Hans van Bokhoven

发表

Faculty of 1000 evaluation for Model of autism: increased ratio of excitation/inhibition in key neural systems.

Hans van Bokhoven, 2017 .

Faculty Opinions recommendation of Ultraconservation identifies a small subset of extremely constrained developmental enhancers.

Hans van Bokhoven, 2008 .

The role of chromatin repressive marks in cognition and disease: A focus on the repressive complex GLP/G9a

Hans van Bokhoven, H. Bokhoven, N. N. Kasri, 2015, Neurobiology of Learning and Memory.

Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice

Yoichi Shinkai, Hans van Bokhoven, Makoto Tachibana, 2010, Behavioural Brain Research.

Asymmetry within and around the human planum temporale is sexually dimorphic and influenced by genes involved in steroid hormone receptor activity

Peter Hagoort, Hans J. Grabe, Alexander Teumer, 2015, Cortex.

Heterozygous Germline Mutations in the p53 Homolog p63 Are the Cause of EEC Syndrome

Michael Bamshad, Gert Vriend, Hans van Bokhoven, 1999, Cell.

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

Steffen Lenzner, Constance Scharff, Kirsten Hoffmann, 2003, Nature Genetics.

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

Andrew Menzies, Sarah Edkins, Sara Widaa, 2009, Nature Genetics.

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2

Gert Matthijs, Dirk Lefeber, Peter Nürnberg, 2008, Nature Genetics.

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome

Birgit Sikkema-Raddatz, Christian R Marshall, Stephen W Scherer, 2010, European Journal of Human Genetics.

Genetic and epigenetic networks in intellectual disabilities.

Hans van Bokhoven, H. Bokhoven, H. van Bokhoven, 2011, Annual review of genetics.

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Han G. Brunner, Hülya Kayserili, Flemming Skovby, 2000, Nature Genetics.

MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome

Hans van Bokhoven, Han G Brunner, Jeroen van Reeuwijk, 2005, Nature Genetics.

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Michael W. Weiner, Anders M. Dale, Robert C. Green, 2017, bioRxiv.