FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

M Tétreault

Research Profile

Physiology

Disorders

Genes & Molecular Sequences

Recessive Genes

Chemicals & Drugs

Concepts & Ideas

Pedigree

Anatomy

Chromosomes, Human, Pair 10

Geographic Areas

Living Beings

European Continental Ancestry Group

Procedures

Chromosome Mapping

Co-author Network

Publications

TOP 3
Hussein Daoud; Janina Gburek-Augustat; William Gibson; Cyril Goizet; Kether Guerrero; Sakkubai Naidu; Rocio Sanchez-Carpintero; Cathy A Stevens; Matthis Synofzik; M Tétreault; Adeline Vanderver; Bernard Brais; Ana Cohen; Geneviève Bernard
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.
Vafa Bayat; Geneviève Bernard; Jean-Pierre Bouchard; Bernard Brais; Julie Demers-Lamarche; Marie-Josée Dicaire; Taraka Donti; Brett H Graham; Claire Haueter; Manish Jaiswal; Zhihong Li; Charles M Lourenco; Jean Mathieu; Marie-France Rioux; Florin Sasarman; Eric A Shoubridge; M Tétreault; Isabelle Thiffault; Michel Vanasse; Hugo J Bellen
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans.
M Tétreault; Isabelle Thiffault; Adeline Venderver; Bernard Brais; Maria Lisa Putorti; Raphael Schiffmann; Michel Sylvain; Geneviève Bernard
TACH leukodystrophy: locus refinement to chromosome 10q22.3-23.1.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of M Tétreault (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Hussein Daoud; Janina Gburek-Augustat; William Gibson; Cyril Goizet; Kether Guerrero; Sakkubai Naidu; Rocio Sanchez-Carpintero; Cathy A Stevens; Matthis Synofzik; M Tétreault; Adeline Vanderver; Bernard Brais; Ana Cohen; Geneviève Bernard
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.
Journal of medical genetics 2013;50(3):194-7.
2012: Vafa Bayat; Geneviève Bernard; Jean-Pierre Bouchard; Bernard Brais; Julie Demers-Lamarche; Marie-Josée Dicaire; Taraka Donti; Brett H Graham; Claire Haueter; Manish Jaiswal; Zhihong Li; Charles M Lourenco; Jean Mathieu; Marie-France Rioux; Florin Sasarman; Eric A Shoubridge; M Tétreault; Isabelle Thiffault; Michel Vanasse; Hugo J Bellen
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans.
PLoS biology 2012;10(3):e1001288.
2012: M Tétreault; Isabelle Thiffault; Adeline Venderver; Bernard Brais; Maria Lisa Putorti; Raphael Schiffmann; Michel Sylvain; Geneviève Bernard
TACH leukodystrophy: locus refinement to chromosome 10q22.3-23.1.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2012;39(1):122-3.
2011: M Tétreault; Davide Tonduti; Adeline Vanderver; Umberto Balottin; Bernard Brais; Karine Choquet; Sébastien Fribourg; Simona Orcesi; Raphael Schiffmann; Martin Teichmann; Geneviève Bernard
Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy.
American journal of human genetics 2011;89(5):652-5.
2011: Geneviève Bernard; Odile Boespflug-Tanguy; Joelle Abou Ghoch; Giovanni Carosso; Eliane Chouery; Isabelle Clément; Valérie Delague; Imen Dorboz; Sebastien Fribourg; Nadine Jalkh; André Megarbane; Maria Lisa Putorti; Diana Rodriguez; Raphael Schiffmann; Asako Takanohashi; Martin Teichmann; M Tétreault; Adeline Vanderver; Bernard Brais
Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy.
American journal of human genetics 2011;89(3):415-23.
2011: M Tétreault; Isabelle Thiffault; Julie Allyson; Jean-Pierre Bouchard; Lina Loisel; Yves Robitaille; M Srour; Bernard Brais
Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian cluster.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2011;38(5):747-52.
2008: Isabelle Gosselin; Isabelle Thiffault; M Tétreault; Vann Chau; Marie-Josée Dicaire; Lina Loisel; Monique Emond; Jan Senderek; Jean Mathieu; Nicolas Dupré; Michel Vanasse; Jack Puymirat; Bernard Brais
Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster.
Neuromuscular disorders : NMD 2008;18(6):483-92.
2007: E Rossignol; Jean Mathieu; I Thiffault; M Tétreault; Marie-Josée Dicaire; Nicolas Chrestian; Nicolas Dupré; Jack Puymirat; Bernard Brais
A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians.
Neurology 2007;69(20):1937-41.
2007: J Jarry; Marie-France Rioux; V Bolduc; Yves Robitaille; V Khoury; I Thiffault; M Tétreault; Lina Loisel; Jean-Pierre Bouchard; Bernard Brais
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12.
Brain : a journal of neurology 2007;130(Pt 2):368-80.
2006: M Tétreault; André Duquette; I Thiffault; C Bherer; J Jarry; Lina Loisel; B Banwell; Guy D'Anjou; Jean Mathieu; Yves Robitaille; Michel Vanasse; Bernard Brais
A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21.
Brain : a journal of neurology 2006;129(Pt 8):2077-84.