Debra S. Regier

Also affiliated with Carolinas Medical Center, Levine Children's Hospital, Advocate Children's Hospital, Advocate Children's Hospital

Biochemistry, Genetics and Molecular BiologyMedicine

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: “GM1 gangliosidosis type II: Results of a 10-year prospective study”.

GM1 gangliosidosis type II: Results of a 10-year prospective study

Genetics in Medicine(2024)10.1016/j.gim.2024.101144

N/A

0.557DataRank · unranked

19 citations

Cristan Farmer, Jean M. Johnston, Sangwoo T. Han, David Adams, Adam L. Hartman +24 more

Assessment of Thyroid Function in Patients With Alkaptonuria

JAMA Network Open(2020)10.1001/jamanetworkopen.2020.1357

N/A

0.442DataRank · unranked

18 citations

Wendy J. Introne, Sungyoung Auh, Steven J. Soldin, Brian Stolze, Debra S. Regier +6 more

The Rare Disease Research Scholars Program: A training curriculum for clinical researchers with mixed methods evaluation study

Translational Science of Rare Diseases(2021)10.3233/trd-210051

N/A

0.229DataRank · unranked

3 citations

Jennifer Weaver, Nancy Cheng, Mark L. Batshaw, Mary Ottolini, Michael E. Shy +2 more

Cation leak through the ATP1A3 pump causes spasticity and intellectual disability

Brain(2023)10.1093/brain/awad124

N/A

0DataRank · unranked

13 citations

Cristina Moreno Vadillo, Seth Berger, Timothy Lotze, Marwan Shinawi, Javaher Poupak +24 more

The clinical geneticist workforce: Community forums to address challenges and opportunities

Genetics in Medicine(2024)10.1016/j.gim.2024.101121

N/A

0DataRank · unranked

5 citations

Shoumita Dasgupta, Debra S. Regier, Benjamin D. Solomon, Wendy K. Chung

Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicing

JIMD Reports(2024)10.1002/jmd2.12459

N/A

0DataRank · unranked

4 citations

Sarah Silverstein, Molly Behan, Cynthia J. Tifft, May Christine V. Malicdan, David R. Adams +4 more

New Phenotypic Features in FGFR1‐Related Osteoglophonic Dysplasia

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64092

N/A

0DataRank · unranked

2 citations

Holly E. Babcock, Corey S. Gill, Jamie L. Fraser, Debra S. Regier, Rajdeep Kaur +3 more