Gerard Merkx

3.2k citations

52 papers · 2.2k indexed · h-index 25

Molecular Biology top 5%
Genetics top 5%
Immunology top 10%
Organic Chemistry top 5%
Pulmonary and Respiratory Medicine top 10%

Co-authors: Ad Geurts van Kessel Henrik Clausen Eric Bennett Dominique Smeets Helle Hassan Michael A. Hollingsworth Steven B. Levery Ulla Mandel
Topics: Genomic variations and chromosomal abnormalities (15 papers)Chromosomal and Genetic Variations (9 papers)Glycosylation and Glycoproteins Research (7 papers)
Cited by: Molecular Biology Genetics Immunology
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry PLoS ONE
Partner nations: Netherlands United States Poland

In The Last Decade

Gerard Merkx

52 papers receiving 2.1k citations

Peers

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

#	Work	Indexed citations
1	A Cytogenetic Study in a Large Population of Intellectually Disabled Indonesians 2011 ·Genetic Testing and Molecular Biomarkers ·(unknown),Tri Indah Winarni,Bregje W.M. van Bon,(unknown),Willy M. Nillesen,Gerard Merkx,(unknown),Ben C.J. Hamel,Sultana MH Faradz,Helger G. Yntema	11
2	Pathogenesis of axonal dystrophy and demyelination in αA‐crystallin‐expressing transgenic mice 2003 ·International Journal of Experimental Pathology ·(unknown),(unknown),Gerard Merkx,Martin Lammens,H. Bloemendal	3
3	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
4	The cancer‐related protein SSX2 interacts with the human homologue of a Ras‐like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP 2002 ·Genes Chromosomes and Cancer ·Diederik R.H. de Bruijn,Nuno R. dos Santos,Ellen Kater‐Baats,José Thijssen,(unknown),(unknown),M. Balemans,Marga Schepens,Gerard Merkx,Ad Geurts van Kessel	50
5	Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15) 2001 ·Genes Chromosomes and Cancer ·Marc J. Eleveld,Daniëlle Bodmer,Gerard Merkx,(unknown),Sandra H. E. Sprenger,Marian A. J. Weterman,Marjolijn J. L. Ligtenberg,(unknown),(unknown),Judith W. M. Jeuken,Dominique Smeets,Arie P.T. Smits,Ad Geurts van Kessel	29
6	Genomic organization, chromosomal localization, and 5′ upstream region of the human DC-STAMP gene 2001 ·Immunogenetics ·Franca C. Hartgers,Maaike W.G. Looman,Bas van der Woning,Gerard Merkx,Carl G. Figdor,Gosse J. Adema	14
7	Molecular cloning and immunogenicity of renal cell carcinoma-associated antigen G250 2000 ·International Journal of Cancer ·(unknown),Joost L. M. Vissers,(unknown),Jeannette Oosterwijk‐Wakka,Adrie van Bokhoven,Ruud H. Brakenhoff,Elfriede Noeßner,(unknown),Gerard Merkx,Carl G. Figdor,Gosse J. Adema,Egbert Oosterwijk	139
8	Towards the isolation of a human malignant extragonadal germ cell tumour‐associated breakpoint in chromosome 11q13 1998 ·Apmis ·Richard J. Sinke,M. van Asseldonk,(unknown),(unknown),Gerard Merkx,D. Olde Weghuis,Bauke M. de Jong,J. Wolter Oosterhuis,Ad Geurts van Kessel	4
9	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 1998 ·Cytogenetic and Genome Research ·Christian Ensinger,Peter Obrist,G. Mikuz,Gerard Merkx,(unknown),(unknown),Felix Bachmann,Max M. Burger	4
10	Cloning of a Human UDP-N-Acetyl-α-d-Galactosamine:PolypeptideN-Acetylgalactosaminyltransferase That Complements Other GalNAc-Transferases in Complete O-Glycosylation of the MUC1 Tandem Repeat 1998 ·Journal of Biological Chemistry ·Eric Bennett,Helle Hassan,Ulla Mandel,(unknown),Peter Roepstorff,Joy Burchell,Joyce Taylor‐Papadimitriou,Michael A. Hollingsworth,Gerard Merkx,Ad Geurts van Kessel,Hans Eiberg,Rudi Steffensen,Henrik Clausen	189
11	Assignment<sup>1</sup> of H7365 (C9orf2) to human chromosome band 9q31 by somatic cell hybrid analysis and fluorescence in situ hybridization 1998 ·Cytogenetic and Genome Research ·Douglas W. Eib,Gerard Merkx,Gerard J.M. Martens,Frans P.M. Cremers	5
12	Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: Polypeptide N-acetylgalactosaminyltransferase family 1998 ·Glycobiology ·Eric Bennett,D. Olde Weghuis,Gerard Merkx,Amit Kessel,Hans Eiberg,Henrik Clausen	32
13	Assignment of the Human Adipocyte Fatty Acid-Binding Protein Gene (FABP4) to Chromosome 8q21 Using Somatic Cell Hybrid and Fluorescencein SituHybridization Techniques 1997 ·Genomics ·Clemens Prinsen,Diederik R.H. de Bruijn,Gerard Merkx,Jacques H. Veerkamp	21
14	Fine Mapping of the Human Renal Oncocytoma-Associated Translocation (5;11)(q35;q13) Breakpoint 1997 ·Cancer Genetics and Cytogenetics ·Richard J. Sinke,(unknown),Bert Janssen,Daniël Olde Weghuis,Gerard Merkx,Anke van den Berg,Ed Schuuring,(unknown),Bauke M. de Jong,Ad Geurts van Kessel	29
15	A Family of Human β4-Galactosyltransferases 1997 ·Journal of Biological Chemistry ·Raquel Almeida,Margarida Amado,Leonor David,Steven B. Levery,Eric H. Holmes,Gerard Merkx,Ad Geurts van Kessel,(unknown),Helle Hassan,Eric Bennett,Henrik Clausen	156
16	Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families 1996 ·Pediatric Nephrology ·Henny H. Lemmink,Lambert P.W.J. van den Heuvel,(unknown),Gerard Merkx,Tineke J. Smilde,Peter E.M. Taschner,L.A.H. Monnens,S. C. Hebert,Nine V.A.M. Knoers	53
17	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 1995 ·Human Molecular Genetics ·(unknown),Gerard Merkx,Silvère M. van der Maarel,I Huber,S Malcolm,H.-H. Ropers,Frans P.M. Cremers	60
18	No imprinting involved in the expression of DM-kinase m RNAs in mouse and human tissues 1993 ·Human Molecular Genetics ·Gert Jansen,(unknown),Vera M. Kalscheuer,Gerard Merkx,(unknown),Edwin C.M. Mariman,Dominique Smeets,Hans‐Hilger Ropers,(unknown)	20
19	Analysis of Chromosome Aberrations and Sister Chromatid Exchanges in Peripheral Blood Lymphocytes of Newborns after Vitamin K Prophylaxis at Birth 1991 ·Pediatric Research ·Elisabeth A. M. Cornelissen,Dominique Smeets,Gerard Merkx,Ronney A. De Abreu,Louis A. A. Kollée,L.A.H. Monnens	13
20	Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes 1991 ·Human Genetics ·Dominique Smeets,Gerard Merkx,(unknown)	21

About Gerard Merkx

Gerard Merkx is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 52 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Chromosomal and Genetic Variations (9 papers) and Glycosylation and Glycoproteins Research (7 papers). The work is most often cited by research in Molecular Biology (1.6k citations), Genetics (570 citations) and Immunology (416 citations). Gerard Merkx has collaborated with scholars based in Netherlands, United States and Poland. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

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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