Copy Number Variations in 6q14.1 and 5q13.2 are Associated with Alcohol Dependence

A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications

(2011) Andrew C. Heath et al.   BIOLOGICAL PSYCHIATRY

Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability

(2011) Eva Also-Rallo et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Copy Number Variation Accuracy in Genome-Wide Association Studies

(2011) Peng Lin et al.   HUMAN HEREDITY

Genome-Wide Linkage Screen for Systolic Blood Pressure in the Veterans Administration Genetic Epidemiology Study (VAGES) of Mexican-Americans and Confirmation of a Major Susceptibility Locus on Chromosome 6q14.1

(2011) Sobha Puppala et al.   HUMAN HEREDITY

Defective Neuromuscular Junction Organization and Postnatal Myogenesis in Mice With Severe Spinal Muscular Atrophy

(2011) Elisabet Dachs et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Genome-Wide Association Study of Alcohol Dependence Implicates a Region on Chromosome 11

(2010) Howard J. Edenberg et al.   ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH

Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria

(2010) Mary C. O'Driscoll et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

(2010) Marilyn C. Cornelis et al.   GENETIC EPIDEMIOLOGY

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

A genome-wide association study of alcohol dependence

(2010) L. J. Bierut et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genome-wide Association Study of Alcohol Dependence

(2009) Jens Treutlein et al.   ARCHIVES OF GENERAL PSYCHIATRY

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Characterization of an interstitial deletion 6q13–q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms

(2008) James Lespinasse et al.   European Journal of Medical Genetics

Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype

(2008) Marilee A. Martens et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

(2008) Sharon J. Diskin et al.   NUCLEIC ACIDS RESEARCH