Publications by authors named "Eva Gak"

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The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations.
Sophia Sominsky, Michael Korostishevsky, Daniel Kurnik, Eleni Aklillu, Yoram Cohen, Eva Gak

J Appl Genet· May 2014

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Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosa.
Efrat Czerniak, Michael Korostishevsky, Amos Frisch, Yoram Cohen, Ninette Amariglio, Eva Gak

Arch Womens Ment Health· October 2013

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Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose prediction.
Daniel Kurnik, Husam Qasim, Sophie Sominsky, Aharon Lubetsky, Noa Markovits, Eva Gak

Thromb Haemost· October 2012

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Ex vivo treatment with a novel synthetic aminoglycoside NB54 in primary fibroblasts from Rett syndrome patients suppresses MECP2 nonsense mutations.
Manuela Vecsler, Bruria Ben Zeev, Igor Nudelman, Yair Anikster, Amos J Simon, Eva Gak

PLoS One· November 2011

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Benign hereditary chorea: an update.
Rivka Inzelberg, Moran Weinberger, Eva Gak

Parkinsonism Relat Disord· June 2011

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Epilepsy in Rett syndrome---the experience of a National Rett Center.
Andreea Nissenkorn, Eva Gak, Manuela Vecsler, Haia Reznik, Shay Menascu

Epilepsia· July 2010

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MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitro.
Manuela Vecsler, Amos J Simon, Ninette Amariglio, Gideon Rechavi, Eva Gak

Epigenetics· January 2010

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10 years of oral anticoagulant pharmacogenomics: what difference will it make? A critical appraisal.
Daniel Kurnik, Ronen Loebstein, Hillel Halkin, Eva Gak, Shlomo Almog

Pharmacogenomics· December 2009

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Shifting paradigms in the pharmacogenetics of warfarin.
Eva Gak, Hillel Halkin

Pharmacogenomics· October 2008

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VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individuals.
Eleni Aklillu, Cheryl Leong, Ronen Loebstein, Hillel Halkin, Eva Gak

Blood· April 2008

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A novel missense mutation in the NDP gene in a child with Norrie disease and severe neurological involvement including infantile spasms.
Dorit Lev, Yuval Weigl, Mariana Hasan, Eva Gak, Michael Davidovich

Am J Med Genet A· May 2007

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A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistance.
Ronen Loebstein, Ilana Dvoskin, Hillel Halkin, Manuela Vecsler, Aharon Lubetsky, Eva Gak

Blood· March 2007

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Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa.
Maya Koronyo-Hamaoui, Amos Frisch, Daniel Stein, Yardena Denziger, Shani Leor, Eva Gak

J Psychiatr Res· February 2007

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Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarin.
Manuela Vecsler, Ronen Loebstein, Shlomo Almog, Daniel Kurnik, Boleslav Goldman, Eva Gak

Thromb Haemost· February 2006

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Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis.
Liron Abuhatzira, Kirill Makedonski, Yael Petel Galil, Eva Gak, Bruria Ben Zeev

Hum Genet· October 2005

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Common genetic variants of microsomal epoxide hydrolase affect warfarin dose requirements beyond the effect of cytochrome P450 2C9.
Ronen Loebstein, Manuela Vecsler, Daniel Kurnik, Naomi Austerweil, Eva Gak

Clin Pharmacol Ther· May 2005

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CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population.
Maya Koronyo-Hamaoui, Eva Gak, Daniel Stein, Amos Frisch, Yardena Danziger

Am J Med Genet B Neuropsychiatr Genet· November 2004

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Association study of CAG repeats in the KCNN3 gene in Israeli patients with major psychosis.
Michael Ritsner, Sharon Amir, Maya Koronyo-Hamaoui, Eva Gak, Hana Ziv

Psychiatr Genet· September 2003

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