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 sort by overperformance

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 R.J.C. Admiraal, Irene M. Janssen et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Eric Schoenmakers	2.5k	2.1k	977	748	705	76	5.2k
Jan P. Dumanski	3.6k 1.5×	2.0k 1.0×	1.3k 1.3×	690 0.9×	931 1.3×	146	7.4k
Lies H. Hoefsloot	3.7k 1.5×	1.7k 0.8×	1.0k 1.0×	1.1k 1.5×	279 0.4×	136	6.6k
David Gisselsson	2.7k 1.1×	966 0.5×	1.0k 1.1×	380 0.5×	1.4k 2.0×	151	5.0k
Athena M. Cherry	2.2k 0.9×	1.3k 0.6×	396 0.4×	512 0.7×	322 0.5×	81	4.7k
Laurence Faivre	2.6k 1.1×	3.3k 1.6×	1.4k 1.4×	344 0.5×	618 0.9×	215	6.3k
Daniel L. Van Dyke	1.8k 0.7×	1.9k 0.9×	271 0.3×	1.4k 1.8×	416 0.6×	183	4.7k
Dominique Smeets	2.6k 1.1×	2.7k 1.3×	439 0.4×	219 0.3×	658 0.9×	112	4.9k
Ludwine Messiaen	2.2k 0.9×	932 0.4×	892 0.9×	213 0.3×	397 0.6×	145	5.0k
John R.W. Yates	2.2k 0.9×	1.5k 0.7×	563 0.6×	162 0.2×	925 1.3×	82	5.4k
Marc Jeanpierre	3.8k 1.5×	1.3k 0.6×	547 0.6×	366 0.5×	242 0.3×	120	4.7k

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

Lira, Maruja E., Tae Min Kim, Donghui Huang, et al.. (2012). Multiplexed Gene Expression and Fusion Transcript Analysis to Detect ALK Fusions in Lung Cancer. Journal of Molecular Diagnostics. 15(1). 51–61. 57 indexed citations

Volpi, Ludovica, Gaia Roversi, Elisa Adele Colombo, et al.. (2010). Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene. The American Journal of Human Genetics. 87(3). 445–445. 2 indexed citations

Volpi, Ludovica, Gaia Roversi, Elisa Adele Colombo, et al.. (2009). Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene. The American Journal of Human Genetics. 86(1). 72–76. 108 indexed citations

Kuiper, Roland P., Lilian Vreede, Ramprasath Venkatachalam, et al.. (2009). The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer. Cancer Genetics and Cytogenetics. 195(2). 105–111. 22 indexed citations

Schraders, Margit, Pedro Jares, Sı́lvia Beà, et al.. (2008). Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene‐dosage regulated candidate genes. British Journal of Haematology. 143(2). 210–221. 21 indexed citations

Woldringh, G.H., Irene M. Janssen, Jayne Y. Hehir‐Kwa, et al.. (2008). Constitutional DNA copy number changes in ICSI children. Human Reproduction. 24(1). 233–240. 7 indexed citations

Adélaı̈de, José, Pascal Finetti, Ismahane Bekhouche, et al.. (2007). Integrated Profiling of Basal and Luminal Breast Cancers. Cancer Research. 67(24). 11565–11575. 221 indexed citations

Looijenga, Leendert H. J., Remko Hersmus, Ad Gillis, et al.. (2006). Genomic and Expression Profiling of Human Spermatocytic Seminomas: Primary Spermatocyte as Tumorigenic Precursor and DMRT1 as Candidate Chromosome 9 Gene. Cancer Research. 66(1). 290–302. 170 indexed citations

Macville, Merryn, et al.. (2006). XX male with sex reversal and a de novo 11;22 translocation. American Journal of Medical Genetics Part A. 140A(18). 1973–1977. 3 indexed citations

10.

Heidenblad, Markus, David Lindgren, Joris A. Veltman, et al.. (2005). 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. 24(10). 1794–1801. 82 indexed citations

11.

Heidenblad, Markus, Eric Schoenmakers, Tord Jonson, et al.. (2004). Genome-Wide Array-Based Comparative Genomic Hybridization Reveals Multiple Amplification Targets and Novel Homozygous Deletions in Pancreatic Carcinoma Cell Lines. Cancer Research. 64(9). 3052–3059. 73 indexed citations

12.

Veltman, Joris A., Yvonne M.H. Versleijen‐Jonkers, Irene M. Janssen, et al.. (2003). Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH. The American Journal of Human Genetics. 72(6). 1578–1584. 83 indexed citations

13.

Belge, Gazanfer, et al.. (2003). Does conventional cytogenetics detect the real frequency of 19q13 aberrations in benign thyroid lesions? A survey of 38 cases. Cancer Genetics and Cytogenetics. 146(1). 70–72. 3 indexed citations

14.

Amant, Frédéric, et al.. (2001). Cumulative dosage effect of a RAD51l1/HMGA2 fusion and RAD51l1 loss in a case of pseudo‐Meigs' syndrome. Genes Chromosomes and Cancer. 32(4). 324–329. 11 indexed citations

15.

Claessens, Frank, Inge Vercaeren, Guy Verrijdt, et al.. (1998). Androgen-Regulated Transcription in the Epithelium of the Rat Lacrimal Gland. Advances in experimental medicine and biology. 438. 43–48. 4 indexed citations

16.

Frints, Suzanna G.M., et al.. (1998). De novo 7q36 deletion: Breakpoint analysis and types of holoprosencephaly. American Journal of Medical Genetics. 75(2). 153–158. 23 indexed citations

17.

Gallego, Marta I., Eric Schoenmakers, Wim J.M. Van de Ven, & Pedro A. Lazo. (1997). Complex genomic rearrangement within the 12q15 multiple aberration region induced by integrated human papillomavirus 18 in a cervical carcinoma cell line. Molecular Carcinogenesis. 19(2). 114–121. 16 indexed citations

18.

Roebroek, Anton, Torik Ayoubi, Helgi J. K. van de Velde, et al.. (1996). Genomic Organization of the HumanNSPGene, Prototype of a Novel Gene Family Encoding Reticulons. Genomics. 32(2). 191–199. 34 indexed citations

19.

Caselitz, J., Sylke Wanschura, Eric Schoenmakers, et al.. (1995). A hamartoma of the breast with an aberration of 12q mapped to the MAR region by fluorescence in situ hybridization. Cancer Genetics and Cytogenetics. 84(1). 82–84. 20 indexed citations

20.

Kas, Koen, Eric Schoenmakers, Wim Van de Ven, et al.. (1993). Assignment of the Human FAU Gene to a Subregion of Chromosome 11q13. Genomics. 17(2). 387–392. 17 indexed citations

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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