M.H. Breuning

4.3k citations
67 papers · 3.4k · h-index 31

Impact in

  • Developmental Biology top 2%
  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
    • Genetics and Neurodevelopmental Disorders

Papers in

  • Genetics 37
    • Genomic variations and chromosomal abnormalities 13
    • Genetic Syndromes and Imprinting 13
    • Genetic and Kidney Cyst Diseases 12
  • Molecular Biology 27
    • Renal and related cancers 7
Co-authors
Egbert Bakker (9 shared papers)Dorien J.M. Peters (6 shared papers)Jasper J. Saris (6 shared papers)Juul Wijnen (3 shared papers)Sarina G. Kant (6 shared papers)Hans F. A. Vasen (3 shared papers)Carli M.J. Tops (2 shared papers)G.J.B. van Ommen (4 shared papers)
Journals
Journal of Medical Genetics (6 papers)Clinical Genetics (4 papers)Hormone Research in Paediatrics (4 papers)Nephrology Dialysis Transplantation (3 papers)Blood (3 papers)
Partner nations
NetherlandsUnited StatesUnited Kingdom

In The Last Decade

M.H. Breuning

66 papers receiving 3.2k citations

Peers

M.H. Breuning
Comparison fields: 5 of 106
  • Developmental Biology 140
  • Genetics 1.6k
  • Pathology and Forensic Medicine 464
  • Molecular Biology 1.3k
  • Pediatrics, Perinatology and Child Health 325
Replace Jürgen Kohlhase with:
Jürgen Kohlhase Germany
Margherita Silengo Italy
Ineke van der Burgt Netherlands
Jean‐Pierre Fryns Belgium
Charles I. Scott United States
David D. Weaver United States
Louise C. Wilson United Kingdom
Sylvie Manouvrier France
Joyce Tannenbaum Turner United States
Livia Garavelli Italy
M.H. Breuning relative to Jürgen Kohlhase Germany Jürgen Kohlhase's profile →
Citations per field
00.5×1.5×
Jürgen Kohlhase · 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 67 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 J.L. de Ravel, Claudia A. L. Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt
2008257
2
Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
European Journal of Medical Genetics ·Emilia K. Bijlsma, A.C.J. Gijsbers, Janneke H. M. Schuurs-Hoeijmakers, Arie van Haeringen, Dietje E. Fransen van de Putte, Britt‐Marie Anderlid, Johanna Lundin, Pablo Daniel Lapunzina
2009226
3
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
1993219
4
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
2001170
5
Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians
CA A Cancer Journal for Clinicians ·Yvonne M. C. Hendriks, Andrea E. van der Meulen‐de Jong, Hans Morreau, Carli M.J. Tops, Hans F. A. Vasen, Juul Wijnen, M.H. Breuning, A. H. J. T. Bröcker-Vriends
2006141
6
Somatic APC mosaicism: an underestimated cause of polyposis coli
Gut ·Frederik Jan Hes, Maartje Nielsen, Elsa C. Bik, David Konvalinka, Juul Wijnen, Egbert Bakker, Hans F. A. Vasen, M.H. Breuning
2007129
7
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis
Clinical Genetics ·Maartje Nielsen, Frederik Jan Hes, FM Nagengast, Marjan M. Weiss, EM Mathus‐Vliegen, Hans Morreau, M.H. Breuning, Job Wijnen
2007123
8
Duplications in theDMD gene
Human Mutation ·Stefan J. White, Annemieke M Aartsma-Rus, Kevin M. Flanigan, Robert B. Weiss, Alexander L.J. Kneppers, Tanja Lalic, Annika Janson, H.B. Ginjaar
2006122
9
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 ·Marie 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 Anthonius Romijn
2006117
10
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
199393
11
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Journal of Medical Genetics ·Deborah Bartholdi, Jeroen H. Roelfsema, Francesco Saverio Papadia, M.H. Breuning, Dunja Niedrist, Raoul C. M. Hennekam, Albert Schinzel, Dorien J.M. Peters
200787
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, Peter Lees Pearson
198780
13
The IGSF1 Deficiency Syndrome: Characteristics of Male and Female Patients
The Journal of Clinical Endocrinology & Metabolism ·Sjoerd D. Joustra, Nadia A. Schoenmakers, Luca Persani, Irene Campi, Marco Bonomi, Giorgio Radetti, P. Beck‐Peccoz, Hongdong Zhu
201380
14
Subtypes of HLA-B27 detected by cytotoxic T lymphocytes and their role in self-recognition
Human Immunology ·M.H. Breuning, C.J. Lucas, Birgitta S. Breur, Marc Y. Engelsma, Gerda G. de Lange, A. Dekker, William E. Biddison, Pavol Ivanyi
198280
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
200973
16
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, Jan Struck, Stephan J. L. Bakker
201270
17
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
199970
18
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. A. Wessels, JJ Saris, A. Hagemeijer, G.C. Beverstock, GJ van Ommen, M.H. Breuning
199269
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. A. Wessels, G.C. Beverstock, Hartmut Doehner, M Jotterand-Bellomo
199765
20
Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2
Hepatology ·Yves Pirson, N. Lannoy, Dorien J.M. Peters, A Geubel, J. F. Gigot, M.H. Breuning, C. Verellen‐Dumoulin
199664

About M.H. Breuning

M.H. Breuning is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 67 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genetic Syndromes and Imprinting (13 papers), Genetic and Kidney Cyst Diseases (12 papers), Chromosomal and Genetic Variations (7 papers), Renal and related cancers (7 papers), Prenatal Screening and Diagnostics (6 papers), Lysosomal Storage Disorders Research (5 papers) and Acute Myeloid Leukemia Research (5 papers). The work is most often cited by research in Developmental Biology (140 citations), Genetics (1.6k citations), Pathology and Forensic Medicine (464 citations), Molecular Biology (1.3k citations) and Pediatrics, Perinatology and Child Health (325 citations). M.H. Breuning has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Egbert Bakker, Dorien J.M. Peters, Jasper J. Saris, Juul Wijnen, Sarina G. Kant, Hans F. A. Vasen, Carli M.J. Tops, G.J.B. van Ommen, Raoul C. M. Hennekam and Hans Morreau. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, Hormone Research in Paediatrics, Nephrology Dialysis Transplantation and Blood.

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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