Eric Schoenmakers

7.1k citations
76 papers · 5.2k · 1 hit paper · h-index 34

Impact in

  • Genetics top 0.5%
    • Genomic variations and chromosomal abnormalities
    • Congenital Ear and Nasal Anomalies
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
  • Cancer Research top 2%

Papers in

  • Molecular Biology 37
    • Renal and related cancers 8
    • Genomics and Chromatin Dynamics 7
  • Genetics 26
    • Genomic variations and chromosomal abnormalities 19
Co-authors
Ad Geurts van Kessel (23 shared papers)Joris A. Veltman (12 shared papers)Irene M. Janssen (10 shared papers)Erik Huys (9 shared papers)Lisenka E.L.M. Vissers (5 shared papers)Jörn Bullerdiek (13 shared papers)Sylke Wanschura (11 shared papers)Bert B.A. de Vries (3 shared papers)
Journals
Genes Chromosomes and Cancer (13 papers)The American Journal of Human Genetics (6 papers)Genomics (5 papers)Oncogene (4 papers)Cancer Research (3 papers)
Partner nations
BelgiumNetherlandsUnited States

In The Last Decade

Eric Schoenmakers

75 papers receiving 5.0k citations

Eric Schoenmakers's Hit Papers

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome 2004 · 881 citations
8810+7+14Years since publication250500750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2004 Nature Genetics

Peers

Eric Schoenmakers
Comparison fields: 5 of 106
  • Genetics 1.9k
  • Genetics 697
  • Cancer Research 601
  • Reproductive Medicine 274
  • Obstetrics and Gynecology 227
Replace Marc Jeanpierre with:
Marc Jeanpierre France
Philippe Jonveaux France
Maurizio Genuardi Italy
Jan P. Dumanski Sweden
Vladimir Joukov Finland
Daniel L. Van Dyke United States
David Gisselsson Sweden
Malek Faham United States
Sahar Mansour United Kingdom
Pamela A. Hoodless Canada
Eric Schoenmakers relative to Marc Jeanpierre France Marc Jeanpierre's profile →
Citations per field
00.5×2×4×6×7.6×
Marc Jeanpierre · 1×
Citations per year

Countries citing papers authored by Eric Schoenmakers

Since Specialization
Citations

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

Fields of papers citing papers by Eric Schoenmakers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 76 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
Nature Genetics ·Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij, R.J.C. Admiraal, Jane A. Hurst, Bert B.A. de Vries, Irene M. Janssen, W A van der Vliet, Erik Huys, Pieter J. de Jong, Ben C.J. Hamel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman, Ad Geurts van Kessel
Hit paper breakdown →		2004881
2
Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours
Nature Genetics ·Eric Schoenmakers, Sylke Wanschura, Raf Mols, Jörn Bullerdiek, Herman Van den Berghe, Wim J.M. Van de Ven
1995475
3
Diagnostic Genome Profiling in Mental Retardation
The American Journal of Human Genetics ·Bert B.A. de Vries, Rolph Pfundt, M.A.R. Leisink, David A. Koolen, Lisenka E.L.M. Vissers, Irene M. Janssen, Simon V. van Reijmersdal, Willy M. Nillesen, Erik Huys, Nicole de Leeuw, Dominique Smeets, Erik A. Sistermans, Ton Feuth, Conny M.A. van Ravenswaaij‐Arts, Ad Geurts van Kessel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman
2005413
4
Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities
The American Journal of Human Genetics ·Lisenka E.L.M. Vissers, Bert B.A. de Vries, Kazutoyo Osoegawa, Irene M. Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik Huys, Anke van Rijk, Dominique Smeets, Conny M.A. van Ravenswaaij‐Arts, Nine V.A.M. Knoers, Ineke van der Burgt, Pieter J. de Jong, Han G. Brunner, Ad Geurts van Kessel, Eric Schoenmakers, Joris A. Veltman
2003348
5
High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression
Leukemia ·Roland P. Kuiper, Eric Schoenmakers, S V van Reijmersdal, Jayne Y. Hehir‐Kwa, Ad Geurts van Kessel, Frank N. van Leeuwen, Peter M. Hoogerbrugge
2007271
6
Integrated Profiling of Basal and Luminal Breast Cancers
Cancer Research ·José Adélaı̈de, Pascal Finetti, Ismahane Bekhouche, Laetitia Repellini, Jeannine Geneix, Fabrice Sircoulomb, Emmanuelle Charafe‐Jauffret, Nathalie Cervera, Jérôme Desplans, Daniel Parzy, Eric Schoenmakers, Patrice Viens, J Jacquemier, Daniel Birnbaum, François Bertucci, Max Chaffanet
2007222
7
Selective DNA binding by the androgen receptor as a mechanism for hormone-specific gene regulation
The Journal of Steroid Biochemistry and Molecular Biology ·Frank Claessens, Guy Verrijdt, Eric Schoenmakers, Annemie Haelens, Benjamin Peeters, Guido Verhoeven, W. Rombauts
2001173
8
Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene
Cancer Research ·Leendert H. J. Looijenga, Remko Hersmus, Ad Gillis, Rolph Pfundt, Hans Stoop, Ruud J. H. L. M. van Gurp, Joris A. Veltman, H. Berna Beverloo, Ellen van Drunen, Ad Geurts van Kessel, Renee A. Reijo Pera, Dominik T. Schneider, Brenda Summersgill, Janet Shipley, Alan McIntyre, Peter J. van der Spek, Eric Schoenmakers, J. Wolter Oosterhuis
2006171
9
High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization
The American Journal of Human Genetics ·Joris A. Veltman, Eric Schoenmakers, Bert H.J. Eussen, Irene M. Janssen, Gerard Merkx, Brigitte van Cleef, Conny Ma van Ravenswaaij, Han G. Brunner, Dominique Smeets, Ad Geurts van Kessel
2002167
10
Identification of Tumor-Specific Molecular Signatures in Intracranial Ependymoma and Association With Clinical Characteristics
Journal of Clinical Oncology ·Piergiorgio Modena, Elena Lualdi, Federica Facchinetti, Joris A. Veltman, James F. Reid, Simone P. Minardi, Irene M. Janssen, Felice Giangaspero, Marco Forni, Gaetano Finocchiaro, Lorenzo Genitori, Flavio Giordano, Riccardo Riccardi, Eric Schoenmakers, Maura Massimino, Gabriella Sozzi
2006157
11
Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene
The American Journal of Human Genetics ·Ludovica Volpi, Gaia Roversi, Elisa Adele Colombo, Nico Leijsten, Daniela Concolino, Andrea Calabria, Maria Antonietta Mencarelli, Michele Fimiani, Fabìo Macciardi, Rolph Pfundt, Eric Schoenmakers, Lidia Larizza
2009108
12
Role of gain of 12p in germ cell tumour development
Apmis ·Leendert H. J. Looijenga, Gaetano Zafarana, Beata Grygalewicz, Brenda Summersgill, Maria Dêbiec‐Rychter, Joris A. Veltman, Eric Schoenmakers, Sandrine Rodriguez, Osman Jafer, Jeremy Clark, Ad Geurts van Kessel, Janet Shipley, Ruud J. H. L. M. van Gurp, Ad Gillis, J. Wolter Oosterhuis
2003105
13
Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines
Oncogene ·Gaia Roversi, Rolph Pfundt, Ramona Frida Moroni, Ivana Magnani, S V van Reijmersdal, Bianca Pollo, Huub Straatman, Lidia Larizza, Eric Schoenmakers
200589
14
Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH
The American Journal of Human Genetics ·Joris A. Veltman, Yvonne M.H. Versleijen‐Jonkers, Inge Nuijten, Irene M. Janssen, Walter van der Vliet, Erik Huys, Joris Vermeesch, Griet Van Buggenhout, Jean‐Pierre Fryns, R.J.C. Admiraal, Paulien A. Terhal, Didier Lacombe, Ad Geurts van Kessel, Dominique Smeets, Eric Schoenmakers, Conny M.A. van Ravenswaaij‐Arts
200383
15
Microarray analyses reveal strong influence of DNA copy number alterations on the transcriptional patterns in pancreatic cancer: implications for the interpretation of genomic amplifications
Oncogene ·Markus Heidenblad, David Lindgren, Joris A. Veltman, Tord Jonson, Eija Mahlamäki, Ludmila Gorunova, Ad Geurts van Kessel, Eric Schoenmakers, Mattias Höglund
200582
16
HMGIC, the gene for an architectural transcription factor, is amplified and rearranged in a subset of human sarcomas
Oncogene ·Jeanne-Marie Berner, Leonardo A. Meza‐Zepeda, Patrick Kools, Anne Forus, Eric Schoenmakers, Wim JM Van de Ven, Øystein Fodstad, Ola Myklebost
199779
17
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation
Journal of Medical Genetics ·Kazutoyo Osoegawa, Gery M. Vessere, Kagistia Hana Utami, M. Adela Mansilla, Marla Johnson, (unknown), Jamie L’Heureux, Rolph Pfundt, Johan Staaf, W A van der Vliet, Andrew C. Lidral, Eric Schoenmakers, Åke Borg, Brian C. Schutte, Edward J. Lammer, Jeffrey C. Murray, Pieter J. de Jong
200776
18
Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines
Cancer Research ·Markus Heidenblad, Eric Schoenmakers, Tord Jonson, Ludmila Gorunova, Joris A. Veltman, Ad Geurts van Kessel, Mattias Höglund
200473
19
Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion
American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Geert Poelmans, J.J.M. Engelen, JCM Van Lent‐Albrechts, Hubert J.M. Smeets, Eric Schoenmakers, Barbara Franke, Jan K. Buitelaar, Mea G.F. Wuisman-Frerker, W. Erens, Jean Steyaert, C. T. R. M. Schrander‐Stumpel
200863
20
12p-Amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH
Oncogene ·Gaetano Zafarana, Beata Grygalewicz, Ad Gillis, Lisenka E.L.M. Vissers, Walter van de Vliet, Ruud J. H. L. M. van Gurp, Hans Stoop, Maria Dêbiec‐Rychter, Jan Wolter Oosterhuis, Ad Geurts van Kessel, Eric Schoenmakers, Leendert H. J. Looijenga, Joris A. Veltman
200358

About Eric Schoenmakers

Eric Schoenmakers is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Pathology and Forensic Medicine and Oncology, having authored 76 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Sarcoma Diagnosis and Treatment (9 papers), Cancer Genomics and Diagnostics (9 papers), Uterine Myomas and Treatments (9 papers), Renal and related cancers (8 papers), Chromosomal and Genetic Variations (8 papers), Genomics and Chromatin Dynamics (7 papers) and Lymphoma Diagnosis and Treatment (6 papers). The work is most often cited by research in Genetics (1.9k citations), Genetics (697 citations), Cancer Research (601 citations), Reproductive Medicine (274 citations) and Obstetrics and Gynecology (227 citations). Eric Schoenmakers has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Ad Geurts van Kessel, Joris A. Veltman, Irene M. Janssen, Erik Huys, Lisenka E.L.M. Vissers, Jörn Bullerdiek, Sylke Wanschura, Bert B.A. de Vries, Han G. Brunner and Raf Mols. Their work appears in journals such as Genes Chromosomes and Cancer, The American Journal of Human Genetics, Genomics, Oncogene and Cancer 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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