These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Developing the "next generation" of genetic association databases for complex diseases. Lill CM; Bertram L Hum Mutat; 2012 Sep; 33(9):1366-72. PubMed ID: 22752977 [TBL] [Abstract][Full Text] [Related]
4. A two-platform design for next generation genome-wide association studies. Sampson JN; Jacobs K; Wang Z; Yeager M; Chanock S; Chatterjee N Genet Epidemiol; 2012 May; 36(4):400-8. PubMed ID: 22508365 [TBL] [Abstract][Full Text] [Related]
10. Amyotrophic Lateral Sclerosis Genetic Studies: From Genome-wide Association Mapping to Genome Sequencing. He J; Mangelsdorf M; Fan D; Bartlett P; Brown MA Neuroscientist; 2015 Dec; 21(6):599-615. PubMed ID: 25378359 [TBL] [Abstract][Full Text] [Related]
11. [Future prospects of molecular epidemiology in tuberculosis]. Matsumoto T; Iwamoto T Kekkaku; 2009 Dec; 84(12):783-4. PubMed ID: 20077862 [TBL] [Abstract][Full Text] [Related]
12. Common statistical issues in genome-wide association studies: a review on power, data quality control, genotype calling and population structure. Teo YY Curr Opin Lipidol; 2008 Apr; 19(2):133-43. PubMed ID: 18388693 [TBL] [Abstract][Full Text] [Related]
13. Human genome sequence variation and the search for genes influencing stroke. Rosand J; Altshuler D Stroke; 2003 Oct; 34(10):2512-6. PubMed ID: 14500931 [TBL] [Abstract][Full Text] [Related]
15. Genetic approaches to studying common diseases and complex traits. Hirschhorn JN Pediatr Res; 2005 May; 57(5 Pt 2):74R-77R. PubMed ID: 15817501 [TBL] [Abstract][Full Text] [Related]
16. Shared genetic factors for age at natural menopause in Iranian and European women. Rahmani M; Earp MA; Ramezani Tehrani F; Ataee M; Wu J; Treml M; Nudischer R; P-Behnami S; ; Perry JR; Murabito JM; Azizi F; Brooks-Wilson A Hum Reprod; 2013 Jul; 28(7):1987-94. PubMed ID: 23592221 [TBL] [Abstract][Full Text] [Related]
17. Strategies to identify genes for complex disorders: a focus on bipolar disorder and chromosome 16p. Byerley W; Badner JA Psychiatr Genet; 2011 Aug; 21(4):173-82. PubMed ID: 20453718 [TBL] [Abstract][Full Text] [Related]
18. The challenge for the next generation of medical geneticists. Frebourg T Hum Mutat; 2014 Aug; 35(8):909-11. PubMed ID: 24838402 [TBL] [Abstract][Full Text] [Related]
19. Unravelling the human genome-phenome relationship using phenome-wide association studies. Bush WS; Oetjens MT; Crawford DC Nat Rev Genet; 2016 Mar; 17(3):129-45. PubMed ID: 26875678 [TBL] [Abstract][Full Text] [Related]
20. On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test. Ionita-Laza I; Perry GH; Raby BA; Klanderman B; Lee C; Laird NM; Weiss ST; Lange C Genet Epidemiol; 2008 Apr; 32(3):273-84. PubMed ID: 18228561 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]