Geneviève Bernard - Concepedia

Author

Geneviève Bernard

Also Known As

Bernard Brais, Bernard, Genevieve, Bernard, Geneviève, G BERNARD, G Bernard, G. Bernard, G. W. Bernard, G.Wesley Bernard, Genevieve Bernard, Geneviève Bernard

258

Publications

7.7K

Citations

H-Index

142

Concepts

All Affiliations

McGill University Montreal Children's Hospital McGill University Health Centre Université de Montréal Université Laval

About

Geneviève Bernard is an author at McGill University specializing in medicine, neuropathology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	47	2.6K
2	Engineering	7	7	278
3	Health Sciences	1	1	23
4	Language Studies	1	1	25
5	Public Health	1	1	131

Geneviève Bernard

101

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
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, Johanna L. Schmidt, American Journal of Medical Genetics Part A	2015	589
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, Marcin Szynkiewicz, The Lancet Neurology Genetic DisorderAicardi-goutières SyndromeGeneticsMedicineImmunology	2013	425
Cancer-associated fibroblasts induce epithelial–mesenchymal transition of bladder cancer cells through paracrine IL-6 signalling Cassandra Ringuette Goulet, Audrey Champagne, Geneviève Bernard, BMC Cancer	2019	320
Exosomes Induce Fibroblast Differentiation into Cancer-Associated Fibroblasts through TGFβ Signaling Cassandra Ringuette Goulet, Geneviève Bernard, Sarah Tremblay, Molecular Cancer Research	2018	317
Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy Geneviève Bernard, Éliane Chouery, Maria Lisa Putorti, The American Journal of Human Genetics GeneticsRecessive Hypomyelinating LeukodystrophyMolecular BiologyDegenerative DiseaseMolecular Genetics	2011	267
Clinical spectrum of 4H leukodystrophy caused by <i>POLR3A</i> and <i>POLR3B</i> mutations Nicole I. Wolf, Adeline Vanderver, Rosalina M.L. van Spaendonk, Neurology	2014	203
Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor Nancy D. Merner, Simon Girard, Hélène Catoire, The American Journal of Human Genetics Essential TremorSomatic VariantGenetic DisorderGeneticsDisease Gene Identification	2012	194
Recessive Mutations in POLR3B, Encoding the Second Largest Subunit of Pol III, Cause a Rare Hypomyelinating Leukodystrophy Martine Tétreault, Karine Choquet, Simona Orcesi, The American Journal of Human Genetics Pol IiiMendelian DisorderGenetic DisorderGeneticsPathology	2011	183
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III Isabelle Thiffault, Nicole I. Wolf, Diane Forget, Nature Communications	2015	176
Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans Vafa Bayat, Isabelle Thiffault, Manish Jaiswal, PLoS Biology	2012	164

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