Publications
Rennert H., Bercovich D., Hubert A., Abeliovich D., Rozovsky U., Bar-Shira A., Soloviov S., Schreiber L., Matzkin H., Rennert G., Kadouri L., Peretz T., Yaron Y., Orr-Urtreger A.: A novel founder mutation in the RNASEL gene, 471delAAAG, is associated with prostate cancer in Ashkenazi Jews. Am J Hum Genet. 7:981-984, 2002.
Goldstein M., Rennert H., Bar-Shira A., Burstein Y., Yaron Y. and Orr-Urtreger A. Combined Cytogenetic and Array-Based CGH Analyses of Wilms Tumors: Amplification and Overexpression of the Multidrug Resistance-Associated Protein 1 Gene in a Metachronous Tumor. Cancer Genetics and Cytogenetics 141:120-127, 2003.
Rennert H., Zeigler-Johnson C.M., Addya K., Spangler E.E., Finely M.F., Walker A.H., Malkowicz S.B., Leonard D.G.B and Rebbeck T.R. Association of Susceptibility Alleles in ELAC2/HPC2, RNASEL/HPC1, and Macrophage Scavenger Receptor 1 with Prostate Cancer Severity in European-American and African-American Men. Can Epi Biomarkers and Prevention. 14:949-957, 2005.
Kesari A., Rennert H., Leonard G.B., Phadke S.R. and Mittal B. Prenatal diagnosis of spinal muscular atrophy: Indian scenario. Prenat Diagen. 25: 641-644, 2005.
