M.H. Breuning
Impact in
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- Genomic variations and chromosomal abnormalities
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- Acute Myeloid Leukemia Research
Papers in
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- RNA modifications and cancer 2
- Muscle Physiology and Disorders 1
- Genetics 4
- Digestive system and related health 2
- Animal Genetics and Reproduction 2
- Co-authors
- G.J.B. van Ommen (3 shared papers)J. Wiegant (3 shared papers)Anton K. Raap (2 shared papers)Johannes G. Dauwerse (1 shared paper)Carel Meijers (1 shared paper)Jan Osinga (1 shared paper)Robert M.W. Hofstra (1 shared paper)Elna W. Moerland (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)British Journal of Cancer (1 paper)Clinical Genetics (1 paper)Journal of Medical Genetics (1 paper)Data Archiving and Networked Services (DANS) (2 papers)
- Partner nations
- NetherlandsItalyUnited States
In The Last Decade
M.H. Breuning
10 papers receiving 227 citations
Peers
Comparison fields: 5 of 47
- Genetics 99
- Hematology 30
- Pediatrics, Perinatology and Child Health 36
- Molecular Biology 123
- Biophysics 8
Countries citing papers authored by M.H. Breuning
This map shows the geographic impact of M.H. Breuning'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 M.H. Breuning with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M.H. Breuning more than expected).
Fields of papers citing papers by M.H. Breuning
This network shows the impact of papers produced by M.H. Breuning. 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 M.H. Breuning. The network helps show where M.H. Breuning may publish in the future.
Co-authors
The 25 scholars most cited alongside M.H. Breuning, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 102 | |
| 2 | 1999 | 49 | |
| 3 | 1993 | 40 | |
| 4 | 2010 | 19 | |
| 5 | 1997 | 15 | |
| 6 | [The frequency of listeria infections in newborn; studies at the gynecological clinic of Leipzig University]. | 1954 | 11 |
| 7 | 2008 | 3 | |
| 8 | NEW PROBES CLOSE TO THE GENE FOR ADULT POLYCYSTIC KIDNEY-DISEASE (PKD1) ON 16P | 1987 | 2 |
| 9 | RAPID GENETIC-ANALYSIS OF POLYCYSTIC KIDNEY DISEASE-1 (PKD1) FAMILIES WITH A CLOSELY LINKED, HIGHLY POLYMORPHIC MICROSATELLITE | 1991 | 2 |
| 10 | Erratum: Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16 (Genomics (1999) 62: 1 (1)) | 2000 | 1 |
| 11 | Targeted disruption of the Cln3 gene provides a mouse model for Batten disease (vol 6, pg 321, 1999) | 2000 | 0 |
| 12 | A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999) | 1999 | 0 |
About M.H. Breuning
M.H. Breuning is a scholar working on Molecular Biology, Genetics, General Health Professions, Philosophy and Surgery, having authored 12 papers that have together received 244 indexed citations. Recurring topics across this work include Hermeneutics and Narrative Identity (3 papers), Aging, Elder Care, and Social Issues (3 papers), Health, Medicine and Society (3 papers), Digestive system and related health (2 papers), Animal Genetics and Reproduction (2 papers), RNA modifications and cancer (2 papers), Acute Myeloid Leukemia Research (1 paper) and Muscle Physiology and Disorders (1 paper). The work is most often cited by research in Genetics (99 citations), Hematology (30 citations), Pediatrics, Perinatology and Child Health (36 citations), Molecular Biology (123 citations) and Biophysics (8 citations). M.H. Breuning has collaborated with scholars based in Netherlands, Italy and United States. Frequent co-authors include G.J.B. van Ommen, J. Wiegant, Anton K. Raap, Johannes G. Dauwerse, Carel Meijers, Jan Osinga, Robert M.W. Hofstra, Elna W. Moerland, A.M. Cleton-Jansen and Cornelisse Cj. Their work appears in journals such as Human Molecular Genetics, British Journal of Cancer, Clinical Genetics, Journal of Medical Genetics and Data Archiving and Networked Services (DANS).
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.