Peter Freisinger
Impact in
- Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
- Molecular Biology top 2%
- Mitochondrial Function and Pathology
Papers in
-
- Metabolism and Genetic Disorders 87
-
- Mitochondrial Function and Pathology 38
- ATP Synthase and ATPases Research 4
- Co-authors
- Johannes Adalbert Mayr (16 shared papers)Jacky Bonaventure (5 shared papers)Wolfgang Sperl (20 shared papers)L Cohen-Solal (2 shared papers)J. Bourguignon (1 shared paper)Catherine Benoist-Lasselin (1 shared paper)N. Kadhom (1 shared paper)Kim Heng Ng (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (24 papers)The American Journal of Human Genetics (12 papers)Neuropediatrics (8 papers)Molecular Genetics and Metabolism (7 papers)Orphanet Journal of Rare Diseases (6 papers)
- Partner nations
- GermanyAustriaUnited States
In The Last Decade
Peter Freisinger
136 papers receiving 6.6k citations
Peter Freisinger's Hit Papers
Peers
Comparison fields: 5 of 133
- Clinical Biochemistry 1.8k
- Molecular Biology 2.7k
- Genetics 1.2k
- Rheumatology 525
- Developmental Biology 76
Countries citing papers authored by Peter Freisinger
This map shows the geographic impact of Peter Freisinger'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 Freisinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Freisinger more than expected).
Fields of papers citing papers by Peter Freisinger
This network shows the impact of papers produced by Peter Freisinger. 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 Freisinger. The network helps show where Peter Freisinger may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Freisinger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 138 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 447 | |
| 2 | Genetic diagnosis of Mendelian disorders via RNA sequencing Hit paper breakdown → | 2017 | 440 |
| 3 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 407 |
| 4 | 2000 | 253 | |
| 5 | 2012 | 161 | |
| 6 | 2013 | 147 | |
| 7 | 2016 | 141 | |
| 8 | Clinical implementation of RNA sequencing for Mendelian disease diagnostics Hit paper breakdown → | 2022 | 139 |
| 9 | 2014 | 134 | |
| 10 | 2007 | 132 | |
| 11 | 2013 | 126 | |
| 12 | 2021 | 118 | |
| 13 | 2016 | 110 | |
| 14 | 1998 | 109 | |
| 15 | 2014 | 106 | |
| 16 | 2015 | 104 | |
| 17 | 2010 | 103 | |
| 18 | 1999 | 101 | |
| 19 | 2015 | 101 | |
| 20 | 2006 | 98 |
About Peter Freisinger
Peter Freisinger is a scholar working on Clinical Biochemistry, Molecular Biology, Genetics, Rheumatology and Developmental Biology, having authored 138 papers that have together received 6.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (87 papers), Mitochondrial Function and Pathology (38 papers), Connective tissue disorders research (13 papers), Genomics and Rare Diseases (10 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Congenital limb and hand anomalies (4 papers), ATP Synthase and ATPases Research (4 papers) and Trace Elements in Health (3 papers). The work is most often cited by research in Clinical Biochemistry (1.8k citations), Molecular Biology (2.7k citations), Genetics (1.2k citations), Rheumatology (525 citations) and Developmental Biology (76 citations). Peter Freisinger has collaborated with scholars based in Germany, Austria and United States. Frequent co-authors include Johannes Adalbert Mayr, Jacky Bonaventure, Wolfgang Sperl, L Cohen-Solal, J. Bourguignon, Catherine Benoist-Lasselin, N. Kadhom, Kim Heng Ng, Thomas Meitinger and Holger Prokisch. Their work appears in journals such as Journal of Inherited Metabolic Disease, The American Journal of Human Genetics, Neuropediatrics, Molecular Genetics and Metabolism and Orphanet Journal of Rare Diseases.
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.