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Human genetics

A New Statistic to Evaluate Imputation Reliability

Peng Lin, Sarah M. Hartz, [ ... ], for the COGA Collaborators COGEND Collaborators, GENEVA

The Cannabinoid 1 Receptor (CNR1) 1359 G/A Polymorphism Modulates Susceptibility to Ulcerative Colitis and the Phenotype in Crohn's Disease

Martin Storr, Dominik Emmerdinger, [ ... ], Stephan Brand

The Dopamine Transporter Gene, a Spectrum of Most Common Risky Behaviors, and the Legal Status of the Behaviors

Guang Guo, Tianji Cai, [ ... ], Kathleen Mullan Harris

Investigation of Type 2 Diabetes Risk Alleles Support CDKN2A/B, CDKAL1, and TCF7L2 As Susceptibility Genes in a Han Chinese Cohort

Jie Wen, Tina Rönn, [ ... ], Renming Hu

Contribution of Genome-Wide HCV Genetic Differences to Outcome of Interferon-Based Therapy in Caucasian American and African American Patients

Maureen J. Donlin, Nathan A. Cannon, [ ... ], for the Virahep-C Study Group

Genome Wide Association for Addiction: Replicated Results and Comparisons of Two Analytic Approaches

Tomas Drgon, Ping-Wu Zhang, [ ... ], George R. Uhl

Application of Gene Network Analysis Techniques Identifies AXIN1/PDIA2 and Endoglin Haplotypes Associated with Bicuspid Aortic Valve

Eric C. Wooten, Lakshmanan K. Iyer, [ ... ], Gordon S. Huggins

Concordant Association of Insulin Degrading Enzyme Gene (IDE) Variants with IDE mRNA, Aß, and Alzheimer's Disease

Minerva M. Carrasquillo, Olivia Belbin, [ ... ], Kevin Morgan

Magnitude of Stratification in Human Populations and Impacts on Genome Wide Association Studies

Ke Hao, Eugene Chudin, Danielle Greenawalt, Eric E. Schadt

Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels

Jinong Feng, Zhifang Zhang, [ ... ], Steve S. Sommer

Investigating the Role of Mitochondrial Haplogroups in Genetic Predisposition to Meningococcal Disease

Antonio Salas, Laura Fachal, [ ... ], Grupo de investigación ESIGEM (Estudio Sobre la Influencia Genética en la Enfermedad Meningocócica) ¶

Genetic Variance in the Spinocerebellar Ataxia Type 2 (ATXN2) Gene in Children with Severe Early Onset Obesity

Karla P. Figueroa, Sadaf Farooqi, [ ... ], Stefan M. Pulst

The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci

Louise V. Wain, Inti Pedroso, [ ... ], Ammar Al-Chalabi

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