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au.\*:("PEYRARD-JANVID, Myriam")

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AMP deaminase deficiency is associated with lower sprint cycling performance in healthy subjectsFISCHER, Heléne; ESBJÖRNSSON, Mona; SABINA, Richard L et al.Journal of applied physiology (1985). 2007, Vol 103, Num 1, pp 315-322, issn 8750-7587, 8 p.Article

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter StructureDARKI, Fahimeh; PEYRARD-JANVID, Myriam; MATSSON, Hans et al.Biological psychiatry (1969). 2012, Vol 72, Num 8, pp 671-676, issn 0006-3223, 6 p.Article

Dopamine, Working Memory, and Training Induced Plasticity: Implications for Developmental Research : Neuromodulation of Behavioral and Cognitive development Across the Life SpanSÖDERQVIST, Stina; BERGMAN NUTLEY, Sissela; PEYRARD-JANVID, Myriam et al.Developmental psychology. 2012, Vol 48, Num 3, pp 836-843, issn 0012-1649, 8 p.Article

Family-based association study of DYX1C1 variants in autismYLISAUKKO-OJA, Tero; PEYRARD-JANVID, Myriam; LINDGREN, Cecilia M et al.European journal of human genetics. 2005, Vol 13, Num 1, pp 127-130, issn 1018-4813, 4 p.Article

Influence of the COMT Genotype on Working Memory and Brain Activity Changes During DevelopmentDUMONTHEIL, Iroise; ROGGEMAN, Chantal; ZIERMANS, Tim et al.Biological psychiatry (1969). 2011, Vol 70, Num 3, pp 222-229, issn 0006-3223, 8 p.Article

The SNAP25 Gene Is Linked to Working Memory Capacity and Maturation of the Posterior Cingulate Cortex During ChildhoodSÖDERQVIST, Stina; MCNAB, Fiona; PEYRARD-JANVID, Myriam et al.Biological psychiatry (1969). 2010, Vol 68, Num 12, pp 1120-1125, issn 0006-3223, 6 p.Article

A locus on 2p12 containing the co-regulated MRPL 19 and C2ORF3 genes is associated to dyslexiaANTHONI, Heidi; ZUCCHELLI, Marco; HOFFMANN, Per et al.Human molecular genetics (Print). 2007, Vol 16, Num 6, pp 667-677, issn 0964-6906, 11 p.Article

ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosisHODGSON, Ulla; PULKKINEN, Ville; TUKIAINEN, Pentti et al.American journal of human genetics. 2006, Vol 79, Num 1, pp 149-154, issn 0002-9297, 6 p.Article

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate genePEYRARD-JANVID, Myriam; ANTHONI, Heidi; KERE, Juha et al.Human genetics. 2004, Vol 114, Num 5, pp 510-516, issn 0340-6717, 7 p.Article

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndromePEYRARD-JANVID, Myriam; PEGELOW, Marie; KOILLINEN, Hannele et al.European journal of human genetics. 2005, Vol 13, Num 12, pp 1261-1267, issn 1018-4813, 7 p.Article

Genomic Strategy Identifies a Missense Mutation in WD-Repeat Domain 65 (WDR65) in an Individual With Van der Woude SyndromeRORICK, Nicholas K; KINOSHITA, Akira; MANSILLA, Maria A et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 6, pp 1314-1321, issn 1552-4825, 8 p.Article

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexiaSCHUMACHER, Johannes; ANTHONI, Heidi; HÜLSMANN, Jutta et al.American journal of human genetics. 2006, Vol 78, Num 1, pp 52-62, issn 0002-9297, 11 p.Article

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