The benefit of diagnostic whole genome sequencing in schizophrenia and other psychotic disorders von Alkelai, Anna, Greenbaum, Lior, Docherty, Anna R., Shabalin, Andrey A., Povysil, Gundula, Malakar, Ayan, Hughes, Daniel, Delaney, Shannon L., Peabody, Emma P., McNamara, James, Gelfman, Sahar, Baugh, Evan H., Zoghbi, Anthony W., Harms, Matthew B., Hwang, Hann-Shyan, Grossman-Jonish, Anat, Aggarwal, Vimla, Heinzen, Erin L., Jobanputra, Vaidehi, Pulver, Ann E., Lerer, Bernard, Goldstein, David B.

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Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations von Yahalom, Gilad, Greenbaum, Lior, Israeli-Korn, Simon, Fay-Karmon, Tsvia, Livneh, Vered, Ruskey, Jennifer A., Roncière, Léanne, Alam, Armaghan, Gan-Or, Ziv, Hassin-Baer, Sharon

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

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Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia von Alkelai, Anna, Shohat, Shahar, Greenbaum, Lior, Schechter, Tanya, Draiman, Benjamin, Chitrit-Raveh, Eti, Rienstein, Shlomit, Dagaonkar, Neha, Hughes, Daniel, Aggarwal, Vimla S, Heinzen, Erin L, Shifman, Sagiv, Goldstein, David B, Kohn, Yoav

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

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A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies von Pode-Shakked, Ben, Barel, Ortal, Singer, Amihood, Regev, Miriam, Poran, Hana, Eliyahu, Aviva, Finezilber, Yael, Segev, Meirav, Berkenstadt, Michal, Yonath, Hagith, Reznik-Wolf, Haike, Gazit, Yael, Chorin, Odelia, Heimer, Gali, Gabis, Lidia V., Tzadok, Michal, Nissenkorn, Andreea, Bar-Yosef, Omer, Zohar-Dayan, Efrat, Ben-Zeev, Bruria, Mor, Nofar, Kol, Nitzan, Nayshool, Omri, Shimshoviz, Noam, Bar-Joseph, Ifat, Marek-Yagel, Dina, Javasky, Elisheva, Einy, Reviva, Gal, Moran, Grinshpun-Cohen, Julia, Shohat, Mordechai, Dominissini, Dan, Raas-Rothschild, Annick, Rechavi, Gideon, Pras, Elon, Greenbaum, Lior

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Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample von Alkelai, Anna, Greenbaum, Lior, Lupoli, Sara, Kohn, Yoav, Sarner-Kanyas, Kyra, Ben-Asher, Edna, Lancet, Doron, Macciardi, Fabio, Lerer, Bernard

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Muscular dystrophy patients show low exercise‐induced blood flow in muscles with normal strength von Gera, Orna, Shavit‐Stein, Efrat, Amichai, Taly, Chapman, Joab, Chorin, Odelia, Greenbaum, Lior, Dori, Amir

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The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons von Jones-Tabah, Jace, He, Kathy, Karpilovsky, Nathan, Senkevich, Konstantin, Deyab, Ghislaine, Pietrantonio, Isabella, Goiran, Thomas, Cousineau, Yuting, Nikanorova, Daria, Goldsmith, Taylor, Del Cid Pellitero, Esther, Chen, Carol X-Q, Luo, Wen, You, Zhipeng, Abdian, Narges, Ahmad, Jamil, Ruskey, Jennifer A, Asayesh, Farnaz, Spiegelman, Dan, Fahn, Stanley, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Miliukhina, Irina, Timofeeva, Alla, Emelyanov, Anton, Pchelina, Sofya, Greenbaum, Lior, Hassin-Baer, Sharon, Alcalay, Roy N, Milnerwood, Austen, Durcan, Thomas M, Gan-Or, Ziv, Fon, Edward A

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

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TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes von Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior

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

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Publisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes von Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior

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

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Vici syndrome in Israel: Clinical and molecular insights von 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

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

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Are rare heterozygous SYNJ1 variants associated with Parkinson’s disease? von Senkevich, Konstantin, Parlar, Sitki Cem, Chantereault, Cloe, Yu, Eric, Ahmad, Jamil, Ruskey, Jennifer A., Asayesh, Farnaz, Spiegelman, Dan, Waters, Cheryl, Monchi, Oury, Dauvilliers, Yves, Dupré, Nicolas, Miliukhina, Irina, Timofeeva, Alla, Emelyanov, Anton, Pchelina, Sofya, Greenbaum, Lior, Hassin-Baer, Sharon, Alcalay, Roy N., Gan-Or, Ziv

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Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features von 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

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LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder von Chettle, James, Louie, Raymond J., Larner, Olivia, Best, Robert, Chen, Kevin, Morris, Josephine, Dedeic, Zinaida, Childers, Anna, Rogers, R. Curtis, DuPont, Barbara R., Skinner, Cindy, Küry, Sébastien, Uguen, Kevin, Planes, Marc, Monteil, Danielle, Li, Megan, Eliyahu, Aviva, Greenbaum, Lior, Mor, Nofar, Besnard, Thomas, Isidor, Bertrand, Cogné, Benjamin, Blesson, Alyssa, Comi, Anne, Wentzensen, Ingrid M., Vuocolo, Blake, Lalani, Seema R., Sierra, Roberta, Berry, Lori, Carter, Kent, Sanders, Stephan J., Blagden, Sarah P.

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

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