Resultats de la cerca - Lior Greenbaum

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  1. 1
    Differential contribution of genetic variation in multiple brain nicotinic cholinergic receptors to nicotine dependence: recent progress and emerging open questions

    Differential contribution of genetic variation in multiple brain nicotinic cholinergic receptors to nicotine dependence: recent progress and emerging open questions per Lior Greenbaum, Bernard Lerer

    Publicat 2009
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  2. 2
    Use of fluorescent probes that form intramolecular excimers to monitor structural changes in model and biological membranes

    Use of fluorescent probes that form intramolecular excimers to monitor structural changes in model and biological membranes per R L Melnick, Howard C. Haspel, Merrill Goldenberg, Lior Greenbaum, S. Weinstein

    Publicat 1981
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  3. 3
    Relationship between Rgs2 gene expression level and anxiety and depression-like behaviour in a mutant mouse model: serotonergic involvement

    Relationship between Rgs2 gene expression level and anxiety and depression-like behaviour in a mutant mouse model: serotonergic involvement per Tzuri Lifschytz, Esther Channah Broner, Polina Zozulinsky, Alexandra Slonimsky, Renana Eitan, Lior Greenbaum, Bernard Lerer

    Publicat 2011
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  4. 4
    DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population

    DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population per Anna Alkelai, Sara Lupoli, Lior Greenbaum, Yoav Kohn, Kyra Kanyas-Sarner, Edna Ben‐Asher, Doron Lancet, Fabìo Macciardi, Bernard Lerer

    Publicat 2011
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  5. 5
    Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample

    Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample per Anna Alkelai, Lior Greenbaum, Sara Lupoli, Yoav Kohn, Kyra Sarner-Kanyas, Edna Ben‐Asher, Doron Lancet, Fabìo Macciardi, Bernard Lerer

    Publicat 2012
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  6. 6
    Targeted sequencing of Parkinson’s disease loci genes highlights <i>SYT11, FGF20</i> and other associations

    Targeted sequencing of Parkinson’s disease loci genes highlights <i>SYT11, FGF20</i> and other associations per Uladzislau Rudakou, Eric Yu, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Yves Dauvilliers, Dan Spiegelman, Lior Greenbaum, Stanley Fahn, Cheryl Waters, Nicolas Dupré, Guy A. Rouleau, Sharon Hassin‐Baer, Edward A. Fon, Roy N. Alcalay, Ziv Gan‐Or

    Publicat 2020
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  7. 7
    Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families

    Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families per Lior Greenbaum, Ben Pode‐Shakked, Shlomit Eisenberg‐Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik‐Wolf, Hana Poran, Amihai Rigbi, Ortal Barel, Aida M. Bertoli‐Avella, Peter Bauer, Miriam Regev, Annick Raas‐Rothschild, Elon Pras, Michal Berkenstadt

    Publicat 2019
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  8. 8
    Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's disease

    Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson's disease per Jennifer A. Ruskey, Lior Greenbaum, Léanne Roncière, Armaghan Alam, Dan Spiegelman, Christopher Liong, Oren Levy, Cheryl Waters, Stanley Fahn, Karen Marder, Wendy K. Chung, Gilad Yahalom, Simon Israeli‐Korn, Vered Livneh, Tsvia Fay‐Karmon, Roy N. Alcalay, Sharon Hassin‐Baer, Ziv Gan‐Or

    Publicat 2018
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  9. 9
    Analysis of Heterozygous <scp><i>PRKN</i></scp> Variants and Copy‐Number Variations in Parkinson's Disease

    Analysis of Heterozygous <scp><i>PRKN</i></scp> Variants and Copy‐Number Variations in Parkinson's Disease per Eric Yu, Uladzislau Rudakou, Lynne Krohn, Kheireddin Mufti, Jennifer A. Ruskey, Farnaz Asayesh, Mehrdad A. Estiar, Dan Spiegelman, Matthew Surface, Stanley Fahn, Cheryl Waters, Lior Greenbaum, Alberto J. Espay, Yves Dauvilliers, Nicolas Dupré, Guy A. Rouleau, Sharon Hassin‐Baer, Edward A. Fon, Roy N. Alcalay, Ziv Gan‐Or

    Publicat 2020
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  10. 10
    Pathological variants in <i>TOP3A</i> cause distinct disorders of mitochondrial and nuclear genome stability

    Pathological variants in <i>TOP3A</i> cause distinct disorders of mitochondrial and nuclear genome stability per Direnis Erdinc, Alejandro Rodríguez‐Luis, Mahmoud R. Fassad, Sarah Mackenzie, Christopher M. Watson, Sebastian Valenzuela, Xie Xie, Katja E. Menger, Kate Sergeant, Kate Craig, Sila Hopton, Gavin Falkous, Joanna Poulton, Héctor García‐Moreno, Paola Giunti, Carlos Alberto de Moura Aschoff, Jonas Alex Morales Saute, Amelia Jeanne Kirby, Camilo Toro, Lynne A. Wolfe, Danica Novacic, Lior Greenbaum, Aviva Eliyahu, Ortal Barel, Yair Anikster, Robert McFarland, Gráinne S. Gorman, Andrew M. Schaefer, Claes M. Gustafsson, Robert W. Taylor, Maria Falkenberg, Thomas J. Nicholls

    Publicat 2023
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  11. 11
    <i>SMPD1</i> mutations, activity, and α‐synuclein accumulation in Parkinson's disease

    <i>SMPD1</i> mutations, activity, and α‐synuclein accumulation in Parkinson's disease per Roy N. Alcalay, Victoria Mallett, Benoît Vanderperre, Omid Tavassoly, Yves Dauvilliers, Richard Y. J. Wu, Jennifer A. Ruskey, Claire S. Leblond, Amirthagowri Ambalavanan, Sandra B. Laurent, Dan Spiegelman, Alexandre Dionne‐Laporte, Christopher Liong, Oren Levy, Stanley Fahn, Cheryl Waters, Sheng‐Han Kuo, Wendy K. Chung, Blair Ford, Karen Marder, Un Jung Kang, Sharon Hassin‐Baer, Lior Greenbaum, Jean‐François Trempe, Pavlina Wolf, Petra Oliva, Xiaokui Kate Zhang, Lorraine N. Clark, Mélanie Langlois, Patrick A. Dion, Edward A. Fon, Nicolas Dupré, Guy A. Rouleau, Ziv Gan‐Or

    Publicat 2019
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  12. 12
    Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia

    Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia per Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, Karl Heilbron, Sara Bandrés‐Ciga, Manuela Tan, J. Raphael Gibbs, Dena Hernández, Ravindran Kumaran, Rebekah G. Langston, Luis Bonet‐Ponce, Roy N. Alcalay, Sharon Hassin‐Baer, Lior Greenbaum, Hirotaka Iwaki, Hampton L. Leonard, Francis P. Grenn, Jennifer A. Ruskey, Marya S. Sabir, Sarah Ahmed, Mary B. Makarious, Lasse Pihlstrøm, Mathias Toft, Jacobus J. van Hilten, Johan Marinus, Claudia Schulte, Kathrin Brockmann, Manu Sharma, Ari Siitonen, Kari Majamaa, Johanna Eerola‐Rautio, Pentti J. Tienari, Alexander Pantelyat, Argye E. Hillis, Ted M. Dawson, Liana S. Rosenthal, Marilyn S. Albert, Susan M. Resnick, Luigi Ferrucci, Christopher M. Morris, Olga Pletnikova, Juan C. Troncoso, Donald G. Grosset, Suzanne Lesage, Jean‐Christophe Corvol, Alexis Brice, Alastair Noyce, Eliezer Masliah, Nicholas Wood, John Hardy, Lisa M. Shulman, Joseph Jankovic, Joshua Shulman, Peter Heutink, Thomas Gasser, Paul J. Cannon, Sonja W. Scholz, Huw R. Morris, Mark Cookson, Mike A. Nalls, Ziv Gan‐Or, Andrew Singleton

    Publicat 2019
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