A. Gulhan Ercan‐Sencicek
Yale University(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Genomics and Rare Diseases, Obsessive-Compulsive Spectrum Disorders
Most-Cited Works
- → De novo mutations revealed by whole-exome sequencing are strongly associated with autism(2012)2,152 cited
- → Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci(2015)1,524 cited
- → Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism(2011)1,287 cited
- → Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism(2013)972 cited
- → Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome(2005)944 cited
- → Molecular Cytogenetic Analysis and Resequencing of Contactin Associated Protein-Like 2 in Autism Spectrum Disorders(2008)541 cited
- → L-Histidine Decarboxylase and Tourette's Syndrome(2010)363 cited
- → Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas(2016)349 cited
- → Integrated genomic characterization of IDH1-mutant glioma malignant progression(2015)346 cited
- → Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy(2012)310 cited