Found: 24

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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

  • Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34732-5
    By:
    • Krohn, Lynne;
    • Heilbron, Karl;
    • Blauwendraat, Cornelis;
    • Reynolds, Regina H.;
    • Yu, Eric;
    • Senkevich, Konstantin;
    • Rudakou, Uladzislau;
    • Estiar, Mehrdad A.;
    • Gustavsson, Emil K.;
    • Brolin, Kajsa;
    • Ruskey, Jennifer A.;
    • Freeman, Kathryn;
    • Asayesh, Farnaz;
    • Chia, Ruth;
    • Arnulf, Isabelle;
    • Hu, Michele T. M.;
    • Montplaisir, Jacques Y.;
    • Gagnon, Jean-François;
    • Desautels, Alex;
    • Dauvilliers, Yves
    Publication type:
    Article

  • 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

  • Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations.

    Published in:
    2021
    By:
    • 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
    Publication type:
    journal article

  • 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

  • Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

    Published in:
    2019
    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:
    journal article

  • Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder.

    Published in:
    2017
    By:
    • Gan-Or, Ziv;
    • Ruskey, Jennifer A.;
    • Spiegelman, Dan;
    • Arnulf, Isabelle;
    • Dauvilliers, Yves;
    • Högl, Birgit;
    • Monaca-Charley, Christelle;
    • Postuma, Ronald B.;
    • Montplaisir, Jacques Y.;
    • Rouleau, Guy A.
    Publication type:
    Letter

  • <italic>TOX3</italic> Variants Are Involved in Restless Legs Syndrome and Parkinson’s Disease with Opposite Effects.

    Published in:
    Journal of Molecular Neuroscience, 2018, v. 64, n. 3, p. 341, doi. 10.1007/s12031-018-1031-4
    By:
    • Mohtashami, Sadaf;
    • He, Qin;
    • Ruskey, Jennifer A.;
    • Zhou, Sirui;
    • Dion, Patrick A.;
    • Allen, Richard P.;
    • Earley, Christopher J.;
    • Fon, Edward A.;
    • Xiong, Lan;
    • Dupre, Nicolas;
    • Dauvilliers, Yves;
    • Rouleau, Guy A.;
    • Gan-Or, Ziv
    Publication type:
    Article

  • HLA in isolated REM sleep behavior disorder and Lewy body dementia.

    Published in:
    Annals of Clinical & Translational Neurology, 2023, v. 10, n. 9, p. 1682, doi. 10.1002/acn3.51841
    By:
    • Yu, Eric;
    • Krohn, Lynne;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Spiegelman, Dan;
    • Shah, Zalak;
    • Chia, Ruth;
    • Arnulf, Isabelle;
    • Hu, Michele T. M.;
    • Montplaisir, Jacques Y.;
    • Gagnon, Jean‐François;
    • Desautels, Alex;
    • Dauvilliers, Yves;
    • Gigli, Gian Luigi;
    • Valente, Mariarosaria;
    • Janes, Francesco;
    • Bernardini, Andrea;
    • Högl, Birgit;
    • Stefani, Ambra;
    • Ibrahim, Abubaker
    Publication type:
    Article

  • Common X‐Chromosome Variants Are Associated with Parkinson Disease Risk.

    Published in:
    Annals of Neurology, 2021, v. 90, n. 1, p. 22, doi. 10.1002/ana.26051
    By:
    • Le Guen, Yann;
    • Napolioni, Valerio;
    • Belloy, Michael E.;
    • Yu, Eric;
    • Krohn, Lynne;
    • Ruskey, Jennifer A.;
    • Gan‐Or, Ziv;
    • Kennedy, Gabriel;
    • Eger, Sarah J.;
    • Greicius, Michael D.
    Publication type:
    Article

  • Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.

    Published in:
    Annals of Neurology, 2021, v. 90, n. 1, p. 35, doi. 10.1002/ana.26090
    By:
    • Blauwendraat, Cornelis;
    • Iwaki, Hirotaka;
    • Makarious, Mary B.;
    • Bandres‐Ciga, Sara;
    • Leonard, Hampton L.;
    • Grenn, Francis P.;
    • Lake, Julie;
    • Krohn, Lynne;
    • Tan, Manuela;
    • Kim, Jonggeol J.;
    • Gibbs, Jesse R.;
    • Hernandez, Dena G.;
    • Ruskey, Jennifer A.;
    • Pihlstrøm, Lasse;
    • Toft, Mathias;
    • Hilten, Jacobus J.;
    • Marinus, Johan;
    • Schulte, Claudia;
    • Brockmann, Kathrin;
    • Sharma, Manu
    Publication type:
    Article

  • Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies.

    Published in:
    2020
    By:
    • Krohn, Lynne;
    • Wu, Richard Y. J.;
    • Heilbron, Karl;
    • Ruskey, Jennifer A.;
    • Laurent, Sandra B.;
    • Blauwendraat, Cornelis;
    • Alam, Armaghan;
    • Arnulf, Isabelle;
    • Hu, Michele T. M.;
    • Dauvilliers, Yves;
    • Högl, Birgit;
    • Toft, Mathias;
    • Bjørnarå, Kari Anne;
    • Stefani, Ambra;
    • Holzknecht, Evi;
    • Monaca, Christelle Charley;
    • Abril, Beatriz;
    • Plazzi, Giuseppe;
    • Antelmi, Elena;
    • Ferini‐Strambi, Luigi
    Publication type:
    journal article

  • Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies.

    Published in:
    2020
    By:
    • Krohn, Lynne;
    • Öztürk, Tuğba Nur;
    • Vanderperre, Benoît;
    • Ouled Amar Bencheikh, Bouchra;
    • Ruskey, Jennifer A.;
    • Laurent, Sandra B.;
    • Spiegelman, Dan;
    • Postuma, Ronald B.;
    • Arnulf, Isabelle;
    • Hu, Michele T. M.;
    • Dauvilliers, Yves;
    • Högl, Birgit;
    • Stefani, Ambra;
    • Monaca, Christelle Charley;
    • Plazzi, Giuseppe;
    • Antelmi, Elena;
    • Ferini‐Strambi, Luigi;
    • Heidbreder, Anna;
    • Rudakou, Uladzislau;
    • Cochen De Cock, Valérie
    Publication type:
    journal article

  • Morphological and genetic analysis of sympatric dace within the Rhinichthys cataractae species complex: a case of isolation lost.

    Published in:
    Biological Journal of the Linnean Society, 2016, v. 117, n. 3, p. 547, doi. 10.1111/bij.12657
    By:
    • Ruskey, Jennifer A.;
    • Taylor, Eric B.
    Publication type:
    Article

  • Triple A syndrome presenting as complicated hereditary spastic paraplegia.

    Published in:
    Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 1134, doi. 10.1002/mgg3.492
    By:
    • Leveille, Etienne;
    • Gonorazky, Hernan D.;
    • Rioux, Marie‐France;
    • Hazrati, Lili‐Naz;
    • Ruskey, Jennifer A.;
    • Carnevale, Amanda;
    • Spiegelman, Dan;
    • Dionne‐Laporte, Alexandre;
    • Rouleau, Guy A.;
    • Yoon, Grace;
    • Gan‐Or, Ziv
    Publication type:
    Article

  • Investigating the relationship between the SNCA gene and cognitive abilities in idiopathic Parkinson's disease using machine learning.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-84316-4
    By:
    • Ramezani, Mehrafarin;
    • Mouches, Pauline;
    • Yoon, Eunjin;
    • Rajashekar, Deepthi;
    • Ruskey, Jennifer A.;
    • Leveille, Etienne;
    • Martens, Kristina;
    • Kibreab, Mekale;
    • Hammer, Tracy;
    • Kathol, Iris;
    • Maarouf, Nadia;
    • Sarna, Justyna;
    • Martino, Davide;
    • Pfeffer, Gerald;
    • Gan-Or, Ziv;
    • Forkert, Nils D.;
    • Monchi, Oury
    Publication type:
    Article

  • Association Between BDNF Val66Met Polymorphism and Mild Behavioral Impairment in Patients With Parkinson's Disease.

    Published in:
    Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.587992
    By:
    • Ramezani, Mehrafarin;
    • Ruskey, Jennifer A.;
    • Martens, Kristina;
    • Kibreab, Mekale;
    • Javer, Zainul;
    • Kathol, Iris;
    • Hammer, Tracy;
    • Cheetham, Jenelle;
    • Leveille, Etienne;
    • Martino, Davide;
    • Sarna, Justyna R.;
    • Gan-Or, Ziv;
    • Pfeffer, Gerald;
    • Ismail, Zahinoor;
    • Monchi, Oury
    Publication type:
    Article

  • 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

  • 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

  • Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder.

    Published in:
    2021
    By:
    • Mufti, Kheireddin;
    • Rudakou, Uladzislau;
    • Yu, Eric;
    • Krohn, Lynne;
    • Ruskey, Jennifer A.;
    • Asayesh, Farnaz;
    • Laurent, Sandra B.;
    • Spiegelman, Dan;
    • Arnulf, Isabelle;
    • Hu, Michele T.M.;
    • Montplaisir, Jacques Y.;
    • Gagnon, Jean‐François;
    • Desautels, Alex;
    • Dauvilliers, Yves;
    • Gigli, Gian Luigi;
    • Valente, Mariarosaria;
    • Janes, Francesco;
    • Högl, Birgit;
    • Stefani, Ambra;
    • Holzknecht, Evi
    Publication type:
    journal article

  • 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

  • SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease.

    Published in:
    2019
    By:
    • Alcalay, Roy N.;
    • Mallett, Victoria;
    • Vanderperre, Benoît;
    • Tavassoly, Omid;
    • Dauvilliers, Yves;
    • Wu, Richard Y.J.;
    • Ruskey, Jennifer A.;
    • Leblond, Claire S.;
    • Ambalavanan, Amirthagowri;
    • Laurent, Sandra B.;
    • Spiegelman, Dan;
    • Dionne‐Laporte, Alexandre;
    • Liong, Christopher;
    • Levy, Oren A.;
    • Fahn, Stanley;
    • Waters, Cheryl;
    • Kuo, Sheng‐Han;
    • Chung, Wendy K.;
    • Ford, Blair;
    • Marder, Karen S.
    Publication type:
    journal article

  • Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.

    Published in:
    2018
    By:
    • Li, Jiao;
    • Ruskey, Jennifer A.;
    • Arnulf, Isabelle;
    • Dauvilliers, Yves;
    • Hu, Michele T. M.;
    • Högl, Birgit;
    • Leblond, Claire S.;
    • Zhou, Sirui;
    • Ambalavanan, Amirthagowri;
    • Ross, Jay P.;
    • Bourassa, Cynthia V.;
    • Spiegelman, Dan;
    • Laurent, Sandra B.;
    • Stefani, Ambra;
    • Charley Monaca, Christelle;
    • Cochen De Cock, Valérie;
    • Boivin, Michel;
    • Ferini‐Strambi, Luigi;
    • Plazzi, Giuseppe;
    • Antelmi, Elena
    Publication type:
    journal article

  • 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