Andrei Verner - Concepedia

Author

Andrei Verner

McGill University and Génome Québec Innovation Centre

Also Known As

A Verner, A. E. Verner, A. Verner, Alexis Verner, Andrei E Verner, Andrei E. Verner, Andrei Verner, Vincent Ferretti, Yungang He

Publications

13.3K

Citations

H-Index

Concepts

All Affiliations

McGill University and Génome Québec Innovation Centre McGill University McGill University Health Centre Temple University Montreal General Hospital

About

Andrei Verner is an author at McGill University and Génome Québec Innovation Centre specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	2.3K
2	Public Health	2	2	53
3	Biology	2	2	160
4	Social Sciences	1	1	648
5	Allergy	1	1	29

Andrei Verner

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy Patrick Cossette, Lidong Liu, Katéri Brisebois, Nature Genetics Molecular NeuroscienceGenetic DisorderGeneticsJuvenile Myoclonic EpilepsyNeurology	2002	648
Susceptibility to leprosy is associated with PARK2 and PACRG Marcelo Távora Mira, Alexandre Alcaïs, Nguyen Van Thuc, Nature LeprosyAutoimmune DiseaseDisease MechanismPathogenesisImmunology	2004	476
Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q Alex Désautels, Gustavo Turecki, Jacques Montplaisir, The American Journal of Human Genetics Clinical DisordersChromosome 12QRestless Legs SyndromeNeurological DisorderGenetic Disorder	2001	274
A survey of genetic and epigenetic variation affecting human gene expression Tomi Pastinen, Robert Sladek, Scott Gurd, Physiological Genomics	2004	262
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population Marcelo Távora Mira, Alexandre Alcaïs, Nguyen Van Thuc, Nature Genetics Disease SusceptibilityVietnamese PopulationAutoimmune DiseaseGenetic DisorderGenetics	2003	188
Spectrum of mutations in<i>mut</i>methylmalonic acidemia and identification of a common Hispanic mutation and haplotype Lisa Worgan, Kirsten M. Niles, Jamie C. Tirone, Human Mutation BiologyAllelic VariantCommon Hispanic MutationGenetic DisorderGenetics	2005	120
Genome-wide scan in Portuguese Island families identifies 5q31–5q35 as a susceptibility locus for schizophrenia and psychosis Pamela Sklar, M T Pato, Andrew Kirby, Molecular Psychiatry Portuguese Island FamiliesPsychiatric DisordersPsychiatryGeneticsPsychiatric Genetics	2003	116
Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome) Martin Hřebı́ček, Lenka Mrázová, Volkan Seyrantepe, The American Journal of Human Genetics Sanfilippo C SyndromeAutoimmune DiseaseGenetic DisorderPathogenesisPathology	2006	95
A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13 Agnieszka Seyda, Robert F. Newbold, Thomas J. Hudson, The American Journal of Human Genetics Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsMicrocell-mediated Transfer	2001	72
A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22 Elise Héon, Andrew D. Paterson, Michael Fraser, The American Journal of Human Genetics OphthalmologyGenetic DisorderGeneticsMolecular GeneticsMedicine	2001	52

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