Ehud Banne - Hebrew Univ Jerusalem, Med Ctr, Monique & Jacques Roboh Dept Genet Res, Jerusalem, Israel

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个人简介

I am both a physician as well as a researcher, with interests in the genetic basis of rare disorders.

研究兴趣

论文共 29 篇作者统计合作学者相似作者

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Autosomal Dominant, Long-Standing Dysglycemia in 2 Families with Unique Phenotypic Features

Aaron Hanukoglu,Ehud Banne,Dorit Lev,Julio Wainstein

CLINICAL MEDICINE INSIGHTS-ENDOCRINOLOGY AND DIABETES (2024)

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National Rapid Genome Sequencing in Neonatal Intensive Care

Daphna Marom,Adi Mory, Sivan Reytan-Miron,Yam Amir,Alina Kurolap, Julia Grinshpun Cohen, Yocheved Morhi,Tatiana Smolkin,Lior Cohen,Shmuel Zangen,Adel Shalata,Arieh Riskin,Amir Peleg,Karen Lavie-Nevo,Dror Mandel,Elana Chervinsky, Clari Felszer Fisch,Vered Fleisher Sheffer,Tzipora C. Falik-Zaccai,Jonathan Rips,Noa Ofek Shlomai,Smadar Eventov 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

JAMA NETWORK OPENno. 2 (2024)

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Variants in SART3 Cause a Spliceosomopathy Characterised by Failure of Testis Development and Neuronal Defects

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 36-37

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Glycerol Phenylbutyrate Treatment of 2 Patients with Monocarboxylate Transporter 8 Deficiency

Amnon Zung, Niklas Sonntag,Ulrich Schweizer,Ehud Banne,Doreen Braun

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISMno. 10 (2024): 2589-2601

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Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics

Amnon Zung,Galia Barash,Ehud Banne,Michael A Levine

Hormone research in paediatricsno. 5 (2023): 473-482

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Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects (vol 14, 3403, 2023)

NATURE COMMUNICATIONSno. 1 (2023)

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The Genetics of Idiopathic Intracranial Hypertension (IIH): Integration of Population Studies and Clinical Data

Roei Zucker, Michael Kovalerchik,Zvika Davidovich,Ehud Banne,Idit Maharshak,Michal Linial

medrxiv（2023）

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Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics

Amnon Zung,Galia Barash,Ehud Banne,Michael A. Levine

HORMONE RESEARCH IN PAEDIATRICSno. 5 (2023): 473-482

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Phenylbutyrate treatment of three patients with Monocarboxylate Transporter 8 deficiency

Amnon Zung,Felix Schreiner,Heike Vollbach,Ulrich Schweizer,Ehud Banne,Doreen Braun

HORMONE RESEARCH IN PAEDIATRICS (2023): 117-117

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