Serkan Erdin

Also affiliated with Massachusetts General Hospital

Biochemistry, Genetics and Molecular BiologyPhysics and Astronomy

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Data integration of bulk and single-cell transcriptomics from cerebral organoids and post-mortem brains to identify cell types and cell type specific driver genes in autism

Research Square(2020)10.21203/rs.3.rs-113869/v1

Top 100%

0DataRank

Top 100%0 citations

Yingleong Chan, Mannix J. Burns, Xiaoge Guo, Serkan Erdin, Derek J.C. Tai +13 more

Papers

Driven by 30 papers — median percentile 0. Top paper: “Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p”.

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice

eLife(2020)10.7554/elife.55911

N/A

0.620DataRank · unranked

21 citations

Serkan Erdin, Marissa A Andrew, Jason St. Claire, Melissa Shaughnessey, Leroy Hubert +9 more

TSC patient-derived isogenic neural progenitor cells reveal altered early neurodevelopmental phenotypes and rapamycin-induced MNK-eIF4E signaling

Molecular Autism(2020)10.1186/s13229-019-0311-3

N/A

0.590DataRank · unranked

50 citations

Vilas Wagh, Surya A. Reis, Serkan Erdin, Roberta L. Beauchamp, Ghalib Shaikh +6 more

Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorder

Nature Communications(2022)10.1038/s41467-022-30968-3

N/A

0.500DataRank · unranked

27 citations

Yingleong Chan, Pepper Dawes, Xiaoge Guo, Serkan Erdin, Derek J.C. Tai +15 more

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing

Nucleic Acids Research(2022)10.1093/nar/gkac1134

N/A

0.494DataRank · unranked

26 citations

Michele Arnoldi, Takshashila Tripathi, Miguel Pellegrini, Samuele Maturi, Serkan Erdin +16 more

Age dependent association of inbreeding with risk for schizophrenia in Egypt

Schizophrenia Research(2020)10.1016/j.schres.2019.10.039

N/A

0DataRank · unranked

5 citations

Hader Mansour, Ibtihal Ibrahim, Lambertus Klei, Warda Fathi, Joel Wood +19 more

A deep learning approach to identify new gene targets of a novel therapeutic for human splicing disorders

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.03.932103

N/A

0DataRank · unranked

7 citations

Elisabetta Morini, Monica Salani, Aram J. Krauson, Ashok Ragavendran, Serkan Erdin +15 more

CHD8 Suppression Impacts on Histone H3 Lysine 36 Trimethylation and Alters RNA Alternative Splicing

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.14.992032

N/A

0DataRank · unranked

0 citations

Takshashila Tripathi, Serkan Erdin, Elisa Salviato, Francesca Di Leva, Endre Sebestyén +9 more

Data integration of bulk and single-cell transcriptomics from cerebral organoids and post-mortem brains to identify cell types and cell type specific driver genes in autism

Research Square(2020)10.21203/rs.3.rs-113869/v1

Top 100%

0DataRank

Top 100%0 citations

Yingleong Chan, Mannix J. Burns, Xiaoge Guo, Serkan Erdin, Derek J.C. Tai +13 more

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52

N/A

0DataRank · unranked

0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

A deep learning approach to identify gene targets of a therapeutic for human splicing disorders

Nature Communications(2021)10.1038/s41467-021-23663-2

N/A

0DataRank · unranked

48 citations

Elisabetta Morini, Monica Salani, Aram J. Krauson, Anil Chekuri, Neeraj Sharma +20 more

Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.09.017

N/A

0DataRank · unranked

23 citations

Rachita Yadav, Shivangi Shah, William T. Hendriks, Serkan Erdin, Dadi Gao +9 more

Physiological Characterization and Transcriptomic Properties of GnRH Neurons Derived From Human Stem Cells

Endocrinology(2021)10.1210/endocr/bqab120

N/A

0DataRank · unranked

18 citations

Andrew J. Petersen, Alexander G. Figueroa, Benjamin I. Fordyce, Jaeweon Shin, Rachita Yadav +6 more

Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage

Journal of genetics and genomics/Journal of Genetics and Genomics(2021)10.1016/j.jgg.2021.11.011

N/A

0DataRank · unranked

12 citations

Dadi Gao, Emily M. Logan, Monica Salani, Aram J. Krauson, Anil Chekuri +9 more

Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.16.440179

N/A

0DataRank · unranked

1 citations

Dadi Gao, Emily M. Logan, Monica Salani, Aram J. Krauson, Anil Chekuri +9 more

Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.22.449452

N/A

0DataRank · unranked

0 citations

Rachita Yadav, Shivangi Shah, William T. Hendriks, Serkan Erdin, Dadi Gao +9 more

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.015

N/A

0DataRank · unranked

30 citations

Rachita Yadav, Eva D’haene, Philip M. Boone, Serkan Erdin, Dadi Gao +18 more

Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p

medRxiv(2022)10.1101/2022.03.23.22272826

N/A

0DataRank · unranked

2 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +15 more

Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.15.480098

N/A

0DataRank · unranked

0 citations

Rachita Yadav, Eva D’haene, Philip M. Boone, Serkan Erdin, Dadi Gao +15 more

Convergent coexpression of autism associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

medRxiv(2022)10.1101/2022.02.28.22271620

N/A

0DataRank · unranked

0 citations

Mariana Moysés‐Oliveira, Celine E. de Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li +14 more

Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies

Cell Genomics(2023)10.1016/j.xgen.2023.100277

N/A

0DataRank · unranked

24 citations

Mariana Moysés‐Oliveira, Celine E.F. De Esch, Riya Bhavsar, Xander Nuttle, Aiqun Li +14 more

Proteasomal pathway inhibition as a potential therapy for NF2-associated meningioma and schwannoma

Neuro-Oncology(2023)10.1093/neuonc/noad037

N/A

0DataRank · unranked

10 citations

Janet L. Oblinger, Roberta L. Beauchamp, Zhenzhen Yin, Serkan Erdin, Priya Koundinya +8 more

Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.28.559870

N/A

0DataRank · unranked

0 citations

Elisabetta Morini, Monica Salani, Emily M. Logan, Emily Kirchner, Jessica Bolduc +7 more

Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system

Scientific Reports(2024)10.1038/s41598-023-51137-6

N/A

0DataRank · unranked

2 citations

Elisabetta Morini, Monica Salani, Emily M. Logan, Emily Kirchner, Jessica Bolduc +8 more

Whole-blood transcriptomic analysis reveals preoperative complement inhibitor deficiencies linked to postoperative delirium

Molecular Psychiatry(2025)10.1038/s41380-025-03063-4

N/A

0DataRank · unranked

4 citations

Jiayi Kang, Haobo Li, Serkan Erdin, Matthew J. Smith, Ariel Mueller +11 more

Therapeutic targeting of alternative splicing caused by a lethal noncoding structural variant in X-linked dystonia parkinsonism

medRxiv(2025)10.1101/2025.10.10.25336355

N/A

0DataRank · unranked

1 citations

Christine A. Vaine, Aloysius Domingo, Sheldon C. Reed, Shivangi Shah, Dadi Gao +23 more

New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders

Current Opinion in Genetics & Development(2020)10.1016/j.gde.2020.07.001

N/A

0DataRank · unranked

49 citations

Rachita Yadav, Serkan Erdin, Michael E. Talkowski, Mariana Moysés‐Oliveira

mTOR kinase inhibition disrupts neuregulin 1-ERBB3 autocrine signaling and sensitizes NF2-deficient meningioma cellular models to IGF1R inhibition

Journal of Biological Chemistry(2020)10.1074/jbc.ra120.014960

N/A

0DataRank · unranked

18 citations

Serkan Erdin, Luke Witt, Justin T. Jordan, Scott R. Plotkin, James F. Gusella +2 more

Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons

Molecular Autism(2020)10.1186/s13229-020-00354-1

N/A

0DataRank · unranked

21 citations

Tatsiana Aneichyk, Serkan Erdin, Derek J.C. Tai, Celine de Esch, Parisa Razaz +10 more

Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51003

N/A

0DataRank · unranked

30 citations

Tadahiro Mitani, Sedat Işıkay, Jozef Hertecant, Mohammed Almannai, Kandamurugu Manickam +19 more

Serkan Erdin

Indexed papers

Top data-sharing exemplar

Papers