Jay P Ross
McGill University
H-index: 19
North America-Canada
Top articles of Jay P Ross
Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome
Genetics in Medicine
2024/1/1
Genomic analysis identifies risk factors in restless legs syndrome
medRxiv
2023/12/20
Exploring the common genetic architecture of autism spectrum disorder using a novel multi-polygenic risk score approach
Journal of the Neurological Sciences
2023/12/1
Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability
Frontiers in Psychiatry
2023/11/29
Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids
PLoS Genetics
2023/2/6
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
Science translational medicine
2022/2/23
Alfredo Iacoangeli
H-Index: 10
Cristina Moglia
H-Index: 33
Maura Brunetti
H-Index: 10
Jay P Ross
H-Index: 13
Sarah Furlong
H-Index: 3
Tian Lin
H-Index: 14
Kelly L Williams
H-Index: 25
Ruben J Cauchi
H-Index: 14
Susana Pinto
H-Index: 6
Christopher E Shaw
H-Index: 82
Ammar Al-Chalabi
H-Index: 65
Philip Van Damme
H-Index: 59
Jonathan Mill
H-Index: 72
Ammar Al-Chalabi
H-Index: 65
Jonathan Mill
H-Index: 72
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis
JAMA neurology
2022/2/1
Moyamoya Disease Susceptibility Gene RNF213 Regulates Endothelial Barrier Function
Stroke
2022/4
Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study
BMC medicine
2022/11/2
Do variants in the coding regions of FOXP2, a gene implicated in speech disorder, confer a risk for congenital amusia?
Annals of the New York Academy of Sciences
2022/11
The value of testing for ATXN2 intermediate repeat expansions in routine clinical practice for amyotrophic lateral sclerosis
European Journal of Human Genetics
2022/11
Copy-number variants in the contactin-5 gene are a potential risk factor for autism spectrum disorder
Research in Autism Spectrum Disorders
2022/11/1
Transcriptomic effects of propranolol and primidone converge on molecular pathways relevant to essential tremor
NPJ Genomic Medicine
2022/8/4
Questioning the Association of the STMN2 Dinucleotide Repeat With Amyotrophic Lateral Sclerosis
Neurology: Genetics
2022/7/13
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome
Communications Biology
2022/3/30
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Nature genetics
2021/12
Niek De Klein
H-Index: 7
Harm-Jan Westra
H-Index: 48
Patrick Deelen
H-Index: 31
Alfredo Iacoangeli
H-Index: 10
John Hardy
H-Index: 9
Michael Sendtner
H-Index: 48
Thomas Meyer
H-Index: 17
Massimiliano Filosto
H-Index: 30
Alessandro Padovani
H-Index: 58
Cristina Moglia
H-Index: 33
Maura Brunetti
H-Index: 10
Jay P Ross
H-Index: 13
David Brenner
H-Index: 4
Simon Topp
H-Index: 3
Stephan Ripke
H-Index: 88
Ruben J Cauchi
H-Index: 14
Caroline Graff
H-Index: 42
Beben Benyamin
H-Index: 25
Sarah Furlong
H-Index: 3
Occurrence of amyotrophic lateral sclerosis in type 1 Gaucher disease
Neurology: Genetics
2021/5/18
Genetic Basis of ALS
2021/4/27
Jay P Ross
H-Index: 13
Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7
Movement Disorders
2021/7
Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project
Movement Disorders
2021/2
Co-Authors
