20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition

Fragile X and X-Linked Intellectual Disability: Four Decades of Discovery

(2012) Herbert A. Lubs et al.   AMERICAN JOURNAL OF HUMAN GENETICS

De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine

(2012) Ryan E. O’Leary et al.   European Journal of Medical Genetics

Monoamine oxidase A and A/B knockout mice display autistic-like features

(2012) Marco Bortolato et al.   INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes

(2012) Claire Redin et al.   JOURNAL OF MEDICAL GENETICS

KD4v: comprehensible knowledge discovery system for missense variant

(2012) Tien-Dao Luu et al.   NUCLEIC ACIDS RESEARCH

Association of the MAOA promoter uVNTR polymorphism with suicide attempts in patients with major depressive disorder

(2011) For-Wey Lung et al.   BMC Medical Genetics

MAOA, abuse exposure and antisocial behaviour: 30-year longitudinal study

(2011) David M. Fergusson et al.   BRITISH JOURNAL OF PSYCHIATRY

Genetics of Early Onset Cognitive Impairment

(2010) Hans Hilger Ropers   Annual Review of Genomics and Human Genetics

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

(2010) A Piton et al.   MOLECULAR PSYCHIATRY

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

MutationTaster evaluates disease-causing potential of sequence alterations

(2010) Jana Marie Schwarz et al.   NATURE METHODS

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

(2009) Patrick S Tarpey et al.   NATURE GENETICS

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

(2009) François-Olivier Desmet et al.   NUCLEIC ACIDS RESEARCH

Reference intervals for urinary catecholamines and metabolites from birth to adulthood

(2008) Eric Pussard et al.   CLINICAL BIOCHEMISTRY

Mutations in human monoamine-related neurotransmitter pathway genes

(2008) Jan Haavik et al.   HUMAN MUTATION

Novel monoamine oxidase A knock out mice with human-like spontaneous mutation

(2008) Anna L. Scott et al.   NEUROREPORT

Structure of human monoamine oxidase A at 2.2-A resolution: The control of opening the entry for substrates/inhibitors

(2008) S.-Y. Son et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA