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Publications by Celia MT Greenwood

How Old Is This Mutation? - A Study of Three Ashkenazi Jewish Founder Mutations

English

Linkage and Association Analysis in Pedigrees From Different Populations

English

Related publications

A Founder Mutation in the Ashkenazi Jewish Population Affecting Messenger RNA Splicing of the CCM2 Gene Causes Cerebral Cavernous Malformations

Genetics in Medicine

English

Signatures of Founder Effects, Admixture, and Selection in the Ashkenazi Jewish Population

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

The Jewish Ashkenazi Founder Mutations in the BRCA1/BRCA2 Genes Are Not Found at an Increased Frequency in Ashkenazi Patients With Prostate Cancer

American Journal of Human Genetics

English

Double Heterozygotes for the Ashkenazi Founder Mutations in BRCA1 and BRCA2 Genes

American Journal of Human Genetics

English

New POMT2 Mutations Causing Congenital Muscular Dystrophy: Identification of a Founder Mutation

English

Rapid One-Step Carrier Detection Assay of Mucolipidosis IV Mutations in the Ashkenazi Jewish Population

Journal of Molecular Diagnostics

Forensic Medicine

Molecular Medicine

English

Phenotypic Characteristics Associated With the APC Gene I1307K Mutation in Ashkenazi Jewish Patients With Colorectal Polyps

JAMA - Journal of the American Medical Association

English

The R245X Mutation of PCDH15 in Ashkenazi Jewish Children Diagnosed With Nonsyndromic Hearing Loss Foreshadows Retinitis Pigmentosa

Pediatric Research

English

Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated With a TMEM216 Mutation

American Journal of Human Genetics

English