Genetic models and approaches to study orofacial clefts-Reference-Cited by-同舟云学术

Genetic models and approaches to study orofacial clefts

Published:2022-01-06 Issue: Volume: Page:
ISSN:1354-523X
Container-title:Oral Diseases
language:en
Short-container-title:Oral Diseases

Author:

Leslie Elizabeth J.¹^ORCID

Affiliation:

1. Emory University School of Medicine Atlanta Georgia USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

General Dentistry,Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/odi.14109

Reference104 articles.

1. Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

2. Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

3. Association of genetic variation of the transforming growth factor‐alpha gene with cleft lip and palate;Ardinger H. H.;American Journal of Human Genetics,1989

4. Mendelian Gene Discovery: Fast and Furious with No End in Sight

5. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Functional analysis of ESRP1/2 gene variants and CTNND1 isoforms in orofacial cleft pathogenesis;Communications Biology;2024-08-23

2. Research Trends in the Relationship Between Orofacial Cleft and Cancer: A Bibliometric and Network Visualization Study;Cancer Investigation;2024-07-12

3. Functional analysis ofESRP1/2gene variants andCTNND1isoforms in orofacial cleft pathogenesis;2024-07-02

4. Investigating gene functions and single-cell expression profiles of de novo variants in orofacial clefts;Human Genetics and Genomics Advances;2024-07

5. Whole-exome sequencing identifies ECPAS as a novel potentially pathogenic gene in multiple hereditary families with nonsyndromic orofacial cleft;Protein & Cell;2024-05-02