Jamil Ahmad

机构：Montreal Neurological Institute and Hospital, McGill University · ORCID：0000-0002-0320-4020

发表论文 51 篇 · 总被引 1500 次 · h-index 19

代表论文

• No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing (2016 · Journal of Medical Genetics · 被引 104)
• GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson’s disease (2022 · Brain · 被引 39)
• The Parkinson’s disease risk gene cathepsin B promotes fibrillar alpha-synuclein clearance, lysosomal function and glucocerebrosidase activity in dopaminergic neurons (2024 · Molecular Neurodegeneration · 被引 36)
• Genetic Characterization of Serotypes A and Asia-1 Foot-and-mouth Disease Viruses in Balochistan, Pakistan, in 2011 (2016 · Transboundary and Emerging Diseases · 被引 26)
• Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly (2019 · Human Genetics · 被引 23)
• Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia (2016 · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 被引 20)