M.H. Breuning
Impact in
- Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Developmental Biology top 5%
Papers in
-
- Renal and related cancers 12
- Genomics and Chromatin Dynamics 2
- Genetics 18
- Genetic and Kidney Cyst Diseases 15
- Genetic Syndromes and Imprinting 6
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Stephen T. Reeders (4 shared papers)D. J. Weatherall (3 shared papers)Kay E. Davies (3 shared papers)P. Pearson (2 shared papers)Dorien J.M. Peters (8 shared papers)Robert D. Nicholls (1 shared paper)Andrew P. Jarman (1 shared paper)Douglas R. Higgs (1 shared paper)
- Journals
- Kidney International (3 papers)Human Molecular Genetics (2 papers)Nephrology Dialysis Transplantation (2 papers)Nature Genetics (1 paper)Nature (1 paper)
- Partner nations
- NetherlandsUnited KingdomGermany
In The Last Decade
M.H. Breuning
25 papers receiving 2.1k citations
M.H. Breuning's Hit Papers
Peers
Comparison fields: 5 of 83
- Genetics 1.7k
- Developmental Biology 85
- Molecular Biology 1.4k
- Nephrology 139
- Gender Studies 120
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
Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome Hit paper breakdown → | 1997 | 701 |
| 2 | A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 Hit paper breakdown → | 1985 | 518 |
| 3 | 2007 | 164 | |
| 4 | 2009 | 117 | |
| 5 | 1997 | 77 | |
| 6 | 1986 | 74 | |
| 7 | 1990 | 67 | |
| 8 | 2000 | 52 | |
| 9 | 2010 | 49 | |
| 10 | Adult, fetal, and polycystic kidney expression of polycystin, the polycystic kidney disease-1 gene product. | 1996 | 46 |
| 11 | 1999 | 43 | |
| 12 | Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects. | 1993 | 43 |
| 13 | 1995 | 37 | |
| 14 | 1990 | 23 | |
| 15 | 1994 | 18 | |
| 16 | 2017 | 17 | |
| 17 | 1990 | 15 | |
| 18 | 1986 | 13 | |
| 19 | 1996 | 11 | |
| 20 | 1991 | 11 |
About M.H. Breuning
M.H. Breuning is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Urology, having authored 26 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (15 papers), Renal and related cancers (12 papers), Genetic Syndromes and Imprinting (6 papers), Genomics and Chromatin Dynamics (2 papers), Prenatal Screening and Diagnostics (2 papers), Chromosomal and Genetic Variations (2 papers), Congenital limb and hand anomalies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (1.7k citations), Developmental Biology (85 citations), Molecular Biology (1.4k citations), Nephrology (139 citations) and Gender Studies (120 citations). M.H. Breuning has collaborated with scholars based in Netherlands, United Kingdom and Germany. Frequent co-authors include Stephen T. Reeders, D. J. Weatherall, Kay E. Davies, P. Pearson, Dorien J.M. Peters, Robert D. Nicholls, Andrew P. Jarman, Douglas R. Higgs, Emile de Heer and Annemieke van der Wal. Their work appears in journals such as Kidney International, Human Molecular Genetics, Nephrology Dialysis Transplantation, Nature Genetics and Nature.
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.