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Chantal F. Morel | Researchclopedia

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Chantal F. Morel

University Health Network ORCID

93

Works

3,710

Citations

31

h-index

50

i10-index

Research Topics

Genomics and Rare Diseases Lysosomal Storage Disorders Research Cardiomyopathy and Myosin Studies

Affiliations

Mount Sinai Hospital2009–2023

Sunnybrook Health Science Centre2018–2018

University Health Network2009–2025

MACOM (United States)2024–2024

University of Toronto2009–2024

Top Works

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Jordan Lerner‐Ellis,Jamie C. Tirone,et al.

2005375 citations

Metabolism and Genetic Disorders

Folate and B Vitamins Research

Reappraisal of Reported Genes for Sudden Arrhythmic Death

S. Mohsen Hosseini,Raymond H. Kim,et al.

2018363 citations

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

Daniel Moreno‐De‐Luca,Jennifer G. Mullé,et al.

2010332 citations

Spectrum of mutations in<i>MMACHC</i>, allelic expression, and evidence for genotypeâphenotype correlations

Jordan Lerner‐Ellis,Natascia Anastasio,et al.

2009210 citations

Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcome

Philippa B. Mills,Stéphane Camuzeaux,et al.

2014175 citations

Genome Sequencing for Diagnosing Rare Diseases

Monica H. Wojcik,Gabrielle Lemire,et al.

2024163 citations

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

Neal K. Lakdawala,Birgit Funke,et al.

2012161 citations

Cardiovascular magnetic resonance demonstration of the spectrum of morphological phenotypes and patterns of myocardial scarring in Anderson-Fabry disease

Djeven P. Deva,Kate Hanneman,et al.

2016135 citations

Combined methylmalonic aciduria and homocystinuria (cblC): Phenotype–genotype correlations and ethnic-specific observations

Chantal F. Morel,Jordan Lerner‐Ellis,et al.

2006133 citations