Literature DB >> 15598223

Replication in genetic studies of complex traits.

M J Sillanpää1, K Auranen.   

Abstract

Disappointments in replicating initial findings in gene mapping for complex traits are often attributed to small sample sizes and inadequate techniques to determine the threshold value. This is clearly not the whole truth. More fundamental reasons lie in the inherent heterogeneity related to disease, including genetic heterogeneity, differences in allele frequencies, and context-dependency in genetic architecture. There are also other reasons related to the data collection and analysis. Replication may remain a source of frustration unless more emphasis is put on controlling these sources of heterogeneity between studies.

Mesh:

Year:  2004        PMID: 15598223     DOI: 10.1046/j.1529-8817.2004.00122.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  19 in total

Review 1.  Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses.

Authors:  M J Sillanpää
Journal:  Heredity (Edinb)       Date:  2010-07-14       Impact factor: 3.821

2.  Association mapping of complex trait loci with context-dependent effects and unknown context variable.

Authors:  Mikko J Sillanpää; Madhuchhanda Bhattacharjee
Journal:  Genetics       Date:  2006-10-08       Impact factor: 4.562

Review 3.  Genome-wide association studies: progress and potential for drug discovery and development.

Authors:  Stephen F Kingsmore; Ingrid E Lindquist; Joann Mudge; Damian D Gessler; William D Beavis
Journal:  Nat Rev Drug Discov       Date:  2008-03       Impact factor: 84.694

4.  Multivariate analysis of regulatory SNPs: empowering personal genomics by considering cis-epistasis and heterogeneity.

Authors:  Stephen D Turner; William S Bush
Journal:  Pac Symp Biocomput       Date:  2011

5.  Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder.

Authors:  Huijuan Li; Hong Chang; Xueqin Song; Weipeng Liu; Lingyi Li; Lu Wang; Yongfeng Yang; Luwen Zhang; Wenqiang Li; Yan Zhang; Dong-Sheng Zhou; Xingxing Li; Chen Zhang; Yiru Fang; Yan Sun; Jia-Pei Dai; Xiong-Jian Luo; Yong-Gang Yao; Xiao Xiao; Luxian Lv; Ming Li
Journal:  Neuropsychopharmacology       Date:  2019-02-16       Impact factor: 7.853

6.  Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease.

Authors:  Joseph H Lee; Rong Cheng; Ekaterina Rogaeva; Yan Meng; Yaakov Stern; Vincent Santana; Rafael Lantigua; Martin Medrano; Ivonne Z Jimenez-Velazquez; Lindsay A Farrer; Peter St George-Hyslop; Richard Mayeux
Journal:  Neurogenetics       Date:  2008-03-14       Impact factor: 2.660

7.  Maternal-zygotic epistasis and the evolution of genetic diseases.

Authors:  Nicholas K Priest; Michael J Wade
Journal:  J Biomed Biotechnol       Date:  2010-05-10

8.  Genome-wide association studies: progress in identifying genetic biomarkers in common, complex diseases.

Authors:  Stephen F Kingsmore; Ingrid E Lindquist; Joann Mudge; William D Beavis
Journal:  Biomark Insights       Date:  2007-08-08

Review 9.  Brain-derived neurotrophic factor as a model system for examining gene by environment interactions across development.

Authors:  B J Casey; C E Glatt; N Tottenham; F Soliman; K Bath; D Amso; M Altemus; S Pattwell; R Jones; L Levita; B McEwen; A M Magariños; M Gunnar; K M Thomas; J Mezey; A G Clark; B L Hempstead; F S Lee
Journal:  Neuroscience       Date:  2009-04-07       Impact factor: 3.590

Review 10.  To replicate or not to replicate: the case of pharmacogenetic studies: Establishing validity of pharmacogenomic findings: from replication to triangulation.

Authors:  Stella Aslibekyan; Steven A Claas; Donna K Arnett
Journal:  Circ Cardiovasc Genet       Date:  2013-08
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