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Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription

Cell Metabolism(2020)10.1016/j.cmet.2020.05.007Source: DataRank Database

Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription is a research paper published in Cell Metabolism (2020). On theSindex it has a DataRank of 0. It has been cited 82 times.

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Enrichment:Funding (19 grants)OA: hybridTopics (29)IDs (PubMed)SDGs (1)

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Authors (21)

Audrey E. Hendricks ORCID,Aliki Perdikari ORCID,Rebecca Bounds ORCID,Felicity Payne ORCID,Julia M. Keogh ORCID

Live enrichment

PubMed:19767382

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Grant: 208363/Z/17/Z

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Grant: P2EZP3_175090

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Grant: WT091310

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Grant: WT098051

National Institute of Neurological Disorders and Stroke

Grant: 207462/Z/17/Z

National Institute of Neurological Disorders and Stroke

Grant: WT206194

British Heart Foundation

Grant: RG/13/13/30194

British Heart Foundation

Grant: RG/18/13/33946

British Heart Foundation

Grant: SP/09/002

Wellcome Trust

Grant: 206194

Provozierte Bewunderung

Wellcome Trust

Grant: BTRU-2014-10024

Medical Research Council

Grant: MC_PC_13046

High Throughput Science - Investigating pathways to metabolic disease using "omic" approaches

Medical Research Council

Grant: MC_UU_12015/1

Aetiology of type 2 diabetes and related metabolic disorders

Medical Research Council

Grant: MR/L003120/1

Large-scale integrative studies of risk factors in coronary heart disease: from discovery to application

Swiss National Science Foundation

Grant: 175090

KSR2-mediated pathways involved in substrate utilization and energy expenditure and the impact of human KSR2 mutations in early onset obesity.

Wellcome Trust

Grant: 091310

10,000 UK genome sequences: accessing the role of rare genetic variants in health and disease.

Wellcome Trust

Grant: 207462

Fundamental mechanisms controlling human energy homeostasis

Wellcome Trust

Grant: 208363

The University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Cambridge

Wellcome Trust

Grant: 098051

Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers

hybridLicense: cc-by

publisherhttp://www.cell.com/article/S1550413120302461/pdf

publisherhttps://api.elsevier.com/content/article/PII:S1550413120302461?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1550413120302461?httpAccept=text/plain

repositoryhttps://www.research.ed.ac.uk/en/publications/c037e386-2063-46d9-a810-0362c24f192f

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7267775

Fields of Study

0301 basic medicine03 medical and health sciences

Keywords

AdultMalePediatric ObesityPro-Opiomelanocortin[SDV]Life Sciences [q-bio]Association ; Function ; Gene Set ; Genetics ; Pomc ; Severe Childhood Obesity610ArticleMicegene setChlorocebus aethiopsAnimalsHumansgeneticsExomesevere childhood obesityChildCells, CulturedfunctionassociationIntracellular Signaling Peptides and ProteinsGenetic VariationPOMCMiddle Aged[SDV] Life Sciences [q-bio]Mice, Inbred C57BLFemale

Sustainable Development Goals

SDG 2: 2. Zero hunger