Peter Scambler
Impact in
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 0.2%
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
-
- Congenital heart defects research 102
- Hedgehog Signaling Pathway Studies 13
- Genetics 89
- Genomic variations and chromosomal abnormalities 24
- Congenital Ear and Nasal Anomalies 23
- Ocular Disorders and Treatments 14
- Co-authors
- John Burn (18 shared papers)David I. Wilson (17 shared papers)Judith Goodship (8 shared papers)Antonio Baldini (14 shared papers)Robert J. Shprintzen (7 shared papers)Rosalie Goldberg (7 shared papers)Bernice E. Morrow (8 shared papers)Eran Meshorer (3 shared papers)
- Journals
- Human Molecular Genetics (13 papers)Genomics (13 papers)Human Genetics (12 papers)Nucleic Acids Research (12 papers)The American Journal of Human Genetics (12 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
Peter Scambler
253 papers receiving 17.2k citations
Peter Scambler's Hit Papers
Peers
Comparison fields: 5 of 158
- Genetics 6.2k
- Molecular Biology 11.7k
- Developmental Biology 334
- Pulmonary and Respiratory Medicine 3.0k
- Genetics 904
Countries citing papers authored by Peter Scambler
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
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-authors
The 25 scholars most cited alongside Peter Scambler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 262 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Localization of the gene for familial adenomatous polyposis on chromosome 5 Hit paper breakdown → | 1987 | 1013 |
| 2 | 22q11.2 deletion syndrome Hit paper breakdown → | 2015 | 810 |
| 3 | Hyperdynamic Plasticity of Chromatin Proteins in Pluripotent Embryonic Stem Cells Hit paper breakdown → | 2006 | 785 |
| 4 | Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice Hit paper breakdown → | 2001 | 749 |
| 5 | The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5 Hit paper breakdown → | 1987 | 501 |
| 6 | 2001 | 440 | |
| 7 | 1985 | 372 | |
| 8 | 1993 | 364 | |
| 9 | 2000 | 354 | |
| 10 | 1992 | 331 | |
| 11 | 1993 | 319 | |
| 12 | 1987 | 278 | |
| 13 | 1997 | 274 | |
| 14 | 1998 | 244 | |
| 15 | 2007 | 227 | |
| 16 | 2006 | 225 | |
| 17 | 2005 | 211 | |
| 18 | 1998 | 205 | |
| 19 | 1993 | 204 | |
| 20 | Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder | 2001 | 196 |
About Peter Scambler
Peter Scambler is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Epidemiology and Surgery, having authored 262 papers that have together received 17.6k indexed citations. Recurring topics across this work include Congenital heart defects research (102 papers), Congenital Heart Disease Studies (28 papers), Genomic variations and chromosomal abnormalities (24 papers), Cystic Fibrosis Research Advances (24 papers), Congenital Ear and Nasal Anomalies (23 papers), Tracheal and airway disorders (20 papers), Ocular Disorders and Treatments (14 papers) and Hedgehog Signaling Pathway Studies (13 papers). The work is most often cited by research in Genetics (6.2k citations), Molecular Biology (11.7k citations), Developmental Biology (334 citations), Pulmonary and Respiratory Medicine (3.0k citations) and Genetics (904 citations). Peter Scambler has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include John Burn, David I. Wilson, Judith Goodship, Antonio Baldini, Robert J. Shprintzen, Rosalie Goldberg, Bernice E. Morrow, Eran Meshorer, David T. Brown and Tom Misteli. Their work appears in journals such as Human Molecular Genetics, Genomics, Human Genetics, Nucleic Acids Research and The American Journal of Human Genetics.
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.