Eric Schoenmakers

7.1k citations

82 papers · 5.8k · 1 hit paper · h-index 34

Impact in

Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Genomics and Rare Diseases
Obstetrics and Gynecology top 2%
- Uterine Myomas and Treatments

Papers in

Genetics 37
- Genomic variations and chromosomal abnormalities 32
Obstetrics and Gynecology 10
- Uterine Myomas and Treatments 10

Co-authors: Ad Geurts van Kessel (26 shared papers)Joris Andre Veltman (12 shared papers)Irene M. Janssen (10 shared papers)Conny M.A. van Ravenswaaij‐Arts (7 shared papers)Erik Huys (11 shared papers)Han G. Brunner (4 shared papers)Lisenka E.L.M. Vissers (5 shared papers)de Vries Bj (3 shared papers)
Journals: Genes Chromosomes and Cancer (13 papers)The American Journal of Human Genetics (6 papers)Genomics (5 papers)Oncogene (4 papers)Leukemia (3 papers)
Partner nations: Belgium Netherlands Germany

In The Last Decade

Eric Schoenmakers

81 papers receiving 5.5k citations

Eric Schoenmakers's Hit Papers

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome 2004 · 1k citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2004 Nature Genetics

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 82 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‐Arts, Ronald J C Admiraal, Jane A. Hurst, de Vries Bj, Irene M. Janssen, W A van der Vliet, Erik Huys Hit paper breakdown →	2004	1019
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	1995	496
3	Diagnostic Genome Profiling in Mental Retardation The American Journal of Human Genetics ·de Vries Bj, Rolph Pfundt, M.A.R. Leisink, David A. Koolen, Lisenka E.L.M. Vissers, Irene M. Janssen, Simon V. van Reijmersdal, Willy M. Nillesen	2005	481
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, de Vries Bj, Kazutoyo Osoegawa, Irene M. Janssen, Ton B. Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet	2003	378
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, Simon V. van Reijmersdal, Jayne Y. Hehir‐Kwa, Ad Geurts van Kessel, Frank N. van Leeuwen, Peter M. Hoogerbrugge	2007	308
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	2007	244
7	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 Andre Veltman, H. B. Beverloo	2006	187
8	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	2001	180
9	High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization The American Journal of Human Genetics ·Joris Andre Veltman, Eric Schoenmakers, Bert H.J. Eussen, Irene M. Janssen, Gerard F. M. Merkx, Brigitte van Cleef, Conny M.A. van Ravenswaaij‐Arts, Han G. Brunner	2002	174
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 Andre Veltman, James F. Reid, Simone Paolo Minardi, Irene M. Janssen, Felice Giangaspero	2006	169
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	2009	127
12	Role of gain of 12p in germ cell tumour development Apmis ·Leendert H. J. Looijenga, Gaetano Zafarana, Beata Grygalewicz, Brenda M. Summersgill, Maria Dêbiec‐Rychter, Joris Andre Veltman, Eric Schoenmakers, Sandrine Rodriguez	2003	118
13	Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH The American Journal of Human Genetics ·Joris Andre Veltman, Yvonne M.H. Versleijen‐Jonkers, Inge Nuijten, Irene M. Janssen, Walter van der Vliet, Erik Huys, Joris Robert Vermeesch, Griet Van Buggenhout	2003	97
14	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, Simon V. van Reijmersdal, Bianca Pollo, Huub Straatman, Lidia Larizza	2005	91
15	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	1997	84
16	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 Andre Veltman, Tord Jonson, Eija Mahlamäki, Ludmila Gorunova, Ad Geurts van Kessel, Eric Schoenmakers	2005	84
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, Maria Adela Mansilla, Marla K. Johnson, Bridget M. Riley-Gillis, Jamie L’Heureux, Rolph Pfundt	2007	81
18	Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome Leukemia ·Marjolijn C.J. Jongmans, Roland P. Kuiper, Catherine Carmichael, Ella Jane Wilkins, Natasja Dors, Amandine Carmagnac, Antoinette Y. N. Schouten‐van Meeteren, Eveline J. Kamping	2009	80
19	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 Andre Veltman, Ad Geurts van Kessel, Mattias Höglund	2004	77
20	Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Geert Poelmans, John J.M. Engelen, J.C.M. Albrechts, Hubert J.M. Smeets, Eric Schoenmakers, Barbara Franke, Jan K. Buitelaar, Mea G.F. Wuisman-Frerker	2008	66

About Eric Schoenmakers

Eric Schoenmakers is a scholar working on Genetics, Obstetrics and Gynecology, Pulmonary and Respiratory Medicine, Pathology and Forensic Medicine and Genetics, having authored 82 papers that have together received 5.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Uterine Myomas and Treatments (10 papers), Sarcoma Diagnosis and Treatment (7 papers), Renal cell carcinoma treatment (7 papers), Lymphoma Diagnosis and Treatment (6 papers), Testicular diseases and treatments (4 papers), Acute Myeloid Leukemia Research (3 papers) and Genomics and Chromatin Dynamics (3 papers). The work is most often cited by research in Genetics (2k citations), Genetics (508 citations), Obstetrics and Gynecology (288 citations), Cancer Research (293 citations) and Pulmonary and Respiratory Medicine (523 citations). Eric Schoenmakers has collaborated with scholars based in Belgium, Netherlands and Germany. Frequent co-authors include Ad Geurts van Kessel, Joris Andre Veltman, Irene M. Janssen, Conny M.A. van Ravenswaaij‐Arts, Erik Huys, Han G. Brunner, Lisenka E.L.M. Vissers, de Vries Bj, Jörn Bullerdiek and Sylke Wanschura. Their work appears in journals such as Genes Chromosomes and Cancer, The American Journal of Human Genetics, Genomics, Oncogene and Leukemia.

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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In The Last Decade

Eric Schoenmakers

Eric Schoenmakers's Hit Papers

Peers

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Fields of papers citing papers by Eric Schoenmakers

All Works

About Eric Schoenmakers

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