Mislen Bauer

1.4k total citations
19 papers, 561 citations indexed

About

Mislen Bauer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mislen Bauer has authored 19 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in Mislen Bauer's work include Neurofibromatosis and Schwannoma Cases (4 papers), Neuroblastoma Research and Treatments (3 papers) and Lysosomal Storage Disorders Research (3 papers). Mislen Bauer is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (4 papers), Neuroblastoma Research and Treatments (3 papers) and Lysosomal Storage Disorders Research (3 papers). Mislen Bauer collaborates with scholars based in United States, Germany and Croatia. Mislen Bauer's co-authors include Nancy D. Leslie, Claire Morgan, John Clancy, Tara O’Meara, Hanna Mandel, Daniel Gruskin, Deya Corzo, Michael Beck, Susan Richards and Rossella Parini and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, American Journal of Neuroradiology and Journal of Medical Genetics.

In The Last Decade

Mislen Bauer

19 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mislen Bauer United States 10 269 208 143 109 107 19 561
Ting‐Rong Hsu Taiwan 16 463 1.7× 178 0.9× 201 1.4× 89 0.8× 217 2.0× 53 780
Paola De Filippi Italy 13 254 0.9× 193 0.9× 112 0.8× 73 0.7× 43 0.4× 25 486
Alexander Broomfield United Kingdom 14 358 1.3× 137 0.7× 205 1.4× 24 0.2× 124 1.2× 54 613
Esmée Oussoren Netherlands 15 383 1.4× 166 0.8× 245 1.7× 26 0.2× 169 1.6× 32 768
Françoise Bouhour France 9 173 0.6× 115 0.6× 239 1.7× 49 0.4× 75 0.7× 18 463
Norberto Guelbert Argentina 16 514 1.9× 232 1.1× 148 1.0× 22 0.2× 216 2.0× 39 651
F. A. Beemer Netherlands 12 293 1.1× 248 1.2× 232 1.6× 27 0.2× 101 0.9× 21 714
Guilhem Solé France 15 119 0.4× 107 0.5× 250 1.7× 176 1.6× 64 0.6× 62 731
K D MacDermot United Kingdom 15 627 2.3× 230 1.1× 287 2.0× 84 0.8× 290 2.7× 27 1.1k
Susanne Gerit Kircher Austria 12 214 0.8× 108 0.5× 81 0.6× 19 0.2× 115 1.1× 48 420

Countries citing papers authored by Mislen Bauer

Since Specialization
Citations

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

Fields of papers citing papers by Mislen Bauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mislen Bauer. 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 Mislen Bauer. The network helps show where Mislen Bauer may publish in the future.

Co-authorship network of co-authors of Mislen Bauer

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

All Works

19 of 19 papers shown
1.
Bauer, Mislen, et al.. (2021). Gastric Adenocarcinoma and Proximal Polyposis of the Stomach in a Hispanic Pediatric Patient With APC Gene Variant c.‐191T>G. JPGN Reports. 2(4). e123–e123. 3 indexed citations
2.
Hung, Christina, et al.. (2019). A novel FAM20C mutation causes a rare form of neonatal lethal Raine syndrome. American Journal of Medical Genetics Part A. 179(9). 1866–1871. 16 indexed citations
3.
4.
Cernichiaro-Espinosa, Linda A., et al.. (2019). Revascularization After Intravitreal Bevacizumab and Laser Therapy of Bilateral Retinal Vascular Occlusions in Incontinentia Pigmenti (Bloch-Sulzberger Syndrome). Ophthalmic surgery, lasers & imaging retina. 50(2). e33–e37. 4 indexed citations
5.
Harmatz, Paul, Chester B. Whitley, Raymond Wang, et al.. (2018). A novel Blind Start study design to investigate vestronidase alfa for mucopolysaccharidosis VII, an ultra-rare genetic disease. Molecular Genetics and Metabolism. 123(4). 488–494. 51 indexed citations
6.
Chang, Ta Chen, et al.. (2017). Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair. Journal of American Association for Pediatric Ophthalmology and Strabismus. 21(6). 514–516. 9 indexed citations
7.
Harmatz, Paul, Chester B. Whitley, Raymond Wang, et al.. (2017). A novel, randomized, placebo-controlled, blind-start, single-crossover phase 3 study to assess the efficacy and safety of UX003 (rhGUS) enzyme replacement therapy in patients with MPS VII. Molecular Genetics and Metabolism. 120(1-2). S63–S63. 6 indexed citations
8.
Bauer, Mislen, et al.. (2016). New JAG1 mutation causing Alagille Syndrome presenting with severe hypercholesterolemia: Case report with emphasis on genetics and lipid abnormalities. The Journal of Clinical Endocrinology & Metabolism. 102(2). jc.2016–3171. 13 indexed citations
9.
Tanaka, Akemi, Renkui Bai, Megan T. Cho, et al.. (2015). De novo mutations in PURA are associated with hypotonia and developmental delay. Molecular Case Studies. 1(1). a000356–a000356. 49 indexed citations
10.
Bauer, Mislen, et al.. (2014). Neonatal diagnosis of a patient with hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) syndrome associated with cerebral infarction. Journal of Pediatric Endocrinology and Metabolism. 27(9-10). 961–5. 3 indexed citations
11.
Bauer, Mislen, Wilmar Saldarriaga, S. Anthony Wolfe, et al.. (2013). Two extraordinarily severe cases of Treacher Collins syndrome. American Journal of Medical Genetics Part A. 161(3). 445–452. 3 indexed citations
12.
Sisk, Robert A., Audina M. Berrocal, Amy C Schefler, Sander R. Dubovy, & Mislen Bauer. (2010). EPIRETINAL MEMBRANES INDICATE A SEVERE PHENOTYPE OF NEUROFIBROMATOSIS TYPE 2. Retina. 30(4). S51–S58. 19 indexed citations
13.
Shaw, Adam, Mislen Bauer, Trevor Cole, et al.. (2010). Phenotype and natural history in Marshall–Smith syndrome. American Journal of Medical Genetics Part A. 152A(11). 2714–2726. 29 indexed citations
14.
Kishnani, Priya S., Deya Corzo, Nancy D. Leslie, et al.. (2009). Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease. Pediatric Research. 66(3). 329–335. 232 indexed citations
15.
Rasmussen, Sonja A., Susanne Thomson, Steven D. Colman, et al.. (2000). Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1. Genes Chromosomes and Cancer. 28(4). 425–431. 86 indexed citations
16.
Rasmussen, Sonja A., Susanne Thomson, Steven D. Colman, et al.. (2000). Chromosome 17 loss‐of‐heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1. Genes Chromosomes and Cancer. 28(4). 425–431. 3 indexed citations
17.
Altman, Nolan, et al.. (1991). Glutaric aciduria type 1: MR findings in two cases.. American Journal of Neuroradiology. 12(5). 966–8. 19 indexed citations
18.
Born, Peter, et al.. (1989). [Gangliocytic paraganglioma of the duodenum].. PubMed. 27(6). 339–40. 2 indexed citations
19.
Kittur, Smita, et al.. (1987). Linkage analysis of neurofibromatosis.. Journal of Medical Genetics. 24(9). 526–527. 4 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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