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Geneviève Bernard | Researchclopedia

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Geneviève Bernard

McGill University Health Centre ORCID

260

Works

7,732

Citations

44

h-index

117

i10-index

Research Topics

RNA regulation and disease RNA Research and Splicing RNA modifications and cancer

Affiliations

Montreal Neurological Institute and Hospital2011–2022

Children's National2012–2012

University of Ottawa2020–2020

York University2014–2014

School of the Art Institute of Chicago2014–2014

Top Works

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow,Diana Chase,et al.

2015602 citations

RNA and protein synthesis mechanisms

Genetics and Neurodevelopmental Disorders

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

Gillian Rice,Gabriella Forte,et al.

2013433 citations

Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

Sarah L. Sawyer,Taila Hartley,et al.

2015391 citations

Cancer-associated fibroblasts induce epithelial–mesenchymal transition of bladder cancer cells through paracrine IL-6 signalling

Cassandra Ringuette Goulet,Audrey Champagne,et al.

2019323 citations

Exosomes Induce Fibroblast Differentiation into Cancer-Associated Fibroblasts through TGFβ Signaling

Cassandra Ringuette Goulet,Geneviève Bernard,et al.

2018318 citations

Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy

Geneviève Bernard,Éliane Chouery,et al.

2011267 citations

Clinical spectrum of 4H leukodystrophy caused by <i>POLR3A</i> and <i>POLR3B</i> mutations

Nicole I. Wolf,Adeline Vanderver,et al.

2014205 citations

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

Nancy D. Merner,Simon Girard,et al.

2012194 citations

A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies

Sumit Parikh,Geneviève Bernard,et al.

2014193 citations