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68 results for Orr‐Urtreger,+Avi

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Select record 21
ArticlesPeer ReviewedFull Text
Biochemical markers for severity and risk in GBA and LRRK2 Parkinson’s disease
Author / Creator:Thaler, Avner ; Omer, Nurit ; Giladi, Nir ; Gurevich, Tanya ; Bar-Shira, Anat ; Gana-Weisz, Mali ; Goldstein, Orly ; Kestenbaum, Meir ; Cedarbaum, Jesse M. ; Orr-Urtreger, Avi ; Shenhar-Tsarfaty, Shani ; Mirelman, Anat
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2021-04, Vol.268 (4), p.1517-1525
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Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson’s disease
Author / Creator:Thaler, Avner ; Shenhar-Tsarfaty, Shani ; Shaked, Yanay ; Gurevich, Tanya ; Omer, Nurit ; Bar-Shira, Anat ; Gana-Weisz, Mali ; Goldstein, Orly ; Kestenbaum, Meir ; Cedarbaum, Jesse M. ; Orr-Urtreger, Avi ; Giladi, Nir ; Mirelman, Anat
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-06, Vol.10 (1), p.9329-9329, Article 9329
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Radiological markers of CSF α-synuclein aggregation in Parkinson’s disease patients
Author / Creator:Droby, Amgad ; Yoffe-Vasiliev, Avital ; Atias, Daniel ; Fraser, Kyle B. ; Mabrouk, Omar S. ; Omer, Nurit ; Bar-Shira, Anat ; Gana-Weisz, Mali ; Goldstein, Orly ; Artzi, Moran ; Ben Bashat, Dafna ; Alcalay, Roy N. ; Orr-Urtreger, Avi ; Shirvan, Julia C. ; Cedarbaum, Jesse M. ; Giladi, Nir ; Mirelman, Anat ; Thaler, Avner
Publisher:London: Nature Publishing Group UK
Journal title:NPJ Parkinson's Disease, 2025-01, Vol.11 (1), p.7-9, Article 7
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Genome-wide case-only analysis of gene-gene interactions with known Parkinson’s disease risk variants reveals link between LRRK2 and SYT10
Author / Creator:Aleknonytė-Resch, Milda ; Trinh, Joanne ; Leonard, Hampton ; Delcambre, Sylvie ; Leitão, Elsa ; Lai, Dongbing ; Smajić, Semra ; Orr-Urtreger, Avi ; Thaler, Avner ; Blauwendraat, Cornelis ; Sharma, Arunabh ; Makarious, Mary B. ; Kim, Jonggeol Jeff ; Lake, Julie ; Rahmati, Pegah ; Freitag-Wolf, Sandra ; Seibler, Philip ; Foroud, Tatiana ; Singleton, Andrew B. ; Grünewald, Anne ; Kaiser, Frank ; Klein, Christine ; Krawczak, Michael ; Dempfle, Astrid
Publisher:London: Nature Publishing Group UK
Journal title:NPJ Parkinson's Disease, 2023-06, Vol.9 (1), p.102-102, Article 102
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Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives
Author / Creator:Gupte, Manisha ; Alcalay, Roy N. ; Mejia-Santana, Helen ; Raymond, Deborah ; Saunders-Pullman, Rachel ; Roos, Ernest ; Orbe-Reily, Martha ; Tang, Ming-X ; Mirelman, Anat ; Ozelius, Laurie ; Orr-Urtreger, Avi ; Clark, Lorraine ; Giladi, Nir ; Bressman, Susan ; Marder, Karen
Publisher:Boston: Springer US
Journal title:Journal of genetic counseling, 2015-04, Vol.24 (2), p.238-246
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Decreased expression of B cell related genes in leukocytes of women with Parkinson's disease
Author / Creator:Kedmi, Merav ; Bar-Shira, Anat ; Gurevich, Tanya ; Giladi, Nir ; Orr-Urtreger, Avi
Publisher:England: BioMed Central Ltd
Journal title:Molecular neurodegeneration, 2011-09, Vol.6 (1), p.66-66, Article 66
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Megacystis, mydriasis, and ion channel defect in mice lacking the α3 neuronal nicotinic acetylcholine receptor
Author / Creator:Xu, Wei ; Gelber, Shari ; Orr-Urtreger, Avi ; Armstrong, Dawna ; Lewis, Richard A. ; Ou, Ching-Nan ; Patrick, James ; Role, Lorna ; De Biasi, Mariella ; Beaudet, Arthur L.
Publisher:National Acad Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1999-05, Vol.96 (10), p.5746-5751
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Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population
Author / Creator:Simchoni, Sharon ; Friedman, Eitan ; Kaufman, Bella ; Gershoni-Baruch, Ruth ; Orr-Urtreger, Avi ; Kedar-Barnes, Inbal ; Shiri-Sverdlov, Ronit ; Dagan, Efrat ; Tsabari, Sigal ; Shohat, Mordechai ; Catane, Raphael ; King, Mary-Claire ; Lahad, Amnon ; Levy-Lahad, Ephrat
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2006-03, Vol.103 (10), p.3770-3774
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Linkage of a Neurophysiological Deficit in Schizophrenia to a Chromosome 15 Locus
Author / Creator:Freedman, Robert ; Coon, Hilary ; Myles-Worsley, Marina ; Orr-Urtreger, Avi ; Olincy, Ann ; Davis, Ashley ; Polymeropoulos, Mihael ; Holik, John ; Hopkins, Jan ; Hoff, Mark ; Rosenthal, Judy ; Waldo, Merilyne C. ; Reimherr, Fred ; Wender, Paul ; Yaw, Jeffrey ; Young, David A. ; Breese, Charles R. ; Adams, Catherine ; Patterson, David ; Adler, Lawrence E. ; Kruglyak, Leonid ; Leonard, Sherry ; Byerley, William
Publisher:United States: National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 1997-01, Vol.94 (2), p.587-592
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A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers
Author / Creator:Bregman, Noa ; Thaler, Avner ; Mirelman, Anat ; Helmich, Rick C. ; Gurevich, Tanya ; Orr-Urtreger, Avi ; Marder, Karen ; Bressman, Susan ; Bloem, Bastiaan R. ; Giladi, Nir
Journal title:Brain structure & function, 2017-04, Vol.222 (3), p.1207-1218
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Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations
Author / Creator:Gavert, Nancy ; Yaron, Yuval ; Naiman, Tova ; Bercovich, Dani ; Rozen, Paul ; Shomrat, Ruth ; Legum, Cyril ; Orr-Urtreger, Avi
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2002-06, Vol.19 (6), p.664-664
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MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome
Author / Creator:Yaron, Yuval ; Ben Zeev, Bruria ; Shomrat, Ruth ; Bercovich, Dani ; Naiman, Tova ; Orr-Urtreger, Avi
Publisher:New York: Wiley Subscription Services, Inc., A Wiley Company
Journal title:Human mutation, 2002-10, Vol.20 (4), p.323-324
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Cellular and humoral immune response to the fourth Pfizer-BioNTech COVID-19 vaccine dose in individuals aged 60 years and older
Author / Creator:Saiag, Esther ; Alcalay, Yifat ; Marudi, Or ; Orr-Urtreger, Avi ; Hagin, David
Publisher:Netherlands: Elsevier Ltd
Journal title:Vaccine, 2023-01, Vol.41 (4), p.914-921
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Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study
Author / Creator:Simuni, Tanya ; Uribe, Liz ; Caspell-Garcia, Chelsea ; Coffey, Christopher S ; Siderowf, Andrew ; Trojanowski, John Q ; Shaw, Leslie M ; Seibyl, John ; Toga, Arthur W ; Galasko, Doug ; Tosun, Duygu ; Poston, Kathleen ; Weintraub, Daniel ; Mollenhauer, Brit ; Tanner, Caroline M ; Kieburtz, Karl ; Hutten, Samantha J ; Bressman, Susan ; Marek, Kenneth ; Chowdhury, Sohini ; Sherer, Todd ; Casaceli, Cynthia ; Dorsey, Ray ; Wilson, Renee ; Mahes, Sugi ; Salerno, Christina ; Crawford, Karen ; Casalin, Paola ; Malferrari, Giulia ; Weisz, Mali Gani ; Orr-Urtreger, Avi ; Montine, Thomas ; Baglieri, Chris ; Russell, David ; Giladi, Nir ; Factor, Stewart ; Hauser, Robert ; Jankovic, Joseph ; Saint-Hilaire, Marie ; Richard, Irene ; Shprecher, David ; Brockmann, Katrina ; Barone, Paolo ; Espay, Alberto ; Santiago, Anthony ; Hu, Shu-Ching ; Isaacson, Stuart ; Corvol, Jean-Christophe ; Ruiz Martinez, Javiar ; Tolosa, Eduardo ; Tai, Yen ; Smejdir, Debra ; Rees, Linda ; Williams, Karen ; Kausar, Farah ; Richardson, Whitney ; Willeke, Diana ; Peacock, Shawnees ; Sommerfeld, Barbara ; Freed, Alison ; Guthrie, Stephanie ; Harrell, Leigh ; Thomas, Cathi-Ann ; James, Raymond ; Zimmerman, Grace ; Mule, Jennifer ; Hilt, Ella ; Ribb, Kori ; Ainscough, Susan ; Ranola, Madelaine ; Mejia Santana, Helen ; Moreno, Juliana ; Raymond, Deborah ; Carvajal, Lisbeth ; Carvalo, Stephanie ; Croitoru, Ioana ; Garrido, Alicia ; Payne, Laura Marie ; Viswanth, Veena ; Severt, Lawrence ; Facheris, Maurizio ; Cedarbaum, Jesse ; Taylor, Peggy ; Haider Sheikh, Zulfiqar ; Fischer, Tanya ; Sardi, Pablo ; Forrat, Remi ; Reith, Alastair ; Ahlberg Hillert, Gabrielle ; Saba, Barbara ; Min, Chris ; Umek, Robert ; Mather, Joe ; De Santi, Susan ; Post, Anke ; Boess, Frank ; Taylor, Kirsten ; Grachev, Igor ; Muglia, Pierandrea ; Merchant, Kaplana
Publisher:England: Elsevier Ltd
Journal title:Lancet neurology, 2020-01, Vol.19 (1), p.71-80
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White matter abnormalities in healthy E200K carriers may serve as an early biomarker for genetic Creutzfeldt-Jakob disease (gCJD)
Author / Creator:Omer, Nurit ; Droby, Amgad ; Silbak, Rawan ; Trablus, Noa ; Bar David, Aya ; Shiner, Tamara ; Alcalay, Yifat ; Alcalay, Roy ; Nathan, Talya ; Thaler, Avner ; Mirelman, Anat ; Gana Weisz, Mali ; Goldstein, Orly ; Glinka, Tal ; Orr-Urtreger, Avi ; Giladi, Nir ; Bregman, Noa
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of neurology, neurosurgery and psychiatry, 2024-07, Vol.96 (3), p.226-230
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Novel mutations in the emerin gene in Israeli families
Author / Creator:Nevo, Yoram ; Ahituv, Sarit ; Yaron, Yuval ; Kedmi, Merav ; Shomrat, Ruth ; Legum, Cyril ; Orr-Urtreger, Avi
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2001-06, Vol.17 (6), p.522-522
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IMAPT/I Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis
Author / Creator:Shani, Shachar ; Gana-Weisz, Mali ; Bar-Shira, Anat ; Thaler, Avner ; Gurevich, Tanya ; Mirelman, Anat ; Giladi, Nir ; Alcalay, Roy N ; Goldstein, Orly ; Orr-Urtreger, Avi
Publisher:MDPI AG
Journal title:Genes, 2023-12, Vol.15 (1)
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MAPT Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis
Author / Creator:Shani, Shachar ; Gana-Weisz, Mali ; Bar-Shira, Anat ; Thaler, Avner ; Gurevich, Tanya ; Mirelman, Anat ; Giladi, Nir ; Alcalay, Roy N. ; Goldstein, Orly ; Orr-Urtreger, Avi
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-01, Vol.15 (1), p.46
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Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson’s Disease and Their First-Degree Unaffected Relatives
Author / Creator:Thaler, Avner ; Kliper, Efrat ; Maidan, Inbal ; Herman, Talia ; Rosenberg-Katz, Keren ; Bregman, Noa ; Gurevich, Tanya ; Shiner, Tamara ; Hausdorff, Jeffrey M. ; Orr-Urtreger, Avi ; Giladi, Nir ; Mirelman, Anat
Publisher:New York: Springer US
Journal title:Brain topography, 2018-11, Vol.31 (6), p.1029-1036
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Altered reward-related neural responses in non-manifesting carriers of the Parkinson disease related LRRK2 mutation
Author / Creator:Thaler, Avner ; Gonen, Tal ; Mirelman, Anat ; Helmich, Rick C. ; Gurevich, Tanya ; Orr-Urtreger, Avi ; Bloem, Bastiaan R. ; Giladi, Nir ; Hendler, Talma
Publisher:New York: Springer US
Journal title:Brain imaging and behavior, 2019-08, Vol.13 (4), p.1009-1020
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Biochemical markers for severity and risk in GBA and LRRK2 Parkinson’s disease

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Metabolic syndrome does not influence the phenotype of LRRK2 and GBA related Parkinson’s disease

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Radiological markers of CSF α-synuclein aggregation in Parkinson’s disease patients

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Genome-wide case-only analysis of gene-gene interactions with known Parkinson’s disease risk variants reveals link between LRRK2 and SYT10

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Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives

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

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Megacystis, mydriasis, and ion channel defect in mice lacking the α3 neuronal nicotinic acetylcholine receptor

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Familial Clustering of Site-Specific Cancer Risks Associated with BRCA1 and BRCA2 Mutations in the Ashkenazi Jewish Population

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Linkage of a Neurophysiological Deficit in Schizophrenia to a Chromosome 15 Locus

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A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers

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Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations

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MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome

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Cellular and humoral immune response to the fourth Pfizer-BioNTech COVID-19 vaccine dose in individuals aged 60 years and older

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Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

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White matter abnormalities in healthy E200K carriers may serve as an early biomarker for genetic Creutzfeldt-Jakob disease (gCJD)

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Novel mutations in the emerin gene in Israeli families

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IMAPT/I Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis

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MAPT Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis

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Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson’s Disease and Their First-Degree Unaffected Relatives

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Altered reward-related neural responses in non-manifesting carriers of the Parkinson disease related LRRK2 mutation

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