Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition

Diverse types of genetic variation converge on functional gene networks involved in schizophrenia

(2012) Sarah R Gilman et al.   NATURE NEUROSCIENCE

Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and pulmonary hypertension

(2011) Manjunath Nimmakayalu et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Common genetic influences on depression, alcohol, and substance use disorders in Mexican-American families

(2011) R.L. Olvera et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Intelligence

(2011) Ian J. Deary   Annual Review of Psychology

Notch signaling proteins HES-1 and Hey-1 bind to insulin degrading enzyme (IDE) proximal promoter and repress its transcription and activity: Implications for cellular Aβ metabolism

(2011) María C. Leal et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes

(2011) David C. Glahn et al.   BIOLOGICAL PSYCHIATRY

Genome-wide association study identifies five new schizophrenia loci

(2011)   NATURE GENETICS

Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities

(2010) Blake C. Ballif et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Neurocognitive Endophenotypes for Bipolar Disorder Identified in Multiplex Multigenerational Families

(2010) David C. Glahn et al.   ARCHIVES OF GENERAL PSYCHIATRY

Impaired Intellect and Memory

(2010) Timothea Toulopoulou et al.   ARCHIVES OF GENERAL PSYCHIATRY

Double-blind, randomized, placebo-controlled 6-week study on the efficacy and safety of the tamoxifen adjunctive to lithium in acute bipolar mania

(2010) Zohreh Amrollahi et al.   JOURNAL OF AFFECTIVE DISORDERS

Phenotypic Complexity, Measurement Bias, and Poor Phenotypic Resolution Contribute to the Missing Heritability Problem in Genetic Association Studies

(2010) Sophie van der Sluis et al.   PLoS One

Genetic overlap between episodic memory deficits and schizophrenia: results from The Maudsley Twin Study

(2010) S. F. Owens et al.   PSYCHOLOGICAL MEDICINE

Genetic foundations of human intelligence

(2009) Ian J. Deary et al.   HUMAN GENETICS

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits

(2009) Yoon Shin Cho et al.   NATURE GENETICS

Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

(2008) Jonathan Mill et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

On multiple-testing correction in genome-wide association studies

(2008) Valentina Moskvina et al.   GENETIC EPIDEMIOLOGY

Cognitive endophenotypes of bipolar disorder: A meta-analysis of neuropsychological deficits in euthymic patients and their first-degree relatives

(2008) Emre Bora et al.   JOURNAL OF AFFECTIVE DISORDERS

Common variants at 30 loci contribute to polygenic dyslipidemia

(2008) Sekar Kathiresan et al.   NATURE GENETICS

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

(2008) Cristen J Willer et al.   NATURE GENETICS