Works by Ruskey, Jennifer A.

Results: 29

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

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

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

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

Correction: The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.

Published in:

2024

By:

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

Publication type:

Correction Notice

The Parkinson's disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons.

Published in:

Molecular Neurodegeneration, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13024-024-00779-9

By:

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

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

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

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

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

<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

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

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

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

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

Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder.

Published in:

Journal of Parkinson's Disease, 2022, v. 12, n. 1, p. 333, doi. 10.3233/JPD-212867

By:

Sosero, Yuri L.;
Yu, Eric;
Estiar, Mehrdad A.;
Krohn, Lynne;
Mufti, Kheireddin;
Rudakou, Uladzislau;
Ruskey, Jennifer A.;
Asayesh, Farnaz;
Laurent, Sandra B.;
Spiegelman, Dan;
Trempe, Jean-François;
Quinnell, Timothy G.;
Oscroft, Nicholas;
Arnulf, Isabelle;
Montplaisir, Jacques Y.;
Gagnon, Jean-François;
Desautels, Alex;
Dauvilliers, Yves;
Gigli, Gian Luigi;
Valente, Mariarosaria

Publication type:

Article

Age at Onset of Parkinson's Disease Among Ashkenazi Jewish Patients: Contribution of Environmental Factors, LRRK2 p.G2019S and GBA p.N370S Mutations.

Published in:

Journal of Parkinson's Disease, 2020, v. 10, n. 3, p. 1123, doi. 10.3233/JPD-191829

By:

Yahalom, Gilad;
Rigbi, Amihai;
Israeli-Korn, Simon;
Krohn, Lynne;
Rudakou, Uladzislau;
Ruskey, Jennifer A.;
Benshimol, Lior;
Tsafnat, Tal;
Gan-Or, Ziv;
Hassin-Baer, Sharon;
Greenbaum, Lior

Publication type:

Article