LRRK2 and Parkinson's disease: from genetics to targeted therapy

por Sosero, Yuri L., Gan‐Or, Ziv
Publicado 2023

Precision medicine in Parkinson’s disease patients with LRRK2 and GBA risk variants – Let’s get even more personal

por von Linstow, Christian U., Gan-Or, Ziv, Brundin, Patrik
Publicado 2020

GBA1 and The Immune System: A Potential Role in Parkinson’s Disease?

por Al-Azzawi, Zaid A.M., Arfaie, Saman, Gan-Or, Ziv
Publicado 2022

Genetics of NLRP3 suggests lack of involvement and inefficient druggability in Parkinson’s disease

por Senkevich, Konstantin, Liu, Lang, Alvarado, Chelsea X., Leonard, Hampton L., Nalls, Mike A., Gan-Or, Ziv
Publicado 2023

Screening of novel restless legs syndrome–associated genes in French-Canadian families

por Akçimen, Fulya, Spiegelman, Dan, Dionne-Laporte, Alexandre, Gan-Or, Ziv, Dion, Patrick A., Rouleau, Guy A.
Publicado 2018

De novo FUS P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia

por Leblond, Claire S., Webber, Alina, Gan-Or, Ziv, Moore, Fraser, Dagher, Alain, Dion, Patrick A., Rouleau, Guy A.
Publicado 2016

Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype

por Estiar, Mehrdad A., Leveille, Etienne, Spiegelman, Dan, Dupre, Nicolas, Trempe, Jean-François, Rouleau, Guy A., Gan‐Or, Ziv
Publicado 2020

Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson Disease

por Galper, Jasmin, Balwani, Manisha, Fahn, Stanley, Waters, Cheryl, Krohn, Lynne, Gan‐Or, Ziv, Dzamko, Nicolas, Alcalay, Roy N.
Publicado 2021

Neuroanatomical correlates of genetic risk for obesity in children

por Morys, Filip, Yu, Eric, Shishikura, Mari, Paquola, Casey, Vainik, Uku, Nave, Gideon, Koellinger, Philipp, Gan-Or, Ziv, Dagher, Alain
Publicado 2023

Hereditary spastic paraplegia initially diagnosed as cerebral palsy

por Suchowersky, Oksana, Ashtiani, Setareh, Au, Ping-Yee Billie, McLeod, Scott, Estiar, Mehrdad A., Gan-Or, Ziv, Rouleau, Guy A.
Publicado 2021

GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis

por Mallett, Victoria, Ross, Jay P., Alcalay, Roy N., Ambalavanan, Amirthagowri, Sidransky, Ellen, Dion, Patrick A., Rouleau, Guy A., Gan-Or, Ziv
Publicado 2016

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

por Tremblay, Christina, Rahayel, Shady, Vo, Andrew, Morys, Filip, Shafiei, Golia, Abbasi, Nooshin, Markello, Ross D, Gan-Or, Ziv, Misic, Bratislav, Dagher, Alain
Publicado 2021

Type 2 Diabetes as a Determinant of Parkinson’s Disease Risk and Progression

por Chohan, Harneek, Senkevich, Konstantin, Patel, Radhika K., Bestwick, Jonathan P., Jacobs, Benjamin M., Ciga, Sara Bandres, Gan-Or, Ziv, Noyce, Alastair J.
Publicado 2021

Heritability Enrichment Implicates Microglia in Parkinson’s Disease Pathogenesis

por Andersen, Maren Stolp, Bandres-Ciga, Sara, Reynolds, Regina H., Hardy, John, Ryten, Mina, Krohn, Lynne, Gan-Or, Ziv, Holtman, Inge R., Pihlstrøm, Lasse
Publicado 2021

Genome-wide association study stratified by MAPT haplotypes identifies potential novel loci in Parkinson’s disease

por Senkevich, Konstantin, Bandres-Ciga, Sara, Cisterna-García, Alejandro, Yu, Eric, Bustos, Bernabe I., Krohn, Lynne, Lubbe, Steven J., Botía, Juan A., Gan-Or, Ziv
Publicado 2023

Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk

por Lake, Julie, Reed, Xylena, Langston, Rebekah G., Nalls, Mike A., Gan‐Or, Ziv, Cookson, Mark R., Singleton, Andrew B., Blauwendraat, Cornelis, Leonard, Hampton L.
Publicado 2021

Effect Modification between Genes and Environment and Parkinson's Disease Risk

por Periñán, Maria Teresa, Brolin, Kajsa, Bandres‐Ciga, Sara, Blauwendraat, Cornelis, Klein, Christine, Gan‐Or, Ziv, Singleton, Andrew, Gomez‐Garre, Pilar, Swanberg, Maria, Mir, Pablo, Noyce, Alastair
Publicado 2022

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

por Surface, Matthew, Balwani, Manisha, Waters, Cheryl, Haimovich, Alexander, Gan‐Or, Ziv, Marder, Karen S., Hsieh, Tammy, Song, Linxia, Padmanabhan, Shalini, Hsieh, Frank, Merchant, Kalpana M., Alcalay, Roy N.
Publicado 2021

RIC3 variants are not associated with Parkinson’s disease in large European, Latin American, or East Asian cohorts

por Brolin, Kajsa, Bandres-Ciga, Sara, Leonard, Hampton, Makarious, Mary B., Blauwendraat, Cornelis, Mata, Ignacio F, Foo, Jia Nee, Pihlstrøm, Lasse, Swanberg, Maria, Gan-Or, Ziv, Tan, Manuela MX
Publicado 2022

Corrigendum: Clinical and genetic analysis of Costa Rican patients with Parkinson's disease

por Torrealba-Acosta, Gabriel, Yu, Eric, Lobo-Prada, Tanya, Ruíz-Martínez, Javier, Gorostidi-Pagola, Ana, Gan-Or, Ziv, Carazo-Céspedes, Kenneth, Trempe, Jean-François, Mata, Ignacio F., Fornaguera-Trías, Jaime
Publicado 2023