Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families

by Lior Greenbaum, Lior Greenbaum, Lior Greenbaum, Ben Pode-Shakked, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik-Wolf, Hana Poran, Amihai Rigbi, Ortal Barel, Aida M. Bertoli-Avella, Peter Bauer, Miriam Regev, Miriam Regev, Annick Raas-Rothschild, Annick Raas-Rothschild, Elon Pras, Elon Pras, Michal Berkenstadt, Michal Berkenstadt
Published 2019-06-01

Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample.

by Anna Alkelai, Lior Greenbaum, Sara Lupoli, Yoav Kohn, Kyra Sarner-Kanyas, Edna Ben-Asher, Doron Lancet, Fabio Macciardi, Bernard Lerer
Published 2012-01-01

Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population

by Lior Greenbaum, Merav Ben‐David, Vera Nikitin, Orna Gera, Ortal Barel, Adi Hersalis‐Eldar, Jana Shamash, Noam Shimshoviz, Haike Reznik‐Wolf, Mordechai Shohat, Dan Dominissini, Elon Pras, Amir Dori
Published 2021-06-01

Investigation of the HSPG2 Gene in Tardive Dyskinesia – New Data and Meta-Analysis

by Clement C. Zai, Clement C. Zai, Clement C. Zai, Clement C. Zai, Frankie H. Lee, Arun K. Tiwari, Arun K. Tiwari, Justin Y. Lu, Vincenzo de Luca, Vincenzo de Luca, Vincenzo de Luca, Miriam S. Maes, Miriam S. Maes, Deanna Herbert, Anashe Shahmirian, Sheraz Y. Cheema, Gwyneth C. Zai, Gwyneth C. Zai, Anupama Atukuri, Michael Sherman, Sajid A. Shaikh, Maria Tampakeras, Natalie Freeman, Nicole King, Daniel J. Müller, Daniel J. Müller, Daniel J. Müller, Lior Greenbaum, Lior Greenbaum, Lior Greenbaum, Bernard Lerer, Aristotle N. Voineskos, Aristotle N. Voineskos, Aristotle N. Voineskos, Steven G. Potkin, Jeffrey A. Lieberman, Herbert Y. Meltzer, Gary Remington, Gary Remington, Gary Remington, James L. Kennedy, James L. Kennedy, James L. Kennedy
Published 2018-09-01

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies

by Ben Pode-Shakked, Ortal Barel, Amihood Singer, Miriam Regev, Hana Poran, Aviva Eliyahu, Yael Finezilber, Meirav Segev, Michal Berkenstadt, Hagith Yonath, Haike Reznik-Wolf, Yael Gazit, Odelia Chorin, Gali Heimer, Lidia V. Gabis, Michal Tzadok, Andreea Nissenkorn, Omer Bar-Yosef, Efrat Zohar-Dayan, Bruria Ben-Zeev, Nofar Mor, Nitzan Kol, Omri Nayshool, Noam Shimshoviz, Ifat Bar-Joseph, Dina Marek-Yagel, Elisheva Javasky, Reviva Einy, Moran Gal, Julia Grinshpun-Cohen, Mordechai Shohat, Dan Dominissini, Annick Raas-Rothschild, Gideon Rechavi, Elon Pras, Lior Greenbaum
Published 2021-09-01