Thomas Werge
0000-0003-1829-0766
Publication & Citation Trends
Publications
0 total
TRANSCRIPTIONAL CHANGES IN MOUSE MODELS OF THE 15Q13.3 MICRODELETION SYNDROME
Cited by 0
Semantic Scholar
Can Animal Models of Copy Number Variants That Predispose to Schizophrenia Elucidate Underlying Biology?
Cited by 40
Semantic Scholar
Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations OA
Cited by 36
Semantic Scholar
Altered auditory processing and effective connectivity in 22q11.2 deletion syndrome. OA
Cited by 26
Semantic Scholar
Individuals with 22q11.2 deletion syndrome show intact prediction but reduced adaptation in responses to repeated sounds: Evidence from Bayesian mapping OA
Cited by 6
Semantic Scholar
Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome OA
Cited by 24
Semantic Scholar
Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice OA
Cited by 72
Semantic Scholar
22q11.2 Deletion Syndrome Is Associated With Impaired Auditory Steady-State Gamma Response OA
Cited by 46
Semantic Scholar
Research Topics
Genetic Associations and Epidemiology
(201)
Genetics and Neurodevelopmental Disorders
(90)
Autism Spectrum Disorder Research
(63)
Genomic variations and chromosomal abnormalities
(63)
Congenital heart defects research
(46)
Affiliations
Statens Serum Institut
Rutgers, The State University of New Jersey
Boston College
University of Notre Dame
Roskilde University