The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip-Reference-Cited by-同舟云学术

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

Published:2021-04 Issue:2 Volume:2 Page:100025
ISSN:2666-2477
Container-title:Human Genetics and Genomics Advances
language:en
Short-container-title:Human Genetics and Genomics Advances

Author:

Curtis Sarah W.,Chang Daniel,Lee Myoung Keun,Shaffer John R.,Indencleef Karlijne,Epstein Michael P.,Cutler David J.,Murray Jeffrey C.,Feingold Eleanor,Beaty Terri H.,Claes Peter,Weinberg Seth M.,Marazita Mary L.,Carlson Jenna C.,Leslie Elizabeth J.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Molecular Medicine

Reference60 articles.

1. Genetics of cleft lip and cleft palate;Leslie;Am. J. Med. Genet. C. Semin. Med. Genet.,2013

2. A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13;Leslie;Hum. Mol. Genet.,2016

3. Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate;Leslie;Hum. Genet.,2017

4. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4;Beaty;Nat. Genet.,2010

5. Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity;Yu;Nat. Commun.,2017

Cited by 16 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. Functional analysis ofESRP1/2gene variants andCTNND1isoforms in orofacial cleft pathogenesis;2024-07-02

3. The heterogeneous genetic architectures of orofacial clefts;Trends in Genetics;2024-05

4. Genetic association and functional validation of ZFP36L2 in non-syndromic orofacial cleft subtypes;Journal of Human Genetics;2024-02-06

5. Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting;Genetics in Medicine;2023-10