Whole Exome Sequencing Identifies Damaging Variants in Indonesians with Clefts

Genetic and Epigenetic Studies in Nonsyndromic Oral Clefts

(2022) Azeez Alade et al.   ORAL DISEASES

Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis

(2022) Lara Slavec et al.   Scientific Reports

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

(2022) Waheed Awotoye et al.   Scientific Reports

Orofacial clefts embryology, classification, epidemiology, and genetics

(2021) Ghenwa Nasreddine et al.   MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH

Orofacial clefts in low‐ and middle‐income countries: A scoping review of quality and quantity of research based on literature between 2010‐2019

(2020) Erli Sarilita et al.   Orthodontics & Craniofacial Research

Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate

(2019) Nicholas J. Marini et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review

(2019) Anwar Baban et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mouse Genome Database (MGD) 2019

(2018) Carol J Bult et al.   NUCLEIC ACIDS RESEARCH

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

(2017) Elizabeth J. Leslie et al.   HUMAN GENETICS

Folate cycle enzyme MTHFD1L confers metabolic advantages in hepatocellular carcinoma

(2017) Derek Lee et al.   JOURNAL OF CLINICAL INVESTIGATION

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity

(2017) Yanqin Yu et al.   Nature Communications

Genetics and genomics etiology of nonsyndromic orofacial clefts

(2017) Wasiu L. Adeyemo et al.   Molecular Genetics & Genomic Medicine

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

(2016) Elizabeth J. Leslie et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification of Functional Variants for Cleft Lip with or without Cleft Palate in or near PAX7, FGFR2, and NOG by Targeted Sequencing of GWAS Loci

(2015) Elizabeth J. Leslie et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Fine Mapping of 6q23.1 Identifies TULP4 as Contributing to Clefts

(2015) Alexandre R. Vieira et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Systematic analysis of copy number variants of a large cohort of orofacial cleft patients identifies candidate genes for orofacial clefts

(2015) Federica Conte et al.   HUMAN GENETICS

Fine Mapping of 6q23.1 Identifies TULP4 as Contributing to Clefts

(2015) Alexandre R. Vieira et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

The Indonesian archipelago: an ancient genetic highway linking Asia and the Pacific

(2013) Meryanne K Tumonggor et al.   JOURNAL OF HUMAN GENETICS