73 related articles for article (PubMed ID: 11968082)
1. GeneTests-GeneClinics: genetic testing information for a growing audience.
Pagon RA; Tarczy-Hornoch P; Baskin PK; Edwards JE; Covington ML; Espeseth M; Beahler C; Bird TD; Popovich B; Nesbitt C; Dolan C; Marymee K; Hanson NB; Neufeld-Kaiser W; Grohs GM; Kicklighter T; Abair C; Malmin A; Barclay M; Palepu RD
Hum Mutat; 2002 May; 19(5):501-9. PubMed ID: 11968082
[TBL] [Abstract][Full Text] [Related]
2. Recent developments in genomewide association scans: a workshop summary and review.
Thomas DC; Haile RW; Duggan D
Am J Hum Genet; 2005 Sep; 77(3):337-45. PubMed ID: 16080110
[TBL] [Abstract][Full Text] [Related]
3. ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden.
Sharo AG; Zou Y; Adhikari AN; Brenner SE
Genome Med; 2023 Jul; 15(1):51. PubMed ID: 37443081
[TBL] [Abstract][Full Text] [Related]
4. Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing.
Mackay ZP; Dukhovny D; Phillips KA; Beggs AH; Green RC; Parad RB; Christensen KD;
Value Health; 2020 May; 23(5):559-565. PubMed ID: 32389220
[TBL] [Abstract][Full Text] [Related]
5. VIPdb, a genetic Variant Impact Predictor Database.
Hu Z; Yu C; Furutsuki M; Andreoletti G; Ly M; Hoskins R; Adhikari AN; Brenner SE
Hum Mutat; 2019 Sep; 40(9):1202-1214. PubMed ID: 31283070
[TBL] [Abstract][Full Text] [Related]
6. Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project.
Christensen KD; Phillips KA; Green RC; Dukhovny D
Value Health; 2018 Sep; 21(9):1054-1061. PubMed ID: 30224109
[TBL] [Abstract][Full Text] [Related]
7. Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.
Christensen KD; Vassy JL; Phillips KA; Blout CL; Azzariti DR; Lu CY; Robinson JO; Lee K; Douglas MP; Yeh JM; Machini K; Stout NK; Rehm HL; McGuire AL; Green RC; Dukhovny D;
Genet Med; 2018 Dec; 20(12):1544-1553. PubMed ID: 29565423
[TBL] [Abstract][Full Text] [Related]
8. A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.
Overby CL; Rasmussen LV; Hartzler A; Connolly JJ; Peterson JF; Hedberg RE; Freimuth RR; Shirts BH; Denny JC; Larson EB; Chute CG; Jarvik GP; Ralston JD; Shuldiner AR; Starren J; Kullo IJ; Tarczy-Hornoch P; Williams MS
AMIA Annu Symp Proc; 2014; 2014():944-53. PubMed ID: 25954402
[TBL] [Abstract][Full Text] [Related]
9. Use of contemporary genetics in cardiovascular diagnosis.
George AL
Circulation; 2014 Nov; 130(22):1971-80. PubMed ID: 25421045
[TBL] [Abstract][Full Text] [Related]
10. Text mining in cancer gene and pathway prioritization.
Luo Y; Riedlinger G; Szolovits P
Cancer Inform; 2014; 13(Suppl 1):69-79. PubMed ID: 25392685
[TBL] [Abstract][Full Text] [Related]
11. A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record.
Tarczy-Hornoch P; Amendola L; Aronson SJ; Garraway L; Gray S; Grundmeier RW; Hindorff LA; Jarvik G; Karavite D; Lebo M; Plon SE; Van Allen E; Weck KE; White PS; Yang Y
Genet Med; 2013 Oct; 15(10):824-32. PubMed ID: 24071794
[TBL] [Abstract][Full Text] [Related]
12. Personalized medicine: challenges and opportunities for translational bioinformatics.
Overby CL; Tarczy-Hornoch P
Per Med; 2013 Jul; 10(5):453-462. PubMed ID: 24039624
[TBL] [Abstract][Full Text] [Related]
13. Development of korean rare disease knowledge base.
Seo H; Kim D; Chae JH; Kang HG; Lim BC; Cheong HI; Kim JH
Healthc Inform Res; 2012 Dec; 18(4):272-8. PubMed ID: 23346478
[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. The UCSC Genome Browser database: extensions and updates 2013.
Meyer LR; Zweig AS; Hinrichs AS; Karolchik D; Kuhn RM; Wong M; Sloan CA; Rosenbloom KR; Roe G; Rhead B; Raney BJ; Pohl A; Malladi VS; Li CH; Lee BT; Learned K; Kirkup V; Hsu F; Heitner S; Harte RA; Haeussler M; Guruvadoo L; Goldman M; Giardine BM; Fujita PA; Dreszer TR; Diekhans M; Cline MS; Clawson H; Barber GP; Haussler D; Kent WJ
Nucleic Acids Res; 2013 Jan; 41(Database issue):D64-9. PubMed ID: 23155063
[TBL] [Abstract][Full Text] [Related]
16. EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease.
Losekoot M; van Belzen MJ; Seneca S; Bauer P; Stenhouse SA; Barton DE;
Eur J Hum Genet; 2013 May; 21(5):480-6. PubMed ID: 22990145
[TBL] [Abstract][Full Text] [Related]
17. The UCSC genome browser and associated tools.
Kuhn RM; Haussler D; Kent WJ
Brief Bioinform; 2013 Mar; 14(2):144-61. PubMed ID: 22908213
[TBL] [Abstract][Full Text] [Related]
18. The genetics and neuropathology of neurodegenerative disorders: perspectives and implications for research and clinical practice.
Van Deerlin VM
Acta Neuropathol; 2012 Sep; 124(3):297-303. PubMed ID: 22875012
[No Abstract] [Full Text] [Related]
19. Translational bioinformatics: linking knowledge across biological and clinical realms.
Sarkar IN; Butte AJ; Lussier YA; Tarczy-Hornoch P; Ohno-Machado L
J Am Med Inform Assoc; 2011; 18(4):354-7. PubMed ID: 21561873
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]