M.H. Breuning

481 total citations
13 papers, 385 citations indexed

About

M.H. Breuning is a scholar working on Molecular Biology, Genetics and General Health Professions. According to data from OpenAlex, M.H. Breuning has authored 13 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in General Health Professions. Recurrent topics in M.H. Breuning's work include RNA modifications and cancer (3 papers), Aging, Elder Care, and Social Issues (3 papers) and Health, Medicine and Society (3 papers). M.H. Breuning is often cited by papers focused on RNA modifications and cancer (3 papers), Aging, Elder Care, and Social Issues (3 papers) and Health, Medicine and Society (3 papers). M.H. Breuning collaborates with scholars based in Netherlands, United States and Russia. M.H. Breuning's co-authors include G.J.B. van Ommen, J. Wiegant, Anton K. Raap, J.G. Dauwerse, Johannes G. Dauwerse, Peter Devilee, Tim Kievits, P. Pearson, David F. Callen and Norman A. Doggett and has published in prestigious journals such as Human Molecular Genetics, British Journal of Cancer and Journal of Medical Genetics.

In The Last Decade

M.H. Breuning

11 papers receiving 371 citations

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	8	219	157	77	51	43	13	385
J.G. Dauwerse Netherlands	6	211 1.0×	129 0.8×	52 0.7×	21 0.4×	17 0.4×	7	307
Claudia Dellavecchia Italy	9	153 0.7×	220 1.4×	87 1.1×	39 0.8×	93 2.2×	11	408
Sparkes Rs United States	11	143 0.7×	132 0.8×	42 0.5×	30 0.6×	72 1.7×	30	382
E. Orye Belgium	14	233 1.1×	311 2.0×	122 1.6×	48 0.9×	137 3.2×	35	590
Bogdan Kałużewski Poland	13	200 0.9×	200 1.3×	88 1.1×	101 2.0×	67 1.6×	59	407
Teresa Vendrell Spain	12	160 0.7×	143 0.9×	34 0.4×	45 0.9×	64 1.5×	25	310
I. López Pajares Spain	12	286 1.3×	316 2.0×	94 1.2×	76 1.5×	106 2.5×	27	493
Pietro Sirleto Italy	12	221 1.0×	137 0.9×	27 0.4×	30 0.6×	33 0.8×	25	399
Heide Seidel Germany	14	182 0.8×	192 1.2×	33 0.4×	45 0.9×	32 0.7×	24	337
Gerald A.J. Gillespie United States	9	228 1.0×	161 1.0×	20 0.3×	18 0.4×	17 0.4×	13	372

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

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13 of 13 papers shown

Breuning, M.H., et al.. (2010). Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?. Clinical Genetics. 79(3). 236–242. 17 indexed citations

Saux, Olivia Le, Zsolt Urbán, Katalin Csiszár, et al.. (2000). Erratum: Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16 (Genomics (1999) 62: 1 (1)). Data Archiving and Networked Services (DANS). 1 indexed citations

Mitchison, Hannah M., et al.. (2000). Targeted disruption of the Cln3 gene provides a mouse model for Batten disease (vol 6, pg 321, 1999). UCL Discovery (University College London).

Vos, Nathalie De, et al.. (1999). A murine model for juvenile NCL: Gene targeting of mouse CLn3 (vol 66, pg 309, 1999). UCL Discovery (University College London).

Breuning, M.H., et al.. (1999). A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome). Journal of Medical Genetics. 36(6). 485–489. 41 indexed citations

Moerland, Elna W., M.H. Breuning, Cornelisse Cj, & A.M. Cleton-Jansen. (1997). Exclusion of BBC1 and CMAR as candidate breast tumour-suppressor genes. British Journal of Cancer. 76(12). 1550–1553. 15 indexed citations

Doggett, Norman A., M.H. Breuning, & David F. Callen. (1996). Report of the Fourth International Workshop on Human Chromosome 16 Mapping 1995. Cytogenetic and Genome Research. 72(4). 271–293. 27 indexed citations

Dauwerse, J.G., J.W. Wessels, Rachel H. Giles, et al.. (1993). Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo. Human Molecular Genetics. 2(10). 1527–1534. 38 indexed citations

Dauwerse, Johannes G., J. Wiegant, Anton K. Raap, M.H. Breuning, & G.J.B. van Ommen. (1992). Multiple colors by fluorescence in situ hybridization using ratio-labelled DNA probes create a molecular karyotype. Human Molecular Genetics. 1(8). 593–598. 96 indexed citations

10.

Harris, Peter C., Sean McKeown, Peter J. Ratcliffe, et al.. (1991). RAPID GENETIC-ANALYSIS OF POLYCYSTIC KIDNEY DISEASE-1 (PKD1) FAMILIES WITH A CLOSELY LINKED, HIGHLY POLYMORPHIC MICROSATELLITE. Oxford University Research Archive (ORA) (University of Oxford). 58. 2000–2000. 2 indexed citations

11.

Kievits, Tim, J.G. Dauwerse, J. Wiegant, et al.. (1990). Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization. Cytogenetic and Genome Research. 53(2-3). 134–136. 137 indexed citations

12.

Breuning, M.H., et al.. (1987). NEW PROBES CLOSE TO THE GENE FOR ADULT POLYCYSTIC KIDNEY-DISEASE (PKD1) ON 16P. Data Archiving and Networked Services (DANS). 2 indexed citations

13.

Breuning, M.H., et al.. (1954). [The frequency of listeria infections in newborn; studies at the gynecological clinic of Leipzig University].. PubMed. 14(12). 1113–24. 9 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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