Works by Gan-Or, Ziv

Results: 93
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    Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7.

    Published in:
    Movement Disorders, 2021, v. 36, n. 7, p. 1664, doi. 10.1002/mds.28528
    By:
    • Estiar, Mehrdad A.;
    • Yu, Eric;
    • Haj Salem, Ikhlass;
    • Ross, Jay P.;
    • Mufti, Kheireddin;
    • Akçimen, Fulya;
    • Leveille, Etienne;
    • Spiegelman, Dan;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Dagher, Alain;
    • Yoon, Grace;
    • Tarnopolsky, Mark;
    • Boycott, Kym M.;
    • Dupre, Nicolas;
    • Dion, Patrick A.;
    • Suchowersky, Oksana;
    • Trempe, Jean‐Francois;
    • Rouleau, Guy A.;
    • Gan‐Or, Ziv
    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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    The Parkinson's Disease Mendelian Randomization Research Portal.

    Published in:
    2019
    By:
    • Noyce, Alastair J.;
    • Bandres‐Ciga, Sara;
    • Kim, Jonggeol;
    • Heilbron, Karl;
    • Kia, Demis;
    • Hemani, Gibran;
    • Xue, Angli;
    • Lawlor, Debbie A.;
    • Smith, George Davey;
    • Duran, Raquel;
    • Gan‐Or, Ziv;
    • Blauwendraat, Cornelis;
    • Gibbs, J. Raphael;
    • Hinds, David A.;
    • Yang, Jian;
    • Visscher, Peter;
    • Cuzick, Jack;
    • Morris, Huw;
    • Hardy, John;
    • Wood, Nicholas W.
    Publication type:
    journal article
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    The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease.

    Published in:
    2019
    By:
    • Bandres‐Ciga, Sara;
    • Saez‐Atienzar, Sara;
    • Bonet‐Ponce, Luis;
    • Billingsley, Kimberley;
    • Vitale, Dan;
    • Blauwendraat, Cornelis;
    • Gibbs, Jesse Raphael;
    • Pihlstrøm, Lasse;
    • Gan‐Or, Ziv;
    • Noyce, Alastair J;
    • Kaiyrzhanov, Rauan;
    • Middlehurst, Ben;
    • Kia, Demis A;
    • Tan, Manuela;
    • Houlden, Henry;
    • Morris, Huw R;
    • Plun‐Favreau, Helene;
    • Holmans, Peter;
    • Hardy, John;
    • Trabzuni, Daniah
    Publication type:
    journal 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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    GCH1 mutations in hereditary spastic paraplegia.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 1, p. 51, doi. 10.1111/cge.13955
    By:
    • Varghaei, Parizad;
    • Yoon, Grace;
    • Estiar, Mehrdad A.;
    • Veyron, Simon;
    • Leveille, Etienne;
    • Dupré, Nicolas;
    • Trempe, Jean‐François;
    • Rouleau, Guy A.;
    • Gan‐Or, Ziv
    Publication type:
    Article
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    Fine mapping of the HLA locus in Parkinson's disease in Europeans.

    Published in:
    NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00231-5
    By:
    • Yu, Eric;
    • Ambati, Aditya;
    • Andersen, Maren Stolp;
    • Krohn, Lynne;
    • Estiar, Mehrdad A.;
    • Saini, Prabhjyot;
    • Senkevich, Konstantin;
    • Sosero, Yuri L.;
    • Sreelatha, Ashwin Ashok Kumar;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Toft, Mathias;
    • Viken, Marte K.;
    • Sharma, Manu;
    • Blauwendraat, Cornelis;
    • Pihlstrøm, Lasse;
    • Mignot, Emmanuel;
    • Gan-Or, Ziv
    Publication type:
    Article
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    Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.

    Published in:
    NPJ Parkinson's Disease, 2019, v. 5, n. 1, p. N.PAG, doi. 10.1038/s41531-019-0080-x
    By:
    • Billingsley, Kimberley J.;
    • Barbosa, Ines A.;
    • Bandrés-Ciga, Sara;
    • Quinn, John P.;
    • Bubb, Vivien J.;
    • Deshpande, Charu;
    • Botia, Juan A.;
    • Reynolds, Regina H.;
    • Zhang, David;
    • Simpson, Michael A.;
    • Blauwendraat, Cornelis;
    • Gan-Or, Ziv;
    • Gibbs, J. Raphael;
    • Nalls, Mike A.;
    • Singleton, Andrew;
    • Ryten, Mina;
    • Koks, Sulev
    Publication type:
    Article
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    RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 21, p. 3729, doi. 10.1093/hmg/ddac120
    By:
    • Paul, Franziska;
    • Ng, Calista;
    • Sahari, Umar Bin Mohamad;
    • Nafissi, Shahriar;
    • Nilipoor, Yalda;
    • Tavasoli, Ali Reza;
    • Bonnard, Carine;
    • Wong, Pui-Mun;
    • Nabavizadeh, Nasrinsadat;
    • Altunoğlu, Umut;
    • Estiar, Mehrdad A;
    • Majoie, Charles B;
    • Lee, Hane;
    • Nelson, Stanley F;
    • Gan-Or, Ziv;
    • Rouleau, Guy A;
    • Veldhoven, Paul P Van;
    • Massie, Rami;
    • Hennekam, Raoul C;
    • Kariminejad, Ariana
    Publication type:
    Article
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    From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants.

    Published in:
    European Journal of Neurology, 2025, v. 32, n. 1, p. 1, doi. 10.1111/ene.70025
    By:
    • Degoutin, Manon;
    • Angelini, Chloé;
    • Bar, Claire;
    • El Khedoud, Wahiba Amer;
    • Barnerias, Christine;
    • Boulariah‐Hadjou, Razika;
    • Estiar, Mehrdad A.;
    • Ewenczyk, Claire;
    • Gan‐Or, Ziv;
    • Lacombe, Didier;
    • Lefeuvre, Claire;
    • Majethia, Purvi;
    • Messaoud‐Khelifi, Mouna;
    • Narayanan, Dhanya Lakshmi;
    • Rouleau, Guy A.;
    • Suchowersky, Oksana;
    • Shukla, Anju;
    • Guillaud‐Bataille, Marine;
    • Stevanin, Giovanni;
    • Goizet, Cyril
    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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    Genotype–phenotype correlation in PRKN-associated Parkinson's disease.

    Published in:
    NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00677-3
    By:
    • Menon, Poornima Jayadev;
    • Sambin, Sara;
    • Criniere-Boizet, Baptiste;
    • Courtin, Thomas;
    • Tesson, Christelle;
    • Casse, Fanny;
    • Ferrien, Melanie;
    • Mariani, Louise-Laure;
    • Carvalho, Stephanie;
    • Lejeune, Francois-Xavier;
    • Rebbah, Sana;
    • Martet, Gaspard;
    • Houot, Marion;
    • Lanore, Aymeric;
    • Mangone, Graziella;
    • Roze, Emmanuel;
    • Vidailhet, Marie;
    • Aasly, Jan;
    • Gan Or, Ziv;
    • Yu, Eric
    Publication type:
    Article
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    Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.

    Published in:
    NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00496-y
    By:
    • Alvarez Jerez, Pilar;
    • Alcantud, Jose Luis;
    • de los Reyes-Ramírez, Lucia;
    • Moore, Anni;
    • Ruz, Clara;
    • Vives Montero, Francisco;
    • Rodriguez-Losada, Noela;
    • Saini, Prabhjyot;
    • Gan-Or, Ziv;
    • Alvarado, Chelsea X.;
    • Makarious, Mary B.;
    • Billingsley, Kimberley J.;
    • Blauwendraat, Cornelis;
    • Noyce, Alastair J.;
    • Singleton, Andrew B.;
    • Duran, Raquel;
    • Bandres-Ciga, Sara
    Publication type:
    Article
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    Genetic and Clinical Predictors of Deep Brain Stimulation in Young-Onset Parkinson's Disease.

    Published in:
    Movement Disorders Clinical Practice, 2016, v. 3, n. 5, p. 465, doi. 10.1002/mdc3.12309
    By:
    • Pal, Gian D.;
    • Hall, Deborah;
    • Ouyang, Bichun;
    • Phelps, Jessica;
    • Alcalay, Roy;
    • Pauciulo, Michael W.;
    • Nichols, William C.;
    • Clark, Lorraine;
    • Mejia‐Santana, Helen;
    • Blasucci, Lucia;
    • Goetz, Christopher G.;
    • Comella, Cynthia;
    • Colcher, Amy;
    • Gan‐Or, Ziv;
    • Rouleau, Guy A.;
    • Marder, Karen;
    • Sharp, Madeleine E.;
    • Caccappolo, Elise;
    • Tang, Ming‐X.;
    • Rosado, Llency
    Publication type:
    Article
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    Rapid eye movement sleep behaviour disorder: Past, present, and future.

    Published in:
    Journal of Sleep Research, 2022, v. 31, n. 4, p. 1, doi. 10.1111/jsr.13612
    By:
    • Högl, Birgit;
    • Arnulf, Isabelle;
    • Bergmann, Melanie;
    • Cesari, Matteo;
    • Gan‐Or, Ziv;
    • Heidbreder, Anna;
    • Iranzo, Alex;
    • Krohn, Lynne;
    • Luppi, Pierre‐Hervé;
    • Mollenhauer, Brit;
    • Provini, Federica;
    • Santamaria, Joan;
    • Trenkwalder, Claudia;
    • Videnovic, Aleksandar;
    • Stefani, Ambra
    Publication type:
    Article
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