Egbert Bakker

20.0k citations
246 papers · 12.3k · h-index 62

Impact in

  • Genetics top 0.2%
    • Neurogenetic and Muscular Disorders Research
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • BRCA gene mutations in cancer
  • Molecular Biology top 0.5%
    • Muscle Physiology and Disorders

Papers in

  • Molecular Biology 130
    • Muscle Physiology and Disorders 64
  • Genetics 67
    • Genomic variations and chromosomal abnormalities 26
    • Neurogenetic and Muscular Disorders Research 25
    • Genetics and Neurodevelopmental Disorders 17
Co-authors
P. Pearson (24 shared papers)Johan T. den Dunnen (35 shared papers)Manuela Simoni (3 shared papers)G.J.B. van Ommen (21 shared papers)Ron G. Rosenfeld (7 shared papers)Christine Van Broeckhoven (9 shared papers)Csilla Krausz (1 shared paper)Martin C. Wapenaar (6 shared papers)
Journals
Journal of Medical Genetics (18 papers)European Journal of Human Genetics (13 papers)Human Genetics (12 papers)Human Mutation (11 papers)Neuromuscular Disorders (10 papers)
Partner nations
NetherlandsUnited StatesUnited Kingdom

In The Last Decade

Egbert Bakker

243 papers receiving 11.9k citations

Peers

Egbert Bakker
Comparison fields: 5 of 151
  • Genetics 3.7k
  • Genetics 1.2k
  • Molecular Biology 6.5k
  • Endocrinology, Diabetes and Metabolism 889
  • Reproductive Medicine 451
Replace Elaine Spector with:
Elaine Spector United States
Sue Richards United Kingdom
Nazneen Aziz United States
Elaine Lyon United States
David Bick United States
Julie M. Gastier‐Foster United States
Madhuri Hegde United States
Sherri J. Bale United States
P. Pearson Netherlands
Gert Matthijs Belgium
Egbert Bakker relative to Elaine Spector United States Elaine Spector's profile →
Citations per field
00.5×1.5×2.0×
Elaine Spector · 1×
Citations per year

Countries citing papers authored by Egbert Bakker

Since Specialization
Citations

This map shows the geographic impact of Egbert Bakker'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 Egbert Bakker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Egbert Bakker more than expected).

Fields of papers citing papers by Egbert Bakker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Egbert Bakker. 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 Egbert Bakker. The network helps show where Egbert Bakker may publish in the future.

Co-authors

The 25 scholars most cited alongside Egbert Bakker, 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 Egbert Bakker Line = papers co-authored together Egbert Bakker links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 246 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.
PubMed ·Johan T. den Dunnen, P.M. Grootscholten, Egbert Bakker, Lau A.J. Blonden, H.B. Ginjaar, Martin C. Wapenaar, H M van Paassen, Christine Van Broeckhoven, P. Pearson, G J van Ommen
1989438
2
EAA/EMQN best practice guidelines for molecular diagnosis of y‐chromosomal microdeletions. State of the art 2004
International Journal of Andrology ·Manuela Simoni, Egbert Bakker, Csilla Krausz
2004378
3
Amyloid β Protein Precursor Gene and Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch)
Science ·Christine Van Broeckhoven, J. Haan, Egbert Bakker, John Hardy, Wim Van Hul, Anita Wehnert, M Vegter-van der Vlis, R. A. C. Roos
1990352
4
Guidelines for diagnostic next-generation sequencing
European Journal of Human Genetics ·Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik A. Sistermans, Marc Sturm, Marjan M. Weiss, Helger G. Yntema, Egbert Bakker, Hans Scheffer, Peter Bauer
2015342
5
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
Nature Genetics ·Anne Petrij-Bosch, Tamara Peelen, Margreethe van Vliet, Ronald van Eijk, Renske Olmer, Marion Drüsedau, Frans B.L. Hogervorst, S. Hageman, Petronella J.W. Arts, Marjolijn J. L. Ligtenberg, Hanne Meijers-Heijboer, Jan G.M. Klijn, Hans F. A. Vasen, Cees J. Cornelisse, Laura J. van’t Veer, Egbert Bakker, Gert‐Jan B. van Ommen, Peter Devilee
1997320
6
PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
The Lancet ·Egbert Bakker, Nicole Goor, Klaus Wrogemann, Louis M. Kunkel, Wayne A. Fenton, Daniëlle Majoor‐Krakauer, M. G. J. Jahoda, G.J.B. van Ommen, Marten H. Hofker, Jean‐Louis Mandel, Kay E. Davies, H.F. Willard, L. A. Sandkuyl, A.J. van Essen, E. S. Sachs, P. Pearson
1985284
7
Population-based incidence and prevalence of facioscapulohumeral dystrophy
Neurology ·Johanna C.W. Deenen, Hisse Arnts, Silvère M. van der Maarel, George W. Padberg, Jan J.G.M. Verschuuren, Egbert Bakker, Stephanie S. Weinreich, André L. M. Verbeek, Baziel G.M. van Engelen
2014271
8
Rapid detection of BRCA1 mutations by the protein truncation test
Nature Genetics ·Frans B.L. Hogervorst, Renée S. Cornelis, Mattie Bout, Margreethe van Vliet, Jan C. Oosterwijk, Renske Olmer, Egbert Bakker, Jan G.M. Klijn, Hans F. A. Vasen, Hanna Meijers-Heijboer, Fred H. Menko, Cees J. Cornelisse, Johan T. den Dunnen, Peter Devilee, Gert‐Jan B. van Ommen
1995251
9
Estimating Y Chromosome Specific Microsatellite Mutation Frequencies using Deep Rooting Pedigrees
Human Molecular Genetics ·Évelyne Heyer, Jack Puymirat, Patrick Dieltjes, Egbert Bakker, Peter de Knijff
1997201
10
Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy
Human Genetics ·Marten H. Hofker, Martin C. Wapenaar, Nicole Goor, Egbert Bakker, G.J.B. van Ommen, P. Pearson
1985194
11
Laboratory guidelines for molecular diagnosis of Y‐chromosomal microdeletions
International Journal of Andrology ·Manuela Simoni, Egbert Bakker, Eurlings, Gert Matthijs, Enrico Moro, Müller, Vogt Vogt
1999191
12
Compliance and Persistence in Pediatric and Adult Patients Receiving Growth Hormone Therapy
Endocrine Practice ·Ron G. Rosenfeld, Egbert Bakker
2008173
13
Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene Mutations
The American Journal of Human Genetics ·Juul Wijnen, P. Meera Khan, Hans F. A. Vasen, Heleen van der Klift, Adri Mulder, Inge van Leeuwen‐Cornelisse, Egbert Bakker, Monique Losekoot, Pål Møller, Riccardo Fodde
1997171
14
Duchenne muscular dystrophy
Neurology ·Richard J. Bartlett, Margaret A. Pericak‐Vance, Jin‐Young Koh, Larry H. Yamaoka, J. C. Chen, Wu-Yen Hung, Marcy C. Speer, Martin C. Wapenaar, G.J.B. van Ommen, Egbert Bakker, P. Pearson, R.S. Kandt, Teepu Siddique, J. R. Gilbert, Judith Lee, Marcia Sirotkin-roses, Allen D. Roses
1988170
15
Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study
The Lancet ·EM Hoogerwaard, Egbert Bakker, PF Ippel, JC Oosterwijk, DF Majoor‐Krakauer, NJ Leschot, AJ Van Essen, HG Brunner, PA van der Wouw, AAM Wilde, Marjolein Visser
1999166
16
Complete sequencing of TP53 predicts poor response to systemic therapy of advanced breast cancer.
PubMed ·E. Berns, John A. Foekens, R. van Vossen, Maxime P. Look, Peter Devilee, S.C. Henzen‐Logmans, Iris L. van Staveren, Wim L.J. van Putten, Mats Inganäs, Marion E. Meijer‐van Gelder, Cees J. Cornelisse, Cassandra J.C. Claassen, Henk Portengen, Egbert Bakker, J.G.M. Klijn
2000162
17
An Extensive Analysis of Y-Chromosomal Microsatellite Haplotypes in Globally Dispersed Human Populations
The American Journal of Human Genetics ·Manfred Kayser, Michael Krawczak, Laurent Excoffier, Patrick Dieltjes, Daniel Corach, Vincente Pascali, Christian Gehrig, Luigi F. Bernini, Jørgen Jespersen, Egbert Bakker, Lutz Roewer, Peter de Knijff
2001158
18
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels
Nature ·Johan T. den Dunnen, Egbert Bakker, E. G. Klein Breteler, P. Pearson, G.J.B. van Ommen
1987157
19
Germline mosaicism and Duchenne muscular dystrophy mutations
Nature ·Egbert Bakker, Christine Van Broeckhoven, E. J. Bonten, M. J. van de Vooren, H Veenema, Wim Van Hul, G.J.B. van Ommen, A. Vandenberghe, P. Pearson
1987155
20
Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses
The American Journal of Human Genetics ·Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, Florindo Mollica, Hermann‐Josef Lüdecke, Bekir Sıtkı Şaylı, Ugo E. Pazzaglia, Geert Mortier, B Hamel, Ernest U. Conrad, Mark Matsushita, W H Raskind, P J Willems
1998155

About Egbert Bakker

Egbert Bakker is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine, having authored 246 papers that have together received 12.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (64 papers), Genetic Neurodegenerative Diseases (27 papers), Genomic variations and chromosomal abnormalities (26 papers), Neurogenetic and Muscular Disorders Research (25 papers), Cardiomyopathy and Myosin Studies (23 papers), Growth Hormone and Insulin-like Growth Factors (18 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (15 papers). The work is most often cited by research in Genetics (3.7k citations), Genetics (1.2k citations), Molecular Biology (6.5k citations), Endocrinology, Diabetes and Metabolism (889 citations) and Reproductive Medicine (451 citations). Egbert Bakker has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include P. Pearson, Johan T. den Dunnen, Manuela Simoni, G.J.B. van Ommen, Ron G. Rosenfeld, Christine Van Broeckhoven, Csilla Krausz, Martin C. Wapenaar, Wim Van Hul and Marten H. Hofker. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Human Genetics, Human Mutation and Neuromuscular Disorders.

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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