Claudia Cozma

1.0k total citations
38 papers, 529 citations indexed

About

Claudia Cozma is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Claudia Cozma has authored 38 papers receiving a total of 529 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Physiology, 18 papers in Cell Biology and 10 papers in Molecular Biology. Recurrent topics in Claudia Cozma's work include Lysosomal Storage Disorders Research (28 papers), Cellular transport and secretion (17 papers) and Carbohydrate Chemistry and Synthesis (9 papers). Claudia Cozma is often cited by papers focused on Lysosomal Storage Disorders Research (28 papers), Cellular transport and secretion (17 papers) and Carbohydrate Chemistry and Synthesis (9 papers). Claudia Cozma collaborates with scholars based in Germany, Israel and United States. Claudia Cozma's co-authors include Arndt Rolfs, Ari Zimran, Sabrina Eichler, Marina Hovakimyan, Shoshana Revel‐Vilk, Tama Dinur, Michal Becker‐Cohen, Jan Lukáš, Anne‐Katrin Giese and Peter Bauer and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Claudia Cozma

36 papers receiving 519 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Claudia Cozma Germany 14 401 214 208 124 105 38 529
Adriane Schilling United States 9 343 0.9× 179 0.8× 149 0.7× 137 1.1× 186 1.8× 12 516
Michal Becker‐Cohen Israel 13 205 0.5× 263 1.2× 154 0.7× 175 1.4× 60 0.6× 31 480
Jennifer A. Wiseman United States 8 383 1.0× 216 1.0× 212 1.0× 86 0.7× 71 0.7× 9 553
Gregory C. Zirzow United States 13 421 1.0× 265 1.2× 220 1.1× 183 1.5× 152 1.4× 13 628
Mukarram El-Banna United States 7 412 1.0× 217 1.0× 222 1.1× 87 0.7× 76 0.7× 8 571
Helen Christomanou Germany 9 608 1.5× 340 1.6× 266 1.3× 236 1.9× 162 1.5× 9 717
E M Prence United States 15 380 0.9× 274 1.3× 168 0.8× 91 0.7× 142 1.4× 27 571
Marielle Boonen Belgium 13 127 0.3× 282 1.3× 225 1.1× 68 0.5× 39 0.4× 21 504
J Kreysing Germany 10 415 1.0× 359 1.7× 100 0.5× 218 1.8× 114 1.1× 12 639
Jaime Anguiano United States 9 54 0.1× 247 1.2× 99 0.5× 191 1.5× 50 0.5× 11 466

Countries citing papers authored by Claudia Cozma

Since Specialization
Citations

This map shows the geographic impact of Claudia Cozma's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Claudia Cozma with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claudia Cozma more than expected).

Fields of papers citing papers by Claudia Cozma

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Claudia Cozma. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Claudia Cozma. The network helps show where Claudia Cozma may publish in the future.

Co-authorship network of co-authors of Claudia Cozma

This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Cozma. A scholar is included among the top collaborators of Claudia Cozma based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Claudia Cozma. Claudia Cozma is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Varga, Lilian, Dorottya Csuka, Ágnes Szilágyi, et al.. (2023). Application of a dried blood spot based proteomic and genetic assay for diagnosing hereditary angioedema. Clinical and Translational Allergy. 13(11). e12317–e12317. 7 indexed citations
2.
Polla, D.L., Sebastiano Di Bucchianico, Steffen Fischer, et al.. (2023). Neuronal progenitor cells-based metabolomics study reveals dysregulated lipid metabolism and identifies putative biomarkers for CLN6 disease. Scientific Reports. 13(1). 18550–18550. 4 indexed citations
3.
Becker‐Cohen, Michal, Shoshana Revel‐Vilk, Dafna Frydman, et al.. (2023). Rapid home therapy infusion of velaglucerase alfa in naïve patients with Gaucher disease. Internal Medicine Journal. 54(3). 398–403. 4 indexed citations
4.
Giugliani, Roberto, Catarina Pereira, Claudia Cozma, et al.. (2022). Fifteen years of enzyme replacement therapy for mucopolysaccharidosis type VI (Maroteaux–Lamy syndrome): a case report. Journal of Medical Case Reports. 16(1). 46–46. 3 indexed citations
5.
Weissensteiner, Thomas, Catarina Pereira, María Eugenia Rocha, et al.. (2022). Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single center. Orphanet Journal of Rare Diseases. 17(1). 179–179. 9 indexed citations
6.
Becker‐Cohen, Michal, Ari Zimran, Tama Dinur, et al.. (2022). A Comprehensive Assessment of Qualitative and Quantitative Prodromal Parkinsonian Features in Carriers of Gaucher Disease—Identifying Those at the Greatest Risk. International Journal of Molecular Sciences. 23(20). 12211–12211. 6 indexed citations
7.
Bucchianico, Sebastiano Di, et al.. (2021). Dried Blood Spot (DBS) Methodology Study for Biomarker Discovery in Lysosomal Storage Disease (LSD). Metabolites. 11(6). 382–382. 7 indexed citations
8.
Dinur, Tama, Ulrike Grittner, Shoshana Revel‐Vilk, et al.. (2021). Impact of Long-Term Enzyme Replacement Therapy on Glucosylsphingosine (Lyso-Gb1) Values in Patients with Type 1 Gaucher Disease: Statistical Models for Comparing Three Enzymatic Formulations. International Journal of Molecular Sciences. 22(14). 7699–7699. 19 indexed citations
9.
Westenberger, Ana, Claudia Cozma, Christian Beetz, et al.. (2020). Genetic characterization of the Albanian Gaucher disease patient population. JIMD Reports. 57(1). 52–57. 4 indexed citations
10.
Cheema, Huma Arshad, Aida M. Bertoli‐Avella, Volha Skrahina, et al.. (2020). Genomic testing in 1019 individuals from 349 Pakistani families results in high diagnostic yield and clinical utility. npj Genomic Medicine. 5(1). 44–44. 29 indexed citations
11.
Arkadir, David, Tama Dinur, Shoshana Revel‐Vilk, et al.. (2019). Prodromal substantia nigra sonography undermines suggested association between substrate accumulation and the risk for GBA‐related Parkinson's disease. European Journal of Neurology. 26(7). 1013–1018. 12 indexed citations
12.
Dinur, Tama, Ari Zimran, Michal Becker‐Cohen, et al.. (2019). Long-term follow-up of 103 untreated adult patients with type 1 Gaucher disease. Molecular Genetics and Metabolism. 126(2). S49–S49. 1 indexed citations
13.
Cozma, Claudia, Marina Hovakimyan, Nawal Makhseed, et al.. (2019). Genetic, clinical and biochemical characterization of a large cohort of patients with hyaline fibromatosis syndrome. Orphanet Journal of Rare Diseases. 14(1). 209–209. 7 indexed citations
14.
Hovakimyan, Marina, et al.. (2019). Plasma adiponectin is a potential biomarker for organ involvement in male Fabry disease patients. Blood Cells Molecules and Diseases. 80. 102379–102379. 2 indexed citations
15.
Lukáš, Jan, Claudia Cozma, Fan Yang, et al.. (2017). Glucosylsphingosine Causes Hematological and Visceral Changes in Mice—Evidence for a Pathophysiological Role in Gaucher Disease. International Journal of Molecular Sciences. 18(10). 2192–2192. 24 indexed citations
16.
Elstein, Deborah, Björn Mellgård, Lan Lan, et al.. (2017). Reductions in glucosylsphingosine (lyso-Gb1) in treatment-naïve and previously treated patients receiving velaglucerase alfa for type 1 Gaucher disease: Data from phase 3 clinical trials. Molecular Genetics and Metabolism. 122(1-2). 113–120. 37 indexed citations
17.
Cozma, Claudia, et al.. (2016). An HLA-B27 Homodimer Specific Antibody Recognizes a Discontinuous Mixed-Disulfide Epitope as Identified by Affinity-Mass Spectrometry. Journal of the American Society for Mass Spectrometry. 27(6). 1105–1112. 10 indexed citations
18.
Cozma, Claudia, et al.. (2015). Diagnosis of Morquio Syndrome in Dried Blood Spots Based on a New MRM-MS Assay. PLoS ONE. 10(7). e0131228–e0131228. 13 indexed citations
19.
Perdivara, Irina, Leesa J. Deterding, Claudia Cozma, Kenneth B. Tomer, & Michael Przybylski. (2009). Glycosylation profiles of epitope-specific anti-β-amyloid antibodies revealed by liquid chromatography–mass spectrometry. Glycobiology. 19(9). 958–970. 13 indexed citations
20.
Cozma, Claudia, et al.. (2009). Structural characterization of ß-amyloid oligomer-aggregates by ion mobility mass spectrometry and electron spin resonance spectroscopy. Analytical and Bioanalytical Chemistry. 395(8). 2509–2519. 29 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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