M.H. Breuning

4.3k citations
60 papers · 2.6k · h-index 29

Impact in

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

Papers in

  • Genetics 34
    • Genomic variations and chromosomal abnormalities 12
    • Genetic Syndromes and Imprinting 12
    • Genetic and Kidney Cyst Diseases 11
    • Genetics and Neurodevelopmental Disorders 4
  • Molecular Biology 25
    • Renal and related cancers 6
Co-authors
Egbert Bakker (9 shared papers)Sarina G. Kant (6 shared papers)Jasper J. Saris (6 shared papers)Juul Wijnen (3 shared papers)Hans F. A. Vasen (3 shared papers)Dorien J.M. Peters (4 shared papers)Carli M.J. Tops (2 shared papers)Johan T. den Dunnen (4 shared papers)
Journals
Clinical Genetics (4 papers)Journal of Medical Genetics (4 papers)Nucleic Acids Research (3 papers)Blood (3 papers)Cytogenetic and Genome Research (3 papers)
Partner nations
NetherlandsUnited KingdomUnited States

In The Last Decade

M.H. Breuning

59 papers receiving 2.5k citations

Peers

M.H. Breuning
Comparison fields: 5 of 97
  • Genetics 1.2k
  • Developmental Biology 81
  • Pathology and Forensic Medicine 382
  • Neurology 222
  • Molecular Biology 1.0k
Replace Dvorah Abeliovich with:
Dvorah Abeliovich Israel
Sigrid Tinschert Germany
Jean‐Pierre Fryns Belgium
Maurizio Genuardi Italy
Arie van Haeringen Netherlands
Gwenaëlle Collod‐Béroud France
M.H. Breuning Netherlands
Jacopo Celli Netherlands
David J. Bunyan United Kingdom
Peter Wieacker Germany
M.H. Breuning relative to Dvorah Abeliovich Israel Dvorah Abeliovich's profile →
Citations per field
00.5×2×3×3.5×
Dvorah Abeliovich · 1×
Citations per year

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

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
2008209
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
1993191
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
2001150
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
2006118
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
2006113
6
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
2007108
7
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, (unknown)
2007107
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
2006101
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
199384
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
198273
11
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
199964
12
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
201264
13
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
198764
14
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
200363
15
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
200963
16
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
199261
17
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
199160
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
200355
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
199755
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
199053

About M.H. Breuning

M.H. Breuning is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Plant Science and Pediatrics, Perinatology and Child Health, having authored 60 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genetic Syndromes and Imprinting (12 papers), Genetic and Kidney Cyst Diseases (11 papers), Chromosomal and Genetic Variations (7 papers), Renal and related cancers (6 papers), Prenatal Screening and Diagnostics (6 papers), Lysosomal Storage Disorders Research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (1.2k citations), Developmental Biology (81 citations), Pathology and Forensic Medicine (382 citations), Neurology (222 citations) and Molecular Biology (1.0k citations). M.H. Breuning has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Egbert Bakker, Sarina G. Kant, Jasper J. Saris, Juul Wijnen, Hans F. A. Vasen, Dorien J.M. Peters, Carli M.J. Tops, Johan T. den Dunnen, G.J.B. van Ommen and Hans Morreau. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Nucleic Acids Research, Blood and Cytogenetic and Genome Research.

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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