The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol von Bregman, Noa, Shiner, Tamara, Kavé, Gitit, Alcalay, Roy, Gana-Weisz, Mali, Goldstein, Orly, Glinka, Tal, Aizenstein, Orna, Bashat, Dafna Ben, Alcalay, Yifat, Mirelman, Anat, Thaler, Avner, Giladi, Nir, Omer, Nurit

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A Possible Modifying Effect of the G2019S Mutation in the LRRK2 Gene on GBA Parkinson's Disease von Omer, Nurit, Giladi, Nir, Gurevich, Tanya, Bar‐Shira, Anat, Gana‐Weisz, Mali, Goldstein, Orly, Kestenbaum, Meir, Cedarbaum, Jesse M., Orr‐Urtreger, Avi, Mirelman, Anat, Thaler, Avner

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Arm swing as a potential new prodromal marker of Parkinson's disease von Mirelman, Anat, Bernad-Elazari, Hagar, Thaler, Avner, Giladi-Yacobi, Eytan, Gurevich, Tanya, Gana-Weisz, Mali, Saunders-Pullman, Rachel, Raymond, Deborah, Doan, Nancy, Bressman, Susan B., Marder, Karen S., Alcalay, Roy N., Rao, Ashwini K., Berg, Daniela, Brockmann, Kathrin, Aasly, Jan, Waro, Bjørg Johanne, Tolosa, Eduardo, Vilas, Dolores, Pont-Sunyer, Claustre, Orr-Urtreger, Avi, Hausdorff, Jeffrey M., Giladi, Nir

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Glucocerebrosidase Activity Is Not Associated with Parkinson's Disease Risk or Severity von Omer, Nurit, Giladi, Nir, Gurevich, Tanya, Bar‐Shira, Anat, Gana‐Weisz, Mali, Glinka, Tal, Goldstein, Orly, Kestenbaum, Meir, Cedarbaum, Jesse M., Mabrouk, Omar S., Fraser, Kyle B., Shirvan, Julia C., Orr‐Urtreger, Avi, Mirelman, Anat, Thaler, Avner

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The Influence of GBA and LRRK2 on Mood Disorders in Parkinson's Disease von DeBroff, Jake, Omer, Nurit, Cohen, Batsheva, Giladi, Nir, Kestenbaum, Meir, Shirvan, Julia C., Cedarbaum, Jesse M., Gana‐Weisz, Mali, Goldstein, Orly, Orr‐Urtreger, Avi, Mirelman, Anat, Thaler, Avner

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R869C mutation in molecular motor KIF17 gene is involved in dementia with Lewy bodies von Goldstein, Orly, Gana‐Weisz, Mali, Shiner, Tamara, Attar, Reut, Mordechai, Yael, Waldman, Yedael Y., Bar‐Shira, Anat, Thaler, Avner, Gurevich, Tanya, Mirelman, Anat, Giladi, Nir, Orr‐Urtreger, Avi

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A “dose” effect of mutations in the GBA gene on Parkinson's disease phenotype von Thaler, Avner, Gurevich, Tanya, Shira, Anat Bar, Weisz, Mali Gana, Ash, Elissa, Shiner, Tamara, Orr-Urtreger, Avi, Giladi, Nir, Mirelman, Anat

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Effect of GBA1 Mutations and APOE Polymorphisms on Survival and Progression Among Ashkenazi Jews with Dementia with Lewy Bodies von Shiner, Tamara, Kavé, Gitit, Mirelman, Anat, Regev, Keren, Piura, Yoav, Goldstein, Orly, Gana Weisz, Mali, Bar-Shira, Anat, Gurevich, Tanya, Orr-Urtreger, Avi, Alcalay, Roy N, Giladi, Nir, Bregman, Noa

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Application of the Movement Disorder Society prodromal criteria in healthy G2019S‐LRRK2 carriers von Mirelman, Anat, Saunders‐Pullman, Rachel, Alcalay, Roy N., Shustak, Shiran, Thaler, Avner, Gurevich, Tanya, Raymond, Deborah, Mejia‐Santana, Helen, Orbe Reilly, Martha, Ozelius, Laurie, Clark, Lorraine, Gana‐Weisz, Mali, Bar‐Shira, Anat, Orr‐Utreger, Avi, Bressman, Susan B., Marder, Karen, Giladi, Nir

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TMEM16F regulates pathologic α-synuclein secretion and spread in cellular and mouse models of Parkinson's disease von Cohen-Adiv, Stav, Amer-Sarsour, Fatima, Berdichevsky, Yevgeny, Boxer, Emily, Goldstein, Orly, Gana-Weisz, Mali, Tripathi, Utkarsh, Rike, Wote Amelo, Prag, Gali, Gurevich, Tanya, Giladi, Nir, Stern, Shani, Orr-Urtreger, Avi, Friedmann-Morvinski, Dinorah, Ashkenazi, Avraham

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Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations von Alcalay, Roy N., Mirelman, Anat, Saunders-Pullman, Rachel, Tang, Ming-X, Mejia Santana, Helen, Raymond, Deborah, Roos, Ernest, Orbe-Reilly, Martha, Gurevich, Tanya, Bar Shira, Anat, Gana Weisz, Mali, Yasinovsky, Kira, Zalis, Maayan, Thaler, Avner, Deik, Andres, Barrett, Matthew James, Cabassa, Jose, Groves, Mark, Hunt, Ann L., Lubarr, Naomi, San Luciano, Marta, Miravite, Joan, Palmese, Christina, Sachdev, Rivka, Sarva, Harini, Severt, Lawrence, Shanker, Vicki, Swan, Matthew Carrington, Soto-Valencia, Jeannie, Johannes, Brooke, Ortega, Robert, Fahn, Stanley, Cote, Lucien, Waters, Cheryl, Mazzoni, Pietro, Ford, Blair, Louis, Elan, Levy, Oren, Rosado, Llency, Ruiz, Diana, Dorovski, Tsvyatko, Pauciulo, Michael, Nichols, William, Orr-Urtreger, Avi, Ozelius, Laurie, Clark, Lorraine, Giladi, Nir, Bressman, Susan, Marder, Karen S.

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Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene von Mirelman, Anat, Alcalay, Roy N., Saunders-Pullman, Rachel, Yasinovsky, Kira, Thaler, Avner, Gurevich, Tanya, Mejia-Santana, Helen, Raymond, Deborah, Gana-Weisz, Mali, Bar-Shira, Anat, Ozelius, Laurie, Clark, Lorraine, Orr-Urtreger, Avi, Bressman, Susan, Marder, Karen, Giladi, Nir

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The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression von Shema, Efrat, Tirosh, Itay, Aylon, Yael, Huang, Jing, Ye, Chaoyang, Moskovits, Neta, Raver-Shapira, Nina, Minsky, Neri, Pirngruber, Judith, Tarcic, Gabi, Hublarova, Pavla, Moyal, Lilach, Gana-Weisz, Mali, Shiloh, Yosef, Yarden, Yossef, Johnsen, Steven A, Vojtesek, Borivoj, Berger, Shelley L, Oren, Moshe

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A new functional Ras antagonist inhibits human pancreatic tumor growth in nude mice von WEISZ, B, GIEHL, K, GANA-WEISZ, M, EGOZI, Y, BEN-BARUCH, G, MARCIANO, D, GIERSCHIK, P, KLOOG, Y

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A novel super-resolution microscopy platform for cutaneous alpha-synuclein detection in Parkinson's disease von Sade, Ofir, Fischel, Daphna, Barak-Broner, Noa, Halevi, Shir, Gottfried, Irit, Bar-On, Dana, Sachs, Stefan, Mirelman, Anat, Thaler, Avner, Gour, Aviv, Kestenbaum, Meir, Gana Weisz, Mali, Anis, Saar, Soto, Claudio, Roitman, Melanie Shanie, Shahar, Shimon, Doppler, Kathrin, Sauer, Markus, Giladi, Nir, Lev, Nirit, Alcalay, Roy N, Hassin-Baer, Sharon, Ashery, Uri

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Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease von Kozlovski, Tal, Mitelpunkt, Alexis, Thaler, Avner, Gurevich, Tanya, Orr-Urtreger, Avi, Gana-Weisz, Mali, Shachar, Netta, Galili, Tal, Marcus-Kalish, Mira, Bressman, Susan, Marder, Karen, Giladi, Nir, Benjamini, Yoav, Mirelman, Anat

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Differential effects of severe vs mild GBA mutations on Parkinson disease von Gan-Or, Ziv, Amshalom, Idan, Kilarski, Laura L, Bar-Shira, Anat, Gana-Weisz, Mali, Mirelman, Anat, Marder, Karen, Bressman, Susan, Giladi, Nir, Orr-Urtreger, Avi

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Dislodgment and Accelerated Degradation of Ras von Haklai, Roni, Weisz, Mali Gana, Elad, Galit, Paz, Ariella, Marciano, Daniele, Egozi, Yaakov, Ben-Baruch, Gilad, Kloog, Yoel

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The Ras Inhibitor S-trans,trans-Farnesylthiosalicylic Acid Chemosensitizes Human Tumor Cells Without Causing Resistance von Gana-Weisz, Mali, Halaschek-Wiener, Julius, Jansen, Burkhard, Elad, Galit, Haklai, Ronit, Kloog, Yoel

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Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics von Goldstein, Orly, Kedmi, Merav, Gana-Weisz, Mali, Twito, Shir, Nefussy, Beatrice, Vainer, Batel, Fainmesser, Yaara, Abraham, Alon, Nayshool, Omri, Orr-Urtreger, Avi, Drory, Vivian E.

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