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.
Localization of the gene for familial adenomatous polyposis on chromosome 5
Countries citing papers authored by Peter Scambler
Since
Specialization
Citations
This map shows the geographic impact of Peter Scambler'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 Peter Scambler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Scambler more than expected).
This network shows the impact of papers produced by Peter Scambler. 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 Peter Scambler. The network helps show where Peter Scambler may publish in the future.
Co-authorship network of co-authors of Peter Scambler
This figure shows the co-authorship network connecting the top 25 collaborators of Peter Scambler.
A scholar is included among the top collaborators of Peter Scambler 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 Peter Scambler. Peter Scambler is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Haelst, Mieke M. van, Geneviève Baujat, Hennie T. Brüggenwirth, et al.. (2005). Familial gigantism caused by an NSD1 mutation. American Journal of Medical Genetics Part A. 139A(1). 40–44.17 indexed citations
Katsanis, Nicholas, et al.. (2001). Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder. UCL Discovery (University College London).196 indexed citations
8.
Scambler, Peter, et al.. (2001). An amino acid substitution in the HOXD13 homeodomain causes a novel brachydactyly-polydactyly syndrome. European Journal of Human Genetics.3 indexed citations
9.
Ross, Andrew S., et al.. (2000). Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene (vol 66, pg 1504, 2000). UCL Discovery (University College London).1 indexed citations
10.
Scambler, Peter, et al.. (1999). Persistent truncus arteriosus is associated with decreased expression of HIRA by cardiac neural crest cells in chick embryos. UCL Discovery (University College London).1 indexed citations
11.
Wynshaw‐Boris, Anthony, et al.. (1997). Comparative mapping of Hu22q11 and the conserved syntenic region of MMU16 reveals disruption to linkage conservation.. UCL Discovery (University College London).1 indexed citations
12.
O‘Donnell, Hilary, et al.. (1997). Detection of a deletion within 22q11 which has no overlap with the DiGeorge syndrome critical region. UCL Discovery (University College London).2 indexed citations
13.
Leatherbury, Linda, et al.. (1996). Morphologic and hemodynamic assessment of TUPLE 1 gene attenuated chick embryos.. UCL Discovery (University College London).1 indexed citations
14.
Scambler, Peter, et al.. (1996). Genomic organization of TUPLE1/HIRA: Alternative splice products of the same gene. UCL Discovery (University College London).1 indexed citations
15.
Rizzu, Patrizia, et al.. (1996). Cloning and comparative mapping of a gene deleted in DiGeorge and velocardiofacial syndromes conserved in the C.elegans genome.. UCL Discovery (University College London).1 indexed citations
16.
Wilson, David I., John Burn, Peter Scambler, & Judith Goodship. (1993). Syndrome of the month: DiGeorge Syndrome. Part of CATCH-22.. UCL Discovery (University College London).11 indexed citations
17.
Scambler, Peter, D. Kelly, R Williamson, Rosalie Goldberg, & Robert J. Shprintzen. (1992). The velo-cardio-facial syndrome is associated with chromosome 22 deletions which encompass the DiGeorge syndrome locus. UCL Discovery (University College London).15 indexed citations
18.
Scambler, Peter, Stephanie Halford, R Wadey, et al.. (1991). MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES. UCL Discovery (University College London).4 indexed citations
19.
Wilson, David I., et al.. (1991). IS MONOSOMY FOR THE DIGEORGE LOCUS ON CHROMOSOME-22 RESPONSIBLE FOR ISOLATED HEART MALFORMATIONS. UCL Discovery (University College London).2 indexed citations
20.
Scambler, Peter, Martin Farrall, Jimmy D. Bell, et al.. (1985). Linkage of the Col1A2 collagen gene to cystic fibrosis. UCL Discovery (University College London).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.