Publications Authored by Moran Gal

Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders.

Authors:

Jasmine Jacob-Hirsch Eran Eyal Binyamin A Knisbacher Jonathan Roth Karen Cesarkas Chen Dor Sarit Farage-Barhom Vered Kunik Amos J Simon Moran Gal Michal Yalon Sharon Moshitch-Moshkovitz Rick Tearle Shlomi Constantini Erez Y Levanon Ninette Amariglio Gideon Rechavi

Cell Res 2018 Feb 12;28(2):187-203. Epub 2018 Jan 12.

Cancer Research Center and the Wohl Institute of Translational Medicine, the Chaim Sheba Medical Center, Tel Hashomer, Israel.

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http://dx.doi.org/10.1038/cr.2018.8	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5799824	PMC

February 2018

Which Anthropometric Measure Best Correlates with Neonatal Fat Mass at Birth?

Authors:

Gal Dubnov-Raz Moran Gal Yeela Landau-Helman Lihi Biderman Romy Nir Ayala Maayan-Metzger

Am J Perinatol 2016 07 23;33(9):826-30. Epub 2016 Feb 23.

Sackler Faculty Medicine, Tel Aviv University, Tel Aviv, Israel.

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http://dx.doi.org/10.1055/s-0036-1572427	DOI Listing

July 2016

Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing.

Authors:

Moran Gal Khen Khermesh Michal Barak Min Lin Hadas Lahat Haike Reznik Wolf Michael Lin Elon Pras Erez Y Levanon

BMC Med Genomics 2016 05 13;9(1):24. Epub 2016 May 13.

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, 52900, Israel.

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http://dx.doi.org/10.1186/s12920-016-0184-7	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865987	PMC

May 2016

A novel homozygous splice site mutation in NALCN identified in siblings with cachexia, strabismus, severe intellectual disability, epilepsy and abnormal respiratory rhythm.

Authors:

Moran Gal Daniella Magen Younan Zahran Sarit Ravid Ayelet Eran Morad Khayat Chen Gafni Erez Y Levanon Hanna Mandel

Eur J Med Genet 2016 Apr 23;59(4):204-9. Epub 2016 Feb 23.

Metabolic Unit, Rambam Health Care Center, Haifa, Israel; Rappaport School of Medicine, Technion, Haifa, Israel.

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http://dx.doi.org/10.1016/j.ejmg.2016.02.007	DOI Listing

April 2016

Novel mutation in TSPAN12 leads to autosomal recessive inheritance of congenital vitreoretinal disease with intra-familial phenotypic variability.

Authors:

Moran Gal Erez Y Levanon Yasir Hujeirat Morad Khayat Jacob Pe'er Stavit Shalev

Am J Med Genet A 2014 Dec 22;164A(12):2996-3002. Epub 2014 Sep 22.

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

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http://dx.doi.org/10.1002/ajmg.a.36739	DOI Listing

December 2014

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2.

Authors:

Efrat Gabai-Kapara Amnon Lahad Bella Kaufman Eitan Friedman Shlomo Segev Paul Renbaum Rachel Beeri Moran Gal Julia Grinshpun-Cohen Karen Djemal Jessica B Mandell Ming K Lee Uziel Beller Raphael Catane Mary-Claire King Ephrat Levy-Lahad

Proc Natl Acad Sci U S A 2014 Sep 5;111(39):14205-10. Epub 2014 Sep 5.

Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem 91031, Israel; Faculty of Medicine, Hebrew University Medical School, Jerusalem 91120, Israel;

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http://dx.doi.org/10.1073/pnas.1415979111	DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191771	PMC

September 2014

Endocrine outcome in long-term survivors of childhood brain tumors.

Authors:

Shlomit Shalitin Moran Gal Yacob Goshen Ian Cohen Isaac Yaniv Moshe Phillip

Horm Res Paediatr 2011 17;76(2):113-22. Epub 2011 Jun 17.

The Jesse Z and Lea Shafer Institute of Endocrinology and Diabetes, National Center for Childhood Diabetes, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.

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