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Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center

Gastroenterology(2020)10.1053/j.gastro.2020.02.023Source: DataRank Database

Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center is a research paper published in Gastroenterology (2020). On theSindex it has a DataRank of 0. It has been cited 119 times.

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datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (11 grants)OA: hybridTopics (91)IDs (PubMed, PMC)SDGs (1)

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Authors (31)

Neil Warner ORCID,Jie Pan ORCID,Sam Khalouei,Abdul Elkadri ORCID,Karoline Fiedler ORCID

Live enrichment

PubMed:32084423 PMC:PMC7283012

NIDDK NIH HHS

Grant: RC2 DK118640

NIDDK NIH HHS

Grant: P30 DK034854

NIDDK NIH HHS

Grant: U01 DK062413

NIDDK NIH HHS

Grant: P01 DK046763

National Institutes of Health

Grant: 5RC2DK118640-05

COngenital Diarrhea and Enteropathy (PediCODE) Consortium and BioRepository

National Institutes of Health

Grant: 2U01DK062413-16

Genetic and genomic approaches to better understand the clinical heterogeneity in inflammatory bowel diseases

National Institutes of Health

Grant: 5P01DK046763-22

IBD: Genetic and Immunopathologic Mechanisms

Canadian Institutes of Health Research

Grant: unidentified

unidentified

National Institutes of Health

CIHR

hybridLicense: CC BY NC ND

publisherhttps://api.elsevier.com/content/article/PII:S001650852030233X?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S001650852030233X?httpAccept=text/plain

https://doi.org/10.1053/j.gastro.2020.02.023

https://pubmed.ncbi.nlm.nih.gov/32084423

https://dx.doi.org/10.1053/j.gastro.2020.02.023

Fields of Study

0301 basic medicine03 medical and health sciences0303 health sciencesAdolescentAge FactorsBiological ProductsChildChild, PreschoolColitis, UlcerativeCrohn DiseaseFemaleGenetic Predisposition to DiseaseGenetic VariationHematopoietic Stem Cell TransplantationHumansInfantInfant, NewbornMaleOntarioPhenotypePrevalenceRisk AssessmentRisk FactorsTransplantation, HomologousTreatment OutcomeExome SequencingPediatric Crohn's diseasePediatric ulcerative colitis

MeSH Terms

HumansColitis, UlcerativeCrohn DiseaseGenetic Predisposition to DiseaseBiological ProductsTreatment OutcomeHematopoietic Stem Cell TransplantationTransplantation, HomologousPrevalenceRisk AssessmentRisk FactorsAge FactorsPhenotypeAdolescentChildChild, PreschoolInfantInfant, NewbornOntarioFemaleMaleGenetic VariationExome Sequencing

Keywords

GeneticsPrevalenceRisk factorHSCTHomologousMaleAdolescent610UlcerativePediatricsRisk AssessmentWhole Exome Sequencing618Crohn DiseaseRisk FactorsgenomicsTransplantation, HomologousHumansGenetic Predisposition to DiseasePreschoolChildOntarioTransplantationBiological ProductsAge FactorsHematopoietic Stem Cell TransplantationInfant, NewbornGenetic VariationInfantColitisNewbornmutationsTreatment OutcomePhenotypeenteropathyChild, PreschoollociepidemiologyColitis, UlcerativeFemale

Sustainable Development Goals

SDG 3: 3. Good health