相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Genomics of human health and aging
Alexander M. Kulminski et al.
AGE (2013)
FOXP2 Targets Show Evidence of Positive Selection in European Populations
Qasim Ayub et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
Dennis Lal et al.
EPILEPSIA (2013)
Distinguishing true from false positives in genomic studies: p values
Linda Broer et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2013)
Genetic Association With Multiple Traits in the Presence of Population Stratification
Ting Yan et al.
GENETIC EPIDEMIOLOGY (2013)
The Impact of Improved Microarray Coverage and Larger Sample Sizes on Future Genome-Wide Association Studies
Karla J. Lindquist et al.
GENETIC EPIDEMIOLOGY (2013)
Comprehensive candidate gene study highlights UGT1A and BNC2 as new genes determining continuous skin color variation in Europeans
Leonie C. Jacobs et al.
HUMAN GENETICS (2013)
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
Dwight Stambolian et al.
HUMAN MOLECULAR GENETICS (2013)
Darned in 2013: inclusion of model organisms and linking with Wikipedia
Anmol M. Kiran et al.
NUCLEIC ACIDS RESEARCH (2013)
GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications
Mulin Jun Li et al.
NUCLEIC ACIDS RESEARCH (2013)
RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
Dennis Lal et al.
PLOS ONE (2013)
Neutralization of terminal differentiation in gliomagenesis
Jian Hu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Mining the Human Phenome Using Allelic Scores That Index Biological Intermediates
David M. Evans et al.
PLOS GENETICS (2013)
KAREBrowser: SNP database of Korea Association REsource Project
Chang Bum Hong et al.
BMB REPORTS (2012)
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies
Daniah Trabzuni et al.
HUMAN MOLECULAR GENETICS (2012)
RBFOX1 regulates both splicing and transcriptional networks in human neuronal development
Brent L. Fogel et al.
HUMAN MOLECULAR GENETICS (2012)
DistiLD Database: diseases and traits in linkage disequilibrium blocks
Albert Palleja et al.
NUCLEIC ACIDS RESEARCH (2012)
Mechanisms of activation and repression by the alternative splicing factors RBFOX1/2
Shuying Sun et al.
RNA (2012)
Discovery and replication of gene influences on brain structure using LASSO regression
Omid Kohannim et al.
FRONTIERS IN NEUROSCIENCE (2012)
Abundant Pleiotropy in Human Complex Diseases and Traits
Shanya Sivakumaran et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
PRIMe: a method for characterization and evaluation of pleiotropic regions from multiple genome-wide association studies
Jie Huang et al.
BIOINFORMATICS (2011)
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study)
Jens K. Hertel et al.
BMC MEDICAL GENETICS (2011)
A Functional Single Nucleotide Polymorphism in Mucin 1, at Chromosome 1q22, Determines Susceptibility to Diffuse-Type Gastric Cancer
Norihisa Saeki et al.
GASTROENTEROLOGY (2011)
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses
Moran N. Cabili et al.
GENES & DEVELOPMENT (2011)
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population
Mohamad Saad et al.
HUMAN MOLECULAR GENETICS (2011)
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Chris C. A. Spencer et al.
HUMAN MOLECULAR GENETICS (2011)
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Guenter U. Hoeglinger et al.
NATURE GENETICS (2011)
A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1
Yongyong Shi et al.
NATURE GENETICS (2011)
System-Wide Temporal Characterization of the Proteome and Phosphoproteome of Human Embryonic Stem Cell Differentiation
Kristoffer T. G. Rigbolt et al.
SCIENCE SIGNALING (2011)
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Chuong B. Do et al.
PLOS GENETICS (2011)
LocusZoom: regional visualization of genome-wide association scan results
Randall J. Pruim et al.
BIOINFORMATICS (2010)
Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study
Weihong Tang et al.
BLOOD (2010)
Genetic Differences between Five European Populations
Valentina Moskvina et al.
HUMAN HEREDITY (2010)
A Sequence Variation (I148M) in PNPLA3 Associated with Nonalcoholic Fatty Liver Disease Disrupts Triglyceride Hydrolysis
Shaoqing He et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C
Jacques Fellay et al.
NATURE (2010)
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma
Christian C. Abnet et al.
NATURE GENETICS (2010)
Genome-Wide Association Studies of Serum Magnesium, Potassium, and Sodium Concentrations Identify Six Loci Influencing Serum Magnesium Levels
Tamra E. Meyer et al.
PLOS GENETICS (2010)
An Open Access Database of Genome-wide Association Results
Andrew D. Johnson et al.
BMC MEDICAL GENETICS (2009)
Genomewide association study for susceptibility genes contributing to familial Parkinson disease
Nathan Pankratz et al.
HUMAN GENETICS (2009)
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
Rosalind A. Eeles et al.
NATURE GENETICS (2009)
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
Julius Gudmundsson et al.
NATURE GENETICS (2009)
Genome-wide association study identifies three loci associated with melanoma risk
D. Timothy Bishop et al.
NATURE GENETICS (2009)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simon-Sanchez et al.
NATURE GENETICS (2009)
HGVbaseG2P: a central genetic association database
Gudmundur A. Thorisson et al.
NUCLEIC ACIDS RESEARCH (2009)
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
Lucia A. Hindorff et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Next generation disparities in human genomics: concerns and remedies
Anna C. Need et al.
TRENDS IN GENETICS (2009)
Basonuclin-2 Requirements for Zebrafish Adult Pigment Pattern Development and Female Fertility
Michael R. Lang et al.
PLOS GENETICS (2009)
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
Andrew D. Johnson et al.
BIOINFORMATICS (2008)
Multiple novel prostate cancer predisposition loci confirmed by an international study:: The PRACTICAL consortium
Zsofia Kote-Jarai et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)
Multiple loci identified in a genome-wide association study of prostate cancer
Gilles Thomas et al.
NATURE GENETICS (2008)
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
Mai M. Abd El-Aziz et al.
NATURE GENETICS (2008)
Multiple newly identified loci associated with prostate cancer susceptibility
Rosalind A. Eeles et al.
NATURE GENETICS (2008)
ORegAnno: an open-access community-driven resource for regulatory annotation
Obi L. Griffith et al.
NUCLEIC ACIDS RESEARCH (2008)
Genomic anatomy of the Tyrp1 (brown) deletion complex
IM Smyth et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Demonstrating stratification in a European American population
CD Campbell et al.
NATURE GENETICS (2005)
分享论文
