Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts

AXIS inhibition protein 2, orofacial clefts and a family history of cancer

(2014) Renato Menezes et al.   JOURNAL OF THE AMERICAN DENTAL ASSOCIATION

Family history of cleft lip and palate in subjects diagnosed with leukemia

(2012) Aditi Jindal et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Risk of cancer in relatives of children born with isolated cleft lip and palate

(2012) Alexandre R. Vieira et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

(2012) Kerstin U Ludwig et al.   NATURE GENETICS

E-Cadherin Destabilization Accounts for the Pathogenicity of Missense Mutations in Hereditary Diffuse Gastric Cancer

(2012) Joana Simões-Correia et al.   PLoS One

Risk of Breast Cancer in Families with Cleft Lip and Palate

(2011) Alexander Dietz et al.   ANNALS OF EPIDEMIOLOGY

Maternal smoking in pregnancy and birth defects: a systematic review based on 173 687 malformed cases and 11.7 million controls

(2011) A. Hackshaw et al.   HUMAN REPRODUCTION UPDATE

CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling

(2011) Irma Kluijt et al.   INTERNATIONAL JOURNAL OF CANCER

Cleft lip and palate: understanding genetic and environmental influences

(2011) Michael J. Dixon et al.   NATURE REVIEWS GENETICS

Breakthroughs in the genetics of orofacial clefting

(2011) Elisabeth Mangold et al.   TRENDS IN MOLECULAR MEDICINE

Maternal Alcohol Consumption, Alcohol Metabolism Genes, and the Risk of Oral Clefts: A Population-based Case-Control Study in Norway, 1996-2001

(2010) A. L. Boyles et al.   AMERICAN JOURNAL OF EPIDEMIOLOGY

Association of CDH1 promoter polymorphism and the risk of non-syndromic orofacial clefts in a Chinese Han population

(2010) Yanbin Song et al.   ARCHIVES OF ORAL BIOLOGY

Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research

(2010) R. C. Fitzgerald et al.   JOURNAL OF MEDICAL GENETICS

Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers

(2010) K. A. Schrader et al.   JOURNAL OF MEDICAL GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

(2009) François-Olivier Desmet et al.   NUCLEIC ACIDS RESEARCH

Folic acid and orofacial clefts: a review of the evidence

(2009) GL Wehby et al.   ORAL DISEASES

Maternal periconceptional smoking and alcohol consumption and risk for select congenital anomalies

(2008) Jagteshwar Grewal et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

AXIN2andCDH1polymorphisms, tooth agenesis, and oral clefts

(2008) Ariadne Letra et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Endoplasmic reticulum quality control: a new mechanism of E-cadherin regulation and its implication in cancer

(2008) J. Simoes-Correia et al.   HUMAN MOLECULAR GENETICS

Transcriptional expression ofcis-acting andtrans-acting splicing mutations cause autosomal dominant retinitis pigmentosa

(2008) María José Gamundi et al.   HUMAN MUTATION

Histopathological and molecular analysis of gastrectomy specimens from hereditary diffuse gastric cancer patients has implications for endoscopic surveillance of individuals at risk

(2008) ME Barber et al.   JOURNAL OF PATHOLOGY

 -Catenin mediates initial E-cadherin-dependent cell-cell recognition and subsequent bond strengthening

(2008) S. Bajpai et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA