Hagit Baris - Concepedia

Author

Hagit Baris

Rambam Health Care Campus

Also Known As

Baris, Hagit, Deguchi, Kentaro, H Baris, H. N. Baris, H.N. Baris, Hagit Baris, Hagit N Baris, Hagit N. Baris

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

Rambam Health Care Campus Tel Aviv University Rabin Medical Center Technion – Israel Institute of Technology Hadassah Medical Center

About

Hagit Baris is an author at Rambam Health Care Campus specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	16	1.1K
2	Health Sciences	1	1	115
3	Natural Sciences	1	1	15
4	Public Health	1	1	60
5	Biology	1	1	15

Hagit Baris

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance Max A. Tischfield, Hagit Baris, Chen Wu, Cell Axon GuidanceProtein FunctionMolecular BiologyCytoskeletonCell Motility	2010	589
VarElect: the phenotype-based variation prioritizer of the GeneCards Suite Gil Stelzer, Inbar Plaschkes, Danit Oz-Levi, BMC Genomics	2016	273
Effect of Oral Eliglustat on Splenomegaly in Patients With Gaucher Disease Type 1 Pramod K. Mistry, Elena Lukina, Hadhami Ben Turkia, JAMA	2015	152
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history. Hagit Baris, Ian J. Cohen, Pramod K. Mistry PubMed Enzyme Replacement TherapyGeneticsPathologySubstrate Reduction TherapyType 1	2014	115
Outcomes after 18 months of eliglustat therapy in treatment‐naïve adults with <scp>G</scp>aucher disease type 1: The phase 3 ENGAGE trial Pramod K. Mistry, Elena Lukina, Hadhami Ben Turkia, American Journal of Hematology	2017	96
Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance Carol Durno, Ayse B. Ercan, Vanessa Bianchi, Journal of Clinical Oncology	2021	95
Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT) Lonneke Haer‐Wigman, Horatio Hackett Newman, Rina Leibu, Human Molecular Genetics Ocular DiseaseGeneticsGlycobiologyMolecular BiologyPathology	2015	75
Diagnostic utility of array‐based comparative genomic hybridization in a clinical setting Hagit Baris, Wen‐Hann Tan, Virginia Kimonis, American Journal of Medical Genetics Part A	2007	69
PI(3,4)P2-mediated cytokinetic abscission prevents early senescence and cataract formation Federico Gulluni, Lorenzo Prever, Huayi Li, Science	2021	68
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction Dov Tiosano, Hagit Baris, Anlu Chen, PLoS Genetics	2019	64

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