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Homozygosity for the MTX1 c.184T>A (p.S63T) alteration modifies the age of onset in GBA-associated Parkinson's diseaseGAN-OR, Ziv; BAR-SHIRA, Anat; GUREVICH, Tanya et al.Neurogenetics (Oxford. Print). 2011, Vol 12, Num 4, pp 325-332, issn 1364-6745, 8 p.Article

The homozygous P582S mutation in the oxygen-dependent degradation domain of HIF-Iα is associated with increased risk for prostate cancerORR-URTREGER, Avi; BAR-SHIRA, Anat; MATZKIN, Haim et al.The Prostate. 2007, Vol 67, Num 1, pp 8-13, issn 0270-4137, 6 p.Article

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuriesBAR-SHIRA, Anat; HUTTER, Carolyn M; GILADI, Nir et al.Neurogenetics (Oxford. Print). 2009, Vol 10, Num 4, pp 355-358, issn 1364-6745, 4 p.Article

Mutation screening and association study of the candidate prostate cancer susceptibility genes MSRI, PTEN, and KLF6BAR-SHIRA, Anat; MATARASSO, Noa; ROSNER, Serena et al.The Prostate. 2006, Vol 66, Num 10, pp 1052-1060, issn 0270-4137, 9 p.Article

Combined cytogenetic and array-based comparative genomic hybridization analyses of Wilms tumors: Amplification and overexpression of the multidrug resistance associated protein 1 gene (MRP1) in a metachronous tumorGOLDSTEIN, Myriam; RENNERT, Hanna; BAR-SHIRA, Anat et al.Cancer genetics and cytogenetics. 2003, Vol 141, Num 2, pp 120-127, issn 0165-4608, 8 p.Article

Gait Alterations in Healthy Carriers of the LRRK2 G2019S MutationMIRELMAN, Anat; GUREVICH, Tanya; GILADI, Nir et al.Annals of neurology. 2011, Vol 69, Num 1, pp 193-197, issn 0364-5134, 5 p.Article

Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograftBAR-SHIRA, Anat; PINTHUS, Jehonathan H; ROZOVSKY, Uri et al.Cancer research (Baltimore). 2002, Vol 62, Num 23, pp 6803-6807, issn 0008-5472, 5 p.Article

Association of Sequence Alterations in the Putative Promoter of RAB7L1 With a Reduced Parkinson Disease RiskGAN-OR, Ziv; BAR-SHIRA, Anat; DAHARY, Dvir et al.Archives of neurology (Chicago). 2012, Vol 69, Num 1, pp 105-110, issn 0003-9942, 6 p.Article

ATM-dependent activation of the gene encoding MAP kinase phosphatase 5 by radiomimetic DNA damageBAR-SHIRA, Anat; RASHI-ELKELES, Sharon; ZLOCHOVER, Liat et al.Oncogene (Basingstoke). 2002, Vol 21, Num 5, pp 849-855, issn 0950-9232Article

Array-based comparative genome hybridization in clinical genetics. CommentaryMCGHEE, Sean A; MCCABE, Edward R. B; BAR-SHIRA, Anat et al.Pediatric research. 2006, Vol 60, Num 3, issn 0031-3998, 243-244,353-358 [8 p.]Article

RNASEL mutation screening and association study in ashkenazi and non-ashkenazi prostate cancer patientsORR-URTREGER, Avi; BAR-SHIRA, Anat; RENNERT, Hanna et al.Cancer epidemiology, biomarkers & prevention. 2006, Vol 15, Num 3, pp 474-479, issn 1055-9965, 6 p.Article

The p.L302P mutation in the lysosom enzyme gene SMPD1 is a risk factor for Parkinson diseaseGAN-OR, Ziv; OZELIUS, Laurie J; GUREVICH, Tanya et al.Neurology. 2013, Vol 80, Num 17, pp 1606-1610, issn 0028-3878, 5 p.Article

A novel founder mutation in the RNASEL gene, 471deIAAAG, is associated with prostate Cancer in Ashkenazi jewsRENNERT, Hanna; BERCOVICH, Dani; KADOURI, Luna et al.American journal of human genetics. 2002, Vol 71, Num 4, pp 981-984, issn 0002-9297, 4 p.Article

Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's diseaseGILADI, Nir; MIRELMAN, Anat; THALER, Avner et al.Journal of the neurological sciences. 2011, Vol 310, Num 1-2, pp 17-20, issn 0022-510X, 4 p.Article

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humansLESAGE, Suzanne; PATIN, Etienne; OUVRARD-HERNANDEZ, Anne-Marie et al.Human molecular genetics (Print). 2010, Vol 19, Num 10, pp 1998-2004, issn 0964-6906, 7 p.Article