Large, rare chromosomal deletions associated with severe early-onset obesity
about
Molecular basis of signaling specificity of insulin and IGF receptors: neglected corners and recent advancesGenome-wide copy number analysis uncovers a new HSCR gene: NRG3Human genetics and genomics a decade after the release of the draft sequence of the human genomeAn integrated approach of comparative genomics and heritability analysis of pig and human on obesity trait: evidence for candidate genes on human chromosome 2Using ERDS to infer copy-number variants in high-coverage genomesA genome-wide study reveals copy number variants exclusive to childhood obesity casesBeyond the fourth wave of genome-wide obesity association studiesObesity genetics in mouse and human: back and forth, and back againRegulation of insulin and type 1 insulin-like growth factor signaling and action by the Grb10/14 and SH2B1/B2 adaptor proteinsObesity in children with autism spectrum disorderLeptin signaling and leptin resistanceBrain regulation of energy balance and body weight.Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approachesConnecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceReciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication SyndromesPhenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse modelsA duplication CNV that conveys traits reciprocal to metabolic syndrome and protects against diet-induced obesity in mice and menOn the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysisExploring the role of copy number variants in human adaptationThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationGenome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesityMultiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismAssociation analyses of 249,796 individuals reveal 18 new loci associated with body mass indexA copy number variation morbidity map of developmental delayDetection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.Genome-wide association study of copy number variations (CNVs) with opioid dependence.Etiology of Obesity Over the Life Span: Ecological and Genetic Highlights from Asian Countries.A new paradigm for the understanding of obesity: the role of stem cells.Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.A survey of copy-number variation detection tools based on high-throughput sequencing data.Analyzing copy number variation using SNP array data: protocols for calling CNV and association tests.Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an 'exome-first' approach.G-CNV: A GPU-Based Tool for Preparing Data to Detect CNVs with Read-Depth Methods.Chromosome 16p11.2 deletions: another piece in the genetic puzzle of childhood obesityParental obesity and risk of autism spectrum disorder.Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsiesGenetic studies in Drosophila and humans support a model for the concerted function of CISD2, PPT1 and CLN3 in disease.Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variantsInfantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.
P2860
Q21131281-09D56A48-191F-4B3D-BF02-D5B47211E481Q21144917-0932D42D-0CD7-4048-9C77-49BC0C139697Q21245451-FBB9AB3B-1ADB-4DF5-85F7-212155A272E3Q21266690-05AE24E1-C775-40F9-82AE-06335A634C45Q24604693-EBE6E104-10D5-4E94-915D-309925286EB6Q24607677-31CE8F21-3BCE-499D-8671-0B641451E1D9Q24627723-1374B759-6191-4812-B7C2-73ECD9C89AD9Q26782027-6ACD1907-3525-475D-BE72-D2CECCDA5BDFQ26849720-B94B4229-A5BA-4FEF-93F9-BF959A525C85Q26860363-CB7F350D-B69B-4FEB-A200-6CB0B8D5D1CCQ26865174-ADE5294E-748A-475C-8466-B1EC77289DB9Q26865811-FE41307D-E35B-4721-A824-20D329C827A3Q27005637-F734872A-8712-4097-9FED-1F61520DA382Q27305223-491D8714-BE18-42FE-9396-98C831DB862DQ27309937-601C0789-1621-4F9F-AFE0-1A87125A3010Q27322785-570D49D9-04CA-4AC5-B584-4984D7277862Q27333802-99AE9FC2-2BF7-431D-BD7C-304AB15A1D7AQ27496612-94FAE64B-68B0-4CA5-9016-EECECBA7D4BFQ28263929-E885ABD4-705A-4FBB-9B04-ACFD776A4273Q28685216-2C48FBC0-63C9-4E04-AA64-5B7A1D0BEB79Q28943380-DE6EFE2F-C27D-4D12-88A8-0DB3876220BDQ29013643-986E1969-6119-4AE4-AD07-6BA75858B381Q29547208-40913781-1D86-445A-8E6B-23992AE7ECC1Q29616033-3CBA098B-BA58-41D1-8E4E-F6CEE96285E6Q30301272-1C503788-C773-4C5E-B88C-F8BBB3AEC313Q30303052-F97C483F-7758-45D4-BD6B-0E7CC78DCED1Q30382106-699881B0-2C41-4256-A863-E9EEF0B1423AQ30402365-C31A3A4E-C798-4C74-80D3-C1D66E4B689AQ30426500-2E34DEAA-AEF1-4CB2-B319-C43EE16B8E01Q30573762-C299F093-5E2E-4D3A-AAFC-30F661DD7D1EQ30752947-51261514-779D-4D41-9EA5-CCB2146044B4Q30885441-5149FC90-0957-4F8A-A3DD-133FAE2EA067Q30915634-32EAC4AD-5F21-4FE9-8EAA-D5C201CC47A6Q33349224-01293361-469B-422A-B43F-F67ACCAD252AQ33551804-16874080-8631-4D00-BDD0-726198DE37E9Q33587483-B06EA31A-ABF9-4004-AFE2-C76AC3FFB720Q33612782-1C1E0DF3-FA5C-4597-8AA1-26C39C351FF1Q33718117-4E039896-958C-4417-BA30-3B1044FD3171Q33724980-2EC07556-EF4A-45CF-B8A3-3A2C2C69CCDFQ33741872-33D7C7A0-515F-4602-B874-2042FD7E41A8
P2860
Large, rare chromosomal deletions associated with severe early-onset obesity
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Large, rare chromosomal deletions associated with severe early-onset obesity
@ast
Large, rare chromosomal deletions associated with severe early-onset obesity
@en
Large, rare chromosomal deletions associated with severe early-onset obesity
@nl
type
label
Large, rare chromosomal deletions associated with severe early-onset obesity
@ast
Large, rare chromosomal deletions associated with severe early-onset obesity
@en
Large, rare chromosomal deletions associated with severe early-onset obesity
@nl
prefLabel
Large, rare chromosomal deletions associated with severe early-onset obesity
@ast
Large, rare chromosomal deletions associated with severe early-onset obesity
@en
Large, rare chromosomal deletions associated with severe early-onset obesity
@nl
P2093
P2860
P50
P3181
P356
P1433
P1476
Large, rare chromosomal deletions associated with severe early-onset obesity
@en
P2093
Carolin Purmann
Elana Henning
I Sadaf Farooqi
Julia Keogh
Kasia Blaszczyk
Matthew E Hurles
P2860
P2888
P304
P3181
P356
10.1038/NATURE08689
P407
P577
2010-02-04T00:00:00Z
P5875
P6179
1048443451