Galit Rozenfeld-Granot

Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes

Karen E. Heath, Ángel Campos‐Barros, Amos Toren et al. · The American Journal of Human Genetics · 2001 · 301 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene

Ninette Cohen, Galit Rozenfeld-Granot, Izhar Hardan et al. · Cancer Genetics and Cytogenetics · 2001 · 103 citations

Life Sciences, Genetics, Hematology +14

A positive feedback mechanism in the transcriptional activation of Apaf-1 by p53 and the coactivator Zac-1

Galit Rozenfeld-Granot, Janakiraman Krishnamurthy, Karuppiah Kannan et al. · Oncogene · 2002 · 71 citations

Life Sciences, Genetics, Molecular Biology +14

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13

Amos Toren, Galit Rozenfeld-Granot, Bianca Rocca et al. · Blood · 2000 · 45 citations

Life Sciences, Genetics, Hematology +15

Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

Amos Toren, Ninette Amariglio, Galit Rozenfeld-Granot et al. · The American Journal of Human Genetics · 1999 · 43 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13