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Egbert Bakker

Active 1985–2023

81
Papers
17,964
Citations
78
h-index
81
i10-index

Citations

Citations per year for Egbert Bakker1960: 1 citations1985: 5 citations1986: 16 citations1987: 28 citations1988: 45 citations1989: 48 citations1990: 41 citations1991: 46 citations1992: 41 citations1993: 29 citations1994: 22 citations1995: 32 citations1996: 71 citations1997: 42 citations1998: 93 citations1999: 71 citations2000: 98 citations2001: 107 citations2002: 98 citations2003: 104 citations2004: 92 citations2005: 109 citations2006: 115 citations2007: 113 citations2008: 122 citations2009: 120 citations2010: 149 citations2011: 111 citations2012: 88 citations2013: 117 citations2014: 138 citations2015: 137 citations2016: 150 citations2017: 121 citations2018: 133 citations2019: 333 citations2020: 349 citations2021: 275 citations2022: 174 citations2023: 128 citations2024: 225 citations2025: 93 citations2026: 7 citations1961–1984: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,472 citing papers, 22.6% of this breakdownUnited Kingdom: 617 citing papers, 9.5% of this breakdownNetherlands: 487 citing papers, 7.5% of this breakdownFrance: 388 citing papers, 6% of this breakdownGermany: 372 citing papers, 5.7% of this breakdownItaly: 360 citing papers, 5.5% of this breakdownChina: 285 citing papers, 4.4% of this breakdownCanada: 237 citing papers, 3.7% of this breakdownJapan: 192 citing papers, 3% of this breakdownAustralia: 189 citing papers, 2.9% of this breakdownSpain: 184 citing papers, 2.8% of this breakdownSweden: 143 citing papers, 2.2% of this breakdown
0%22.6%Other 24.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology45.9%
  • Medicine32%
  • Engineering16.8%
  • Computer Science1.3%
  • Neuroscience1.2%
  • Agricultural and Biological Sciences1.1%
  • Other1.7%

Topics

  • Muscle Physiology and Disorders5.3%
  • Vehicle Dynamics and Control Systems4.8%
  • Genomic variations and chromosomal abnormalities2.5%
  • Genetic factors in colorectal cancer2.2%
  • Genomics and Rare Diseases2.1%
  • Alzheimer's disease research and treatments2%
  • Other81.1%

Coauthors

All papers

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  1. THE MAGIC FORMULA TYRE MODEL

    Authors: Hans B. Pacejka, Egbert Bakker - Vehicle System Dynamics 1992 cited by 1,293

  2. Population-based incidence and prevalence of facioscapulohumeral dystrophy

    Authors: 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 - Neurology 2014 cited by 387

  3. Tyre Modelling for Use in Vehicle Dynamics Studies

    Authors: Egbert Bakker, Lars Nyborg, Hans B. Pacejka - SAE technical papers on CD-ROM/SAE technical paper series 1987 cited by 927

  4. Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

    Authors: Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek, Judit Balog, Gregory J. Block, Gijs W.E. Santen, Amanda M. Amell, Patrick J. van der Vliet, Rowida Almomani, Kirsten R. Straasheijm, Yvonne D. Krom, Rinse Klooster, Yu Sun, Johan T. den Dunnen, Quinta Helmer, Colleen M. Donlin‐Smith, George W. Padberg, Baziel G.M. van Engelen, Jessica C. de Greef, Annemieke Aartsma‐Rus, Rune R. Frants, Marianne de Visser, Claude Desnuelle, Sabrina Sacconi, Galina N. Filippova, Egbert Bakker, Michael J. Bamshad, Stephen J. Tapscott, Daniel G. Miller, Silvère M. van der Maarel - Nature Genetics 2012 cited by 664

  5. Guidelines for diagnostic next-generation sequencing

    Authors: 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 - European Journal of Human Genetics 2015 cited by 519

  6. Erratum: Guidelines for diagnostic next-generation sequencing

    Authors: 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 - European Journal of Human Genetics 2016 cited by 425

  7. Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2

    Authors: Richard J.L.F. Lemmers, Jelle J. Goeman, Patrick J. van der Vliet, Merlijn P. van Nieuwenhuizen, Judit Balog, Marianne Vos-Versteeg, Pilar Camaño, María Antonia Ramos Arroyo, Ivonne Jericó, Mark T. Rogers, Daniel G. Miller, Meena Upadhyaya, Jan J.G.M. Verschuuren, Adolfo López de Munaín Arregui, Baziel G.M. van Engelen, George W. Padberg, Sabrina Sacconi, Rabi Tawil, Stephen J. Tapscott, Egbert Bakker, Silvère M. van der Maarel - Human Molecular Genetics 2014 cited by 166

  8. The FSHD2 Gene SMCHD1 Is a Modifier of Disease Severity in Families Affected by FSHD1

    Authors: Sabrina Sacconi, Richard J.L.F. Lemmers, Judit Balog, Patrick J. van der Vliet, Pauline Lahaut, Merlijn P. van Nieuwenhuizen, Kirsten R. Straasheijm, Rashmie D. Debipersad, Marianne Vos-Versteeg, Leonardo Salviati, Alberto Casarin, Elena Pegoraro, Rabi Tawil, Egbert Bakker, Stephen J. Tapscott, Claude Desnuelle, Silvère M. van der Maarel - The American Journal of Human Genetics 2013 cited by 189

  9. De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10

    Authors: Silvère M. van der Maarel, Giancarlo Deidda, Richard J.L.F. Lemmers, Petra G.M. van Overveld, Michiel van der Wielen, Jane Hewitt, Lodewijk A. Sandkuijl, Egbert Bakker, Gert‐Jan B. van Ommen, George W. Padberg, Rune R. Frants - The American Journal of Human Genetics 2000 cited by 167

  10. A New Tire Model with an Application in Vehicle Dynamics Studies

    Authors: Egbert Bakker, Hans B. Pacejka, Lars Lidner - SAE technical papers on CD-ROM/SAE technical paper series 1989 cited by 721

  11. Genome-wide association study identifies three loci associated with melanoma risk

    Authors: D. Timothy Bishop, Florence Démenais, Mark M. Iles, Mark Harland, John Taylor, Eve Corda, Juliette A. Randerson‐Moor, Joanne F. Aitken, Marie‐Françoise Avril, Esther Azizi, Egbert Bakker, Giovanna Bianchi‐Scarrà, Brigitte Bressac–de Paillerets, Donato Calista, Lisa Cannon‐Albright, Thomas F. C. Chin‐A‐Woeng, Tadeusz Dębniak, Gilli Galore-Haskel, Paola Ghiorzo, Marta Gut, Johan Hansson, Marko Hočevar, Veronica Höiom, John L. Hopper, Christian Ingvar, Peter A. Kanetsky, Richard Kefford, Maria Teresa Landi, Julie Lang, Jan Lubiński, Rona M. MacKie, Josep Malvehy, Graham J. Mann, Nicholas G. Martin, Grant W. Montgomery, Frans A. van Nieuwpoort, Srdjan Novaković, Håkan Olsson, Susana Puig, Marjan M. Weiss, Wilbert van Workum, Diana Zélénika, Kevin M Brown, Alisa M. Goldstein, Elizabeth M. Gillanders, Anne Boland, Pilar Galán, David E. Elder, Nelleke A. Gruis, Nicholas K. Hayward, G.M. Lathrop, Jennifer H. Barrett, Julia Newton‐Bishop - Nature Genetics 2009 cited by 464

  12. Risk of clozapine-associated agranulocytosis and mandatory white blood cell monitoring: Can the regulations be relaxed?

    Authors: Peter F.J. Schulte, Selene Veerman, Egbert Bakker, Jan Bogers, Amy Jongkind, Dan Cohen - Schizophrenia Research 2023 cited by 16

  13. A variant in FTO shows association with melanoma risk not due to BMI

    Authors: Juliette A. Randerson‐Moor, D. Timothy Bishop, John Taylor, Mark Harland, Mark M. Iles, Julia Newton‐Bishop, Helen Snowden, Jennifer H. Barrett, Nicholas K. Hayward, Nicholas G. Martin, Stuart MacGregor, Matthew H. Law, Simon Stacey, Patrick Sulem, Patrick Sulem, Kari Stefansson, Mingfeng Zhang, Fengju Song, Jiali Han, Jiali Han, Jiali Han, Shenying Fang, Christopher I. Amos, Maria Teresa Landi, Ruth M. Pfeiffer, Alisa M. Goldstein, Anne C de Waal, Lars A Akslen, Anders Molven, Marie-Françoise Avril, Esther Azizi, Anders Molven, Lars A. Akslen, Anders Molven, Lars A. Akslen, Marie-Françoise Avril, Esther Azizi, Esther Azizi, Eitan Friedman, Egbert Bakker, Nienke van der Stoep, Valérie Chaudru, Florence Demenais, G Mark Lathrop, Wilma Bergman, Nelleke A. Gruis, Giovanna Bianchi‐Scarrà, Paola Ghiorzo, Giovanna Bianchi‐Scarrà, Paola Ghiorzo, David E Elder, Donato Calista, Florence Démenais, Valérie Chaudru, Valérie Chaudru, Rainer Tuominen, Florence Démenais, Valérie Chaudru, Ketty Peris, Maria Concetta Fargnoli, Anne Ε. Cust, Florence Démenais, Michelle M. van Rossum, Peter A Kanetsky, Jan Lubiński, Tadeusz Dębniak, David E. Elder, Pilar Galán, Elizabeth M. Gillanders, Rainer Tuominen, Veronica Höiom, Johan Hansson, Per Helsing, Marko Hočevar, John L. Hopper, Mark A. Jenkins, Christian Ingvar, Suzanne Mulder, Marjolein J. F. W. Janssen, Peter A. Kanetsky, Peter A. Kanetsky, Hubert Pehamberger, Julie Lang, Diana Zélénika, Joan Anton Puig-Butille, Sancy A. Leachman, Jeffrey E. Lee, Rona M. MacKie, Graham J. Mann, Maria Pilar Grasa - Nature Genetics 2013 cited by 132

  14. Clozapine Underutilization in the Treatment of Schizophrenia

    Authors: Jan Bogers, Peter F.J. Schulte, D. van Dijk, Egbert Bakker, Dan Cohen - Journal of Clinical Psychopharmacology 2016 cited by 86

  15. Amyloid β Protein Precursor Gene and Hereditary Cerebral Hemorrhage with Amyloidosis (Dutch)

    Authors: Christine Van Broeckhoven, J. Haan, Egbert Bakker, John Hardy, Wim Van Hul, Anita Wehnert, M Vegter-van der Vlis, R. A. C. Roos - Science 1990 cited by 477

  16. Complete sequencing of TP53 predicts poor response to systemic therapy of advanced breast cancer.

    Authors: 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 - 2000 cited by 197

  17. Beyond White Blood Cell Monitoring

    Authors: Dan Cohen, Jan Bogers, D. van Dijk, Egbert Bakker, Peter F.J. Schulte - The Journal of Clinical Psychiatry 2012 cited by 142

  18. Facioscapulohumeral muscular dystrophy in the dutch population

    Authors: G.W. Padberg, Rune R. Frants, Oebele F. Brouwer, Cisca Wijmenga, Egbert Bakker, Lodewijk A. Sandkuijl - Muscle & Nerve 1995 cited by 122

  19. Acromegaly: the disease, its impact on patients, and managing the burden of long-term treatment

    Authors: Daphne T. Adelman, Liebert, Nachtigall, Lamerson, Egbert Bakker - International Journal of General Medicine 2013 cited by 76

  20. Calpainopathy—A Survey of Mutations and Polymorphisms

    Authors: I. Richard, Carinne Roudaut, Amets Sáenz, Robert Pogue, Joke Grimbergen, Louise V.B. Anderson, Cyriaque Beley, A.-M. Cobo, Chiappe Diego, B. Eymard, P. Gallano, H.B. Ginjaar, Adriana Lasa, C. Pollitt, Haluk Topaloğlu, J. Andoni Urtizberea, Marianne de Visser, Anneke J. van der Kooi, K. Bushby, Egbert Bakker, Adolfo López de Munaín, Michel Fardeau, J. Beckmann - The American Journal of Human Genetics 1999 cited by 206

  21. Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb)

    Authors: Ivy Jennes, Elena Pedrini, Monia Zuntini, Marina Mordenti, Sahila Balkassmi, Carla Asteggiano, Brett Casey, Egbert Bakker, Luca Sangiorgi, Wim Wuyts - Human Mutation 2009 cited by 199

  22. Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

    Authors: 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 - The American Journal of Human Genetics 1998 cited by 197

  23. Compliance and Persistence in Pediatric and Adult Patients Receiving Growth Hormone Therapy

    Authors: Ron G. Rosenfeld, Egbert Bakker - Endocrine Practice 2008 cited by 199

  24. Best Practice Guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies

    Authors: Stephen Abbs, Sylvie Tuffery‐Giraud, Egbert Bakker, Alessandra Ferlini, Thomas Sejersen, Clemens R. Mueller - Neuromuscular Disorders 2010 cited by 112