Hagit Baris

Rambam Health Care Campus — Israel

Medicine · Health Sciences

28h-index3.3kcitations82works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Lysosomal Storage Disorders Research(20), Genetic factors in colorectal cancer(15), Cellular transport and secretion(13), Carbohydrate Chemistry and Synthesis(10), Genomic variations and chromosomal abnormalities(9)

Publications82 total

PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formation
Science·2021· 68 citedOpen Access
Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance
Journal of Clinical Oncology·2021· 96 citedOpen Access
ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid Leukemia
Scientific Reports·2020· 9 citedOpen Access
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects: HUMAN MUTATION
UNC Libraries·2020Open Access
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction
PLoS Genetics·2019· 64 citedOpen Access
Addendum to Letter to the Editor: Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Blood Cells Molecules and Diseases·2019· 2 cited
Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population
European Journal of Medical Genetics·2019· 7 cited
Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Nature Communications·2018· 53 citedOpen Access
Successful eculizumab therapy for clinical syndromes caused by CD59 and CD55 deficiencies
Molecular Immunology·2018
Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt
Rambam Maimonides Medical Journal·2018· 5 citedOpen Access
No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency
Frontiers in Immunology·2018· 26 citedOpen Access
Establishing the role of <i>PLVAP</i> in protein-losing enteropathy: a homozygous missense variant leads to an attenuated phenotype
Journal of Medical Genetics·2018· 28 cited
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1
Blood Cells Molecules and Diseases·2018· 30 citedOpen Access
Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency
Human Molecular Genetics·2018· 60 citedOpen Access
Microarray analysis in pregnancies with isolated echogenic bowel
Early Human Development·2018· 22 cited
Prenatal microarray analysis in right aortic arch—a retrospective cohort study and review of the literature
Journal of Perinatology·2018· 19 cited
Microarray analysis in pregnancies with isolated unilateral kidney agenesis
Pediatric Research·2018· 15 citedOpen Access
Outcomes after 18 months of eliglustat therapy in treatment‐naïve adults with <scp>G</scp>aucher disease type 1: The phase 3 ENGAGE trial
American Journal of Hematology·2017· 96 citedOpen Access
Loss of CD55 in Eculizumab-Responsive Protein-Losing Enteropathy
New England Journal of Medicine·2017· 63 citedOpen Access
Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel
Familial Cancer·2017· 9 cited
page 1 of 5Next →

Frequent Co-authors

Yael Goldberg(9), Adi Mory(8), Wen‐Hann Tan(7), Zohar Levi(7), Alina Kurolap(6), Ian J. Cohen(5), Virginia Kimonis(5), Inbal Kedar(5), Israela Lerer(5), Tamar Peretz(5), Pramod K. Mistry(4), Atul Mehta(4), Dov Tiosano(4), Tova Hershkovitz(4), Tamar Paperna(4), Hanna Mandel(4), Elizabeth Half(4), Idit Maya(4), Revital Kariv(4), Mira Irons(3)