Work

Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome

Year: 2020

Type: article

Source: Biological Psychiatry

DOI: 10.1016/j.biopsych.2020.05.005

Authors: Kagistia Hana Utami, Niels H. Skotte, Ana R. Colaço, Nur Amirah Binte Mohammad Yusof, Bernice Sim, Xin Yi Yeo, Han-Gyu Bae, Marta Garcia-Miralles, Carola I. Radulescu, Qiyu Chen, Georgia Chaldaiopoulou, Herty Liany, Srikanth Nama, Ulla-Kaisa A. Peteri, Prabha Sampath, Maija L. Castrén, Sangyong Jung, Matthias Mann, Mahmoud A. Pouladi

Institutions: Agency for Science, Technology and Research, University of Copenhagen, Novo Nordisk Foundation, National University of Singapore, Singapore Bioimaging Consortium, National University Hospital, UK Dementia Research Institute, Imperial College London, Genome Institute of Singapore, Institute of Medical Biology, University of Helsinki

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: FRAXA Research Foundation, Agency for Science, Technology and Research, Novo Nordisk, Novo Nordisk Fonden, Weill Cornell Medical College, Australian Research Council

Awards: G1076064052, G4282887365, G5568672882, G6445383465

OpenAlex ID: W3024746958

FWCI: 3.619

Cites: 97

Cited by: 48

Related to: 10