Angela L. Duker

Also affiliated with 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 8 papers. Top paper: “Defining the clinical phenotype of Saul–Wilson syndrome”.

Defining the clinical phenotype of Saul–Wilson syndrome

Genetics in Medicine(2020)10.1038/s41436-019-0737-1

N/A

0DataRank · unranked

21 citations

Wadih M. Zein, Laryssa A. Huryn, Andrea Merker, Seth Berger, William G. Wilson +26 more

Growth in individuals with Saul–Wilson syndrome

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.61754

N/A

0DataRank · unranked

7 citations

Timothy Niiler, Angela L. Duker, Andrew P. Jackson, Michael B. Bober, Carlos R. Ferreira

Collagen X Marker Levels are Decreased in Individuals with Achondroplasia

Calcified Tissue International(2022)10.1007/s00223-022-00966-0

N/A

0DataRank · unranked

10 citations

Robert C. Olney, Angela L. Duker, Ryan F. Coghlan, William G. Mackenzie, Colleen Ditro +8 more

Collagen X Marker Levels are Decreased in Individuals with Achondroplasia

Zenodo (CERN European Organization for Nuclear Research)(2022)10.5281/zenodo.6607639

N/A

0DataRank · unranked

0 citations

Robert C. Olney, Angela L. Duker, Ryan F. Coghlan, William G. Mackenzie, Colleen Ditro +8 more

Identification of potential non-invasive biomarkers in diastrophic dysplasia

Bone(2023)10.1016/j.bone.2023.116838

N/A

0DataRank · unranked

4 citations

Ricki Carroll, Chiara Gramegna Tota, Andrea J. Schelhaas, Alessandra Leone, Angela L. Duker +14 more

RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.009

N/A

0DataRank · unranked

4 citations

Yang Li, Nandina Paria, Ryan J. Bohlender, Chad Huff, Jill A. Rosenfeld +17 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

C-type natriuretic peptide and collagen X marker are aberrant in skeletal dysplasias

Journal of Bone and Mineral Research(2025)10.1093/jbmr/zjaf085

N/A

0DataRank · unranked

3 citations

Robert C. Olney, Angela L. Duker, Ryan F. Coghlan, Andrea Schelhaas, William G. Mackenzie +9 more