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

Catherine Rehder

Duke University

ORCID: 0000-0003-4924-9010

Also affiliated with Duke Medical Center, Duke University Health System

MedicineBiochemistry, Genetics and Molecular Biology

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 7 papers. Top paper: “Two years of newborn screening for Duchenne muscular dystrophy as a part of the statewide Early Check research program in North Carolina”.

Two years of newborn screening for Duchenne muscular dystrophy as a part of the statewide Early Check research program in North Carolina

Genetics in Medicine(2023)10.1016/j.gim.2023.101009
N/A
0.464DataRank · unranked
21 citations

Beth Lincoln Boyea, Brooke Migliore, Sarah Nelson Potter, Veronica Robles, Oksana Kutsa +7 more

Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1665
N/A
0DataRank · unranked
18 citations

Hayk Barseghyan, Surajit Bhattacharya, Yulong Fu, Nicole L. Hoppman, Cherisse A. Marcou +8 more

Evaluation of X-Linked Adrenoleukodystrophy Newborn Screening in North Carolina

JAMA Network Open(2020)10.1001/jamanetworkopen.2019.20356
N/A
0DataRank · unranked
66 citations

Kristin Clinard, Sarah P. Young, Catherine Rehder, Zheng Fan, Ali S. Çalıkoğlu +10 more

Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IX

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.14.654043
N/A
0DataRank · unranked
0 citations

Xue Zou, Jian Dai, R. A. Francis, Alexias Safi, Karynne Patterson +13 more

Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary Dyskinesia

UNC Libraries(2025)10.17615/eftt-rm75
N/A
0DataRank · unranked
0 citations

Maimoona A. Zariwala, Kenneth N. Olivier, Amanda Smith, Hong Dang, Weining Yin +20 more

Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IX

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103474
N/A
0DataRank · unranked
0 citations

Xue Zou, Jian Dai, R. A. Francis, Alexias Safi, Karynne Patterson +14 more

Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary Dyskinesia

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63880
N/A
0DataRank · unranked
1 citations

Weining Yin, Amanda Smith, Patrick R. Sears, Margaret W. Leigh, Thomas W. Ferkol +20 more