Serkan Erdin

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

33h-index10.0kcitations123works1.02yr avg
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Research Topics

Genetics and Neurodevelopmental Disorders(21), Physics of Superconductivity and Magnetism(13), RNA Research and Splicing(13), CRISPR and Genetic Engineering(13), Congenital heart defects research(12)

Publications122 total

CRISPR-engineered deletion of <i>POGZ</i> alters transcription factor binding at promoters of genes involved in synaptic signaling
2025· 1 citedOpen Access
Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonism
2025Open Access
Aberrant recursive splicing in a human disease locus
2025Open Access
Functional consequences of genetic risk for neuropsychiatric conditions at chr22q
2025· 1 citedOpen Access
Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium
Molecular Psychiatry·2025· 3 cited
TSC2 loss in neural progenitor cells suppresses mRNA translation of neurodevelopmental genes
Brain·2025· 1 cited
Therapeutic Targeting of Alternative Splicing Caused by a Lethal Noncoding Structural Variant in X-Linked Dystonia Parkinsonism
SSRN Electronic Journal·2025Open Access
<i>TSC2</i> loss in neural progenitor cells suppresses translation of ASD/NDD-associated transcripts in an mTORC1- and MNK1/2-reversible fashion
2024· 1 citedOpen Access
Author Correction: Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
Scientific Reports·2024· 1 citedOpen Access
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
The American Journal of Human Genetics·2024· 1 citedOpen Access
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
Scientific Reports·2024· 2 citedOpen Access
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system
2023Open Access
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Cell Genomics·2023· 20 citedOpen Access
Proteasomal pathway inhibition as a potential therapy for NF2-associated meningioma and schwannoma
Neuro-Oncology·2023· 9 citedOpen Access
P159: Variants in cohesin release factors WAPL, PDS5A, and PDS5B define a new class of cohesinopathies*
Genetics in Medicine Open·2023· 2 citedOpen Access
<i>CHD8</i> suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing
Nucleic Acids Research·2022· 25 citedOpen Access
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
Nature Genetics·2022· 54 citedOpen Access
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
The American Journal of Human Genetics·2022· 27 citedOpen Access
STATISTICAL AND FUNCTIONAL CONVERGENCE OF COMMON AND RARE VARIANT RISK FOR AUTISM SPECTRUM DISORDERS AT CHROMOSOME 16P
European Neuropsychopharmacology·2022· 3 cited
Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models
The American Journal of Human Genetics·2022· 36 citedOpen Access
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Frequent Co-authors

Michael E. Talkowski(22), James F. Gusella(15), Olivier Lichtarge(12), Ashok Ragavendran(9), Alexei Stortchevoi(7), Shalini N. Jhangiani(7), James R. Lupski(7), R. Matthew Ward(7), Stephen J. Haggarty(6), Ender Karaca(6), Davut Pehli̇van(6), Richard A. Gibbs(6), Derek J.C. Tai(6), Andreas Martin Lisewski(5), Eric Venner(5), Ryan L. Collins(5), Poornima Manavalan(5), Diane Lucente(5), Tomasz Gambin(5), Yavuz Bayram(5)