Peter Bauer

21.5k total citations · 5 hit papers
250 papers, 11.6k citations indexed

About

Peter Bauer is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Peter Bauer has authored 250 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Molecular Biology, 51 papers in Genetics and 38 papers in Cellular and Molecular Neuroscience. Recurrent topics in Peter Bauer's work include Genomics and Rare Diseases (31 papers), Lysosomal Storage Disorders Research (28 papers) and Parkinson's Disease Mechanisms and Treatments (21 papers). Peter Bauer is often cited by papers focused on Genomics and Rare Diseases (31 papers), Lysosomal Storage Disorders Research (28 papers) and Parkinson's Disease Mechanisms and Treatments (21 papers). Peter Bauer collaborates with scholars based in Germany, Austria and United States. Peter Bauer's co-authors include Philipp Metnitz, Rui P. Moreno, Wilfred Druml, Maurizia Capuzzo, T Radaszkiewicz, B Dragosics, M. Hiesmayr, Barbara Jordan, D. Schmidlin and Andrea Lassnigg and has published in prestigious journals such as Nature, The Lancet and Journal of Clinical Oncology.

In The Last Decade

Peter Bauer

243 papers receiving 11.2k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Minimal Changes of Serum Creatinine Predict Prognosis in Patients after Cardiothoracic Surgery

2004 1.0k citations Peter Bauer et al. Journal of the American Society of Nephrology profile →
SAPS 3—From evaluation of the patient to evaluation of the intensive care unit. Part 2: Development of a prognostic model for hospital mortality at ICU admission

2005 965 citations Peter Bauer et al. profile →
Mortality after surgery in Europe: a 7 day cohort study

2012 809 citations Peter Bauer et al. profile →
A draft genome of Yersinia pestis from victims of the Black Death

2011 442 citations Peter Bauer et al. profile →
A Revised Timescale for Human Evolution Based on Ancient Mitochondrial Genomes

2013 346 citations Peter Bauer et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter Bauer Germany	47	2.2k	2.1k	2.0k	1.9k	1.6k	250	11.6k
Javier Llorca Spain	62	1.5k 0.7×	1.9k 0.9×	2.3k 1.2×	2.2k 1.2×	558 0.3×	479	15.7k
George J. Schwartz United States	53	1.6k 0.8×	2.1k 1.0×	3.8k 1.9×	1.8k 0.9×	734 0.5×	275	18.8k
Matthieu Resche‐Rigon France	53	686 0.3×	1.4k 0.7×	2.2k 1.1×	1.9k 1.0×	827 0.5×	231	10.9k
James R. Stone United States	60	1.7k 0.8×	2.1k 1.0×	4.8k 2.4×	2.4k 1.3×	376 0.2×	348	14.0k
Ingeborg van der Tweel Netherlands	45	867 0.4×	2.7k 1.3×	952 0.5×	2.3k 1.2×	566 0.4×	152	10.5k
Olaf M. Dekkers Netherlands	80	2.7k 1.3×	6.7k 3.3×	1.6k 0.8×	4.1k 2.1×	1.6k 1.0×	398	22.9k
Howard T. Thaler United States	76	1.6k 0.7×	4.2k 2.0×	2.3k 1.2×	1.9k 1.0×	964 0.6×	233	19.6k
John Eng United States	56	1.9k 0.9×	3.4k 1.7×	2.1k 1.1×	1.2k 0.6×	378 0.2×	224	11.4k
Francis D. Moore United States	63	850 0.4×	4.2k 2.0×	1.6k 0.8×	1.3k 0.7×	874 0.5×	388	13.2k
David A. Lane United Kingdom	60	2.3k 1.1×	1.8k 0.9×	2.4k 1.2×	761 0.4×	704 0.4×	340	13.9k

Countries citing papers authored by Peter Bauer

Since Specialization

Citations

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

Fields of papers citing papers by Peter Bauer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Bauer

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Bauer, Peter, Kathy Keyvani, Rolf R. Diehl, et al.. (2024). Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literature. Journal of Neurology. 271(6). 3328–3339. 2 indexed citations

Pardo, Luba M., et al.. (2023). Adding to the evidence of gene‐disease association of RAP1B and syndromic thrombocytopenia. Clinical Genetics. 105(2). 196–201.

Kraft, Florian, Anna Benet‐Pagès, Daniel Berner, et al.. (2023). Quality assurance within the context of genome diagnostics (a german perspective). Medizinische Genetik. 35(2). 91–104. 1 indexed citations

Marais, Anett, Aida M. Bertoli‐Avella, Christian Beetz, et al.. (2022). Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics. 65(8). 104537–104537. 4 indexed citations

Boutin, Michel, et al.. (2022). Lysosphingolipid Urine Screening Test using Mass Spectrometry for the Early Detection of Lysosomal Storage Disorders. Bioanalysis. 14(5). 289–306. 1 indexed citations

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

Khan, Suliman, Ayman W. El‐Hattab, Ratna Dua Puri, et al.. (2020). Biallelic Pathogenic GFRA1 Variants Cause Autosomal Recessive Bilateral Renal Agenesis. Journal of the American Society of Nephrology. 32(1). 223–228. 12 indexed citations

Mayer, Anja K., Muhammad Mahajnah, Mervyn G. Thomas, et al.. (2019). Homozygous stop mutation in AHR causes autosomal recessive foveal hypoplasia and infantile nystagmus. Brain. 142(6). 1528–1534. 25 indexed citations

Beetz, Christian, Najim Ameziane, Vasiliki Karageorgou, et al.. (2019). VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features. Clinical Genetics. 97(4). 644–648. 4 indexed citations

10.

Bauer, Peter, Thomas Klopstock, Yann Nadjar, et al.. (2019). Recommendations for patient screening in ultra-rare inherited metabolic diseases: what have we learned from Niemann-Pick disease type C?. Orphanet Journal of Rare Diseases. 14(1). 20–20. 11 indexed citations

11.

Hühns, Maja, et al.. (2019). High mutational burden in colorectal carcinomas with monoallelic POLE mutations: absence of allelic loss and gene promoter methylation. Modern Pathology. 33(6). 1220–1231. 7 indexed citations

12.

Schicks, Julia, Jennifer Müller vom Hagen, Peter Bauer, et al.. (2013). Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy. Neurology. 80(12). 1169–1170. 24 indexed citations

13.

Faust, Ulrike, et al.. (2013). Characterisation of novel uveal melanoma cell lines under serum-free conditions. Graefe s Archive for Clinical and Experimental Ophthalmology. 251(8). 2063–2070. 6 indexed citations

14.

Schoenenberger, Andreas W., Peter Bauer, Richard Kobza, et al.. (2013). Improvement of Cardiac Function with Device-Based Diaphragmatic Stimulation in Chronic Heart Failure Patients: The Randomized, Open-Label, Crossover Epiphrenic II Pilot Trial. European Journal of Heart Failure. 16(3). 342–349. 11 indexed citations

15.

Seidel, Kay, Peter Bauer, Wilfred F.A. den Dunnen, et al.. (2009). Widespread thalamic and cerebellar degeneration in a patient with a complicated hereditary spastic paraplegia (HSP). Annals of Anatomy - Anatomischer Anzeiger. 191(2). 203–211. 9 indexed citations

16.

Winkler, Wolfgang, Maria Zellner, Rita Babeluk, et al.. (2007). Biological Variation of the Platelet Proteome in the Elderly Population and Its Implication for Biomarker Research. Molecular & Cellular Proteomics. 7(1). 193–203. 64 indexed citations

17.

Lockwood, G., et al.. (1999). Characterization of the highly variable bioavailability of tiludronate in normal volunteers using population pharmacokinetic methodologies. European Journal of Drug Metabolism and Pharmacokinetics. 24(3). 249–254. 8 indexed citations

18.

Radaszkiewicz, T, B Dragosics, & Peter Bauer. (1992). Gastrointestinal malignant lymphomas of the mucosa-associated lymphoid tissue: Factors relevant to prognosis. Gastroenterology. 102(5). 1628–1638. 349 indexed citations

19.

Bauer, Peter, et al.. (1973). Serumeisen-Normalwerte und statistische Verteilung der Einzelwerte bei Mann und Frau. Annals of Hematology. 27(4). 261–269. 8 indexed citations

20.

Bauer, Peter, et al.. (1971). Normalwerte und Verteilung von Hämoglobin F im Nabelschnurblut. Annals of Hematology. 23(1). 39–41. 2 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.

Explore authors with similar magnitude of impact