Works by Hassin-Baer, Sharon

Results: 68
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    Adult-onset Alexander disease among patients of Jewish Syrian descent.

    Published in:
    Neurogenetics, 2023, v. 24, n. 4, p. 303, doi. 10.1007/s10048-023-00732-w
    By:
    • Anis, Saar;
    • Fay-Karmon, Tsvia;
    • Lassman, Simon;
    • Shbat, Fadi;
    • Lesman-Segev, Orit;
    • Mor, Nofar;
    • Barel, Ortal;
    • Dominissini, Dan;
    • Chorin, Odelia;
    • Pras, Elon;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon
    Publication type:
    Article
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    A diagnostic ceiling for exome sequencing in cerebellar ataxia and related neurological disorders.

    Published in:
    Human Mutation, 2020, v. 41, n. 2, p. 487, doi. 10.1002/humu.23946
    By:
    • Ngo, Kathie J.;
    • Rexach, Jessica E.;
    • Lee, Hane;
    • Petty, Lauren E.;
    • Perlman, Susan;
    • Valera, Juliana M.;
    • Deignan, Joshua L.;
    • Mao, Yuanming;
    • Aker, Mamdouh;
    • Posey, Jennifer E.;
    • Jhangiani, Shalini N.;
    • Coban‐Akdemir, Zeynep H.;
    • Boerwinkle, Eric;
    • Muzny, Donna;
    • Nelson, Alexandra B.;
    • Hassin‐Baer, Sharon;
    • Poke, Gemma;
    • Neas, Katherine;
    • Geschwind, Michael D.;
    • Grody, Wayne W.
    Publication type:
    Article
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    Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 11, p. 1416, doi. 10.1001/jamaneurol.2018.1885
    By:
    • Blauwendraat, Cornelis;
    • Reed, Xylena;
    • Kia, Demis A.;
    • Gan-Or, Ziv;
    • Lesage, Suzanne;
    • Pihlstrøm, Lasse;
    • Guerreiro, Rita;
    • Gibbs, J. Raphael;
    • Sabir, Marya;
    • Ahmed, Sarah;
    • Ding, Jinhui;
    • Alcalay, Roy N.;
    • Hassin-Baer, Sharon;
    • Pittman, Alan M.;
    • Brooks, Janet;
    • Edsall, Connor;
    • Hernandez, Dena G.;
    • Chung, Sun Ju;
    • Goldwurm, Stefano;
    • Toft, Mathias
    Publication type:
    Article
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    The impact of early versus late levodopa administration.

    Published in:
    Journal of Neural Transmission, 2017, v. 124, n. 4, p. 471, doi. 10.1007/s00702-016-1669-4
    By:
    • Yahalom, Gilad;
    • Cohen, Oren;
    • Warmann-Alaluf, Naama;
    • Shabat, Chen;
    • Strauss, Hanna;
    • Elincx-Benizri, Sandra;
    • Israeli-Korn, Simon;
    • Stein, Esther;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon
    Publication type:
    Article
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    LRRK2 rare-variant per-domain genetic burden in Parkinson's Disease: association confined to the kinase domain.

    Published in:
    NPJ Parkinson's Disease, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41531-025-00934-z
    By:
    • Parlar, Sitki Cem;
    • Senkevich, Konstantin;
    • Yu, Eric;
    • Ruskey, Jennifer A.;
    • Ahmad, Jamil;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Waters, Cheryl;
    • Monchi, Oury;
    • Dauvilliers, Yves;
    • Dupré, Nicolas;
    • Greenbaum, Lior;
    • Hassin-Baer, Sharon;
    • Miliukhina, Irina;
    • Timofeeva, Alla;
    • Emelyanov, Anton;
    • Pchelina, Sofya;
    • Alcalay, Roy N.;
    • Fon, Edward A.;
    • Trempe, Jean-François
    Publication type:
    Article
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    Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

    Published in:
    NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00809-9
    By:
    • 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
    Publication type:
    Article
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    GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 1859, doi. 10.1093/brain/awac413
    By:
    • 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
    Publication type:
    Article
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    Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

    Published in:
    Brain: A Journal of Neurology, 2020, v. 143, n. 1, p. 234, doi. 10.1093/brain/awz350
    By:
    • Blauwendraat, Cornelis;
    • Reed, Xylena;
    • Krohn, Lynne;
    • Heilbron, Karl;
    • Bandres-Ciga, Sara;
    • Tan, Manuela;
    • Gibbs, J Raphael;
    • Hernandez, Dena G;
    • Kumaran, Ravindran;
    • Langston, Rebekah;
    • Bonet‐Ponce, Luis;
    • Alcalay, Roy N;
    • Hassin-Baer, Sharon;
    • Greenbaum, Lior;
    • Iwaki, Hirotaka;
    • Leonard, Hampton L;
    • Grenn, Francis P;
    • Ruskey, Jennifer A;
    • Sabir, Marya;
    • Ahmed, Sarah
    Publication type:
    Article
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    Novel PINK1 mutations in early‐onset parkinsonism.

    Published in:
    Annals of Neurology, 2004, v. 56, n. 3, p. 424
    By:
    • Yasuko Hatano;
    • Yuanzhe Li;
    • Kenichi Sato;
    • Shuichi Asakawa;
    • Yasuhiro Yamamura;
    • Hiroyuki Tomiyama;
    • Hiroyo Yoshino;
    • Masato Asahina;
    • Susumu Kobayashi;
    • Sharon Hassin‐Baer;
    • Chin‐Song Lu;
    • Arlene R. Ng;
    • Raymond L. Rosales;
    • Nobuyoshi Shimizu;
    • Tatsushi Toda;
    • Yoshikuni Mizuno;
    • Nobutaka Hattori
    Publication type:
    Article
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    Association of Rare Variants in ARSA with Parkinson's Disease.

    Published in:
    Movement Disorders, 2023, v. 38, n. 10, p. 1806, doi. 10.1002/mds.29521
    By:
    • 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
    Publication type:
    Article
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    Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease.

    Published in:
    Movement Disorders, 2021, v. 36, n. 1, p. 178, doi. 10.1002/mds.28299
    By:
    • 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
    Publication type:
    Article
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    Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls.

    Published in:
    2019
    By:
    • Agalliu, Ilir;
    • Ortega, Roberto A.;
    • Luciano, Marta San;
    • Mirelman, Anat;
    • Pont‐Sunyer, Claustre;
    • Brockmann, Kathrin;
    • Vilas, Dolores;
    • Tolosa, Eduardo;
    • Berg, Daniela;
    • Warø, Bjørg;
    • Glickman, Amanda;
    • Raymond, Deborah;
    • Inzelberg, Rivka;
    • Ruiz‐Martinez, Javier;
    • Mondragon, Elisabet;
    • Friedman, Eitan;
    • Hassin‐Baer, Sharon;
    • Alcalay, Roy N.;
    • Mejia‐Santana, Helen;
    • Aasly, Jan
    Publication type:
    journal article
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