M.H. Breuning

3.0k total citations · 2 hit papers
26 papers, 2.1k citations indexed

About

M.H. Breuning is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M.H. Breuning has authored 26 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M.H. Breuning's work include Genetic and Kidney Cyst Diseases (15 papers), Renal and related cancers (12 papers) and Genetic Syndromes and Imprinting (6 papers). M.H. Breuning is often cited by papers focused on Genetic and Kidney Cyst Diseases (15 papers), Renal and related cancers (12 papers) and Genetic Syndromes and Imprinting (6 papers). M.H. Breuning collaborates with scholars based in Netherlands, United Kingdom and Germany. M.H. Breuning's co-authors include Stephen T. Reeders, Kay E. Davies, D. J. Weatherall, P. Pearson, Dorien J.M. Peters, Andrew P. Jarman, Douglas R. Higgs, Robert D. Nicholls, Emile de Heer and Wouter N. Leonhard and has published in prestigious journals such as Nature, Nucleic Acids Research and Nature Genetics.

In The Last Decade

M.H. Breuning

25 papers receiving 2.1k citations

Hit 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.

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1997 701 citations Ercole Rao, Birgit Weiß et al. Nature Genetics profile →
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1985 518 citations Stephen T. Reeders, M.H. Breuning et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.H. Breuning Netherlands	16	1.7k	1.4k	207	183	160	26	2.1k
Koji Muroya Japan	28	1.9k 1.1×	1.9k 1.4×	301 1.5×	62 0.3×	296 1.9×	119	3.1k
David J. Bunyan United Kingdom	23	979 0.6×	991 0.7×	113 0.5×	304 1.7×	95 0.6×	60	2.0k
Jay W. Ellison United States	23	1.2k 0.7×	1.2k 0.9×	438 2.1×	63 0.3×	210 1.3×	52	2.6k
Lester Weiss United States	29	1.4k 0.8×	918 0.7×	448 2.2×	135 0.7×	416 2.6×	82	2.3k
Jean‐Pierre Fryns Belgium	21	909 0.5×	1.2k 0.9×	202 1.0×	130 0.7×	73 0.5×	25	2.0k
A. Moseley United States	5	890 0.5×	834 0.6×	92 0.4×	127 0.7×	63 0.4×	10	1.6k
Michael Oldridge United Kingdom	19	2.1k 1.2×	1.8k 1.3×	190 0.9×	58 0.3×	120 0.8×	29	3.0k
Hermann‐Josef Lüdecke Germany	19	864 0.5×	937 0.7×	117 0.6×	116 0.6×	167 1.0×	39	1.8k
Jacqueline Schoumans Sweden	29	1.6k 0.9×	1.2k 0.8×	442 2.1×	99 0.5×	458 2.9×	73	2.5k
Simone Schuffenhauer Germany	23	964 0.6×	1.0k 0.7×	308 1.5×	41 0.2×	181 1.1×	42	1.7k

Countries citing papers authored by M.H. Breuning

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of M.H. Breuning

This figure shows the co-authorship network connecting the top 25 collaborators of M.H. Breuning. A scholar is included among the top collaborators of M.H. Breuning 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 M.H. Breuning. M.H. Breuning 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

Hiemstra, Yasmine L., Regina Bökenkamp, Anneke M. van Mil, et al.. (2017). A Dutch MYH7 founder mutation, p.(Asn1918Lys), is associated with early onset cardiomyopathy and congenital heart defects. Netherlands Heart Journal. 25(12). 675–681. 17 indexed citations

Aten, Emmelien, Dorothea Bornholdt, Ingeborg B. Hooijkaas, et al.. (2010). Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2. Human Mutation. 31(10). 1125–1133. 49 indexed citations

Happe, H. Kevin, Wouter N. Leonhard, Annemieke van der Wal, et al.. (2009). Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathways. Human Molecular Genetics. 18(14). 2532–2542. 117 indexed citations

Leeuwen, Irma S Lantinga‐van, Wouter N. Leonhard, Annemieke van der Wal, et al.. (2007). Kidney-specific inactivation of the Pkd1 gene induces rapid cyst formation in developing kidneys and a slow onset of disease in adult mice. Human Molecular Genetics. 16(24). 3188–3196. 164 indexed citations

Giordano, Paola & M.H. Breuning. (2000). [From gene to disease; from hemoglobin genes to thalassemia and sickle cell anemia].. PubMed. 144(40). 1910–3. 7 indexed citations

Hateboer, Nick, Barbera Veldhuisen, Dorien J.M. Peters, et al.. (2000). Location of mutations within the PKD2 gene influences clinical outcome. Kidney International. 57(4). 1444–1451. 52 indexed citations

Monnens, L.A.H., et al.. (1999). Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin. Kidney International. 55(4). 1217–1224. 43 indexed citations

Veldhuisen, Barbera, Jasper J. Saris, Simone de Haij, et al.. (1997). A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2). The American Journal of Human Genetics. 61(3). 547–555. 77 indexed citations

Rao, Ercole, Birgit Weiß, Maki Fukami, et al.. (1997). Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nature Genetics. 16(1). 54–63. 701 indexed citations breakdown →

10.

Veldhuisen, Barbera, et al.. (1996). Analysis of a large family with the second type of autosomal dominant polycystic kidney disease. Nephrology Dialysis Transplantation. 11(supp6). 13–17. 11 indexed citations

11.

Roelfsema, Jeroen, Dorien J.M. Peters, & M.H. Breuning. (1996). Detection of translation terminating mutations in the PKD1 gene. Nephrology Dialysis Transplantation. 11(supp6). 5–9. 10 indexed citations

12.

Masuno, Mitsuo, et al.. (1994). Submicroscopic deletion of chromosome region 16p13.3 in a Japanese patient with Rubinstein‐Taybi syndrome. American Journal of Medical Genetics. 53(4). 352–354. 18 indexed citations

13.

Hennekam, Raoul C. M., Marcel G.J. Tilanus, Ben C.J. Hamel, et al.. (1993). Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspects.. PubMed. 52(2). 255–62. 43 indexed citations

14.

Breuning, M.H., Marcella Devoto, & G. Romeo. (1992). Polycystic kidney disease. KARGER eBooks. 1 indexed citations

15.

Dauwerse, Hans G., et al.. (1991). Inversion 16 and translocation (16;16) in ANLL M4eo break in the same subregion of the short arm of chromosome 16. Cancer Genetics and Cytogenetics. 57(2). 225–228. 11 indexed citations

16.

Cobben, Jan M., M.H. Breuning, Coen Schoots, Leo P. ten Kate, & Klaus Zerres. (1990). Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease. Kidney International. 38(5). 880–885. 67 indexed citations

17.

Hyland, V.J., Graeme Suthers, Kathryn Friend, et al.. (1990). Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1. Human Genetics. 84(3). 286–8. 23 indexed citations

18.

Breuning, M.H., et al.. (1990). A TaqI polymorphism identified by 26–6 (D16S125) proximal to the locus affecting adult polycystic kidney disease (PKD1) on chromosome 16. Nucleic Acids Research. 18(10). 3106–3106. 15 indexed citations

19.

Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.. BMJ. 292(6524). 851–853. 74 indexed citations

20.

Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two Genetic Markers Closely Linked to Adult Polycystic Kidney Disease on Chromosome 16. The Journal of Urology. 136(4). 987–987. 13 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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