Veronica van Heyningen

23.7k total citations · 5 hit papers
212 papers, 15.9k citations indexed

About

Veronica van Heyningen is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Veronica van Heyningen has authored 212 papers receiving a total of 15.9k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Molecular Biology, 74 papers in Genetics and 25 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Veronica van Heyningen's work include Renal and related cancers (47 papers), Developmental Biology and Gene Regulation (45 papers) and Genomics and Chromatin Dynamics (25 papers). Veronica van Heyningen is often cited by papers focused on Renal and related cancers (47 papers), Developmental Biology and Gene Regulation (45 papers) and Genomics and Chromatin Dynamics (25 papers). Veronica van Heyningen collaborates with scholars based in United Kingdom, United States and France. Veronica van Heyningen's co-authors include Isabel M. Hanson, Nicholas D. Hastie, Dirk A. Kleinjan, Penny Rashbass, Anne Seawright, Jane Prosser, Tim Jordan, Dieter Engelkamp, Wendy A. Bickmore and Andreas Schedl and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Veronica van Heyningen

208 papers receiving 15.5k citations

Hit Papers

Mouse Small eye results from mutations in a paired-like h... 1990 2026 2002 2014 1991 1997 1990 1991 2004 250 500 750

Peers

Veronica van Heyningen
Thomas Gridley United States
Mitchell Goldfarb United States
Rudolf Grosschedl United States
Peter W. Andrews United Kingdom
Harold Weintraub United States
Frank Costantini United States
Thomas Gridley United States
Veronica van Heyningen
Citations per year, relative to Veronica van Heyningen Veronica van Heyningen (= 1×) peers Thomas Gridley

Countries citing papers authored by Veronica van Heyningen

Since Specialization
Citations

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

Fields of papers citing papers by Veronica van Heyningen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veronica van Heyningen. 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 Veronica van Heyningen. The network helps show where Veronica van Heyningen may publish in the future.

Co-authorship network of co-authors of Veronica van Heyningen

This figure shows the co-authorship network connecting the top 25 collaborators of Veronica van Heyningen. A scholar is included among the top collaborators of Veronica van Heyningen 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 Veronica van Heyningen. Veronica van Heyningen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bhatia, Shipra, Jack Monahan, Vydianathan Ravi, et al.. (2014). A survey of ancient conserved non-coding elements in the PAX6 locus reveals a landscape of interdigitated cis-regulatory archipelagos. Developmental Biology. 387(2). 214–228. 31 indexed citations
2.
Hart, Alan, et al.. (2013). The Developmental Regulator Pax6 Is Essential for Maintenance of Islet Cell Function in the Adult Mouse Pancreas. PLoS ONE. 8(1). e54173–e54173. 60 indexed citations
3.
Coutinho, Pedro M., et al.. (2011). Discovery and assessment of conserved Pax6 target genes and enhancers. Genome Research. 21(8). 1349–1359. 37 indexed citations
4.
Robinson, David, et al.. (2008). Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia. American Journal of Medical Genetics Part A. 146A(5). 558–569. 95 indexed citations
5.
Fantes, Judith A., Jacqueline Ramsay, Dian Donnai, et al.. (2008). FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality. The American Journal of Human Genetics. 82(4). 916–926. 31 indexed citations
6.
Asai-Coakwell, Mika, et al.. (2007). Involvement of GDF6 in Oculo-Skeletal Development. Investigative Ophthalmology & Visual Science. 48(13). 3211–3211. 1 indexed citations
7.
Yeyati, Patricia L., et al.. (2007). Hsp90 Selectively Modulates Phenotype in Vertebrate Development. PLoS Genetics. 3(3). e43–e43. 119 indexed citations
8.
Ragge, Nicola, Birgit Lorenz, Adele Schneider, et al.. (2005). SOX2 anophthalmia syndrome. American Journal of Medical Genetics Part A. 135A(1). 1–7. 160 indexed citations
9.
Crolla, John A. & Veronica van Heyningen. (2002). Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia. The American Journal of Human Genetics. 71(5). 1138–1149. 128 indexed citations
10.
Sellar, Grant C., Siobhán A. Jordan, Wendy A. Bickmore, et al.. (1994). The Human Serum Amyloid A Protein (SAA) Superfamily Gene Cluster: Mapping to Chromosome 11p15.1 by Physical and Genetic Linkage Analysis. Genomics. 19(2). 221–227. 43 indexed citations
11.
Browne, D.L., Veronica van Heyningen, Wendy A. Bickmore, & M. Litt. (1993). Dinucleotide repeat polymorphism at the D11S995 locus. Human Molecular Genetics. 2(8). 1332–1332.
12.
Rassoulzadegan, Minoo, Véronique Paquis‐Flucklinger, Béatrice Bertino, et al.. (1993). Transmeiotic differentiation of male germ cells in culture. Cell. 75(5). 997–1006. 147 indexed citations
13.
Junien, Claudine, et al.. (1992). Report of the Second Chromosome 11 Workshop. Genomics. 12(3). 620–625. 15 indexed citations
14.
Pritchard‐Jones, Kathy, Stewart Fleming, Duncan Davidson, et al.. (1990). The candidate Wilms' tumour gene is involved in genitourinary development. Nature. 346(6280). 194–197. 718 indexed citations breakdown →
16.
Spurr, Nigel K., Alan C. Gough, John R. Gosden, et al.. (1988). Restriction fragment length polymorphism analysis and assignment of the metalloproteinases stromelysin and collagenase to the long arm of chromosome 11. Genomics. 2(2). 119–127. 48 indexed citations
17.
Carachi, Robert, Tasleem Raza, Daniel J. Robertson, et al.. (1987). Biological properties of a tumour cell line (NB1-G) derived from human neuroblastoma. British Journal of Cancer. 55(4). 407–411. 17 indexed citations
18.
Porteous, David J., John Morten, Gwen Cranston, et al.. (1986). Molecular and Physical Arrangements of Human DNA in HRAS1 -Selected, Chromosome-Mediated Transfectants. Molecular and Cellular Biology. 6(6). 2223–2232. 14 indexed citations
19.
Jones, Elizabeth, Veronica van Heyningen, E. Solomon, et al.. (1975). Linkage relationships of the HL-A system and beta 2 microglobulin.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 11(3). 162–7. 1 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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