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

Stephen G. Kaler

Nationwide Children's Hospital

ORCID: 0000-0002-7522-926X

Also affiliated with Columbia University

NursingBiochemistry, Genetics and Molecular BiologyMedicineEnvironmental Science

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 9 papers. Top paper: “Estimated birth prevalence of Menkes disease and ATP7A-related disorders based on the Genome Aggregation Database (gnomAD)”.

Estimated birth prevalence of Menkes disease and ATP7A-related disorders based on the Genome Aggregation Database (gnomAD)

Molecular Genetics and Metabolism Reports(2020)10.1016/j.ymgmr.2020.100602
N/A
0DataRank · unranked
47 citations

Carlos R. Ferreira, Lung S. Yam, Stephen G. Kaler

Targeted next generation sequencing for newborn screening of Menkes disease

Molecular Genetics and Metabolism Reports(2020)10.1016/j.ymgmr.2020.100625
N/A
0DataRank · unranked
20 citations

Stephen G. Kaler, Evan Mauceli, Tanya Sokolsky, Ling Yi, Arindam Bhattacharjee +1 more

Neck masses due to internal jugular vein phlebectasia: Frequency in Menkes disease and literature review of 85 pediatric subjects

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61572
N/A
0DataRank · unranked
7 citations

Julienne E. Price, Jamie Marko, Stephen G. Kaler, Kristen Stevens

Connecting copper and cancer: from transition metal signalling to metalloplasia

Nature reviews. Cancer(2021)10.1038/s41568-021-00417-2
N/A
0DataRank · unranked
1289 citations

Ashley I. Bush, Angela Casini, Paul A. Cobine, Justin R. Cross, Gina M. DeNicola +19 more

Detection of precisely edited CRISPR/Cas9 alleles through co-introduced restriction-fragment length polymorphisms

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.20.440537
N/A
0DataRank · unranked
0 citations

Sydney Hertafeld, Yvonne Rosario, James Iben, Eric H. Chang, Ling Yi +5 more

Newly identified disorder of copper metabolism caused by variants in CTR1, a high-affinity copper transporter

Human Molecular Genetics(2022)10.1093/hmg/ddac156
N/A
0DataRank · unranked
42 citations

Galit Tal, Andrew T DiStasio, Yanyan Peng, Christiana Charalambous, Paola Nicolaides +10 more

Transduction characteristics of alternative adeno-associated virus serotypes in the cat brain by intracisternal delivery

Molecular Therapy — Methods & Clinical Development(2022)10.1016/j.omtm.2022.07.007
N/A
0DataRank · unranked
6 citations

Caitlyn Molony, Jessica Bagel, Patricia A. O’Donnell, Stephen G. Kaler, John H. Wolfe +1 more

Expanding the Clinical Phenotype of FGFR1 Internal Tandem Duplication

Molecular Case Studies(2022)10.1101/mcs.a006174
N/A
0DataRank · unranked
10 citations

Kathleen M. Schieffer, Sean McGrath, Anthony R. Miller, Maria Elena Hernandez Gonzalez, Samantha Choi +13 more

Choroid plexus-targeted viral gene therapy for alpha-mannosidosis, a prototypical neurometabolic lysosomal storage disease

Human Molecular Genetics(2025)10.1093/hmg/ddae201
N/A
0DataRank · unranked
1 citations

John H. Wolfe, Stephen G. Kaler, Eunyoung Choi