Peter Scambler

34.6k total citations · 5 hit papers
262 papers, 17.6k citations indexed

About

Peter Scambler is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Peter Scambler has authored 262 papers receiving a total of 17.6k indexed citations (citations by other indexed papers that have themselves been cited), including 188 papers in Molecular Biology, 91 papers in Genetics and 60 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Peter Scambler's work include Congenital heart defects research (105 papers), Congenital Heart Disease Studies (34 papers) and Cystic Fibrosis Research Advances (24 papers). Peter Scambler is often cited by papers focused on Congenital heart defects research (105 papers), Congenital Heart Disease Studies (34 papers) and Cystic Fibrosis Research Advances (24 papers). Peter Scambler collaborates with scholars based in United Kingdom, United States and India. Peter Scambler's co-authors include John Burn, David I. Wilson, Judith Goodship, Antonio Baldini, Rosalie Goldberg, Bernice E. Morrow, Brandon J. Wainwright, Eran Meshorer, Tom Misteli and David T. Brown and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Peter Scambler

258 papers receiving 17.2k citations

Hit Papers

5 papers align trajectories

What are hit papers?

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

1987 1.0k citations Peter Scambler et al. profile →
22q11.2 deletion syndrome

2015 791 citations Bernice E. Morrow, Peter Scambler et al. profile →
Hyperdynamic Plasticity of Chromatin Proteins in Pluripotent Embryonic Stem Cells

2006 785 citations Eran Meshorer, Peter Scambler et al. profile →
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

2001 747 citations Peter Scambler, Antonio Baldini et al. profile →
The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

1987 502 citations Peter Scambler et al. Science profile →

Peers

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).

Fields of papers citing papers by Peter Scambler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Hyperdynamic plasticity in pluripotent embryonic of chromatin proteins stem cells 2006 ·UCL Discovery (University College London) ·Eran Meshorer, Dhananjay Yellajoshyula, (unknown), Peter Scambler, (unknown), (unknown)	2
2	Velo-cardio-facial syndrome a model for understanding microdeletion disorders 2005 ·UCL Discovery (University College London) ·Kieran C. Murphy, Peter Scambler	2
3	Familial gigantism caused by an NSD1 mutation 2005 ·American Journal of Medical Genetics Part A ·Mieke M. van Haelst, (unknown), Geneviève Baujat, Hennie T. Brüggenwirth, Ingrid M.B.H. van de Laar, Kim Coleman, Nazneen Rahman, Martinus F. Niermeijer, S L S Drop, Peter Scambler	17
4	Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder 2001 ·Science ·Nicholas Katsanis, Stephen J. Ansley, José L. Badano, Erica R. Eichers, Richard A. Lewis, Bethan E. Hoskins, Peter Scambler, William S. Davidson, Philip L. Beales, James R. Lupski	438
5	Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder 2001 ·UCL Discovery (University College London) ·Nicholas Katsanis, (unknown), (unknown), (unknown), Lewis Ra, (unknown), Peter Scambler, W. S. Davidson, (unknown), (unknown)	196
6	An amino acid substitution in the HOXD13 homeodomain causes a novel brachydactyly-polydactyly syndrome 2001 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Peter Scambler	3
7	Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene (vol 66, pg 1504, 2000) 2000 ·UCL Discovery (University College London) ·(unknown), Andrew S. Ross, (unknown), Sally Ann Lynch, (unknown), (unknown), Peter Scambler	1
8	Persistent truncus arteriosus is associated with decreased expression of HIRA by cardiac neural crest cells in chick embryos 1999 ·UCL Discovery (University College London) ·(unknown), (unknown), Peter Scambler, (unknown), Linda Leatherbury, (unknown)	1
9	Comparative mapping of Hu22q11 and the conserved syntenic region of MMU16 reveals disruption to linkage conservation. 1997 ·UCL Discovery (University College London) ·(unknown), (unknown), (unknown), Anthony Wynshaw‐Boris, Peter Scambler	1
10	Detection of a deletion within 22q11 which has no overlap with the DiGeorge syndrome critical region 1997 ·UCL Discovery (University College London) ·Hilary O‘Donnell, (unknown), Clive Gould, Bernice E. Morrow, Peter Scambler	2
11	Morphologic and hemodynamic assessment of TUPLE 1 gene attenuated chick embryos. 1996 ·UCL Discovery (University College London) ·(unknown), Linda Leatherbury, Peter Scambler, (unknown), (unknown), (unknown)	1
12	Genomic organization of TUPLE1/HIRA: Alternative splice products of the same gene 1996 ·UCL Discovery (University College London) ·(unknown), Peter Scambler, Xavier Estivill, Melanie Pritchard	1
13	Cloning and comparative mapping of a gene deleted in DiGeorge and velocardiofacial syndromes conserved in the C.elegans genome. 1996 ·UCL Discovery (University College London) ·Patrizia Rizzu, (unknown), (unknown), Hilary O‘Donnell, Peter Scambler, Antonio Baldini	1
14	Syndrome of the month: DiGeorge Syndrome. Part of CATCH-22. 1993 ·UCL Discovery (University College London) ·David I. Wilson, John Burn, Peter Scambler, Judith Goodship	11
15	The velo-cardio-facial syndrome is associated with chromosome 22 deletions which encompass the DiGeorge syndrome locus 1992 ·UCL Discovery (University College London) ·Peter Scambler, D. Kelly, R Williamson, Rosalie Goldberg, Robert J. Shprintzen	15
16	MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES 1991 ·UCL Discovery (University College London) ·Peter Scambler, Stephanie Halford, R Wadey, Elizabeth Lindsay, (unknown), (unknown), JA Goodship, John Burn, Rosalie Goldberg, Robert J. Shprintzen, Robin E. Williamson, (unknown)	4
17	IS MONOSOMY FOR THE DIGEORGE LOCUS ON CHROMOSOME-22 RESPONSIBLE FOR ISOLATED HEART MALFORMATIONS 1991 ·UCL Discovery (University College London) ·David I. Wilson, JA Goodship, Peter Scambler, (unknown), Ismael Cross, John Burn	2
18	Localisation of a sequence, 7C22, showing close linkage to the cystic fibrosis locus 1987 ·Cytogenetic and Genome Research ·Veronica J. Buckle, Peter Scambler, Brandon J. Wainwright	7
19	Cystic fibrosis linkage exclusion data 1986 ·Cytogenetic and Genome Research ·Peter Scambler, G. Bell, Eila Watson, Martin Farrall, Gillian P. Bates, Kay E. Davies, Nicholas Lench, (unknown), R. Williamson, P. Tippett, Brandon J. Wainwright	7
20	Linkage of the Col1A2 collagen gene to cystic fibrosis 1985 ·UCL Discovery (University College London) ·Peter Scambler, (unknown), Martin Farrall, Jimmy D. Bell, Philip Stanier, Nicholas Lench, George W. Bell, H. Kruyer, (unknown), R Williamson	1

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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