Tamar Paperna

A single nucleotide polymorphism in the <i>RAD51</i> gene modifies cancer risk in <i>BRCA2</i> but not <i>BRCA1</i> carriers

Ephrat Levy‐Lahad, Amnon Lahad, Shlomit Eisenberg et al. · Proceedings of the National Academy of Sciences · 2001 · 181 citations · Full text

Genome Instability, Oncology, Single Nucleotide Polymorphism +14

A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23

Risa Peoples, Yvonne Franke, Yu-Ker Wang et al. · The American Journal of Human Genetics · 2000 · 180 citations · Full text

Urology, Bac/pac Clone Contig, Williams-beuren Syndrome–deletion Region +7

The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

Karin Weiss, Hayley P. Lazar, Alina Kurolap et al. · Genetics in Medicine · 2019 · 97 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Patterns of sensory intermodality relationships in the cerebral cortex of the rat

Tamar Paperna, Rafael Malach · The Journal of Comparative Neurology · 1991 · 93 citations

Characterization and Expression Pattern of thefrizzledGeneFzd9,the Mouse Homolog ofFZD9Which Is Deleted in Williams–Beuren Syndrome

Yu-Ker Wang, Ralf Spörle, Tamar Paperna et al. · Genomics · 1999 · 82 citations