Tamar Paperna
Rambam Health Care Campus(IL)
Publications by Year
Research Areas
Congenital heart defects research, Multiple Sclerosis Research Studies, Genomics and Rare Diseases, BRCA gene mutations in cancer, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers(2001)181 cited
- → A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23(2000)180 cited
- → The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis(2019)97 cited
- → Patterns of sensory intermodality relationships in the cerebral cortex of the rat(1991)93 cited
- → Characterization and Expression Pattern of thefrizzledGeneFzd9,the Mouse Homolog ofFZD9Which Is Deleted in Williams–Beuren Syndrome(1999)82 cited
- → Internet Usage by Patients with Multiple Sclerosis: Implications to Participatory Medicine and Personalized Healthcare(2010)77 cited
- → Cathepsins and their endogenous inhibitors cystatins: expression and modulation in multiple sclerosis(2010)74 cited
- → Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers(2007)72 cited
- → The ubiquitin–proteasome pathway regulates claudin 5 degradation(2012)69 cited
- → Tight junction proteins expression and modulation in immune cells and multiple sclerosis(2011)64 cited