Barbara Molz

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 4

Top Topics

Autism Spectrum Disorder

Induced Pluripotent Stem Cells

Genome Wide Association Study

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Catherine Doust, Pierre Fontanillas, Else Eising, Scott D Gordon, Zhengjun Wang, Gökberk Alagöz, Barbara Molz, null null, null null, Beate St Pourcain, Clyde Francks, Riccardo E Marioni, Jingjing Zhao, Silvia Paracchini, Joel B Talcott, Anthony P Monaco, John F Stein, Jeffrey R Gruen, Richard K Olson, Erik G Willcutt, John C DeFries, Bruce F Pennington, Shelley D Smith, Margaret J Wright, Nicholas G Martin, Adam Auton, Timothy C Bates, Simon E Fisher, Michelle Luciano
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia. Nature genetics (2023)
Gökberk Alagöz, Barbara Molz, Else Eising, Dick Schijven, Clyde Francks, Jason L Stein, Simon E Fisher
Using neuroimaging genomics to investigate the evolution of human brain structure. Proceedings of the National Academy of Sciences of the United States of America 119 (40) (2022)
Catherine Doust, Pierre Fontanillas, Else Eising, Scott D Gordon, Zhengjun Wang, Gökberk Alagöz, Barbara Molz, null null, null null, Beate St Pourcain, Clyde Francks, Riccardo E Marioni, Jingjing Zhao, Silvia Paracchini, Joel B Talcott, Anthony P Monaco, John F Stein, Jeffrey R Gruen, Richard K Olson, Erik G Willcutt, John C DeFries, Bruce F Pennington, Shelley D Smith, Margaret J Wright, Nicholas G Martin, Adam Auton, Timothy C Bates, Simon E Fisher, Michelle Luciano
Discovery of 42 genome-wide significant loci associated with dyslexia. Nature genetics 54 (11) (2022)
Else Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, Carol A Wang, Dongnhu T Truong, Andrea G Allegrini, Chin Yang Shapland, Gu Zhu, Karen G Wigg, Margot L Gerritse, Barbara Molz, Gökberk Alagöz, Alessandro Gialluisi, Filippo Abbondanza, Kaili Rimfeld, Marjolein van Donkelaar, Zhijie Liao, Philip R Jansen, Till F M Andlauer, Timothy C Bates, Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S Dale, Peter F de Jong, John C DeFries, Jean-François Démonet, Ditte Demontis, Yu Feng, Scott D Gordon, Sharon L Guger, Marianna Emma Hayiou-Thomas, Juan A Hernández-Cabrera, Jouke-Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N Kerr, Tanner Koomar, Karin Landerl, Gabriel T Leonard, Maureen W Lovett, Heikki Lyytinen, Nicholas G Martin, Angela Martinelli, Urs Maurer, Jacob J Michaelson, Kristina Moll, Anthony P Monaco, Angela T Morgan, Markus Maria Nöthen, Zdenka Pausova, Craig E Pennell, Bruce F Pennington, Kaitlyn M Price, Veera Manikandan Rajagopal, Franck Ramus, Louis Richer, Nuala H Simpson, Shelley D Smith, Margaret J Snowling, John F Stein, Lisa J Strug, Joel B Talcott, Henning Tiemeier, Marc P van der Schroeff, Ellen Verhoef, Kate E Watkins, Margaret Wilkinson, Margaret J Wright, Cathy L Barr, Dorret I Boomsma, Manuel Carreiras, Marie-Christine J Franken, Jeffrey R Gruen, Michelle Luciano, Bertram Müller-Myhsok, Dianne F Newbury, Richard K Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte-Körne, J Bruce Tomblin, Elsje van Bergen, Andrew J O Whitehouse, Erik G Willcutt, Beate St Pourcain, Clyde Francks, Simon E Fisher
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America 119 (35) (2022)