Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Identification of shared and unique gene families associated with oral clefts.

International journal of oral science - 1 Jun 2017

Funato Noriko, Nakamura Masataka

Abstract excerpt

Oral clefts, the most frequent congenital birth defects in humans, are multifactorial disorders caused by genetic and environmental factors. Epidemiological studies point to different etiologies underlying the oral cleft phenotypes, cleft lip (CL), CL and/or palate (CL/P) and cleft palate (CP). More than 350 genes have syndromic and/or nonsyndromic oral cleft associations in humans. Although genes related to...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cleft Lip
Share to Cleft Palate
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genotype

Share to Phenotype

Share to Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 28106045
DOI: 10.1038/ijos.2016.56
PMCID: PMC5518969

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of shared and unique gene families associated with oral clefts.PMID 28106045Read ↗

Genetics of cleft lip and cleft palate.Semantic proximity Read ↗

The heterogeneous genetic architectures of orofacial clefts.Semantic proximity Read ↗

Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesSemantic proximity Read ↗

Exploration of Genetic Variants of Non-syndromic Cleft Lip with or without Palate and Underlying Mechanisms.Semantic proximity Read ↗

An integrative, genomic, transcriptomic and network-assisted study to identify genes associated with human cleft lip with or without cleft palate.Semantic proximity Read ↗

Distinct genetic architecture and multiple omics features between non-syndromic cleft lip only and non-syndromic cleft lip with cleft palateSemantic proximity Read ↗

Genetic etiology of cleft lip and cleft palateSemantic proximity Read ↗

Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes.Semantic proximity Read ↗

[Progress in genetic epidemiology of non-syndromic cleft palate only].Semantic proximity Read ↗

Genetic and epigenetic studies in non‐syndromic oral cleftsSemantic proximity Read ↗

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingSemantic proximity Read ↗

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.