Gerard Merkx

3.2k total citations
52 papers, 2.2k citations indexed

About

Gerard Merkx is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Gerard Merkx has authored 52 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 23 papers in Genetics and 10 papers in Plant Science. Recurrent topics in Gerard Merkx's work include Genomic variations and chromosomal abnormalities (15 papers), Chromosomal and Genetic Variations (9 papers) and Glycosylation and Glycoproteins Research (7 papers). Gerard Merkx is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Chromosomal and Genetic Variations (9 papers) and Glycosylation and Glycoproteins Research (7 papers). Gerard Merkx collaborates with scholars based in Netherlands, United States and Poland. Gerard Merkx's co-authors include Ad Geurts van Kessel, Henrik Clausen, Eric Bennett, Dominique Smeets, Helle Hassan, Michael A. Hollingsworth, Steven B. Levery, Ulla Mandel, Han G. Brunner and Tilo Schwientek and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Gerard Merkx

52 papers receiving 2.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Gerard Merkx Netherlands	25	1.6k	570	416	336	262	52	2.2k
Feyruz V. Rassool United States	36	2.5k 1.6×	435 0.8×	275 0.7×	63 0.2×	162 0.6×	80	3.7k
Els Schollen Belgium	30	2.1k 1.3×	530 0.9×	604 1.5×	676 2.0×	29 0.1×	58	2.6k
Philip D. Cotter United States	26	1.3k 0.8×	994 1.7×	153 0.4×	26 0.1×	116 0.4×	95	2.4k
Pedro J. Real Spain	24	2.3k 1.5×	209 0.4×	417 1.0×	41 0.1×	132 0.5×	58	3.5k
Małgorzata Bielińska United States	29	1.7k 1.1×	857 1.5×	120 0.3×	29 0.1×	214 0.8×	41	2.4k
Gail Chuck United States	20	1.3k 0.9×	290 0.5×	70 0.2×	46 0.1×	432 1.6×	36	3.0k
Eissa Faqeih Saudi Arabia	28	1.5k 0.9×	920 1.6×	143 0.3×	49 0.1×	75 0.3×	80	2.2k
Sabine Mazerbourg France	22	1.4k 0.9×	313 0.5×	113 0.3×	75 0.2×	247 0.9×	35	2.4k
Kyoichi Isono Japan	29	2.2k 1.4×	357 0.6×	192 0.5×	19 0.1×	62 0.2×	58	2.6k
Holger Kissel United States	13	830 0.5×	219 0.4×	369 0.9×	60 0.2×	61 0.2×	13	1.5k

Countries citing papers authored by Gerard Merkx

Since Specialization

Citations

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

Fields of papers citing papers by Gerard Merkx

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerard Merkx

This figure shows the co-authorship network connecting the top 25 collaborators of Gerard Merkx. A scholar is included among the top collaborators of Gerard Merkx 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 Gerard Merkx. Gerard Merkx 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

Vries, Marieke de, Gerard Merkx, Kathleen D’Hauwers, et al.. (2012). Human Male Meiotic Sex Chromosome Inactivation. PLoS ONE. 7(2). e31485–e31485. 29 indexed citations

Schoenmakers, Eric, Jens Bunt, Marga Schepens, et al.. (2012). Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma. Genes Chromosomes and Cancer. 52(1). 11–23. 27 indexed citations

Winarni, Tri Indah, Bregje W.M. van Bon, Willy M. Nillesen, et al.. (2011). A Cytogenetic Study in a Large Population of Intellectually Disabled Indonesians. Genetic Testing and Molecular Biomarkers. 16(5). 412–417. 11 indexed citations

Merkx, Gerard, et al.. (2003). Pathogenesis of axonal dystrophy and demyelination in αA‐crystallin‐expressing transgenic mice. International Journal of Experimental Pathology. 84(2). 91–99. 3 indexed citations

Bruijn, Diederik R.H. de, Nuno R. dos Santos, Ellen Kater‐Baats, et al.. (2002). The cancer‐related protein SSX2 interacts with the human homologue of a Ras‐like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP. Genes Chromosomes and Cancer. 34(3). 285–298. 50 indexed citations

Eleveld, Marc J., Daniëlle Bodmer, Gerard Merkx, et al.. (2001). Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15). Genes Chromosomes and Cancer. 31(1). 23–32. 29 indexed citations

Hartgers, Franca C., Maaike W.G. Looman, Bas van der Woning, et al.. (2001). Genomic organization, chromosomal localization, and 5′ upstream region of the human DC-STAMP gene. Immunogenetics. 53(2). 145–149. 14 indexed citations

Weterman, Marian A. J., M. Wilbrink, Marc J. Eleveld, et al.. (2001). Genomic structure, chromosomal localization, and embryonic expression of the mouse homolog of PRCC, a gene associated with papillary renal cell carcinoma. Cytogenetic and Genome Research. 92(3-4). 326–332. 4 indexed citations

Vissers, Joost L. M., Jeannette Oosterwijk‐Wakka, Adrie van Bokhoven, et al.. (2000). Molecular cloning and immunogenicity of renal cell carcinoma-associated antigen G250. International Journal of Cancer. 85(6). 865–870. 139 indexed citations

10.

Sinke, Richard J., M. van Asseldonk, Gerard Merkx, et al.. (1998). Towards the isolation of a human malignant extragonadal germ cell tumour‐associated breakpoint in chromosome 11q13. Apmis. 106(1-6). 73–79. 4 indexed citations

11.

Ensinger, Christian, Peter Obrist, G. Mikuz, et al.. (1998). Assignment<footref rid="foot01"><sup>1</sup></footref> of the p150 subunit of the eukaryotic initiation factor 3A gene (EIF3A) to human chromosome band 10q26 by in situ hybridisation. Cytogenetic and Genome Research. 83(1-2). 74–75. 4 indexed citations

12.

Bennett, Eric, D. Olde Weghuis, Gerard Merkx, et al.. (1998). Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: Polypeptide N-acetylgalactosaminyltransferase family. Glycobiology. 8(6). 547–555. 32 indexed citations

13.

Prinsen, Clemens, Diederik R.H. de Bruijn, Gerard Merkx, & Jacques H. Veerkamp. (1997). Assignment of the Human Adipocyte Fatty Acid-Binding Protein Gene (FABP4) to Chromosome 8q21 Using Somatic Cell Hybrid and Fluorescencein SituHybridization Techniques. Genomics. 40(1). 207–209. 21 indexed citations

14.

Sinke, Richard J., Bert Janssen, Daniël Olde Weghuis, et al.. (1997). Fine Mapping of the Human Renal Oncocytoma-Associated Translocation (5;11)(q35;q13) Breakpoint. Cancer Genetics and Cytogenetics. 96(2). 95–101. 29 indexed citations

15.

Lemmink, Henny H., Lambert P.W.J. van den Heuvel, Gerard Merkx, et al.. (1996). Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families. Pediatric Nephrology. 10(4). 403–407. 53 indexed citations

16.

Merkx, Gerard, Silvère M. van der Maarel, I Huber, et al.. (1995). A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene. Human Molecular Genetics. 4(11). 2145–2150. 60 indexed citations

17.

Smeets, Dominique, et al.. (1991). Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes. Human Genetics. 87(1). 45–48. 21 indexed citations

18.

Cornelissen, Elisabeth A. M., Dominique Smeets, Gerard Merkx, et al.. (1991). Analysis of Chromosome Aberrations and Sister Chromatid Exchanges in Peripheral Blood Lymphocytes of Newborns after Vitamin K Prophylaxis at Birth. Pediatric Research. 30(6). 550–552. 13 indexed citations

19.

Crooijmans, R.P.M.A., J. Hoogenhout, Gerard Merkx, et al.. (1990). Cell lines of human oral squamous‐cell carcinomas retaining their differentiated phenotype. International Journal of Cancer. 45(5). 945–951. 7 indexed citations

20.

Scheres, J. M. J. C., T. W. J. Hustinx, & Gerard Merkx. (1980). Nomarski-optical studies of human chromosomes R-banded with barium hydroxide. Human Genetics. 53(2). 255–9. 2 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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