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All papers authored by Ziv Gan-Or

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2023 Emma N. Somerville, Lynne Krohn, Eric Yu, Uladzislau Rudakou, Konstantin Senkevich, Jennifer A. Ruskey, Farnaz Asayesh, Jamil Ahmad, Dan Spiegelman, Yves Dauvilliers, Isabelle Arnulf, Michele T. M. Hu, Jacques Y. Montplaisir, Jean-François Gagnon, Alex Desautels and 31 other authors

NPC1 variants are not associated with Parkinson’s disease, REM-sleep behavior disorder or dementia with Lewy bodies in European cohorts

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2021 Matthew Surface, Manisha Balwani, Cheryl Waters, Alexander Haimovich, Ziv Gan‐Or

ORCID

, Karen S. Marder, Tammy Hsieh, Linxia Song, Shalini Padmanabhan

ORCID

, Frank Hsieh, Kalpana M. Merchant, Roy N. Alcalay

ORCID

Plasma Glucosylsphingosine in GBA1 Mutation Carriers with and without Parkinson's Disease

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Ziv Gan‐Or

ORCID

, Nicholas W. Wood

ORCID

Mendelian Randomization Studies: A Path to Better Understand Sex and Gender Differences in Parkinson's Disease?

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Christina Tremblay, Shady Rahayel

ORCID

, Andrew Vo, Filip Morys, Golia Shafiei

ORCID

, Nooshin Abbasi

ORCID

, Ross D. Markello

ORCID

, Ziv Gan-Or

ORCID

, Bratislav Misic

ORCID

ORCID

Brain atrophy progression in Parkinson’s disease is shaped by connectivity and local vulnerability

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Yuri L. Sosero, Eric Yu

ORCID

, Lynne Krohn, Uladzislau Rudakou, Kheireddin Mufti

ORCID

, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent, Dan Spiegelman, Stanley Fahn, Cheryl Waters, S. Pablo Sardi

ORCID

, Sara Bandres-Ciga, Roy N. Alcalay, Ziv Gan-Or

ORCID

and 1 other authors

LRRK2 p.M1646T is associated with glucocerebrosidase activity and with Parkinson's disease

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Yann Le Guen

ORCID

, Valerio Napolioni, Michael E. Belloy

ORCID

, Eric Yu

ORCID

ORCID

, Jennifer A. Ruskey, Ziv Gan‐Or

ORCID

, Gabriel Kennedy

ORCID

, Sarah J. Eger, Michael D. Greicius

Common X‐Chromosome Variants Are Associated with Parkinson Disease Risk

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2020 Bernabe I. Bustos

ORCID

, Sara Bandres-Ciga, J. Raphael Gibbs, J. Raphael Gibbs, Dimitri Krainc, Niccolo E. Mencacci

ORCID

, Ziv Gan-Or

ORCID

, Steven J. Lubbe

Replication assessment of NUS1 variants in Parkinson’s Disease

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Eric Yu, Uladzislau Rudakou, Lynne Krohn, U. Rudakov, Kheireddin Mufti

ORCID

, Jennifer A. Ruskey, Farnaz Asayesh, Mehrdad A. Estiar, Dan Spiegelman, Matthew Surface, Stanley Fahn, Cheryl H. Waters, Lior Greenbaum, Alberto J. Espay, Yves Dauvilliers and 6 other authors

Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease

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Bouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, Eric Yu, Kheireddin Mufti

ORCID

, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent, Dan Spiegelman, Stanley Fahn, Cheryl Waters, Oury Monchi, Yves Dauvilliers, Alberto J. Espay, Nicolas Dupré and 6 other authors

Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease

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2019 Hampton Leonard

ORCID

, Cornelis Blauwendraat, Lynne Krohn, Faraz Faghri, Hirotaka Iwaki, Glen Ferguson, Aaron G. Day-Williams, David J. Stone, Andrew B. Singleton, Mike A. Nalls, Ziv Gan-Or

ORCID

Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease

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Ziv Gan-Or

ORCID

, Niccolò E. Mencacci

ORCID

, Mike A. Nalls

Dystonia; a roadmap is needed for future genetic studies

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2017 Ziv Gan-Or

ORCID

, Grace Yoon, Oksana Suchowersky, Nicolas Dupré, Guy A. Rouleau

KCNA2 mutations are rare in hereditary spastic paraplegia

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2016 Ziv Gan-Or

ORCID

, Jacques Y. Montplaisir, Jay P. Ross, Judes Poirier, Simon C. Warby, Isabelle Arnulf, Stephanie Strong, Yves Dauvilliers, Claire S. Leblond, Michele T. M. Hu, Birgit Högl, Ambra Stefani, Christelle Charley Monaca, Valérie Cochen De Cock, Valérie Cochen De Cock and 15 other authors

The dementia-associated APOE e4 allele is not associated with rapid eye movement sleep behavior disorder

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Ziv Gan-Or

ORCID

, Guy A. Rouleau

Calpain 1 in neurodegeneration: a therapeutic target?

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Liron Rozenkrantz, Ziv Gan-Or

ORCID

, Mali Gana-Weisz, Anat Mirelman, Nir Giladi, Anat Bar-Shira, Avi Orr-Urtreger

SEPT14 Is Associated with a Reduced Risk for Parkinson’s Disease and Expressed in Human Brain

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Ziv Gan-Or

ORCID

, Noreen Mohsin, Simon L. Girard, Jacques Y. Montplaisir, Amirthagowri Ambalavanan, Stéphanie Strong, Victoria Mallett, Sandra B. Laurent, Cynthia V. Bourassa, Michel Boivin

ORCID

, Mélanie Langlois, Isabelle Arnulf, Birgit Högl, Birgit Frauscher, Christelle Monaca and 8 other authors

The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder

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Claire S. Leblond, Alina Webber, Ziv Gan-Or

ORCID

, Fraser Moore, Alain Dagher, Patrick A. Dion, Guy A. Rouleau

De novoFUSP525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

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Roy N. Alcalay, Oren A. Levy, Pavlina Wolf, Petra Oliva, Xiaokui Kate Zhang, Cheryl H. Waters, Stanley Fahn, Un Jung Kang, Christopher Liong, Blair Ford, Pietro Mazzoni, Sheng Kuo, Amelie Johnson, Lan Xiong, Guy A. Rouleau and 3 other authors

SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease

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Jessica Phelps, Michael W. Pauciulo, Guy A. Rouleau, Deborah Hall, Bichun Ouyang, Roy Alcalay, William C. Nichols, Lorraine Clark, Gian D. Pal

ORCID

, Helen Mejia-Santana, Lucia Blasucci, Christopher G. Goetz, Cynthia Comella, Amy Colcher, Ziv Gan-Or

ORCID

and 1 other authors

Genetic and Clinical Predictors of Deep Brain Stimulation in Young-Onset Parkinson's Disease

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Ziv Gan-Or

ORCID

, Naima Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B. Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B. Laurent, Daniel Rochefort, Dan Spiegelman, Alexandre Dionne-Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche and 12 other authors

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

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