Eric Schoenmakers

7.1k total citations · 1 hit paper
76 papers, 5.2k citations indexed

About

Eric Schoenmakers is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Eric Schoenmakers has authored 76 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 27 papers in Genetics and 17 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Eric Schoenmakers's work include Genomic variations and chromosomal abnormalities (20 papers), Cancer Genomics and Diagnostics (10 papers) and Sarcoma Diagnosis and Treatment (10 papers). Eric Schoenmakers is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Cancer Genomics and Diagnostics (10 papers) and Sarcoma Diagnosis and Treatment (10 papers). Eric Schoenmakers collaborates with scholars based in Belgium, Netherlands and United States. Eric Schoenmakers's co-authors include Ad Geurts van Kessel, Joris A. Veltman, Irene M. Janssen, Erik Huys, Jörn Bullerdiek, Lisenka E.L.M. Vissers, Sylke Wanschura, Bert B.A. de Vries, Han G. Brunner and Raf Mols and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

In The Last Decade

Eric Schoenmakers

76 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

2004 876 citations Irene M. Janssen, Erik Huys et al. Nature Genetics profile →

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-authorship network of co-authors of Eric Schoenmakers

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Schoenmakers. A scholar is included among the top collaborators of Eric Schoenmakers based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eric Schoenmakers. Eric Schoenmakers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene‐dosage regulated candidate genes 2008 ·British Journal of Haematology ·Margit Schraders, Pedro Jares, Sı́lvia Beà, Eric Schoenmakers, J. Han van Krieken, Elı́as Campo, Patricia J.T.A. Groenen	21
2	Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Geert Poelmans, J.J.M. Engelen, (unknown), Hubert J.M. Smeets, Eric Schoenmakers, Barbara Franke, Jan K. Buitelaar, (unknown), (unknown), Jean Steyaert, C. T. R. M. Schrander‐Stumpel	63
3	Integrated Profiling of Basal and Luminal Breast Cancers 2007 ·Cancer Research ·José Adélaı̈de, Pascal Finetti, Ismahane Bekhouche, (unknown), 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	221
4	High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression 2007 ·Leukemia ·Roland P. Kuiper, Eric Schoenmakers, (unknown), Jayne Y. Hehir‐Kwa, Ad Geurts van Kessel, Frank N. van Leeuwen, Peter M. Hoogerbrugge	271
5	Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene 2007 ·Cancer Genetics and Cytogenetics ·(unknown), Lilian Vreede, Roland P. Kuiper, Daniëlle Bodmer, (unknown), Marc J. Eleveld, (unknown), Ger J. A. Arkesteijn, Nicoline Hoogerbrugge, Conny van Ravenswaaij, Eric Schoenmakers, Ad Geurts van Kessel	17
6	Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene 2006 ·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	170
7	XX male with sex reversal and a de novo 11;22 translocation 2006 ·American Journal of Medical Genetics Part A ·Merryn Macville, (unknown), (unknown), Erik Huys, Eric Schoenmakers, (unknown), Beverly S. Emanuel, J.J.M. Engelen	3
8	Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines 2005 ·Oncogene ·Gaia Roversi, Rolph Pfundt, Ramona Frida Moroni, Ivana Magnani, (unknown), Bianca Pollo, Huub Straatman, Lidia Larizza, Eric Schoenmakers	88
9	Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines 2004 ·Cancer Research ·Markus Heidenblad, Eric Schoenmakers, Tord Jonson, Ludmila Gorunova, Joris A. Veltman, Ad Geurts van Kessel, Mattias Höglund	73
10	Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies 2004 ·Cancer Genetics and Cytogenetics ·Montserrat González, Norma C. Gutiérrez, Juan Luis Garcı́a, Eric Schoenmakers, Françesc Solé, Marı́a José Calasanz, Jesús F. San Miguel, Jesús María Hernández‐Rivas	12
11	High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization 2002 ·The American Journal of Human Genetics ·Joris A. Veltman, Eric Schoenmakers, Bert H.J. Eussen, Irene M. Janssen, Gerard Merkx, (unknown), (unknown), Han G. Brunner, Dominique Smeets, Ad Geurts van Kessel	167
12	Cumulative dosage effect of a RAD51l1/HMGA2 fusion and RAD51l1 loss in a case of pseudo‐Meigs' syndrome 2001 ·Genes Chromosomes and Cancer ·Frédéric Amant, Maria Dêbiec‐Rychter, Eric Schoenmakers, (unknown), Ignace Vergote	11
13	Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors 2001 ·Genes Chromosomes and Cancer ·Maria Dêbiec‐Rychter, Raf Sciot, Patrick Pauwels, Eric Schoenmakers, Paola Dal Cin, Anne Hagemeijer	38
14	Deletion 7q in Uterine Leiomyoma 1999 ·Cancer Genetics and Cytogenetics ·Roberta Vanni, Eric Schoenmakers, (unknown)	8
15	Complex genomic rearrangement within the 12q15 multiple aberration region induced by integrated human papillomavirus 18 in a cervical carcinoma cell line 1997 ·Molecular Carcinogenesis ·Marta I. Gallego, Eric Schoenmakers, Wim J.M. Van de Ven, Pedro A. Lazo	16
16	Genomic Organization of the HumanNSPGene, Prototype of a Novel Gene Family Encoding Reticulons 1996 ·Genomics ·Anton Roebroek, Torik Ayoubi, Helgi J. K. van de Velde, Eric Schoenmakers, Ilse G.L. Pauli, Wim J.M. Van de Ven	34
17	Mapping of the translocation breakpoints of primary pleomorphic adenomas and lipomas within a common region of chromosome 12 1996 ·Cancer Genetics and Cytogenetics ·Sylke Wanschura, Gazanfer Belge, Göran Stenman, Patrick Kools, Paola Dal Cin, Eric Schoenmakers, C. Huysmans, (unknown), (unknown), Wim J.M. Van de Ven, Jörn Bullerdiek	15
18	Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours 1995 ·Nature Genetics ·Eric Schoenmakers, Sylke Wanschura, Raf Mols, Jörn Bullerdiek, Herman Van den Berghe, Wim J.M. Van de Ven	475
19	Molecular-cytogenetic refinement of the 12q14→q15 breakpoint region affected in uterine leiomyomas 1995 ·Cytogenetic and Genome Research ·Sylke Wanschura, Yvonne Hennig, U. Deichert, Eric Schoenmakers, Wim J.M. Van de Ven, Sabine Bartnitzke, Jörn Bullerdiek	6
20	Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas 1994 ·Genes Chromosomes and Cancer ·Eric Schoenmakers, Raf Mols, Sylke Wanschura, Patrick Kools, Jan M.W. Geurts, Sabine Bartnitzke, Jörn Bullerdiek, (unknown), (unknown)	33

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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