🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

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Joshua E. Motelow

Joshua E. Motelow

Morgan Stanley Children's Hospital

ORCID: 0000-0002-4367-4182

Also affiliated with Columbia University

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals”.

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions

Human Molecular Genetics(2021)10.1093/hmg/ddab366

N/A

0DataRank · unranked

20 citations

Joshua E. Motelow, Mark F. Bennett, Zimeng Ye, Caitlin A. Bennett, Nicole G. Griffin +17 more

COVID-19 Mortality in a Pediatric Patient with Hemoglobin SC Disease and Alpha-Thalassemia Trait

Case Reports in Critical Care(2021)10.1155/2021/6617362

N/A

0DataRank · unranked

3 citations

Stacie Kahn, Patrick T. Wilson, Joshua E. Motelow

Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

Epilepsia(2022)10.1111/epi.17166

N/A

0DataRank · unranked

13 citations

Joshua E. Motelow, Kate E. Stanley, Dheeraj Reddy Bobbili, Ryan S. Dhindsa, Patrick May +3 more

Investigation into the genetics of fetal congenital lymphatic anomalies

Prenatal Diagnosis(2023)10.1002/pd.6345

N/A

0DataRank · unranked

28 citations

Anna Alkelai, Jessica L. Giordano, Madhulatha Pantrangi, Meng‐Chang Hsiao, Chia‐Ling Nhan‐Chang +6 more

The Contribution of Commonly Diagnosed Genetic Disorders to Small for Gestational Age Birth and Subsequent Morbidity and Mortality in Preterm Infants

medRxiv(2023)10.1101/2023.07.14.23292682

N/A

0DataRank · unranked

0 citations

Selin Everett, Alex Lyford, Rakesh Sahni, Faith Kim, Caitlin Baptiste +5 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Interstitial Cystitis: a phenotype and rare variant exome sequencing study

medRxiv(2025)10.1101/2025.02.16.25322147

N/A

0DataRank · unranked

0 citations

Ayan Malakar, Sarath Babu Krishna Murthy, Miguel Verbitsky, Atlas Kahn, Elicia Estrella +10 more