A genome-wide association study of suicidal behavior

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

(2014) Beate St Pourcain et al.   Molecular Autism

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

(2013) S Hong Lee et al.   NATURE GENETICS

Regulation of Neuronal Cell Death by c-Abl-Hippo/MST2 Signaling Pathway

(2012) Weizhe Liu et al.   PLoS One

CTNNA3 (α-Catenin) Gene Variants Are Associated With Diisocyanate Asthma: A Replication Study in a Caucasian Worker Population

(2012) David I. Bernstein et al.   TOXICOLOGICAL SCIENCES

The Relationships Between FAM5C SNP (rs10920501) Variability and Metabolic Syndrome and Inflammation in Women With Coronary Heart Disease

(2011) J. L. Cline et al.   Biological Research for Nursing

Two-marker association tests yield new disease associations for coronary artery disease and hypertension

(2011) Thomas P. Slavin et al.   HUMAN GENETICS

A genome-wide association study of attempted suicide

(2011) V L Willour et al.   MOLECULAR PSYCHIATRY

Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression

(2011) Alexandra Schosser et al.   PLoS One

A pilot genome wide association and gene expression array study of suicide with and without major depression

(2011) Hanga Galfalvy et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients

(2010) Roy H. Perlis et al.   AMERICAN JOURNAL OF PSYCHIATRY

Stress, genetics and epigenetic effects on the neurobiology of suicidal behavior and depression

(2010) J.J. Mann et al.   EUROPEAN PSYCHIATRY

Broadening our horizons: Gene expression profiling to help better understand the neurobiology of suicide and depression

(2010) Laura M. Fiori et al.   NEUROBIOLOGY OF DISEASE

FAM5C Contributes to Aggressive Periodontitis

(2010) Flavia M. Carvalho et al.   PLoS One

Unifying Candidate Gene and GWAS Approaches in Asthma

(2010) Sven Michel et al.   PLoS One

A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

(2009) M. G. Posch et al.   JOURNAL OF MEDICAL GENETICS

Association of a nsSNP in ADAMTS14 to some osteoarthritis phenotypes

(2008) J. Rodriguez-Lopez et al.   OSTEOARTHRITIS AND CARTILAGE