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

Ruqaiah Altassan

Alfaisal University

ORCID: 0000-0003-0146-8169

Also affiliated with King Faisal Specialist Hospital & Research Centre

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 5 papers. Top paper: “International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1‐CDG): Diagnosis, follow‐up, and management”.

International consensus guidelines for phosphoglucomutase 1 deficiency (PGM1‐CDG): Diagnosis, follow‐up, and management

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12286
N/A
0DataRank · unranked
66 citations

Silvia Radenkovic, Andrew C. Edmondson, Rita Barone, Sandra Brasil, Anna Čechová +31 more

Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12241
N/A
0DataRank · unranked
64 citations

Ruqaiah Altassan, Delphine Borgel, Arnaud Bruneel, Joana Correia, M Girard +16 more

Neurological manifestations in PMM2-congenital disorders of glycosylation (PMM2-CDG): Insights into clinico-radiological characteristics, recommendations for follow-up, and future directions

Genetics in Medicine(2023)10.1016/j.gim.2023.101027
N/A
0DataRank · unranked
17 citations

Judit Perez Ortiz, Anna N. Ligezka, Ruqaiah Altassan, Christin Johnsen, Matthew Schultz +3 more

ALG13-Congenital Disorder of Glycosylation (ALG13-CDG): Updated clinical and molecular review and clinical management guidelines

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108472
N/A
0DataRank · unranked
11 citations

Erik A. Eklund, Silvia Radenkovic, Mustafa Sadek, Ibrahim Shammas, Sanne Verberkmoes +8 more

Phenotypic and genotypic description of GMPPA-congenital disorder of glycosylation: A review of 26 cases

Molecular Genetics and Metabolism(2025)10.1016/j.ymgme.2025.109196
N/A
0DataRank · unranked
0 citations

Sarah K Aldhahri, Georgia MacDonald, Rameen Shah, Éva Morava, Ruqaiah Altassan