Iannuzzi, Stéphanie
32  Ergebnisse:
Personensuche X
?
3

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

Gialluisi, Alessandro ; Andlauer, Till F. M ; Mirza-Schreiber, Nazanin...
https://cris.maastrichtuniversity.nl/en/publications/8b76c901-ca76-4687-8b5d-daa0dad811ec.  , 2021
 
?
4

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

Gialluisi, Alessandro ; Andlauer, Till F.M ; Mirza-Schreiber, Nazanin...
https://publications.aston.ac.uk/id/eprint/42022/1/s41380_020_00898_x.pdf.  , 2021
 
?
5

Sporadic and Familial Variants in NF1: An Explanation of th..:

Biotteau, Maëlle ; Dejean, Sébastien ; Lelong, Sandrine...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.00368.  , 2020
 
?
6

Sporadic and Familial Variants in NF1: An Explanation of th..:

Biotteau, Maëlle ; Dejean, Sébastien ; Lelong, Sandrine...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.00368.  , 2020
 
?
7

Sporadic and Familial Variants in NF1: An Explanation of th..:

Biotteau, Maëlle ; Dejean, Sébastien ; Lelong, Sandrine...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.00368.  , 2020
 
?
8

Genome Wide Association Study reveals new insights into the..:

Gialluisi, Alessandro ; Andlauer, Till F M ; Mirza-Schreiber, Nazanin...
https://research-portal.st-andrews.ac.uk/en/researchoutput/genome-wide-association-study-reveals-new-insights-into-the-heritability-and-genetic-correlates-of-developmental-dyslexia(be047dd1-4235-448f-ba0f-9041d4ebdf5e).html.  , 2020
 
?
10

Sporadic and Familial Variants in NF1: An Explanation of th..:

Biotteau, Maëlle ; Dejean, Sébastien ; Lelong, Sandrine...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2020.00368.  , 2020
 
?
 
?
12

Genome Wide Association Study reveals new insights into the..:

Gialluisi, Alessandro ; Andlauer, Till F M ; Mirza-Schreiber, Nazanin...
Gialluisi , A , Andlauer , T F M , Mirza-Schreiber , N , Moll , K , Becker , J , Hoffman , P , Ludwig , K U , Czamara , D , St Pourcain , B , Honbolygó , F , Tóth , D , Csépe , V , Huguet , G , Chaix , Y , Iannuzzi , S , Demonet , J-F , Morris , A P , Hulslander , J , Willcutt , E G , DeFries , J C , Olson , R K , Smith , S D , Pennington , B F , Vaessen , A , Maurer , U , Lyytinen , H , Peyrard-Janvid , M , Leppänen , P H T , Brandeis , D , Bonte , M , Stein , J F , Talcott , J B , Fauchereau , F , Wilcke , A , Kirsten , H , Müller , B , Francks , C , Bourgeron , T , Monaco , A P , Ramus , F , Landerl , K , Kere , J , Scerri , T S , Paracchini , S , Fisher , S E , Schumacher , J , Nöthen , M M , Müller-Myhsok , B & Schulte-Körne , G 2020 , ' Genome Wide Association Study reveals new insights into the heritability and genetic correlates of developmental dyslexia ' , Molecular Psychiatry . https://doi.org/10.1038/s41380-020-00898-....  , 2020
 
?
 
?
 
1-15