A Genome-Wide Copy Number Variant Study of Suicidal Behavior

Identification of copy number variants from exome sequence data

(2014) Pubudu Samarakoon et al.   BMC GENOMICS

Ribosomal Protein s15 Phosphorylation Mediates LRRK2 Neurodegeneration in Parkinson’s Disease

(2014) Ian Martin et al.   CELL

Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation

(2013) Claudia Manzoni et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

TheLRRK2R1628P Variant Plays a Protective Role in Han Chinese Population with Alzheimer's Disease

(2013) Hong-Lei Li et al.   CNS Neuroscience & Therapeutics

Life events: a complex role in the timing of suicidal behavior among depressed patients

(2013) M A Oquendo et al.   MOLECULAR PSYCHIATRY

TDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPT

(2013) Helen Ling et al.   NEUROBIOLOGY OF AGING

Parkinson-related LRRK2 mutation R1441C/G/H impairs PKA phosphorylation of LRRK2 and disrupts its interaction with 14-3-3

(2013) K. Muda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Bipolar Disorder and a History of Suicide Attempts With a Duplication in 5HTR1A

(2012) Roy H. Perlis et al.   AMERICAN JOURNAL OF PSYCHIATRY

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

Copy Number Variation in Subjects with Major Depressive Disorder Who Attempted Suicide

(2012) Roy H. Perlis et al.   PLoS One

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample

(2011) Andrew McQuillin et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

(2011) Dheeraj Malhotra et al.   NEURON

Familial clustering of suicide risk: a total population study of 11.4 million individuals

(2011) D. Tidemalm et al.   PSYCHOLOGICAL MEDICINE

The neurodevelopmental origins of suicidal behavior

(2011) Gustavo Turecki et al.   TRENDS IN NEUROSCIENCES

Taking qPCR to a higher level: Analysis of CNV reveals the power of high throughput qPCR to enhance quantitative resolution

(2010) Suzanne Weaver et al.   METHODS

Accurate and objective copy number profiling using real-time quantitative PCR

(2010) Barbara D’haene et al.   METHODS

Pathogenic LRRK2 negatively regulates microRNA-mediated translational repression

(2010) Stephan Gehrke et al.   NATURE

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

(2010) Dalila Pinto et al.   NATURE

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

(2010) Simone Berkel et al.   NATURE GENETICS

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

(2010) Joseph T. Glessner et al.   PLoS One

Familial Aggregation of Suicide Explained by Cluster B Traits: A Three-Group Family Study of Suicide Controlling for Major Depressive Disorder

(2009) Alexander McGirr et al.   AMERICAN JOURNAL OF PSYCHIATRY

High Frequency of Occurrence of CYP2D6 Gene Duplication/Multiduplication Indicating Ultrarapid Metabolism Among Suicide Cases

(2009) A L Zackrisson et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

(2009) A Ingason et al.   MOLECULAR PSYCHIATRY

Suicide neurobiology

(2009) Carl Ernst et al.   PROGRESS IN NEUROBIOLOGY

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE