Mali Gana-Weisz

Mali Gana-Weisz

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Mali Gana-Weisz

Mali Gana-Weisz

Publications by authors named "Mali Gana-Weisz"

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25Publications

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Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics.

J Neurol Sci 2019 Jul 8;402:62-68. Epub 2019 May 8.

Neuromuscular Unit, Department of Neurology, Tel-Aviv Sourasky Medical Center, 6 Weizmann Street, Tel Aviv 64239, Israel; Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

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http://dx.doi.org/10.1016/j.jns.2019.05.006DOI Listing
July 2019

Parkinson's disease phenotype is influenced by the severity of the mutations in the GBA gene.

Parkinsonism Relat Disord 2018 10 17;55:45-49. Epub 2018 May 17.

Sackler School of Medicine, Tel-Aviv University, Israel; Sagol School of Neuroscience, Tel-Aviv University, Israel; Laboratory of Early Markers of Neurodegeneration, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.

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http://dx.doi.org/10.1016/j.parkreldis.2018.05.009DOI Listing
October 2018

Survival rates among Parkinson's disease patients who carry mutations in the LRRK2 and GBA genes.

Mov Disord 2018 10 4;33(10):1656-1660. Epub 2018 Oct 4.

Movement Disorders Unit, Neurological Institute, Tel-Aviv Medical Center, Tel-Aviv, Israel.

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http://dx.doi.org/10.1002/mds.27490DOI Listing
October 2018

High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype.

Neurobiol Aging 2018 04 27;64:160.e1-160.e7. Epub 2017 Dec 27.

The Genetic Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

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http://dx.doi.org/10.1016/j.neurobiolaging.2017.12.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931221PMC
April 2018

A "dose" effect of mutations in the GBA gene on Parkinson's disease phenotype.

Parkinsonism Relat Disord 2017 03 16;36:47-51. Epub 2016 Dec 16.

Movement Disorders Unit, Neurological Institute, Tel-Aviv Sourasky Medical Center, Israel; Sackler School of Medicine, Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.

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http://dx.doi.org/10.1016/j.parkreldis.2016.12.014DOI Listing
March 2017

High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews.

JAMA Neurol 2016 Dec;73(12):1448-1453

Center for Neurodegeneration, Neurological Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel2Sagol School for Neuroscience, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

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http://dx.doi.org/10.1001/jamaneurol.2016.1593DOI Listing
December 2016

SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.

J Mol Neurosci 2016 Jul 26;59(3):343-50. Epub 2016 Apr 26.

The Genetic Institute, Tel-Aviv Sourasky Medical Center, Weizmann 10, 64239, Tel Aviv, Israel.

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http://dx.doi.org/10.1007/s12031-016-0738-3DOI Listing
July 2016

OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes.

Neurology 2016 Feb 6;86(5):446-53. Epub 2016 Jan 6.

From The Genetic Institute (O.G., O.N., M.G.-W., A.O.-U.) and the Neuromuscular Service, Department of Neurology (B.N., V.E.D.), Tel Aviv Sourasky Medical Center, Israel; the Laboratory of Neurogenetics (B.J.T., A.E.R.), National Institute on Aging, Bethesda, MD; and the Sackler Faculty of Medicine (V.E.D., A.O.-U.), Tel Aviv University, Israel.

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http://dx.doi.org/10.1212/WNL.0000000000002334DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773945PMC
February 2016

Genetic markers of Restless Legs Syndrome in Parkinson disease.

Parkinsonism Relat Disord 2015 Jun 17;21(6):582-5. Epub 2015 Mar 17.

Montreal Neurological Institute, McGill University, Montreal, QC, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2015.03.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4441838PMC
June 2015

Differential effects of severe vs mild GBA mutations on Parkinson disease.

Neurology 2015 Mar 4;84(9):880-7. Epub 2015 Feb 4.

From The Genetic Institute (Z.G.-O., I.A., A.B.-S., M.G.-W., A.O.-R.) and Movement Disorders Unit, Parkinson Center, and Department of Neurology (A.M., N.G.), Tel Aviv Sourasky Medical Center; The Sackler Faculty of Medicine (N.G., A.O.-U.), Tel Aviv University, Israel; Stroke and Dementia Research Centre (L.L.K.), St. George's, University of London, UK; Columbia University (K.M.), Columbia Presbyterian Medical Center, New York; and Beth Israel Medical Center (S.B.), New York, NY. Z.G.-O. is currently affiliated with the Department of Human Genetics and Montreal Neurological Institute, McGill University, Montreal, Canada.

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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000131
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http://dx.doi.org/10.1212/WNL.0000000000001315DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351661PMC
March 2015

CHRNB3 c.-57A>G functional promoter change affects Parkinson's disease and smoking.

Neurobiol Aging 2014 Sep 20;35(9):2179.e1-6. Epub 2014 Mar 20.

The Genetic Institute, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel; The Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2014.03.014DOI Listing
September 2014

Imatinib binding and cKIT inhibition is abrogated by the cKIT kinase domain I missense mutation Val654Ala.

Mol Cancer Ther 2005 Dec;4(12):2008-15

Cancer Research UK Viral Oncology Group, Wolfson Institute for Biomedical Research, University College London, London WC1E 6BT, United Kingdom.

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http://dx.doi.org/10.1158/1535-7163.MCT-05-0070DOI Listing
December 2005

The Ras inhibitor S-trans,trans-farnesylthiosalicylic acid chemosensitizes human tumor cells without causing resistance.

Clin Cancer Res 2002 Feb;8(2):555-65

Department of Neurobiochemistry, The George S. Wise Faculty of Life Sciences, Tel-Aviv University, 69978 Tel Aviv, Israel.

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February 2002