Pharmacogenetics of Antipsychotic-Induced Movement Disorders as a Resource for Better Understanding Parkinson’s Disease Modifier Genes

por Greenbaum, Lior, Lerer, Bernard
Publicado 2015

Perspective: Identification of genetic variants associated with dopaminergic compensatory mechanisms in early Parkinson's disease

por Greenbaum, Lior, Lorberboym, Mordechai, Melamed, Eldad, Rigbi, Amihai, Barhum, Yael, Kohn, Yoav, Khlebtovsky, Alexander, Lerer, Bernard, Djaldetti, Ruth
Publicado 2013

Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10‐year period

por Eyal, Ori, Berkenstadt, Michal, Reznik‐Wolf, Haike, Poran, Hana, Ziv‐Baran, Tomer, Greenbaum, Lior, Yonath, Hagit, Pras, Elon
Publicado 2019

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

por Alkelai, Anna, Greenbaum, Lior, Lupoli, Sara, Kohn, Yoav, Sarner-Kanyas, Kyra, Ben-Asher, Edna, Lancet, Doron, Macciardi, Fabio, Lerer, Bernard
Publicado 2012

TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

por Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior
Publicado 2019

Publisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

por Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior
Publicado 2020

Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa Anomalies

por Greenbaum, Lior, Maya, Idit, Sagi-Dain, Lena, Sukenik-Halevy, Rivka, Berkenstadt, Michal, Yonath, Hagith, Rienstein, Shlomit, Shalata, Adel, Katorza, Eldad, Singer, Amihood
Publicado 2021

Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population

por Greenbaum, Lior, Ben‐David, Merav, Nikitin, Vera, Gera, Orna, Barel, Ortal, Hersalis‐Eldar, Adi, Shamash, Jana, Shimshoviz, Noam, Reznik‐Wolf, Haike, Shohat, Mordechai, Dominissini, Dan, Pras, Elon, Dori, Amir
Publicado 2021

Neural correlates of subjective cognitive decline in adults at high risk for Alzheimer’s disease

por Ben-Ami, Liat, Ravona-Springer, Ramit, Tsarfaty, Galia, Raizman, Reut, Shumacher, Aleeza, Sharvit-Ginon, Inbal, Greenbaum, Lior, Bendlin, Barbara B., Okun, Eitan, Heymann, Anthony, Schnaider Beeri, Michal, Livny, Abigail
Publicado 2023

Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin

por Wilf-Yarkoni, Adi, Shor, Oded, Fellner, Avi, Hellmann, Mark Andrew, Pras, Elon, Yonath, Hagit, Shkedi-Rafid, Shiri, Basel-Salmon, Lina, Bazak, Lili, Eliahou, Ruth, Greenbaum, Lior, Stiebel-Kalish, Hadas, Benninger, Felix, Goldberg, Yael
Publicado 2021

Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features

por Dori, Amir, Arad, Michael, Wasserstrum, Yishay, Pollak, Arthur, Nikitin, Vera, Ben‐David, Merav, Shamash, Jana, Nahum, Ayelet Hashachar, Shavit‐Stein, Efrat, Domachevsky, Liran, Kuperstein, Rafael, Dominissini, Dan, Shelestovich, Natalia, Sadeh, Menachem, Pras, Elon, Greenbaum, Lior
Publicado 2023

Alzheimer’s Disease Polygenic Risk Score Is Not Associated With Cognitive Decline Among Older Adults With Type 2 Diabetes

por Manzali, Sigalit B., Yu, Eric, Ravona-Springer, Ramit, Livny, Abigail, Golan, Sapir, Ouyang, Yuxia, Lesman-Segev, Orit, Liu, Lang, Ganmore, Ithamar, Alkelai, Anna, Gan-Or, Ziv, Lin, Hung-Mo, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior
Publicado 2022

Haptoglobin 1-1 Genotype Modulates the Association of Glycemic Control With Hippocampal Volume in Elderly Individuals With Type 2 Diabetes

por Livny, Abigail, Ravona-Springer, Ramit, Heymann, Anthony, Priess, Rachel, Kushnir, Tammar, Tsarfaty, Galia, Rabinov, Leeron, Moran, Reut, Tik, Niv, Moshier, Erin, Cooper, Itzik, Greenbaum, Lior, Silverman, Jeremy, Levy, Andrew, Sano, Mary, Bendlin, Barbara B., Buchman, Aron S., Schnaider-Beeri, Michal
Publicado 2017

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

por Greenbaum, Lior, Pode-Shakked, Ben, Eisenberg-Barzilai, Shlomit, Dicastro-Keidar, Michal, Bar-Ziv, Anat, Goldstein, Nurit, Reznik-Wolf, Haike, Poran, Hana, Rigbi, Amihai, Barel, Ortal, Bertoli-Avella, Aida M., Bauer, Peter, Regev, Miriam, Raas-Rothschild, Annick, Pras, Elon, Berkenstadt, Michal
Publicado 2019

Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay

por Eliyahu, Aviva, Barel, Ortal, Greenbaum, Lior, Zaks Hoffer, Gal, Goldberg, Yael, Raas-Rothschild, Annick, Singer, Amihood, Bar-Joseph, Ifat, Kunik, Vered, Javasky, Elisheva, Staretz-Chacham, Orna, Pode-Shakked, Naomi, Bazak, Lily, Ruhrman-Shahar, Noa, Pras, Elon, Frydman, Moshe, Shohat, Mordechai, Pode-Shakked, Ben
Publicado 2022

Vici syndrome in Israel: Clinical and molecular insights

por Chorin, Odelia, Hirsch, Yoel, Rock, Rachel, Salzer Sheelo, Liat, Goldberg, Yael, Mandel, Hanna, Hershkovitz, Tova, Fleischer, Nicole, Greenbaum, Lior, Katz, Uriel, Barel, Ortal, Hamed, Nasrin, Ben-Zeev, Bruria, Greenberger, Shoshana, Nasser Samra, Nadra, Stern Zimmer, Michal, Raas-Rothschild, Annick, Pode-Shakked, Ben
Publicado 2022

Association of rare variants in ARSA with Parkinson’s disease

por Senkevich, Konstantin, Beletskaia, Mariia, Dworkind, Aliza, Yu, Eric, Ahmad, Jamil, Ruskey, Jennifer A., Asayesh, Farnaz, Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Nagornov, Ilya, Tyurin, Alexandr, Miliukhina, Irina, Timofeeva, Alla, Emelyanov, Anton, Zakharova, Ekaterina, Alcalay, Roy N., Pchelina, Sofya, Gan-Or, Ziv
Publicado 2023

Analysis of common and rare VPS13C variants in late-onset Parkinson disease

por Rudakou, Uladzislau, Ruskey, Jennifer A., Krohn, Lynne, Laurent, Sandra B., Spiegelman, Dan, Greenbaum, Lior, Yahalom, Gilad, Desautels, Alex, Montplaisir, Jacques Y., Fahn, Stanley, Waters, Cheryl H., Levy, Oren, Kehoe, Caitlin M., Narayan, Sushma, Dauvilliers, Yves, Dupré, Nicolas, Hassin-Baer, Sharon, Alcalay, Roy N., Rouleau, Guy A., Fon, Edward A., Gan-Or, Ziv
Publicado 2020

Investigation of the HSPG2 Gene in Tardive Dyskinesia – New Data and Meta-Analysis

por Zai, Clement C., Lee, Frankie H., Tiwari, Arun K., Lu, Justin Y., de Luca, Vincenzo, Maes, Miriam S., Herbert, Deanna, Shahmirian, Anashe, Cheema, Sheraz Y., Zai, Gwyneth C., Atukuri, Anupama, Sherman, Michael, Shaikh, Sajid A., Tampakeras, Maria, Freeman, Natalie, King, Nicole, Müller, Daniel J., Greenbaum, Lior, Lerer, Bernard, Voineskos, Aristotle N., Potkin, Steven G., Lieberman, Jeffrey A., Meltzer, Herbert Y., Remington, Gary, Kennedy, James L.
Publicado 2018

GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson’s disease

por Senkevich, Konstantin, Zorca, Cornelia E, Dworkind, Aliza, Rudakou, Uladzislau, Somerville, Emma, Yu, Eric, Ermolaev, Alexey, Nikanorova, Daria, Ahmad, Jamil, Ruskey, Jennifer A, Asayesh, Farnaz, Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Greenbaum, Lior, Hassin-Baer, Sharon, Grenn, Francis P, Chiang, Ming Sum Ruby, Sardi, S Pablo, Vanderperre, Benoît, Blauwendraat, Cornelis, Trempe, Jean-François, Fon, Edward A, Durcan, Thomas M, Alcalay, Roy N, Gan-Or, Ziv
Publicado 2022