William Allan Award Address: On the role and soul of a statistical geneticist.
作者信息
Ott Jürg
机构信息
Institute of Psychology, Chinese Academy of Sciences, Beijing, China.
出版信息
Am J Hum Genet. 2011 Mar 11;88(3):264-8. doi: 10.1016/j.ajhg.2011.02.013.
Abstract
摘要
相似文献
1
William Allan Award Address: On the role and soul of a statistical geneticist.
Am J Hum Genet. 2011 Mar 11;88(3):264-8. doi: 10.1016/j.ajhg.2011.02.013.
2
2006 William Allan Award Address. Introductory speech for Dorothy Warburton.
Am J Hum Genet. 2007 Oct;81(4):646-7. doi: 10.1086/521403.
3
2006 William Allan Award Address. Having it all.
Am J Hum Genet. 2007 Oct;81(4):648-56. doi: 10.1086/521405.
4
2016 William Allan Award: Human Disease Research: Genetic Cycling and Re-cycling.
Am J Hum Genet. 2017 Mar 2;100(3):387-394. doi: 10.1016/j.ajhg.2017.01.008.
5
2017 William Allan Award.
Am J Hum Genet. 2018 Mar 1;102(3):351-353. doi: 10.1016/j.ajhg.2018.01.012.
6
2016 William Allan Award Introduction: James Gusella.
Am J Hum Genet. 2017 Mar 2;100(3):385-386. doi: 10.1016/j.ajhg.2017.01.016.
7
2005 William Allan Award address. Introductory speech for Francis S. Collins.
Am J Hum Genet. 2006 Sep;79(3):419-20. doi: 10.1086/500276.
8
2005 William Allan Award address. No longer just looking under the lamppost.
Am J Hum Genet. 2006 Sep;79(3):421-6. doi: 10.1086/507611.
9
2017 William Allan Award Introduction: Kári Stefansson.
Am J Hum Genet. 2018 Mar 1;102(3):350. doi: 10.1016/j.ajhg.2018.01.010.
10
2014 William Allan Award introduction: Stuart Orkin.
Am J Hum Genet. 2015 Mar 5;96(3):352-3. doi: 10.1016/j.ajhg.2014.11.018.
本文引用的文献
1
Systematic removal of outliers to reduce heterogeneity in case-control association studies.
Hum Hered. 2010;70(4):227-31. doi: 10.1159/000320422. Epub 2010 Oct 6.
2
Associations of six single nucleotide polymorphisms in obesity-related genes with BMI and risk of obesity in Chinese children.
Diabetes. 2010 Dec;59(12):3085-9. doi: 10.2337/db10-0273. Epub 2010 Sep 15.
3
China's research culture.
Science. 2010 Sep 3;329(5996):1128. doi: 10.1126/science.1196916.
4
Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer.
Pharmacogenet Genomics. 2010 Jun;20(6):389-95. doi: 10.1097/FPC.0b013e32833a6890.
5
Genome-wide conditional search for epistatic disease-predisposing variants in human association studies.
Hum Hered. 2010;70(1):34-41. doi: 10.1159/000293722. Epub 2010 Apr 23.
6
Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16.
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S96. doi: 10.1186/1753-6561-3-s7-s96.
7
Recent decline in nonpaternity rates: a cross-temporal meta-analysis.
Psychol Rep. 2008 Dec;103(3):799-811. doi: 10.2466/pr0.103.3.799-811.
8
Detecting disease-associated genotype patterns.
BMC Bioinformatics. 2009 Jan 30;10 Suppl 1(Suppl 1):S75. doi: 10.1186/1471-2105-10-S1-S75.
9
Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus.
Invest Ophthalmol Vis Sci. 2009 Feb;50(2):654-61. doi: 10.1167/iovs.08-2437. Epub 2008 Sep 29.
10
Collapsing SNP genotypes in case-control genome-wide association studies increases the type I error rate and power.
Stat Appl Genet Mol Biol. 2008;7(1):Article23. doi: 10.2202/1544-6115.1325. Epub 2008 Jul 25.
Zotero 插件