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Peyrard-Janvid, Myriam
78  Ergebnisse:
Personensuche X
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1

Genome-wide association study reveals new insights into the..:

Gialluisi, Alessandro ; Andlauer, Till F. M. ; Mirza-Schreiber, Nazanin...
Molecular Psychiatry.  26 (2020)  7 - p. 3004-3017 , 2020
Link: https://doi.org/10.1038/..
 
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2

Genome-wide association scan identifies new variants associ..:

Gialluisi, Alessandro ; Andlauer, Till F. M. ; Mirza-Schreiber, Nazanin...
Translational Psychiatry.  9 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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3

Identification of NCAN as a candidate gene for developmenta..:

Einarsdottir, Elisabet ; Peyrard-Janvid, Myriam ; Darki, Fahimeh...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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4

Human ROBO1 regulates white matter structure in corpus call..:

Darki, Fahimeh ; Massinen, Satu ; Salmela, Elina...
Brain Structure and Function.  222 (2016)  2 - p. 707-716 , 2016
Link: https://doi.org/10.1007/..
 
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5

Mutation in CEP63 co-segregating with developmental dyslexi..:

Einarsdottir, Elisabet ; Svensson, Idor ; Darki, Fahimeh...
Human Genetics.  134 (2015)  11-12 - p. 1239-1248 , 2015
Link: https://doi.org/10.1007/..
 
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6

Polymorphisms in DCDC2 and S100B associate with development..:

Matsson, Hans ; Huss, Mikael ; Persson, Helena...
Journal of Human Genetics.  60 (2015)  7 - p. 399-401 , 2015
Link: https://doi.org/10.1038/..
 
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7

DCDC2Polymorphism Is Associated with Left Temporoparietal G..:

Darki, Fahimeh ; Peyrard-Janvid, Myriam ; Matsson, Hans..
The Journal of Neuroscience.  34 (2014)  43 - p. 14455-14462 , 2014
Link: https://doi.org/10.1523/..
 
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8

Nonword Repetition – A Clinical Marker for Specific Languag..:

Kalnak, Nelli ; Peyrard-Janvid, Myriam ; Forssberg, Hans..
PLoS ONE.  9 (2014)  2 - p. e89544 , 2014
Link: https://doi.org/10.1371/..
 
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9

Dominant Mutations in GRHL3 Cause Van der Woude Syndrome an..:

Peyrard-Janvid, Myriam ; Leslie, Elizabeth J. ; Kousa, Youssef A....
The American Journal of Human Genetics.  94 (2014)  1 - p. 23-32 , 2014
Link: https://doi.org/10.1016/..
 
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10

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIA..:

Darki, Fahimeh ; Peyrard-Janvid, Myriam ; Matsson, Hans..
Biological Psychiatry.  72 (2012)  8 - p. 671-676 , 2012
Link: https://doi.org/10.1016/..
 
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11

The Dyslexia Candidate Locus on 2p12 Is Associated with Gen..:

Scerri, Thomas S. ; Darki, Fahimeh ; Newbury, Dianne F....
PLoS ONE.  7 (2012)  11 - p. e50321 , 2012
Link: https://doi.org/10.1371/..
 
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12

Dopamine, working memory, and training induced plasticity: ..:

Söderqvist, Stina ; Nutley, Sissela Bergman ; Peyrard-Janvid, Myriam...
Developmental Psychology.  48 (2012)  3 - p. 836-843 , 2012
Link: https://doi.org/10.1037/..
 
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13

SNP Variations in the 7q33 Region Containing DGKI are Assoc..:

Matsson, Hans ; Tammimies, Kristiina ; Zucchelli, Marco...
Behavior Genetics.  41 (2011)  1 - p. 134-140 , 2011
Link: https://doi.org/10.1007/..
 
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14

Increased Expression of the Dyslexia Candidate Gene DCDC2 A..:

Massinen, Satu ; Hokkanen, Marie-Estelle ; Matsson, Hans...
PLoS ONE.  6 (2011)  6 - p. e20580 , 2011
Link: https://doi.org/10.1371/..
 
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15

Influence of the COMT Genotype on Working Memory and Brain ..:

Dumontheil, Iroise ; Roggeman, Chantal ; Ziermans, Tim...
Biological Psychiatry.  70 (2011)  3 - p. 222-229 , 2011
Link: https://doi.org/10.1016/..
 
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