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Kheireddin Mufti
Kheireddin Mufti
BC Children's Hospital, Department of Medical Genetics, University of British Columbia
Verified email at bcchr.ca - Homepage
Title
Cited by
Cited by
Year
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
CS Storm, DA Kia, MM Almramhi, S Bandres-Ciga, C Finan, AD Hingorani, ...
Nature communications 12 (1), 7342, 2021
542021
Investigation of autosomal genetic sex differences in Parkinson's disease
C Blauwendraat, H Iwaki, MB Makarious, S Bandres‐Ciga, HL Leonard, ...
Annals of neurology 90 (1), 35-42, 2021
432021
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
E Yu, U Rudakou, L Krohn, K Mufti, JA Ruskey, F Asayesh, MA Estiar, ...
Movement Disorders 36 (1), 178-187, 2021
402021
Comprehensive analysis of familial parkinsonism genes in rapid‐eye‐movement sleep behavior disorder
K Mufti, U Rudakou, E Yu, L Krohn, JA Ruskey, F Asayesh, SB Laurent, ...
Movement Disorders 36 (1), 235-240, 2021
17*2021
LRRK2 p. M1646T is associated with glucocerebrosidase activity and with Parkinson's disease
YL Sosero, E Yu, L Krohn, U Rudakou, K Mufti, JA Ruskey, F Asayesh, ...
Neurobiology of aging 103, 142. e1-142. e5, 2021
142021
Evidence for non‐Mendelian inheritance in spastic paraplegia 7
MA Estiar, E Yu, I Haj Salem, JP Ross, K Mufti, F Akçimen, E Leveille, ...
Movement Disorders 36 (7), 1664-1675, 2021
132021
Novel associations of BST1 and LAMP3 with rapid eye movement sleep behavior disorder
K Mufti, E Yu, U Rudakou, L Krohn, JA Ruskey, F Asayesh, SB Laurent, ...
Neurology, 2021
132021
Lack of evidence for genetic association of saposins A, B, C and D with Parkinson’s disease
YL Sosero, S Bandres-Ciga, S Hassin-Baer, RN Alcalay, Z Gan-Or, ...
Brain 143 (9), e72-e72, 2020
132020
Variants in the Niemann–Pick type C gene NPC1 are not associated with Parkinson's disease
BOA Bencheikh, K Senkevich, U Rudakou, E Yu, K Mufti, JA Ruskey, ...
Neurobiology of aging 93, 143. e1-143. e4, 2020
132020
The Parkinson's disease DNA variant browser
JJ Kim, MB Makarious, S Bandres‐Ciga, JR Gibbs, J Ding, DG Hernandez, ...
Movement Disorders 36 (5), 1250-1258, 2021
112021
Genetic, structural and clinical analysis of spastic paraplegia 4
P Varghaei, MA Estiar, S Ashtiani, S Veyron, K Mufti, E Leveille, E Yu, ...
Parkinsonism & Related Disorders 98, 62-69, 2022
92022
Rare PSAP variants and possible interaction with GBA in REM sleep behavior disorder
YL Sosero, E Yu, MA Estiar, L Krohn, K Mufti, U Rudakou, JA Ruskey, ...
Journal of Parkinson's disease 12 (1), 333-340, 2022
52022
Finding drug targeting mechanisms with genetic evidence for Parkinson’s disease
CS Storm, DA Kia, M Almramhi, S Bandres-Ciga, C Finan, AD Hingorani, ...
Biorxiv, 2020.07. 24.208975, 2020
22020
Analysis of dominant and recessive parkinsonism genes in REM sleep behavior disorder
K Mufti, U Rudakou, E Yu, JA Ruskey, F Asavesh, SB Laurent, I Arnulf, ...
Parkinsonism & Related Disorders 79, e27-e28, 2020
12020
GENETIC VARIATIONS RELATED TO NERVE MYELINATION AND SYNAPSE ASSEMBLY ARE ASSOCIATED WITH THE RISK OF VINCRISTINE-INDUCED PERIPHERAL NEUROPATHY
K Mufti, E Scott, M Cordova-Delgado, J Trueman, J Lovnicki, C Loucks, ...
PEDIATRIC BLOOD & CANCER 70, S153-S154, 2023
2023
Transcriptome analysis highlights common pathways between Alzheimer’s disease, dementia with Lewy bodies and Parkinson’s disease
K Senkevich, D Nikanorova, L Protsenko, E Yu, L Krohn, K Mufti, ...
Alzheimer's & Dementia 17, e050014, 2021
2021
Evidence of shared biological pathway between Parkinson's disease and psychiatric disorders.
K Senkevich, D Nikanorova, L Protsenko, E Yu, L Krohn, K Mufti, M Estiar, ...
EUROPEAN JOURNAL OF NEUROLOGY 28, 191-191, 2021
2021
NPC1 variants are not associated with Parkinson's disease
K Senkevich, BOA Bencheikh, U Rudakou, E Yu, K Mufti, JA Ruskey, ...
Parkinsonism & Related Disorders 79, e31, 2020
2020
Low lymphocyte count is a risk factor for Parkinson’s disease
MP Jensen, BM Jacobs, R Dobson, S Bandres-Ciga, C Blauwendraat, ...
medRxiv, 2020.09. 13.20189530, 2020
2020
LRRK2 p. G2019S and p. N2081D variants as modifiers of glucocerebrosidase activity
K Senkevich, E Yu, L Krohn, U Rudakou, J Ruskey, F Asayesh, K Mufti, ...
MOVEMENT DISORDERS 35, S211-S211, 2020
2020
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