M.H. Breuning

4.3k citations

60 papers · 2.6k indexed · h-index 29

Impact in

Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
Developmental Biology top 5%

Papers in ⓘ

Genetics 36
- Genetic Syndromes and Imprinting 13
- Genomic variations and chromosomal abnormalities 12
- Genetic and Kidney Cyst Diseases 11
- Genetics and Neurodevelopmental Disorders 5
Developmental Biology 1

Co-authors: Egbert Bakker (9 shared papers)Hans F. A. Vasen (4 shared papers)Sarina G. Kant (6 shared papers)Jasper J. Saris (6 shared papers)Juul Wijnen (3 shared papers)Dorien J.M. Peters (4 shared papers)G.J.B. van Ommen (4 shared papers)Johan T. den Dunnen (4 shared papers)
Journals: Journal of Medical Genetics (4 papers)Clinical Genetics (4 papers)Nucleic Acids Research (3 papers)Cytogenetic and Genome Research (3 papers)Hormone Research in Paediatrics (3 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

M.H. Breuning

59 papers receiving 2.5k citations

Peers

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-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.

Border = papers with M.H. Breuning Line = papers co-authored together M.H. Breuning links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 60 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant Journal of Medical Genetics ·Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch	2008	207
2	Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease Nature Genetics ·Dorien J.M. Peters, Lia Spruit, Jasper J. Saris, David Ravine, Lodewijk A. Sandkuijl, Ragnheiður Fossdal, J. Boersma, Ronald van Eijk, Søren Nørby, Constantinos Deltas, Alkis Pierides, J.E. Briessenden, RuneR. Frants, G.J.B. van Ommen, M.H. Breuning	1993	192
3	Cerebral microbleeds in CADASIL Neurology ·Saskia A.J. Lesnik Oberstein, Rivka van den Boom, Mark A. van Buchem, Hans C. van Houwelingen, Egbert Bakker, Ellen Vollebregt, Michel D. Ferrari, M.H. Breuning, J. Haan	2001	150
4	Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians CA A Cancer Journal for Clinicians ·Yvonne Hendriks, Andrea E. van der Meulen‐de Jong, Hans Morreau, Carli M.J. Tops, Hans F. A. Vasen, Juul Wijnen, M.H. Breuning, A Bröcker-Vriends	2006	116
5	Duplications in theDMD gene Human Mutation ·Stefan J. White, Annemieke Aartsma‐Rus, Kevin M. Flanigan, Robert B. Weiss, Alexander L.J. Kneppers, Tanja Lalic, Annika Janson, H.B. Ginjaar, M.H. Breuning, Johan T. den Dunnen	2006	113
6	Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis Clinical Genetics ·Maartje Nielsen, Frederik J. Hes, FM Nagengast, Marjan M. Weiss, EM Mathus‐Vliegen, Hans Morreau, M.H. Breuning, J. Wijnen, CMJ Tops, Hans F. A. Vasen	2007	107
7	Somatic APC mosaicism: an underestimated cause of polyposis coli Gut ·Frederik J. Hes, Maartje Nielsen, Elsa C. Bik, David Konvalinka, Juul Wijnen, Egbert Bakker, Hans F. A. Vasen, M.H. Breuning, Carli M.J. Tops	2007	106
8	A Variable Degree of Intrauterine and Postnatal Growth Retardation in a Family with a Missense Mutation in the Insulin-Like Growth Factor I Receptor The Journal of Clinical Endocrinology & Metabolism ·M.J.E. Walenkamp, H.J. van der Kamp, Alberto M. Pereira, Sarina G. Kant, Hermine A. van Duyvenvoorde, M. Femke Kruithof, M.H. Breuning, Johannes A. Romijn, Marcel Karperien, J. M. Wit	2006	100
9	Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3. PubMed ·M.H. Breuning, Hans G. Dauwerse, G Fugazza, Jasper J. Saris, Lia Spruit, Herman Wijnen, Niels Tommerup, C. B. van der Hagen, K Imaizumi, Yoshikazu Kuroki, M. J. van den Boogaard, Jennie M. Pater, Edwin C.M. Mariman, Ben C.J. Hamel, Heinz Himmelbauer, A.-M. Frischauf, R. Stallings, G.C. Beverstock, G J van Ommen, Raoul C. M. Hennekam	1993	84
10	Subtypes of HLA-B27 detected by cytotoxic T lymphocytes and their role in self-recognition Human Immunology ·M.H. Breuning, C.J. Lucas, B. S. Breur, M.Y. Engelsma, G. G. de Lange, A. Dekker, William E. Biddison, P. Iványi	1982	73
11	Copeptin, a surrogate marker for vasopressin, is associated with kidney function decline in subjects with autosomal dominant polycystic kidney disease Nephrology Dialysis Transplantation ·Wendy E. Boertien, Esther Meijer, Debbie Zittema, Marjan A. van Dijk, Ton J. Rabelink, M.H. Breuning, J. Struck, Stephan J. L. Bakker, Dorien J.M. Peters, Paul E. de Jong, Ron T. Gansevoort	2012	64
12	IMPROVED EARLY DIAGNOSIS OF ADULT POLYCYSTIC KIDNEY DISEASE WITH FLANKING DNA MARKERS The Lancet ·M.H. Breuning, HG Brunner, Jasper J. Saris, G.J.B. van Ommen, Stephen T. Reeders, Jacob W. IJdo, A. Verwest, P. Pearson	1987	64
13	Recurrence risk due to germ line mosaicism: Duchenne and Becker muscular dystrophy Clinical Genetics ·A. Helderman-van den Enden, Renate de Jong, Johan T. den Dunnen, Jeanine J. Houwing‐Duistermaat, ALJ Kneppers, H.B. Ginjaar, M.H. Breuning, Egbert Bakker	2009	64
14	Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients Neurology ·Saskia A.J. Lesnik Oberstein, Michel D. Ferrari, Egbert Bakker, J. van Gestel, Alexander L.J. Kneppers, Rune R. Frants, M.H. Breuning, J. Haan	1999	63
15	Genetic counselling and the intention to undergo prophylactic mastectomy: effects of a breast cancer risk assessment British Journal of Cancer ·Sandra van Dijk, Wilma Otten, Moniek Zoeteweij, Daniëlle R. M. Timmermans, Christi J. van Asperen, M.H. Breuning, Rob A.�E.�M. Tollenaar, J. Kievit	2003	63
16	Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker The Lancet ·Peter C. Harris, Spencer A. Thomas, Peter J. Ratcliffe, M.H. Breuning, Eliécer Coto, Carlos López‐Larrea	1991	61
17	Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations Blood ·JG Dauwerse, E.A. Jumelet, J. Wessels, JJ Saris, A. Hagemeijer, G.C. Beverstock, GJ van Ommen, M.H. Breuning	1992	61
18	Bannayan–Riley–Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases Familial Cancer ·Yvonne Hendriks, J.T.C.M. Verhallen, Jasper J. van der Smagt, Sarina G. Kant, Yvonne Hilhorst, Lies H. Hoefsloot, Kerstin Hansson, P. J. C. van der Straaten, H. Boutkan, M.H. Breuning, Hans F. A. Vasen, A Bröcker-Vriends	2003	55
19	Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16) Leukemia ·Rachel H. Giles, JG Dauwerse, Christine M. Higgins, Fred Petrij, J. Wessels, G.C. Beverstock, Hartmut Döhner, M Jotterand-Bellomo, JHF Falkenburg, R Släter, G-J.B. van Ommen, A. Hagemeijer, BA van der Reijden, M.H. Breuning	1997	55
20	Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). Journal of Medical Genetics ·M.H. Breuning, F.G.M. Snijdewint, HG Brunner, A. Verwest, Jacob W. IJdo, Jasper J. Saris, Johannes G. Dauwerse, Lau Blonden, Tim P. Keith, David F. Callen	1990	53

About M.H. Breuning

M.H. Breuning is a scholar working on Genetics, Developmental Biology, Pathology and Forensic Medicine, Molecular Biology and Rheumatology, having authored 60 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (13 papers), Genomic variations and chromosomal abnormalities (12 papers), Genetic and Kidney Cyst Diseases (11 papers), Renal and related cancers (8 papers), Chromosomal and Genetic Variations (7 papers), Prenatal Screening and Diagnostics (6 papers), Lysosomal Storage Disorders Research (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Biology (82 citations), Pathology and Forensic Medicine (408 citations), Molecular Biology (1.1k citations) and Neurology (229 citations). M.H. Breuning has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Egbert Bakker, Hans F. A. Vasen, Sarina G. Kant, Jasper J. Saris, Juul Wijnen, Dorien J.M. Peters, G.J.B. van Ommen, Johan T. den Dunnen, Carli M.J. Tops and Saskia A.J. Lesnik Oberstein. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Nucleic Acids Research, Cytogenetic and Genome Research and Hormone Research in Paediatrics.

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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