Frits Meijlink

4.4k total citations
58 papers, 3.6k citations indexed

About

Frits Meijlink is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Frits Meijlink has authored 58 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 21 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Frits Meijlink's work include Developmental Biology and Gene Regulation (19 papers), Congenital heart defects research (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Frits Meijlink is often cited by papers focused on Developmental Biology and Gene Regulation (19 papers), Congenital heart defects research (12 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers). Frits Meijlink collaborates with scholars based in Netherlands, United States and France. Frits Meijlink's co-authors include Jacqueline Deschamps, Antje Brouwer, Inder M. Verma, Jeroen Korving, Derk ten Berge, Sanne Kuijper, Annemiek Beverdam, Olivier Destrée, Mark Reijnen and Hans Clevers and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Frits Meijlink

58 papers receiving 3.5k citations

Peers

Countries citing papers authored by Frits Meijlink

Since Specialization

Citations

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

Fields of papers citing papers by Frits Meijlink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frits Meijlink

This figure shows the co-authorship network connecting the top 25 collaborators of Frits Meijlink. A scholar is included among the top collaborators of Frits Meijlink 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 Frits Meijlink. Frits Meijlink 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	An ENU-induced point mutation in the mouse Btaf1 gene causes post-gastrulation embryonic lethality and protein instability 2011 ·Mechanisms of Development ·Carolien Wansleeben, Léon van Gurp, Petra de Graaf, Florence Mousson, H. T. Marc Timmers, Frits Meijlink	3
2	Genetic Analysis of Hedgehog Signaling in Ventral Body Wall Development and the Onset of Omphalocele Formation 2011 ·PLoS ONE ·Daisuke Matsumaru, Ryuma Haraguchi, Shinichi Miyagawa, Jun Motoyama, Naomi Nakagata, Frits Meijlink, Gen Yamada	26
3	β -catenin tyrosine 654 phosphorylation increases Wnt signalling and intestinal tumorigenesis 2011 ·Gut ·Wendy van Veelen, (unknown), (unknown), Lau Blonden, (unknown), Elvira R. M. Bakker, Patrick Franken, Léon van Gurp, Frits Meijlink, Martin A. van der Valk, Ernst J. Kuipers, Riccardo Fodde, Ron Smits	139
4	Planar cell polarity defects and defective Vangl2 trafficking in mutants for the COPII gene Sec24b 2010 ·Development ·Carolien Wansleeben, Harma Feitsma, Mireille Montcouquiol, C.C.M. Kroon, Edwin Cuppen, Frits Meijlink	78
5	A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction 2010 ·The International Journal of Developmental Biology ·Carolien Wansleeben, Harma Feitsma, (unknown), C.C.M. Kroon, Victor Guryev, Edwin Cuppen, Frits Meijlink	8
6	Function and regulation of Alx4 in limb development: Complex genetic interactions with Gli3 and Shh 2005 ·Developmental Biology ·Sanne Kuijper, Harma Feitsma, Rushikesh Sheth, Jeroen Korving, Mark Reijnen, Frits Meijlink	42
7	The OAR/aristaless domain of the homeodomain protein Cart1 has an attenuating role in vivo 2003 ·Mechanisms of Development ·Antje Brouwer, Derk ten Berge, (unknown), Frits Meijlink	40
8	The Direct Context of a Hox Retinoic Acid Response Element Is Crucial for its Activity 2003 ·Journal of Biological Chemistry ·Tony Oosterveen, Patrick van Vliet, Jacqueline Deschamps, Frits Meijlink	19
9	Progression of Vertebrate Limb Development Through SHH-Mediated Counteraction of GLI3 2002 ·Science ·(unknown), Aimée Zúñiga, Sanne Kuijper, (unknown), (unknown), Frits Meijlink, Rolf Zeller	310
10	Expression patterns of group-I aristaless-related genes during craniofacial and limb development 2001 ·Mechanisms of Development ·Annemiek Beverdam, Frits Meijlink	48
11	Automated topographical cell proliferation analysis 2001 ·Cytometry ·(unknown), Derk ten Berge, W. J. Hage, (unknown), Frits Meijlink, J. B. Antoine Maintz, Fons J. Verbeek	2
12	Vertebrate aristaless-related genes 1999 ·The International Journal of Developmental Biology ·Frits Meijlink, Annemiek Beverdam, Abraham Brouwer, Tony Oosterveen, Derk ten Berge	85
13	MouseAlx3:Anaristaless-like Homeobox Gene Expressed during Embryogenesis in Ectomesenchyme and Lateral Plate Mesoderm 1998 ·Developmental Biology ·Derk ten Berge, Antje Brouwer, (unknown), Jean‐Louis Guénet, (unknown), Frits Meijlink	66
14	Expression patterns of the paired-related homeobox genes MHox/Prx1 and S8/Prx2 suggest roles in development of the heart and the forebrain 1995 ·Mechanisms of Development ·(unknown), Antje Brouwer, Mohamed El Khattabi, Rob E. Poelmann, Adriana C. Gittenberger–de Groot, Frits Meijlink	113
15	Regulation of the Hoxb-8 Gene: Synergism between Multimerized cis-Acting Elements Increases Responsiveness to Positional Information 1995 ·Developmental Biology ·Jeroen Charité, Wim de Graaff, Ronald Vogels, Frits Meijlink, Jacqueline Deschamps	43
16	The Homeobox Gene S8: Mesoderm-Specific Expression in Presomite Embryos and in Cells Cultured in Vitro and Modulation in Differentiating Pluripotent Cells 1993 ·Developmental Biology ·Ron de Jong, Frits Meijlink	36
17	Induction of HOX-2 Genes in P19 Embryocarcinoma Cells Is Dependent on Retinoic Acid Receptor α 1993 ·Experimental Cell Research ·Fried Zwartkruis, Frank A.E. Kruyt, Paul T. van der Saag, Frits Meijlink	9
18	DNA-binding activity of the murine homeodomain protein Hox-2.3 produced by a hybrid phage T7/vaccinia virus system 1992 ·Gene ·Ron de Jong, (unknown), Harry Vennema, Frits Meijlink	2
19	Cloning of murine TCF-1, a T cell-specific transcription factor interacting with functional motifs in the CD3-epsilon and T cell receptor alpha enhancers. 1991 ·The Journal of Experimental Medicine ·Mariëtte A. Oosterwegel, Marc van de Wetering, Dennis Dooijes, Leo W. J. Klomp, Astar Winoto, Katia Georgopoulos, Frits Meijlink, Hans Clevers	122
20	A mouse homeobox containing gene on chromosome 11: sequence and tissue-specific expression 1987 ·Nucleic Acids Research ·Frits Meijlink, (unknown), Peter Verrijzer, Olivier Destrée, V. Kroezen, John Hilkens, Jacqueline Deschamps	53

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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