Serkan Erdin
Harvard University
H-index: 28
North America-United States
Top articles of Serkan Erdin
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system | Scientific Reports | Ricardo Harripaul Elisabetta Morini Monica Salani Emily Logan Emily Kirchner | 2024/1/4 |
P159: Variants in cohesin release factors WAPL, PDS5A, and PDS5B define a new class of cohesinopathies | Genetics in Medicine Open | Philip Boone Kamli Faour Kiana Mohajeri John Lemanski Bimal Jana | 2023/1/1 |
Proteasomal pathway inhibition as a potential therapy for NF2-associated meningioma and schwannoma | Neuro-oncology | Srirupa Bhattacharyya Janet L Oblinger Roberta L Beauchamp Zhenzhen Yin Serkan Erdin | 2023/9/1 |
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies | Cell Genomics | Calwing Liao Mariana Moyses-Oliveira Celine EF De Esch Riya Bhavsar Xander Nuttle | 2023/4/12 |
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder | Nature Communications | Elaine T Lim Yingleong Chan Pepper Dawes Xiaoge Guo Serkan Erdin | 2022/6/10 |
CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing | Nucleic Acids Research | Emanuela Kerschbamer Michele Arnoldi Takshashila Tripathi Miguel Pellegrini Samuele Maturi | 2022/12/9 |
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models | The American Journal of Human Genetics | Kiana Mohajeri Rachita Yadav Eva D'haene Philip M Boone Serkan Erdin | 2022/11/3 |
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p | Nature genetics | Daniel J Weiner Emi Ling Serkan Erdin Derek JC Tai Rachita Yadav | 2022/11 |
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 | Derek JC Tai Parisa Razaz Serkan Erdin Dadi Gao Jennifer Wang | 2022/10/6 |
Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage | Journal of Genetics and Genomics | Elisabetta Morini Dadi Gao Emily M Logan Monica Salani Aram J Krauson | 2022/7/1 |
De novo variants in SIAH1, encoding an E3 ubiquitin ligase, are associated with developmental delay, hypotonia and dysmorphic features | Journal of Medical Genetics | Julien Buratti Lei Ji Boris Keren Youngha Lee Stephanie Booke | 2021/3/1 |
mTOR kinase inhibition disrupts neuregulin 1-ERBB3 autocrine signaling and sensitizes NF2-deficient meningioma cellular models to IGF1R inhibition | Journal of Biological Chemistry | Roberta L Beauchamp Serkan Erdin Luke Witt Justin T Jordan Scott R Plotkin | 2021/1/1 |
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin | The American Journal of Human Genetics | Aloysius Domingo Rachita Yadav Shivangi Shah William T Hendriks Serkan Erdin | 2021/11/4 |
Physiological characterization and transcriptomic properties of GnRH neurons derived from human stem cells | Endocrinology | Kim L Keen Andrew J Petersen Alexander G Figueroa Benjamin I Fordyce Jaeweon Shin | 2021/9 |
Brigatinib causes tumor shrinkage in both NF2-deficient meningioma and schwannoma through inhibition of multiple tyrosine kinases but not ALK | PLoS One | Long-Sheng Chang Janet L Oblinger Abbi E Smith Marc Ferrer Steven P Angus | 2021/7/15 |
A deep learning approach to identify gene targets of a therapeutic for human splicing disorders | Nature communications | Dadi Gao Elisabetta Morini Monica Salani Aram J Krauson Anil Chekuri | 2021/6/7 |
Mechanistic dissection of chromatin topology disruption in the 5q14. 3 MEF2C locus as an indirect driver of neurodevelopmental disorders | Kiana Mohajeri Eva D'haene Rachita Yadav Huiya Gu Björn Menten | 2020 | |
TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling | Molecular autism | Pauline Martin Vilas Wagh Surya A Reis Serkan Erdin Roberta L Beauchamp | 2020/12 |
De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic features | American Journal of Medical Genetics Part A | Jonathan Rips Hagar Mor‐Shaked Serkan Erdin Shira Yanovsky‐Dagan Smadar Eventov‐Friedman | 2020 |
Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice | Elife | Marina Kovalenko Serkan Erdin Marissa A Andrew Jason St Claire Melissa Shaughnessey | 2020/9/29 |
