Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. - sprookjes - yvandenbroek - TriplyDB

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

http://www.wikidata.org/entity/Q34212342

about

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder Beyond the fourth wave of genome-wide obesity association studies The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder Characterizing autism spectrum disorders by key biochemical pathways.Obesity genetics in mouse and human: back and forth, and back again Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches CNVs: harbingers of a rare variant revolution in psychiatric genetics Impact of the gut microbiota on the development of obesity and type 2 diabetes mellitus Genetic and epigenetic control of metabolic health The impact of human copy number variation on gene expression Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes A duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and men On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis Structural variation mutagenesis of the human genome: Impact on disease and evolution.Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms Exploring the role of copy number variants in human adaptation The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation CNVs conferring risk of autism or schizophrenia affect cognition in controls Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions.Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications.A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.Genetic analysis of low BMI phenotype in the Utah Population Database.Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.Biological relevance of CNV calling methods using familial relatedness including monozygotic twins.Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.Identification of structural variation in mouse genomes.Genetic identification of thiosulfate sulfurtransferase as an adipocyte-expressed antidiabetic target in mice selected for leanness.Genomics, intellectual disability, and autism Genetic architectures of psychiatric disorders: the emerging picture and its implications.The genetic variability and commonality of neurodevelopmental disease.Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families SH2B1 regulation of energy balance, body weight, and glucose metabolism.Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.A higher mutational burden in females supports a "female protective model" in neurodevelopmental disorders.Opposing brain differences in 16p11.2 deletion and duplication carriers.Opposite effects on facial morphology due to gene dosage sensitivity

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

http://www.wikidata.org/entity/Q34212342

description

2011 nî lūn-bûn

@nan

2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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type

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

@nl

prefLabel

Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

@ast

Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

@en

Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

@nl

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Mirror extreme BMI phenotypes ...... the chromosome 16p11.2 locus.

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Agnès Guichet

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Albert David

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Alessandra Ferrarini

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Alexandra I F Blakemore

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Alexandre Moerman

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Anita Kloss-Brandstätter

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Anita Rauch

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Anne Faudet

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Anneke T Vulto-van Silfhout

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Armand Bottani

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Genetic structure of Europeans: a view from the North-East

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97-102

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10.1038/NATURE10406

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7367

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478

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Stylianos Antonarakis

James F. Gusella

Thomas Meitinger

Christian Gieger

Peter Vollenweider

Florian Kronenberg

Hreinn Stefansson

Gudmar Thorleifsson

Marjo-Riitta Järvelin

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2011-08-31T00:00:00Z

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