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Myriam Peyrard-Janvid

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Fahimeh Darki; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Stina Söderqvist; Sissela Bergman Nutley; Keith Humphreys; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Dopamine, working memory, and training induced plasticity: implications for developmental research.
Thomas Scerri; John Stein; Joel B Talcott; Andrew J O Whitehouse; Craig E Pennell; Myriam Peyrard-Janvid; Susan Ring; Qi W Ang; Fahimeh Darki; Juha Kere; Torkel Klingberg; Hans Matsson; Anthony P Monaco; Andrew P Morris; Dianne F Newbury; Silvia Paracchini
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.

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All Publications

2012: Fahimeh Darki; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure.
Biological psychiatry 2012;72(8):671-6.
2012: Stina Söderqvist; Sissela Bergman Nutley; Keith Humphreys; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Torkel Klingberg
Dopamine, working memory, and training induced plasticity: implications for developmental research.
Developmental psychology 2012;48(3):836-43.
2012: Thomas Scerri; John Stein; Joel B Talcott; Andrew J O Whitehouse; Craig E Pennell; Myriam Peyrard-Janvid; Susan Ring; Qi W Ang; Fahimeh Darki; Juha Kere; Torkel Klingberg; Hans Matsson; Anthony P Monaco; Andrew P Morris; Dianne F Newbury; Silvia Paracchini
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.
PloS one 2012;7(11):e50321.
2012: T Ziermans; Iroise Dumontheil; J Kere; H Matsson; Myriam Peyrard-Janvid; C Roggeman; Torkel Klingberg
Working memory brain activity and capacity link MAOA polymorphism to aggressive behavior during development.
Translational psychiatry 2012;2():e85.
2011: Iroise Dumontheil; Juha Kere; Hans Matsson; Myriam Peyrard-Janvid; Chantal Roggeman; Tim Ziermans; Torkel Klingberg
Influence of the COMT genotype on working memory and brain activity changes during development.
Biological psychiatry 2011;70(3):222-9.
2011: Nicholas K Rorick; Akira Kinoshita; Jason L Weirather; Myriam Peyrard-Janvid; Renata L L Ferreira de Lima; Martine Dunnwald; Alan L Shanske; Danilo Moretti-Ferreira; Hannele Koillinen; Juha Kere; Maria A Mansilla; Jeffrey C Murray; Steve L Goudy; Brian C Schutte
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndrome.
American journal of medical genetics. Part A 2011;155A(6):1314-21.
2011: Satu Massinen; Hans Matsson; Myriam Peyrard-Janvid; Peter Swoboda; Kristiina Tammimies; Isabel Tapia-Páez; Rune Toftgård; Jan Burghoorn; Eero Castrén; Vanina Dahlström-Heuser; Marie-Estelle Hokkanen; Kristian E Jeppsson; Juha Kuja-Panula; Juha Kere
Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons.
PloS one 2011;6(6):e20580.
2011: Hans Matsson; Kristiina Tammimies; Marco Zucchelli; Heidi Anthoni; Päivi Onkamo; Jaana Nopola-Hemmi; Heikki Lyytinen; Paavo H T Leppanen; Nina Neuhoff; Andreas Warnke; Gerd Schulte-Körne; Johannes Schumacher; Markus M Nöthen; Juha Kere; Myriam Peyrard-Janvid
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Behavior genetics 2011;41(1):134-40.
2010: Stina Söderqvist; Fiona McNab; Myriam Peyrard-Janvid; Hans Matsson; Keith Humphreys; Juha Kere; Torkel Klingberg
The SNAP25 gene is linked to working memory capacity and maturation of the posterior cingulate cortex during childhood.
Biological psychiatry 2010;68(12):1120-5.
2009: Faten Dahdouh; Heidi Anthoni; Isabel Tapia-Páez; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Andreas Warnke; Helmut Remschmidt; Andreas Ziegler; Juha Kere; Bertram Müller-Myhsok; Markus M Nöthen; Johannes Schumacher; Marco Zucchelli
Further evidence for DYX1C1 as a susceptibility factor for dyslexia.
Psychiatric genetics 2009;19(2):59-63.
2008: Kerstin U Ludwig; Johannes Schumacher; Gerd Schulte-Körne; Inke R König; Andreas Warnke; Ellen Plume; Heidi Anthoni; Myriam Peyrard-Janvid; Haiying Meng; Andreas Ziegler; Helmut Remschmidt; Juha Kere; Jeffrey R Gruen; Bertram Müller-Myhsok; Markus M Nöthen; Per Hoffmann
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample.
Psychiatric genetics 2008;18(6):310-2.
2008: M Pegelow; Myriam Peyrard-Janvid; Marco Zucchelli; Ingegerd Fransson; Ola Larson; Juha Kere; Catharina Larsson; Agneta Karsten
Familial non-syndromic cleft lip and palate--analysis of the IRF6 gene and clinical phenotypes.
European journal of orthodontics 2008;30(2):169-75.
2007: Isa Cavaco; Sara Asimus; Myriam Peyrard-Janvid; Pedro E Ferreira; Maria Veiga; Trinh Ngoc Hai; Vera Ribeiro; Michael Ashton; J Pedro Gil
The Vietnamese Khin population harbors particular N-acetyltransferase 2 allele frequencies.
Clinical chemistry 2007;53(11):1977-9.
2007: Heléne Fischer; Mona Esbjörnsson; Richard L Sabina; Anna Strömberg; Myriam Peyrard-Janvid; Barbara Norman
AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjects.
Journal of applied physiology (Bethesda, Md. : 1985) 2007;103(1):315-22.
2007: Heidi Anthoni; Marco Zucchelli; Hans Matsson; Bertram Müller-Myhsok; Ingegerd Fransson; Johannes Schumacher; Satu Massinen; Päivi Onkamo; Andreas Warnke; Heide Griesemann; Per Hoffmann; Jaana Nopola-Hemmi; Heikki Lyytinen; Gerd Schulte-Körne; Juha Kere; Markus M Nöthen; Myriam Peyrard-Janvid
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Human molecular genetics 2007;16(6):667-77.
2006: Ulla Hodgson; Ville Pulkkinen; Morag Dixon; Myriam Peyrard-Janvid; Marko Rehn; Päivi Lahermo; Vesa Ollikainen; Kaisa Salmenkivi; Vuokko Kinnula; Juha Kere; Pentti Tukiainen; Tarja Laitinen
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.
American journal of human genetics 2006;79(1):149-54.
2006: Johannes Schumacher; Heidi Anthoni; Faten Dahdouh; Inke R König; Axel M Hillmer; Nadine Kluck; Malou Manthey; Ellen Plume; Andreas Warnke; Helmut Remschmidt; Jutta Hülsmann; Sven Cichon; Cecilia M Lindgren; Peter Propping; Marco Zucchelli; Andreas Ziegler; Myriam Peyrard-Janvid; Gerd Schulte-Körne; Markus M Nöthen; Juha Kere
Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.
American journal of human genetics 2006;78(1):52-62.
2005: Myriam Peyrard-Janvid; Marie Pegelow; Hannele Koillinen; Catharina Larsson; Ingegerd Fransson; Jorma Rautio; Jyri Hukki; Ola Larson; Agneta Karsten; Juha Kere
Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
European journal of human genetics : EJHG 2005;13(12):1261-7.
2005: James A Timmons; Ola Larsson; Eva Jansson; Helene Fischer; Gustafsson Thomas; Paul L Greenhaff; John Ridden; Jonathan Rachman; Myriam Peyrard-Janvid; Claes Wahlestedt; Carl Johan Sundberg
Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(7):750-60.
2005: Hannele Koillinen; Päivi Lahermo; Jorma Rautio; Jyri Hukki; Myriam Peyrard-Janvid; Juha Kere
A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.
Journal of medical genetics 2005;42(2):177-84.
2005: Tero Ylisaukko-Oja; Myriam Peyrard-Janvid; Cecilia M Lindgren; Karola Rehnström; Raija Vanhala; Leena Peltonen; Irma Järvelä; Juha Kere
Family-based association study of DYX1C1 variants in autism.
European journal of human genetics : EJHG 2005;13(1):127-30.
2004: Myriam Peyrard-Janvid; Heidi Anthoni; Päivi Onkamo; Päivi Lahermo; Marco Zucchelli; Nina Kaminen; Katariina Hannula-Jouppi; Jaana Nopola-Hemmi; Arja Voutilainen; Heikki Lyytinen; Juha Kere
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Human genetics 2004;114(5):510-6.