Hagit Baris Feldman - Tel Aviv Sourasky Medical Center

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Bio

Hagit Baris Feldman is the Director of The Genetics Institute and The Gaucher Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel. The Baris Feldman research group studies Mendelian monogenic syndromes and their molecular biology and has special research interest in Gaucher disease. Current research interests involve 'Deciphering the causative genes and their function in monogenic Mendelian disorders' and 'fatigue in Gaucher disease'.

Research Interests

Papers共 166 篇Author StatisticsCo-AuthorSimilar Experts

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Evaluation of the Digital Genetic Assistant in Technology Assisted Genetic Counseling for Genetic Carrier Screening

Yuval Yaron, Vered Ofen Glassner,Michal Berkenstadt,Nurit Goldstein,Haike Reznik Wolf, Liat Ries Levavi, Liat Abo Gutstein, Yael Furman, Mori Anouchi, Galit Delmar,Doron M Behar,Elon Pras,Adi Reches,Alina Kurolap,Hagit Baris Feldman

NPJ digital medicineno. 1 (2025): 183-183

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Long-Read Structural and Epigenetic Profiling of a Kidney Tumor-matched Sample with Nanopore Sequencing and Optical Genome Mapping

Sapir Margalit,Zuzana Tulpova,Tahir Detinis Zur,Yael Michaeli,Jasline Deek,Gil Nifker,Rita Haldar,Yehudit Gnatek,Dorit Omer,Benjamin Dekel,Hagit Baris Feldman,Assaf Grunwald,Yuval Ebenstein

NAR GENOMICS AND BIOINFORMATICSno. 1 (2025)

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Deletion of RAI1 Noncoding Exons 1–2 Causes Smith–Magenis Syndrome

Uri Hamiel,Alina Kurolap, Chofit Chai Gadot,Adi Mory, Anat Bar Shira,Hagit Baris Feldman,Daphna Marom

Journal of Geneticsno. 1 (2025): 1-5

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High Genetic Diagnostic Yield for Patients with Rare Movement Disorders at a Single-Center Neurogenetics Clinic

Dvir Penn, Yam Amir, Gil Ben David, Alina Kuralop, Dalit Barel,Uri Hamiel, Michal Bach, Emil Elhanan, Tali Barkan,Daphna Marom,Adi Mory, Noga Simantov, Gadi Maayan Eshed,Achinoam Faust-Socher, Vered Livneh,Avner Thaler,Nurit Omer,Tamara Shiner,Nir Giladi,Tanya Gurevich,Hagit Baris Feldman,Roy N Alcalay,Yuval Yaron,Penina Ponger

Movement disorders clinical practice (2025)

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LSM1 C.231+4a>c Hotspot Variant is Associated with a Novel Neurodevelopmental Syndrome: First Patient Cohort

Sivan Reytan Miron,Alina Kurolap, Bassam Abu-Libdeh, Abdel Salam Abu-Libdeh,Clara Velmans,Florian Erger,Vera Riehmer, Tzung-Chien Hsieh,Hellen Lesmann,Adi Reches, Chofit Chai Gadot,Adi Mory, Motee Al-Ashhab,Christian Netzer, Nadirah Damseh,Hagit Baris Feldman

Journal of medical geneticsno. 7 (2025): 441-449

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Changes in Glycinergic Neurotransmission Alter Mammalian Retinal Information Processing

Anneka Joachimsthaler, Katharina Hauf, Anja Armbruster,Shiri Zayit-Soudry, Efrat Naaman,Ido Perlman,Rina Leibu,Alina Kurolap,Hagit Baris Feldman,Jan Kremers,Volker Eulenburg

Frontiers in molecular neuroscience (2025): 1564870-1564870

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The Patient Experience of CHAPLE Disease: Results from Interviews Conducted As Part of a Clinical Trial for an Ultra-Rare Condition

Leighann Litcher-Kelly,Ahmet Ozen,Sarah Ollis,Hagit Baris Feldman,Andrew Yaworsky, Paolo Medrano,Voranush Chongsrisawat,Lorah Perlee,Marisa Walker, Sharanya Pradeep,Diane M. Turner-Bowker,Alina Kurolap,Orly Eshach Adiv,Michael J. Lenardo,Olivier A. Harari,Jessica J. Jalbert

Orphanet Journal of Rare Diseasesno. 1 (2025): 1-9

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National Rapid Genome Sequencing in Neonatal Intensive Care

Daphna Marom,Adi Mory, Sivan Reytan-Miron,Yam Amir,Alina Kurolap, Jonathan Cohen, Yocheved Morhi,Tatiana Smolkin,Lior Cohen,Shmuel Zangen,Adel Shalata,Arieh Riskin,Amir Peleg,Karen Lavie‐Nevo,Dror Mandel,Elana Chervinsky, Charlés Fisch,Vered Fleisher Sheffer,Tzipora C. Falik‐Zaccai,Jonathan Rips,Noa Ofek Shlomai, Smadar Friedman, Calanit Hershkovich Shporen, Sagie Josefsberg Ben-Yehoshua,Aryeh Simmonds, Racheli Goldfarb Yaacobi,Sofia Bauer‐Rusek, Hussam Omari,Karin Weiss,Ori Hochwald,Arie Koifman,Omer Globus,Nurit Assia Batzir, Naveh Yaron,Reeval Segel,Iris Morag,Orit Reish,Aviva Eliyahu,Leah Leibovitch,Marina Eskin Schwartz,Ramy Abramsky,Amit Hochberg,Anat Oron,Ehud Banne,Igor Portnov,Nadra Nasser Samra,Amihood Singer,Hagit Baris Feldman

Obstetrical & Gynecological Surveyno. 8 (2024): 452-454

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Declassification of an RB1 Splice Site Variant Detected As a Potential Secondary Finding in Prenatal Exome Sequencing

Sharon Simchoni,Adi Mory,Alina Kurolap,Anat Bar Shira,Yuval Yaron,Hagit Baris Feldman

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 364-364

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Yield of a Genetic Diagnosis in Complex and Essential Autism

Uri Hamiel,Chen Patt,Yam Amir,Hagit Baris Feldman,Daphna Marom

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 488-489

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