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Nature Neuroscience|February 2, 2016
Engineering microdeletions and microduplications by targeting segmental duplications with CRISPRDerek J C Tai, Ashok Ragavendran, Poornima Manavalan, et al.
Molecular Autism|June 7, 2020
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neuronsCatarina M Seabra, Tatsiana Aneichyk, Serkan Erdin, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Multi-omics profiling reveals MAGEL2-driven defects in human corticogenesis shared across Prader-Willi and Schaaf-Yang syndromesJannis Buecking, Baran Enes Güler, Michael Eibl, et al.
Nature Communications|June 10, 2022
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorderElaine T Lim, Yingleong Chan, Pepper Dawes, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CRISPR-engineered deletion of <i>POGZ</i> alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
HGG Advances|July 11, 2026
CRISPR-engineered deletion of POGZ alters transcription factor binding at promoters of genes involved in synaptic signalingMariana Moyses-Oliveira, Yating Liu, Serkan Erdin, et al.
Nature Genetics|October 25, 2022
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16pDaniel J Weiner, Emi Ling, Serkan Erdin, et al.
Biological Psychiatry|December 29, 2022
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived NeuronsEuan Parnell, Lorenza Culotta, Marc P Forrest, et al.
American Journal of Human Genetics|October 25, 2022
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal modelsKiana Mohajeri, Rachita Yadav, Eva D'haene, et al.
American Journal of Human Genetics|September 24, 2022
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal modelsDerek J C Tai, Parisa Razaz, Serkan Erdin, et al.
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