwa Y; Iwasaki Y; Aoi T; Hakozaki N; Takata S; Suzuki K; Terao C; Hatakeyama M; Hirata M; Sugano K; Yoshida T; Kamatani Y; Nakagawa H; Matsuda K; Murakami Y; Spurdle AB; Matsuo K; Momozawa Y
N Engl J Med; 2023 Mar; 388(13):1181-1190. PubMed ID: 36988593
[TBL] [Abstract][Full Text] [Related]
13. Polygenic architecture of rare coding variation across 394,783 exomes.
Weiner DJ; Nadig A; Jagadeesh KA; Dey KK; Neale BM; Robinson EB; Karczewski KJ; O'Connor LJ
Nature; 2023 Feb; 614(7948):492-499. PubMed ID: 36755099
[TBL] [Abstract][Full Text] [Related]
14. Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Ghouse J; Tragante V; Ahlberg G; Rand SA; Jespersen JB; Leinøe EB; Vissing CR; Trudsø L; Jonsdottir I; Banasik K; Brunak S; Ostrowski SR; Pedersen OB; Sørensen E; Erikstrup C; Bruun MT; Nielsen KR; Køber L; Christensen AH; Iversen K; Jones D; Knowlton KU; Nadauld L; Halldorsson GH; Ferkingstad E; Olafsson I; Gretarsdottir S; Onundarson PT; Sulem P; Thorsteinsdottir U; Thorgeirsson G; Gudbjartsson DF; Stefansson K; Holm H; Olesen MS; Bundgaard H
Nat Genet; 2023 Mar; 55(3):399-409. PubMed ID: 36658437
[TBL] [Abstract][Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
