Silvia Radenkovic

Also affiliated with WinnMed, University Medical Center Utrecht, Mayo Clinic in Florida

Biochemistry, Genetics and Molecular BiologyMedicineChemistry

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 14 papers. Top paper: “Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation”.

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

0.628DataRank · unranked

65 citations

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

Liposome-encapsulated mannose-1-phosphate therapy improves global N-glycosylation in different congenital disorders of glycosylation

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108487

N/A

0.425DataRank · unranked

16 citations

Silvia Radenkovic, Anu Jain, Irena Muffels, Moulay Hicham Alaoui Ismaili, Tamás Kozicz +3 more

A complement C4–derived glycopeptide is a biomarker for PMM2-CDG

JCI Insight(2024)10.1172/jci.insight.172509

N/A

0.388DataRank · unranked

10 citations

Rohit Budhraja, Mayank Saraswat, Jin Yong Kim, Neha Joshi, Gunveen S. Sachdeva +18 more

O-GlcNAcylation modulates expression and abundance of N-glycosylation machinery in an inherited glycosylation disorder

Cell Reports(2024)10.1016/j.celrep.2024.114976

N/A

0.387DataRank · unranked

10 citations

Sneha S. Mokashi, Silvia Radenkovic, Kali Wiggins, Lynn Dukes‐Rimsky, Peggi M. Angel +6 more

Dysregulated proteome and N‐glycoproteome in ALG1‐deficient fibroblasts

PROTEOMICS(2024)10.1002/pmic.202400012

N/A

0.385DataRank · unranked

12 citations

Neha Joshi, Silvia Radenkovic, Tamás Kozicz, Éva Morava, Akhilesh Pandey +1 more

Coagulation abnormalities and vascular complications are common in PGM1-CDG

Molecular Genetics and Metabolism(2024)10.1016/j.ymgme.2024.108530

N/A

0.269DataRank · unranked

5 citations

Sofie Bleukx, Nicole Engelhardt, Erik A. Eklund, Saadet Mercimek‐Andrews, Andrew C. Edmondson +2 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

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

Novel mouse model reveals neurodevelopmental origin of PMM2-CDG brain pathology

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.01.657261

N/A

0DataRank · unranked

2 citations

Rohit Budhraja, Zijie Xia, Ashley Melendez-Perez, Cadmus Cai, Silvia Radenkovic +15 more

Expanding the clinical and metabolic phenotype of DPM2 deficient congenital disorders of glycosylation

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.10.007

N/A

0DataRank · unranked

25 citations

Taylor Fitzpatrick‐Schmidt, Seul Kee Byeon, Anil K. Madugundu, Mayank Saraswat, Angie Lichty +13 more

Impaired glucose-1,6-biphosphate production due to bi-allelic PGM2L1 mutations is associated with a neurodevelopmental disorder

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.017

N/A

0DataRank · unranked

26 citations

Ulrich A. Schatz, Pernille Mathiesen Tørring, Mary-Alice Abbott, Matthias Baumann, Charlotte Brasch‐Andersen +11 more

Novel insights into the phenotype and long-term D-gal treatment in PGM1-CDG: a case series

Therapeutic Advances in Rare Disease(2023)10.1177/26330040221150269

N/A

0DataRank · unranked

11 citations

Christin Johnsen, Andreas Schulze, Gurnoor Lail, Laura Guilder, Kaitlin Schwartz +5 more

Nucleotide metabolism in cancer cells fuels a UDP-driven macrophage cross-talk, promoting immunosuppression and immunotherapy resistance

Nature Cancer(2024)10.1038/s43018-024-00771-8

N/A

0DataRank · unranked

62 citations

Marta Manco, Mathieu Pecqueux, Ricardo Amorim, Rosa Trotta, Heleen H. Van Acker +33 more

Neural and metabolic dysregulation in PMM2-deficient human in vitro neural models

Cell Reports(2024)10.1016/j.celrep.2024.113883

N/A

0DataRank · unranked

26 citations

Rohit Budhraja, Teun M. Klein Gunnewiek, Alexia King, Tarun N. Bhatia, Anna N. Ligezka +9 more