1660 related articles for article (PubMed ID: 24234437)
1. ClinVar: public archive of relationships among sequence variation and human phenotype.
Landrum MJ; Lee JM; Riley GR; Jang W; Rubinstein WS; Church DM; Maglott DR
Nucleic Acids Res; 2014 Jan; 42(Database issue):D980-5. PubMed ID: 24234437
[TBL] [Abstract][Full Text] [Related]
2. ClinVar: public archive of interpretations of clinically relevant variants.
Landrum MJ; Lee JM; Benson M; Brown G; Chao C; Chitipiralla S; Gu B; Hart J; Hoffman D; Hoover J; Jang W; Katz K; Ovetsky M; Riley G; Sethi A; Tully R; Villamarin-Salomon R; Rubinstein W; Maglott DR
Nucleic Acids Res; 2016 Jan; 44(D1):D862-8. PubMed ID: 26582918
[TBL] [Abstract][Full Text] [Related]
3. ClinVar: improvements to accessing data.
Landrum MJ; Chitipiralla S; Brown GR; Chen C; Gu B; Hart J; Hoffman D; Jang W; Kaur K; Liu C; Lyoshin V; Maddipatla Z; Maiti R; Mitchell J; O'Leary N; Riley GR; Shi W; Zhou G; Schneider V; Maglott D; Holmes JB; Kattman BL
Nucleic Acids Res; 2020 Jan; 48(D1):D835-D844. PubMed ID: 31777943
[TBL] [Abstract][Full Text] [Related]
4. ClinVar: improving access to variant interpretations and supporting evidence.
Landrum MJ; Lee JM; Benson M; Brown GR; Chao C; Chitipiralla S; Gu B; Hart J; Hoffman D; Jang W; Karapetyan K; Katz K; Liu C; Maddipatla Z; Malheiro A; McDaniel K; Ovetsky M; Riley G; Zhou G; Holmes JB; Kattman BL; Maglott DR
Nucleic Acids Res; 2018 Jan; 46(D1):D1062-D1067. PubMed ID: 29165669
[TBL] [Abstract][Full Text] [Related]
5. Using ClinVar as a Resource to Support Variant Interpretation.
Harrison SM; Riggs ER; Maglott DR; Lee JM; Azzariti DR; Niehaus A; Ramos EM; Martin CL; Landrum MJ; Rehm HL
Curr Protoc Hum Genet; 2016 Apr; 89():8.16.1-8.16.23. PubMed ID: 27037489
[TBL] [Abstract][Full Text] [Related]
6. Database resources of the National Center for Biotechnology Information.
NCBI Resource Coordinators
Nucleic Acids Res; 2014 Jan; 42(Database issue):D7-17. PubMed ID: 24259429
[TBL] [Abstract][Full Text] [Related]
7. The value of genomic variant ClinVar submissions from clinical providers: Beyond the addition of novel variants.
Wain KE; Palen E; Savatt JM; Shuman D; Finucane B; Seeley A; Challman TD; Myers SM; Martin CL
Hum Mutat; 2018 Nov; 39(11):1660-1667. PubMed ID: 30311381
[TBL] [Abstract][Full Text] [Related]
8. Database resources of the National Center for Biotechnology Information.
NCBI Resource Coordinators
Nucleic Acids Res; 2015 Jan; 43(Database issue):D6-17. PubMed ID: 25398906
[TBL] [Abstract][Full Text] [Related]
9. ClinVar at five years: Delivering on the promise.
Landrum MJ; Kattman BL
Hum Mutat; 2018 Nov; 39(11):1623-1630. PubMed ID: 30311387
[TBL] [Abstract][Full Text] [Related]
10. ClinVar database of global familial hypercholesterolemia-associated DNA variants.
Iacocca MA; Chora JR; Carrié A; Freiberger T; Leigh SE; Defesche JC; Kurtz CL; DiStefano MT; Santos RD; Humphries SE; Mata P; Jannes CE; Hooper AJ; Wilemon KA; Benlian P; O'Connor R; Garcia J; Wand H; Tichy L; Sijbrands EJ; Hegele RA; Bourbon M; Knowles JW;
Hum Mutat; 2018 Nov; 39(11):1631-1640. PubMed ID: 30311388
[TBL] [Abstract][Full Text] [Related]
11. Database resources of the National Center for Biotechnology Information.
Sayers EW; Beck J; Bolton EE; Brister JR; Chan J; Comeau DC; Connor R; DiCuccio M; Farrell CM; Feldgarden M; Fine AM; Funk K; Hatcher E; Hoeppner M; Kane M; Kannan S; Katz KS; Kelly C; Klimke W; Kim S; Kimchi A; Landrum M; Lathrop S; Lu Z; Malheiro A; Marchler-Bauer A; Murphy TD; Phan L; Prasad AB; Pujar S; Sawyer A; Schmieder E; Schneider VA; Schoch CL; Sharma S; Thibaud-Nissen F; Trawick BW; Venkatapathi T; Wang J; Pruitt KD; Sherry ST
Nucleic Acids Res; 2024 Jan; 52(D1):D33-D43. PubMed ID: 37994677
[TBL] [Abstract][Full Text] [Related]
12. ClinVar Miner: Demonstrating utility of a Web-based tool for viewing and filtering ClinVar data.
Henrie A; Hemphill SE; Ruiz-Schultz N; Cushman B; DiStefano MT; Azzariti D; Harrison SM; Rehm HL; Eilbeck K
Hum Mutat; 2018 Aug; 39(8):1051-1060. PubMed ID: 29790234
[TBL] [Abstract][Full Text] [Related]
13. NCBI GEO: archive for functional genomics data sets--update.
Barrett T; Wilhite SE; Ledoux P; Evangelista C; Kim IF; Tomashevsky M; Marshall KA; Phillippy KH; Sherman PM; Holko M; Yefanov A; Lee H; Zhang N; Robertson CL; Serova N; Davis S; Soboleva A
Nucleic Acids Res; 2013 Jan; 41(Database issue):D991-5. PubMed ID: 23193258
[TBL] [Abstract][Full Text] [Related]
14. The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency.
Rubinstein WS; Maglott DR; Lee JM; Kattman BL; Malheiro AJ; Ovetsky M; Hem V; Gorelenkov V; Song G; Wallin C; Husain N; Chitipiralla S; Katz KS; Hoffman D; Jang W; Johnson M; Karmanov F; Ukrainchik A; Denisenko M; Fomous C; Hudson K; Ostell JM
Nucleic Acids Res; 2013 Jan; 41(Database issue):D925-35. PubMed ID: 23193275
[TBL] [Abstract][Full Text] [Related]
15. Database resources of the National Center for Biotechnology Information.
NCBI Resource Coordinators
Nucleic Acids Res; 2016 Jan; 44(D1):D7-19. PubMed ID: 26615191
[TBL] [Abstract][Full Text] [Related]
16. dbSNP: the NCBI database of genetic variation.
Sherry ST; Ward MH; Kholodov M; Baker J; Phan L; Smigielski EM; Sirotkin K
Nucleic Acids Res; 2001 Jan; 29(1):308-11. PubMed ID: 11125122
[TBL] [Abstract][Full Text] [Related]
17. Go!Poly: A gene-oriented polymorphism database.
Zhang G; Zhang S; Chen W; Qiu W; Wu H; Wang J; Luo J; Gu X; Cotton RG
Hum Mutat; 2001 Nov; 18(5):382-7. PubMed ID: 11668631
[TBL] [Abstract][Full Text] [Related]
18. tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.
Wei CH; Phan L; Feltz J; Maiti R; Hefferon T; Lu Z
Bioinformatics; 2018 Jan; 34(1):80-87. PubMed ID: 28968638
[TBL] [Abstract][Full Text] [Related]
19. Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database.
Pérez-Palma E; Gramm M; Nürnberg P; May P; Lal D
Nucleic Acids Res; 2019 Jul; 47(W1):W99-W105. PubMed ID: 31114901
[TBL] [Abstract][Full Text] [Related]
20. SPDI: data model for variants and applications at NCBI.
Holmes JB; Moyer E; Phan L; Maglott D; Kattman B
Bioinformatics; 2020 Mar; 36(6):1902-1907. PubMed ID: 31738401
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
