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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 16, 2006
RNASEL mutation screening and association study in Ashkenazi and non-Ashkenazi prostate cancer patientsAvi Orr-Urtreger, Anat Bar-Shira, Dani Bercovich, et al.
Familial Cancer|December 23, 2008
Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type IHelen Toledano, Yael Goldberg, Inbal Kedar-Barnes, et al.
Journal of Human Genetics|February 27, 2008
Genotype-phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) geneDani Bercovich, Arava Elimelech, Joel Zlotogora, et al.
Experimental Cell Research|March 17, 2004
Synergistic control of keratinocyte adhesion through muscarinic and nicotinic acetylcholine receptor subtypesVu Thuong Nguyen, Alexander I Chernyavsky, Juan Arredondo, et al.
European Thyroid Journal|June 28, 2021
High Prevalence of Hearing Impairment in Primary Congenital HypothyroidismTal Almagor, Shoshana Rath, Dan Nachtigal, et al.
Journal of Medical Genetics|April 16, 2015
Minichromosome maintenance complex component 8 (MCM8) gene mutations result in primary gonadal failureYardena Tenenbaum-Rakover, Ariella Weinberg-Shukron, Paul Renbaum, et al.
BMC Cancer|January 20, 2007
A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancerLuna Kadouri, Dani Bercovich, Arava Elimelech, et al.
American Journal of Human Genetics|July 30, 2002
A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi JewsHanna Rennert, Dani Bercovich, Ayala Hubert, et al.
American Journal of Human Genetics|September 9, 2006
Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14Jennie Lugassy, Peter Itin, Akemi Ishida-Yamamoto, et al.
Harefuah|September 7, 2007
[A new oncogenetic service of counseling and diagnosing for hereditary non-polyposis colorectal cancer (HNPCC)]Yael Goldberg, Rinnat Porat, Michal Sagi, et al.
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