E-LIB Suche - Ergebnisse für: Ross, Jay P

1

Rare-variant and polygenic analyses of amyotrophic lateral ..:

Ross, Jay P. ; Akçimen, Fulya ; Liao, Calwing...
Genetics in Medicine. 26 (2024) 1 - p. 100967 , 2024

Link: https://doi.org/10.1016/..

2

Copy-number variants and polygenic risk for intelligence co..:

Schmilovich, Zoe ; Bourque, Vincent-Raphaël ; Douard, Elise...
Frontiers in Psychiatry. 15 (2024) - p. , 2024

Link: https://doi.org/10.3389/..

3

Spinal cord extracts of amyotrophic lateral sclerosis sprea..:

Tamaki, Yoshitaka ; Ross, Jay P. ; Alipour, Paria...
PLOS Genetics. 19 (2023) 2 - p. e1010606 , 2023

Link: https://doi.org/10.1371/..

4

Transcriptomic effects of propranolol and primidone converg..:

Castonguay, Charles-Etienne ; Liao, Calwing ; Khayachi, Anouar...
npj Genomic Medicine. 7 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

5

Copy-number variants in the contactin-5 gene are a potentia..:

Schmilovich, Zoe ; Huguet, Guillaume ; He, Qin...
Research in Autism Spectrum Disorders. 99 (2022) - p. 102055 , 2022

Link: https://doi.org/10.1016/..

6

Investigation of the causal relationship between ALS and au..:

Alipour, Paria ; Senkevich, Konstantin ; Ross, Jay P....
BMC Medicine. 20 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

7

Transcriptome-wide association study reveals increased neur..:

Liao, Calwing ; Vuokila, Veikko ; Catoire, Hélène...
Communications Biology. 5 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

8

The value of testing for ATXN2 intermediate repeat expansio..:

Salmon, Kristiana ; Ross, Jay P. ; Bertone, Vanessa...
European Journal of Human Genetics. 30 (2022) 11 - p. 1205-1207 , 2022

Link: https://doi.org/10.1038/..

9

Evidence for Non‐Mendelian Inheritance in Spastic Paraplegi..:

Estiar, Mehrdad A. ; Yu, Eric ; Haj Salem, Ikhlass...
Movement Disorders. 36 (2021) 7 - p. 1664-1675 , 2021

Link: https://doi.org/10.1002/..

10

Exome sequencing in genetic disease: recent advances and co..:

Ross, Jay P. ; Dion, Patrick A. ; Rouleau, Guy A.
F1000Research. 9 (2020) - p. 336 , 2020

Link: https://doi.org/10.12688..

11

Oligogenicity, C9orf72 expansion, and variant severity in A..:

Ross, Jay P. ; Leblond, Claire S. ; Laurent, Sandra B....
neurogenetics. 21 (2020) 3 - p. 227-242 , 2020

Link: https://doi.org/10.1007/..

12

Assessing the NOTCH2NLC GGC expansion in European patients ..:

Liao, Calwing ; Akçimen, Fulya ; Diez-Fairen, Monica...
Brain. 143 (2020) 11 - p. e89-e89 , 2020

Link: https://doi.org/10.1093/..

13

Transcriptome-wide association study for restless legs synd..:

Akçimen, Fulya ; Sarayloo, Faezeh ; Liao, Calwing...
Communications Biology. 3 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..

14

Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the..:

Akçimen, Fulya ; Ross, Jay P. ; Liao, Calwing...
Movement Disorders. 36 (2020) 2 - p. 514-518 , 2020

Link: https://doi.org/10.1002/..

15

Mutations in ATP13A2 (PARK9) are associated with an amyotro..:

Spataro, Rossella ; Kousi, Maria ; Farhan, Sali M. K....
Human Genomics. 13 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..