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Author Details
Full Name
Lorne Clarke
Affiliation
University of British Columbia
ORCID
Career Start Year
2016
Papers
9
H Index
6
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36714130
The practice of genomic medicine: A delineation of the process and its governing principles.
Front Med (Lausanne)
2023
37907381
Variant Classification for Pompe disease; ACMG/AMP specifications from the ClinGen Lysosomal Diseases Variant Curation Expert Panel.
Mol Genet Metab
2023
35599849
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
HGG Adv
2022
35442193
The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice.
Genet Med
2022
34186028
Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.
Am J Hum Genet
2021
32376980
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7.
Genet Med
2020
31965078
Mobile element insertion detection in 89,874 clinical exomes.
Genet Med
2020
31639289
Growth patterns for untreated individuals with MPS I: Report from the international MPS I registry.
Am J Med Genet A
2019
26569098
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials.
JAMA Neurol
2016
1 - 9 of 9
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Zaheer Valivullah
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Caroline M Tanner
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Iulia Handra
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