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Andrei Verner

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James C Engert; Mathieu Lemire; Janet Faith; Diane Brisson; T Mary Fujiwara; Nicole M Roslin; Carl G Brewer; Alexandre Montpetit; Corinne Darmond-Zwaig; Yannick Renaud; Carole Doré; Swneke D Bailey; Andrei Verner; Gérald Tremblay; Julie St-Pierre; Christine Bétard; Jill Platko; John D Rioux; Kenneth Morgan; Thomas J Hudson; Daniel Gaudet
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
Martin Hrebícek; Lenka Mrázová; Volkan Seyrantepe; Stéphanie Durand; Nicole M Roslin; Lenka Nosková; Hana Hartmannová; Robert Ivanek; Alena Cízkova; Helena Poupetová; Jakub Sikora; Jana Urinovská; Viktor Stranecký; Jirí Zeman; Pierre Lepage; David Roquis; Andrei Verner; Jérôme Ausseil; Clare E Beesley; Irène Maire; B J H M Poorthuis; Jiddeke van de Kamp; Otto P van Diggelen; Ron A Wevers; Thomas J Hudson; T Mary Fujiwara; Jacek Majewski; Kenneth Morgan; Stanislav Kmoch; Alexey V Pshezhetsky
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
Lisa C Worgan; Kirsten Niles; Jamie C Tirone; Adam Hofmann; Andrei Verner; Alya'a Sammak; Terrence Kucic; Pierre Lepage; David S Rosenblatt
Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.

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All Publications

2008: James C Engert; Mathieu Lemire; Janet Faith; Diane Brisson; T Mary Fujiwara; Nicole M Roslin; Carl G Brewer; Alexandre Montpetit; Corinne Darmond-Zwaig; Yannick Renaud; Carole Doré; Swneke D Bailey; Andrei Verner; Gérald Tremblay; Julie St-Pierre; Christine Bétard; Jill Platko; John D Rioux; Kenneth Morgan; Thomas J Hudson; Daniel Gaudet
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
European journal of human genetics : EJHG 2008;16(1):105-14.
2006: Martin Hrebícek; Lenka Mrázová; Volkan Seyrantepe; Stéphanie Durand; Nicole M Roslin; Lenka Nosková; Hana Hartmannová; Robert Ivanek; Alena Cízkova; Helena Poupetová; Jakub Sikora; Jana Urinovská; Viktor Stranecký; Jirí Zeman; Pierre Lepage; David Roquis; Andrei Verner; Jérôme Ausseil; Clare E Beesley; Irène Maire; B J H M Poorthuis; Jiddeke van de Kamp; Otto P van Diggelen; Ron A Wevers; Thomas J Hudson; T Mary Fujiwara; Jacek Majewski; Kenneth Morgan; Stanislav Kmoch; Alexey V Pshezhetsky
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
American journal of human genetics 2006;79(5):807-19.
2006: Lisa C Worgan; Kirsten Niles; Jamie C Tirone; Adam Hofmann; Andrei Verner; Alya'a Sammak; Terrence Kucic; Pierre Lepage; David S Rosenblatt
Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.
Human mutation 2006;27(1):31-43.
2005: Thomas G Saba; Alexandre Montpetit; Andrei Verner; Pierre Rioux; Thomas J Hudson; Régen Drouin; Christian A Drouin
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.
Human genetics 2005;116(3):167-71.
2004: Jérôme Ausseil; J Concepción Loredo-Osti; Andrei Verner; Corinne Darmond-Zwaig; Irène Maire; B J H M Poorthuis; Otto P van Diggelen; Thomas J Hudson; T Mary Fujiwara; Kenneth Morgan; Alexey V Pshezhetsky
Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.
Journal of medical genetics 2004;41(12):941-5.
2004: Marcelo T Mira; Alexandre Alcaïs; Van Thuc Nguyen; Milton O Moraes; Celestino Di Flumeri; Hong Thai Vu; Chi Phuong Mai; Thu Huong Nguyen; Ngoc Ba Nguyen; Xuan Khoa Pham; Euzenir N Sarno; Andrea Alter; Alexandre Montpetit; Maria Moraes; José R Moraes; Carole Doré; Caroline J Gallant; Pierre Lepage; Andrei Verner; Esther van de Vosse; Thomas J Hudson; Laurent Abel; Erwin Schurr
Susceptibility to leprosy is associated with PARK2 and PACRG.
Nature 2004;427(6975):636-40.
2004: Marie-Thérèse Berthier; Patrick Couture; Alain Houde; Ann-Marie Paradis; Alya'a Sammak; Andrei Verner; Jean-Pierre Deprés; Claude Gagné; Daniel Gaudet; Marie-Claude Vohl
The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians.
Molecular genetics and metabolism 2004;81(2):140-3.
2004: Tomi Pastinen; Robert Sladek; Scott Gurd; Alya'a Sammak; Bing Ge; Pierre Lepage; Karine Lavergne; Amelie Villeneuve; Tiffany Gaudin; Helena Brändström; Allon Beck; Andrei Verner; Jade Kingsley; Eef Harmsen; Damian Labuda; Kenneth Morgan; Marie-Claude Vohl; Anna K Naumova; Daniel Sinnett; Thomas J Hudson
A survey of genetic and epigenetic variation affecting human gene expression.
Physiological genomics 2004;16(2):184-93.
2003: Marcelo T Mira; Alexandre Alcaïs; Nguyen Van Thuc; Vu Hong Thai; Nguyen Thu Huong; Nguyen Ngoc Ba; Andrei Verner; Thomas J Hudson; Laurent Abel; Erwin Schurr
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population.
Nature genetics 2003;33(3):412-5.
2002: Patrick Cossette; Lidong Liu; Kateri Brisebois; Haiheng Dong; Anne Lortie; Michel Vanasse; Jean-Marc Saint-Hilaire; Lionel Carmant; Andrei Verner; Wei-Yang Lu; Yu Tian Wang; Guy Rouleau
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Nature genetics 2002;31(2):184-9.
2001: Alex Desautels; Gustavo Turecki; Jacques Montplaisir; Pedro Adolfo Sequeira; Andrei Verner; Guy Rouleau
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
American journal of human genetics 2001;69(6):1266-70.
2000: Christine Bétard; Andrée Rasquin-Weber; Carl G Brewer; Eric Drouin; S Clark; Andrei Verner; Corinne Darmond-Zwaig; J Fortin; Jocelyne Mercier; Pierre Chagnon; T Mary Fujiwara; Kenneth Morgan; Andrea Richter; Thomas J Hudson; Grant A Mitchell
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.
American journal of human genetics 2000;67(1):222-8.
2000: E de la Casa-Esperon; Fernando Pardo-Manuel de Villena; Andrei Verner; Tammi L Briscoe; Jan Michel Malette; M Rosa; W H Jin; Carmen Sapienza
Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X.
Genetics 2000;154(1):343-50.
1999: Fernando Pardo-Manuel de Villena; Elena de La Casa-Esperón; Andrei Verner; Kenneth Morgan; Carmen Sapienza
The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(5):492-7.
1998: Anna K Naumova; L Olien; L M Bird; M Smith; Andrei Verner; Mark Leppert; Kenneth Morgan; Carmen Sapienza
Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human.
European journal of human genetics : EJHG 1998;6(6):552-62.
1997: Fernando Pardo-Manuel de Villena; Anna K Naumova; Andrei Verner; W H Jin; Carmen Sapienza
Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(9):642-6.
1996: F Pardo-Manual de Villena; C Slamka; M Fonseca; Anna K Naumova; J Paquette; P Pannunzio; M Smith; Andrei Verner; Kenneth Morgan; Carmen Sapienza
Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome.
Genetics 1996;142(4):1299-304.
1995: Anna K Naumova; L Olien; L M Bird; C Slamka; M Fonseca; Andrei Verner; M Wang; Mark Leppert; Kenneth Morgan; Carmen Sapienza
Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation.
Developmental genetics 1995;17(3):198-205.