Müge Güçsavaş‐Çalıkoğlu

1.5k total citations
10 papers, 1.1k citations indexed

About

Müge Güçsavaş‐Çalıkoğlu is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Müge Güçsavaş‐Çalıkoğlu has authored 10 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Clinical Biochemistry, 4 papers in Physiology and 3 papers in Molecular Biology. Recurrent topics in Müge Güçsavaş‐Çalıkoğlu's work include Metabolism and Genetic Disorders (4 papers), Lysosomal Storage Disorders Research (3 papers) and Genomics and Rare Diseases (2 papers). Müge Güçsavaş‐Çalıkoğlu is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Lysosomal Storage Disorders Research (3 papers) and Genomics and Rare Diseases (2 papers). Müge Güçsavaş‐Çalıkoğlu collaborates with scholars based in United States, United Kingdom and South Sudan. Müge Güçsavaş‐Çalıkoğlu's co-authors include Joseph Muenzer, Alan Kimura, Shawn E. McCandless, Thomas Schuetz, Paul Harmatz, Christine M. Eng, Michael Beck, Marwan Shinawi, Uma Ramaswami and Rick Martin and has published in prestigious journals such as Human Molecular Genetics, The Journal of Pediatrics and Epidemiology.

In The Last Decade

Müge Güçsavaş‐Çalıkoğlu

9 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Müge Güçsavaş‐Çalıkoğlu United States 7 797 415 277 232 143 10 1.1k
Agnieszka Jurecka Poland 21 649 0.8× 446 1.1× 293 1.1× 405 1.7× 180 1.3× 63 1.2k
María Josep Coll Spain 19 703 0.9× 228 0.5× 180 0.6× 370 1.6× 158 1.1× 37 1.1k
Ai-Chu Huang Taiwan 11 608 0.8× 195 0.5× 337 1.2× 290 1.3× 280 2.0× 15 940
Vũ Chí Dũng Vietnam 18 729 0.9× 319 0.8× 222 0.8× 298 1.3× 110 0.8× 38 1.1k
Ana Cristina Puga United States 17 1.1k 1.3× 422 1.0× 200 0.7× 379 1.6× 58 0.4× 45 1.3k
Deyanira Corzo United States 18 1.0k 1.3× 260 0.6× 739 2.7× 393 1.7× 105 0.7× 25 1.5k
I Maire France 17 785 1.0× 279 0.7× 287 1.0× 341 1.5× 82 0.6× 85 1.2k
Serena Gasperini Italy 16 443 0.6× 146 0.4× 282 1.0× 223 1.0× 185 1.3× 64 880
Celeste Decker United States 17 550 0.7× 258 0.6× 236 0.9× 82 0.4× 69 0.5× 21 685
Esmée Oussoren Netherlands 15 383 0.5× 169 0.4× 166 0.6× 245 1.1× 89 0.6× 32 768

Countries citing papers authored by Müge Güçsavaş‐Çalıkoğlu

Since Specialization
Citations

This map shows the geographic impact of Müge Güçsavaş‐Çalıkoğlu'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 Müge Güçsavaş‐Çalıkoğlu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Müge Güçsavaş‐Çalıkoğlu more than expected).

Fields of papers citing papers by Müge Güçsavaş‐Çalıkoğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Müge Güçsavaş‐Çalıkoğlu. 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 Müge Güçsavaş‐Çalıkoğlu. The network helps show where Müge Güçsavaş‐Çalıkoğlu may publish in the future.

Co-authorship network of co-authors of Müge Güçsavaş‐Çalıkoğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Müge Güçsavaş‐Çalıkoğlu. A scholar is included among the top collaborators of Müge Güçsavaş‐Çalıkoğlu 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 Müge Güçsavaş‐Çalıkoğlu. Müge Güçsavaş‐Çalıkoğlu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Martin, Chantel L., Suzan L. Carmichael, Müge Güçsavaş‐Çalıkoğlu, et al.. (2023). Are individual‐level risk factors for gastroschisis modified by neighborhood‐level socioeconomic factors?. Birth Defects Research. 115(15). 1438–1449. 1 indexed citations
2.
Desrosiers, Tania A., Chantel L. Martin, Suzan L. Carmichael, et al.. (2023). Neighborhood-level Socioeconomic Position During Early Pregnancy and Risk of Gastroschisis. Epidemiology. 34(4). 576–588. 6 indexed citations
3.
Milko, Laura V., Julianne O’Daniel, Stephanie B. Crowley, et al.. (2019). An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening. The Journal of Pediatrics. 209. 68–76. 44 indexed citations
4.
Marchuk, Daniel S., Laurie D. Smith, Alexandra Arreola, et al.. (2017). Co‐occurring Down syndrome and SUCLA2‐related mitochondrial depletion syndrome. American Journal of Medical Genetics Part A. 173(10). 2720–2724.
5.
Chinsky, Jeffrey M., Rani H. Singh, Can Fıçıcıoğlu, et al.. (2017). Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations. Genetics in Medicine. 19(12). 1380–1395. 150 indexed citations
6.
Houten, Sander M., Simone Denis, Heleen te Brinke, et al.. (2014). Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia. Human Molecular Genetics. 23(18). 5009–5016. 54 indexed citations
7.
Muenzer, Joseph, Michael Beck, Christine M. Eng, et al.. (2010). Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome. Genetics in Medicine. 13(2). 95–101. 173 indexed citations
8.
Kranz, Christian, Alice Basinger, Müge Güçsavaş‐Çalıkoğlu, et al.. (2007). Expanding spectrum of congenital disorder of glycosylation Ig (CDG‐Ig): Sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality. American Journal of Medical Genetics Part A. 143A(12). 1371–1378. 65 indexed citations
9.
Muenzer, Joseph, J. E. Wraith, Michael Beck, et al.. (2006). A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome). Genetics in Medicine. 8(8). 465–473. 457 indexed citations
10.
Muenzer, Joseph, Müge Güçsavaş‐Çalıkoğlu, Shawn E. McCandless, Thomas Schuetz, & Alan Kimura. (2006). A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome). Molecular Genetics and Metabolism. 90(3). 329–337. 180 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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