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Author

Meron Teferra

ORCID: 0009-0007-6033-8475
Observed ORCID: 0009-0007-6033-8475
OpenAlex ID: A5119600956
Patient Safety and Quality of Care are Everybody's Business: Evaluating the Impact of a Continuing Professional Development Program beyond Satisfaction
2019 · Francesca Luconi, Miriam Boillat, et al. · MedEdPublish · 10
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Pathology and Genetics in a Global Cohort of Parkinsonian Disorders
2026 · Lesley Y. Wu, Tessa du Toit, et al. · JAMA Neurology · 4
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An Innovative Needs Assessment Approach to Develop Relevant Continuing Professional Development for Psychiatrists
2021 · Francesca Luconi, Richard Montoro, et al. · Academic Psychiatry · 4
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Shared Pathogenic Pathways Between REM Sleep Behavior Disorder and Neurodegenerative and Psychiatric Disorders
2026 · Zhao Zhang, Emma N. Somerville, et al. · medRxiv · 1
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GALC variants affect glucocerebrosidase to galactosylceramidase activity ratio
2026 · Amirhossein Rajabi Vajargah, Konstantin Senkevich, et al. · medRxiv
Lack of genetic evidence for a role of SLC25A46 in alpha-synucleinopathies
2026 · Han Yu, Sitki Cem Parlar, et al. · Journal of Parkinson s Disease
No genetic evidence for SLC7A11 involvement in Parkinson’s Disease
2026 · Yoomin Lee, Sitki Cem Parlar, et al. · medRxiv
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The GBA1 p. E427K (p. E388K ) Variant Is a Risk Factor for Synucleinopathies: A Meta‐Analysis
2026 · Leah V. Chifamba, Sitki Cem Parlar, et al. · Movement Disorders
Genetic associations between post-traumatic stress disorder and REM-sleep behavior disorder
2026 · Morvarid Ghamgosar Shahkhali, Lang Liu, et al. · npj Parkinson s Disease
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Evaluating ANO6 as a Parkinson’s disease candidate gene: a human genetic investigation of common and rare variant associations
2026 · Sitki Cem Parlar, Hampton Leonard, et al. · medRxiv
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Evaluating ANO6 as a Parkinson’s disease candidate gene: a human genetic investigation of common and rare variant associations
2026 · Sitki Cem Parlar, Hampton Leonard, et al. · SSRN Electronic Journal
Genome-wide association study of REM-sleep behaviour disorder identifies new risk loci
2025 · Emma N. Somerville, Lang Liu, et al. · medRxiv
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Loss‐of‐Function Variants in CPT1C : No Support for a Causal Role in Hereditary Spastic Paraplegia
2025 · Rui Zhu, Lang Liu, et al. · Movement Disorders
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Loss-of-function Variants in CPT1C : No Support for a Causal Role in Hereditary Spastic Paraplegia
2025 · Rui Zhu, Lang Liu, et al. · medRxiv
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Post-traumatic stress disorder and REM-sleep behavior disorder: exploring genetic associations and causal links
2025 · Morvarid Ghamgosar Shahkhali, Lang Liu, et al. · medRxiv
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Dedicated Poster Abstracts
2019 · Kelly Dore, D Fedorkow, et al. · Canadian Medical Education Journal
Works count: 16
Citation count: 19
H-index: 3
I10-index: 1
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