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Ronald Lafrenière

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Masoud Shekarabi; Patrick A Dion; Rébecca Gaudet; Ronald G Lafrenière; Josée Laganière; Martin M Marcinkiewicz; Guy A Rouleau
Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissues.
Valérie Bercier; Edna Brustein; Patrick A Dion; Ronald G Lafrenière; Meijiang Liao; Guy A Rouleau; Pierre Drapeau
WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio).
Ronald G Lafrenière; Guy A Rouleau
Identification of novel genes involved in migraine.

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2013: Masoud Shekarabi; Patrick A Dion; Rébecca Gaudet; Ronald G Lafrenière; Josée Laganière; Martin M Marcinkiewicz; Guy A Rouleau
Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissues.
PloS one 2013;8(2):e57807.
2013: Valérie Bercier; Edna Brustein; Patrick A Dion; Ronald G Lafrenière; Meijiang Liao; Guy A Rouleau; Pierre Drapeau
WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio).
PLoS genetics 2013;9(1):e1003124.
2012: Ronald G Lafrenière; Guy A Rouleau
Identification of novel genes involved in migraine.
Headache 2012;52 Suppl 2():107-10.
2012: Sean A Wiltshire; Lawrence W Castellani; Eduardo Diez; Marie-Pierre Dubé; Mireille Gagné; Ronald G Lafrenière; Qianqian Miao; Momar Ndao; Olivier Paquette; Emil Skamene; Silvia M Vidal; Anny Fortin
Genetic control of high density lipoprotein-cholesterol in AcB/BcA recombinant congenic strains of mice.
Physiological genomics 2012;44(17):843-52.
2012: Isabelle Andres-Enguix; Zameel M Cader; George C Ebers; Lyn R Griffiths; Ronald G Lafrenière; Julia M Morahan; Guy A Rouleau; Bishakha Roy; Mark S P Sansom; Lijun Shang; Phillip J Stansfeld; Stephen J Tucker
Functional analysis of missense variants in the TRESK (KCNK18) K channel.
Scientific reports 2012;2():237.
2011: Ronald G Lafrenière; Guy A Rouleau
Migraine: Role of the TRESK two-pore potassium channel.
The international journal of biochemistry & cell biology 2011;43(11):1533-6.
2011: Julie Gauthier; Fadi F Hamdan; Peng Huashan; Ridha Joober; Marie-Odile Krebs; Ronald G Lafrenière; Mathieu Lapointe; Jacques L Michaud; Laurent Mottron; Anne Noreau; Salvatore Carbonetto; Nathalie Champagne; Ann Marie Craig; Lynn E DeLisi; Pierre Drapeau; Ferid Fathalli; Eric Fombonne; Tabrez J Siddiqui; Dan Spiegelman; Daisaku Yokomaku; Guy A Rouleau
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia.
Human genetics 2011;130(4):563-73.
2011: Rachel A Myers; Ferran Casals; Julie Gauthier; Fadi F Hamdan; Jon Keebler; Adam R Boyko; Carlos D Bustamante; Amelie M Piton; Dan Spiegelman; Edouard Henrion; Martine Zilversmit; Julie Hussin; Jacklyn Quinlan; Yan Yang; Ronald G Lafrenière; Alexander R Griffing; Eric A Stone; Guy A Rouleau; Philip Awadalla
A population genetic approach to mapping neurological disorder genes using deep resequencing.
PLoS genetics 2011;7(2):e1001318.
2010: Fadi F Hamdan; Hussein Daoud; Daniel Rochefort; Amélie Piton; Julie Gauthier; Mathieu Langlois; Gila Foomani; Sylvia Dobrzeniecka; Marie-Odile Krebs; Ridha Joober; Ronald G Lafrenière; Jean-Claude Lacaille; Laurent Mottron; Pierre Drapeau; Miriam H Beauchamp; Michael S Phillips; Eric Fombonne; Guy Rouleau; Jacques L Michaud
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
American journal of human genetics 2010;87(5):671-8.
2010: Ronald G Lafrenière; M Zameel Cader; Jean-François Poulin; Isabelle Andres-Enguix; Maryse Simoneau; Namrata Gupta; Karine Boisvert; François Lafrenière; Shannon McLaughlan; Marie-Pierre Dubé; Martin M Marcinkiewicz; Sreeram Ramagopalan; Olaf Ansorge; Bernard Brais; Jorge Sequeiros; Jose Maria Pereira-Monteiro; Lyn R Griffiths; Stephen J Tucker; George Ebers; Guy A Rouleau
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Nature medicine 2010;16(10):1157-60.
2010: Julien Tarabeux; Nathalie Champagne; Edna Brustein; Fadi F Hamdan; Julie Gauthier; Mathieu Lapointe; Claudia Maios; Amélie Piton; Dan Spiegelman; Edouard Henrion; Bruno Millet; Judith L Rapoport; Lynn E Delisi; Ridha Joober; Ferid Fathalli; Eric Fombonne; Laurent Mottron; Nadine Forget-Dubois; Michel Boivin; Jacques L Michaud; Ronald G Lafrenière; Pierre Drapeau; Marie-Odile Krebs; Guy Rouleau
De novo truncating mutation in Kinesin 17 associated with schizophrenia.
Biological psychiatry 2010;68(7):649-56.
2010: Julie Gauthier; Nathalie Champagne; Ronald G Lafrenière; Lan Xiong; Dan Spiegelman; Edna Brustein; Mathieu Lapointe; Huashan Peng; Mélanie Côté; Anne Noreau; Fadi F Hamdan; Anjené M Addington; Judith L Rapoport; Lynn E Delisi; Marie-Odile Krebs; Ridha Joober; Ferid Fathalli; Fayçal Mouaffak; Ali P Haghighi; Christian Néri; Marie-Pierre Dubé; Mark E Samuels; Claude Marineau; Eric A Stone; Philip Awadalla; Philip A Barker; Salvatore Carbonetto; Pierre Drapeau; Guy Rouleau
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(17):7863-8.
2009: Fadi F Hamdan; Amélie Piton; Julie Gauthier; Anne Lortie; François Dubeau; Sylvia Dobrzeniecka; Dan Spiegelman; Anne Noreau; Stéphanie Pellerin; Mélanie Côté; Edouard Henrion; Eric Fombonne; Laurent Mottron; Claude Marineau; Pierre Drapeau; Ronald G Lafrenière; Jean Claude Lacaille; Guy Rouleau; Jacques L Michaud
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
Annals of neurology 2009;65(6):748-53.
2009: Fadi F Hamdan; Julie Gauthier; Stéphanie Pellerin; Sylvia Dobrzeniecka; Claude Marineau; Eric Fombonne; Laurent Mottron; Ronald G Lafrenière; Pierre Drapeau; Jean-Claude Lacaille; Guy A Rouleau; Jacques L Michaud
No association between SRGAP3/MEGAP haploinsufficiency and mental retardation.
Archives of neurology 2009;66(5):675-6.
2009: Julie Gauthier; Dan Spiegelman; Amélie Piton; Ronald G Lafrenière; Sandra Laurent; Judith St-Onge; Line Lapointe; Fadi F Hamdan; Patrick Cossette; Laurent Mottron; Eric Fombonne; Ridha Joober; Claude Marineau; Pierre Drapeau; Guy Rouleau
Novel de novo SHANK3 mutation in autistic patients.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(3):421-4.
2009: Lan Xiong; Hélène Catoire; Patrick Dion; Claudia Gaspar; Ronald G Lafrenière; Simon L Girard; Anastasia Levchenko; Jean-Baptiste Rivière; Laura Fiori; Judith St-Onge; Isabelle Bachand; Pascale Thibodeau; Richard Allen; Christopher J Earley; Gustavo Turecki; Jacques Montplaisir; Guy A Rouleau
MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.
Human molecular genetics 2009;18(6):1065-74.
2009: Jean-Baptiste Rivière; Patrick Dion; Masoud Shekarabi; Nathalie Girard; Laurence Faivre; Ronald G Lafrenière; Mark Samuels; Guy Rouleau
[Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II].
Médecine sciences : M/S 2009;25(3):235-8.
2009: Fadi F Hamdan; Julie Gauthier; Dan Spiegelman; Anne Noreau; Yan Yang; Stéphanie Pellerin; Sylvia Dobrzeniecka; Mélanie Côté; Elizabeth Perreau-Linck; Elizabeth Perreault-Linck; Lionel Carmant; Guy D'Anjou; Eric Fombonne; Anjene M Addington; Judy Rapoport; Lynn E Delisi; Marie-Odile Krebs; Faycal Mouaffak; Ridha Joober; Laurent Mottron; Pierre Drapeau; Claude Marineau; Ronald G Lafrenière; Jean-Claude Lacaille; Guy Rouleau; Jacques L Michaud
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
The New England journal of medicine 2009;360(6):599-605.
2008: Amélie Piton; Jacques L Michaud; Huashan Peng; Swaroop Aradhya; Julie Gauthier; Laurent Mottron; Nathalie Champagne; Ronald G Lafrenière; Fadi F Hamdan; Ridha Joober; Eric Fombonne; Claude Marineau; Patrick Cossette; Marie-Pierre Dubé; Pejmun Haghighi; Pierre Drapeau; Philip A Barker; Salvatore Carbonetto; Guy Rouleau
Mutations in the calcium-related gene IL1RAPL1 are associated with autism.
Human molecular genetics 2008;17(24):3965-74.
2008: Masoud Shekarabi; Nathalie Girard; Jean-Baptiste Rivière; Patrick Dion; Martin Houle; André Toulouse; Ronald G Lafrenière; Freya Vercauteren; Pascale Hince; janet laganiere; Daniel Rochefort; Laurence Faivre; Mark Samuels; Guy Rouleau
Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.
The Journal of clinical investigation 2008;118(7):2496-505.
2005: Eric Shink; Mario Harvey; Monique Tremblay; Bernard Gagné; Pascal Belleau; Catherine Raymond; Michel Labbé; Marie-Pierre Dubé; Ronald G Lafrenière; Nicholas Barden
Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;135B(1):50-8.
2004: Jean-Baptiste Rivière; Dominique J Verlaan; Masoud Shekarabi; Ronald G Lafrenière; Mélanie Bénard; Vazken M Der Kaloustian; Zuhayr Shbaklo; Guy Rouleau
A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family.
Annals of neurology 2004;56(4):572-5.
2003: Patrick Cossette; Andrew Loukas; Ronald G Lafrenière; Daniel Rochefort; Erik Harvey-Girard; David S Ragsdale; Robert J Dunn; Guy Rouleau
Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS).
Epilepsy research 2003;53(1-2):107-17.
2000: Gustavo Turecki; Martin Alda; Paul Grof; Ridha Joober; Ronald G Lafrenière; Patrizia Cavazzoni; Anne Duffy; Eva Grof; Bernd Ahrens; Anne Berghöfer; Bruno Müller-Oerlinghausen; M Dvoráková; E Libigerová; M Vojtechovský; P Zvolský; A Nilsson; H Prochazka; Rasmus W Licht; NA Rasmussen; M Schou; P Vestergaard; Anita Holzinger; C Schumann; K Thau; Guy Rouleau
Polyglutamine coding genes in bipolar disorder: lack of association with selected candidate loci.
Journal of affective disorders 2000;58(1):63-8.
1999: Ridha Joober; Chawki Benkelfat; André Toulouse; Ronald G Lafrenière; Samarthji Lal; S Ajroud; Gustavo Turecki; David Bloom; Alain Labelle; Pierre Lalonde; Martin Alda; Kenneth Morgan; Roberta Palmour; Guy Rouleau
Analysis of 14 CAG repeat-containing genes in schizophrenia.
American journal of medical genetics 1999;88(6):694-9.
1999: Ridha Joober; Chawki Benkelfat; Kateri Brisebois; André Toulouse; Ronald G Lafrenière; Gustavo Turecki; Samarthji Lal; David Bloom; Alain Labelle; Pierre Lalonde; D Fortin; Martin Alda; Roberta Palmour; Guy Rouleau
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia.
American journal of medical genetics 1999;88(2):154-7.
1999: Zoha Kibar; Ronald G Lafrenière; Aravinda Chakravarti; J C Wang; M Chevrette; Vazken M Der Kaloustian; Guy Rouleau
A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.
Genomics 1999;56(1):127-30.
1998: Bernard Brais; Jean-Pierre Bouchard; Ya-Gang Xie; Daniel Rochefort; N Chrétien; Fernando M S Tomé; Ronald G Lafrenière; Johanna M Rommens; Eiichiro Uyama; O Nohira; Sergiu C Blumen; Amos D Korczyn; Peter Heutink; Jean Mathieu; André Duranceau; François Codère; M Fardeau; Guy Rouleau; A D Korcyn
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
Nature genetics 1998;18(2):164-7.
1997: Ronald G Lafrenière; Zoha Kibar; Daniel Rochefort; Fei-Yu Han; Edward A Fon; Marie-Pierre Dubé; X Kang; S Baird; Robert G Korneluk; Johanna M Rommens; Guy Rouleau
Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3.
Gene 1997;198(1-2):313-21.
1997: Ronald G Lafrenière; Daniel Rochefort; N Chrétien; Johanna M Rommens; J I Cochius; Reetta Kälviäinen; U Nousiainen; G Patry; K Farrell; B Söderfeldt; A Federico; B R Hale; O H Cossio; T Sørensen; M A Pouliot; T Kmiec; P Uldall; J Janszky; M R Pranzatelli; F Andermann; Eva Andermann; Guy Rouleau
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
Nature genetics 1997;15(3):298-302.
1996: Ronald G Lafrenière; Daniel Rochefort; Zoha Kibar; E A Fon; Fei-Yu Han; J Cochius; X Kang; S Baird; R G Korneluk; Eva Andermann; Johanna M Rommens; Guy Rouleau
Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.
Genomics 1996;38(3):264-72.
1996: Ronald G Lafrenière; Daniel Rochefort; N Chrétien; C E Neville; R G Korneluk; L Zuo; Y Wei; J Lichter; Guy Rouleau
Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3.
Genome research 1996;6(12):1216-26.
1995: Ronald G Lafrenière; P J de Jong; Guy Rouleau
A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3.
Genomics 1995;29(1):288-90.