Olaf A. Bodamer

9.8k total citations
156 papers, 4.2k citations indexed

About

Olaf A. Bodamer is a scholar working on Physiology, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Olaf A. Bodamer has authored 156 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Physiology, 55 papers in Molecular Biology and 47 papers in Clinical Biochemistry. Recurrent topics in Olaf A. Bodamer's work include Lysosomal Storage Disorders Research (53 papers), Metabolism and Genetic Disorders (47 papers) and Glycogen Storage Diseases and Myoclonus (23 papers). Olaf A. Bodamer is often cited by papers focused on Lysosomal Storage Disorders Research (53 papers), Metabolism and Genetic Disorders (47 papers) and Glycogen Storage Diseases and Myoclonus (23 papers). Olaf A. Bodamer collaborates with scholars based in United States, Austria and Germany. Olaf A. Bodamer's co-authors include Adolf Mühl, Sylvia Stöckler‐Ipsiroglu, Maurizio Scarpa, Georg F. Hoffmann, J Zeman, Christina Hung, Michael Beck, Raymond Wang, Gunilla Malm and Michael S. Watson and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Olaf A. Bodamer

153 papers receiving 4.1k citations

Peers

Olaf A. Bodamer

PHYSI

RHEUM

GENET

Vassili Valayannopoulos France

Rossella Parini Italy

Hanna Mandel Israel

Melissa Wasserstein United States

Sarah P. Young United States

Kurt Ullrich Germany

Emil Kakkis United States

René Santer Germany

Barbara Plecko Austria

Marco Spada Italy

Vassili Valayannopoulos France

Olaf A. Bodamer

2.0k ×1.1

PHYSI

1.5k ×1.1

1.4k ×1.4

900 ×1.0

RHEUM

562 ×0.8

GENET

Citations per year, relative to Olaf A. Bodamer Olaf A. Bodamer (= 1×) peers Vassili Valayannopoulos

Countries citing papers authored by Olaf A. Bodamer

Since Specialization

Citations

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

Fields of papers citing papers by Olaf A. Bodamer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Olaf A. Bodamer. 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 Olaf A. Bodamer. The network helps show where Olaf A. Bodamer may publish in the future.

Co-authorship network of co-authors of Olaf A. Bodamer

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

All Works

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20 of 20 papers shown

Al‐Hertani, Walla, et al.. (2025). Levacetylleucine (N-acetyl-l-leucine) for Niemann-Pick disease type C. Trends in Pharmacological Sciences. 46(4). 386–387.

Potter, Sarah J., Li Zhang, Yuehong Wu, et al.. (2024). KMT2D regulates activation, localization, and integrin expression by T-cells. Frontiers in Immunology. 15. 1341745–1341745. 2 indexed citations

Bodamer, Olaf A., et al.. (2023). A case of Aicardi syndrome associated with duplication event of Xp22 including SHOX. Ophthalmic Genetics. 44(6). 591–594.

Rashid, Asma, et al.. (2023). Multidisciplinary clinical and translational approach for optimizing management for complex and rare conditions using Kabuki syndrome as example. SHILAP Revista de lepidopterología. 1. 100008–100008. 3 indexed citations

Fulton, Anne B., et al.. (2023). Insights into the genotype–phenotype relationship of ocular manifestations in Kabuki syndrome. American Journal of Medical Genetics Part A. 191(5). 1325–1338. 5 indexed citations

Goodlett, Benjamin D., Fan Zhang, Adam P. Vogel, et al.. (2023). Characterization of central manifestations in patients with Niemann-Pick disease type C. Genetics in Medicine. 26(3). 101053–101053. 7 indexed citations

Hartman, Deborah, et al.. (2022). From Genotype to Phenotype—A Review of Kabuki Syndrome. Genes. 13(10). 1761–1761. 26 indexed citations

Kenna, Margaret A., Thomas E. Mullen, Olaf A. Bodamer, et al.. (2021). Neuroimaging in Kabuki syndrome and another KMT2D‐related disorder. American Journal of Medical Genetics Part A. 185(12). 3770–3783. 4 indexed citations

Bodamer, Olaf A., et al.. (2021). The otolaryngologic manifestations of Sotos syndrome 1: A systematic review. International Journal of Pediatric Otorhinolaryngology. 143. 110649–110649. 2 indexed citations

10.

Yang, Edward, Frank H. Guenther, Benjamin D. Goodlett, et al.. (2021). Targeting neurological abnormalities in lysosomal storage diseases. Trends in Pharmacological Sciences. 43(6). 495–509. 9 indexed citations

11.

Rashid, Asma, et al.. (2020). Congenital microgastria‐limb reduction association: A case report and review of the literature. American Journal of Medical Genetics Part A. 182(12). 2976–2981. 3 indexed citations

12.

McGowan, Caroline, et al.. (2020). Autosomal‐dominant WFS1‐related disorder—Report of a novel WFS1 variant and review of the phenotypic spectrum of autosomal recessive and dominant forms. American Journal of Medical Genetics Part A. 185(2). 528–533. 7 indexed citations

13.

Wang, Yirou, Niu Li, Zhe Su, et al.. (2019). The phenotypic spectrum of Kabuki syndrome in patients of Chinese descent: A case series. American Journal of Medical Genetics Part A. 182(4). 640–651. 10 indexed citations

14.

Hung, Christina, et al.. (2019). Prenatal and perinatal history in Kabuki Syndrome. American Journal of Medical Genetics Part A. 182(1). 85–92. 7 indexed citations

15.

Yang, Edward, et al.. (2019). Holoprosencephaly in Kabuki syndrome. American Journal of Medical Genetics Part A. 182(3). 441–445. 6 indexed citations

16.

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

17.

Hung, Christina, James D. Baker, Johann Bauer, et al.. (2017). A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure. PLoS ONE. 12(12). e0189324–e0189324. 9 indexed citations

18.

Johnson, Britt, Otto P. van Diggelen, Angéla Dajnoki, & Olaf A. Bodamer. (2013). Diagnosing Lysosomal Storage Disorders: Mucopolysaccharidosis Type II. Current Protocols in Human Genetics. 79(1). 17.14.1–17.14.9. 10 indexed citations

19.

Wurm, Martin, Martin Hermann, Stefano Buttiglieri, et al.. (2008). Introduction of a Novel Prototype Bioartificial Liver Support System Utilizing Small Human Hepatocytes in Rotary Culture. Tissue Engineering Part A. 15(5). 1063–1073. 9 indexed citations

20.

Bodamer, Olaf A., et al.. (2005). Microarray-based Detection of Mannose-binding Lectin 2 ( MBL2 ) Polymorphisms in a Routine Clinical Setting. Genetic Testing. 9(1). 6–13. 5 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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