List of works - Anat Bar-Shira

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

scientific article published on 16 December 2016

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

scientific article published on 30 March 2018

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

scientific article published on 13 March 2009

Association of sequence alterations in the putative promoter of RAB7L1 with a reduced parkinson disease risk

scientific article published in January 2012

Decreased expression of B cell related genes in leukocytes of women with Parkinson's disease

scientific article

Differential effects of severe vs mild GBA mutations on Parkinson disease

scientific article

Distinguishing Dementia With Lewy Bodies From Alzheimer Disease: What is the Influence of the GBA Genotype in Ashkenazi Jews?

scientific article published on 01 July 2019

Down-regulation of B cell-related genes in peripheral blood leukocytes of Parkinson's disease patients with and without GBA mutations

scientific article published on 14 September 2015

Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation.

scientific article

Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease.

scientific article

GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

scientific article

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

scientific article

Genetic markers of Restless Legs Syndrome in Parkinson disease

scientific article published on 17 March 2015

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

scientific article

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

scientific article

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

scientific article published on 21 March 2015

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

scientific article published on 15 October 2013

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

article

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

scientific article

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

scientific article

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

article

The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction

scientific article published on 06 September 2011

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

scientific article

Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites

scientific article

List of works by Anat Bar-Shira

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

Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

Association of sequence alterations in the putative promoter of RAB7L1 with a reduced parkinson disease risk

Decreased expression of B cell related genes in leukocytes of women with Parkinson's disease

Differential effects of severe vs mild GBA mutations on Parkinson disease

Distinguishing Dementia With Lewy Bodies From Alzheimer Disease: What is the Influence of the GBA Genotype in Ashkenazi Jews?

Down-regulation of B cell-related genes in peripheral blood leukocytes of Parkinson's disease patients with and without GBA mutations

Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation.

Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease.

GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

Genetic markers of Restless Legs Syndrome in Parkinson disease

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

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

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene

Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

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

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

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

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

The age at motor symptoms onset in LRRK2-associated Parkinson's disease is affected by a variation in the MAPT locus: a possible interaction

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Two Ethnic Clusters with Huntington Disease in Israel: The Case of Mountain Jews and Karaites