RERE deficiency contributes to the development of orofacial clefts in humans and mice

PAX 7 nucleotide variants and the risk of non‐syndromic orofacial clefts in the Polish population

(2019) Agnieszka Gaczkowska et al.   ORAL DISEASES

Genotype-phenotype correlations in individuals with pathogenic RERE variants

(2018) Valerie K. Jordan et al.   HUMAN MUTATION

RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects

(2018) Bum Jun Kim et al.   Disease Models & Mechanisms

De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions

(2016) Brieana Fregeau et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate

(2016) Elisabeth Mangold 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

Retinoic acid controls body axis extension by directly repressing Fgf8 transcription

(2014) S. Kumar et al.   DEVELOPMENT

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

(2013) Myriam Peyrard-Janvid et al.   AMERICAN JOURNAL OF HUMAN GENETICS

An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions

(2013) Bum Jun Kim et al.   PLoS One

Median facial clefts in Xenopus laevis: Roles of retinoic acid signaling and homeobox genes

(2012) Allyson E. Kennedy et al.   DEVELOPMENTAL BIOLOGY

Palatogenesis: morphogenetic and molecular mechanisms of secondary palate development

(2011) J. O. Bush et al.   DEVELOPMENT

Rere controls retinoic acid signalling and somite bilateral symmetry

(2010) Gonçalo C. Vilhais-Neto et al.   NATURE

Prdm16 is required for normal palatogenesis in mice

(2009) Bryan C. Bjork et al.   HUMAN MOLECULAR GENETICS

Atrophin recruits HDAC1/2 and G9a to modify histone H3K9 and to determine cell fates

(2008) Lei Wang et al.   EMBO REPORTS

Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation

(2008) A. Battaglia et al.   PEDIATRICS