Christopher P. A. Bennett

2.6k citations
26 papers · 1.9k · 1 hit paper · h-index 17

Impact in

  • Genetics top 2%
    • Genomics and Rare Diseases
    • Genetic and Kidney Cyst Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
    • Dermatological and Skeletal Disorders
  • Rheumatology top 5%
    • Hypertrophic osteoarthropathy and related conditions

Papers in

  • Genetics 11
    • Genomics and Rare Diseases 4
    • Genetics and Neurodevelopmental Disorders 3
    • Genetic and Kidney Cyst Diseases 3
    • Genomic variations and chromosomal abnormalities 2
    • Genetic Syndromes and Imprinting 2
  • Molecular Biology 11
    • Genomics and Chromatin Dynamics 2
Co-authors
Mushtaq Ahmed (4 shared papers)Ian Carr (2 shared papers)David T. Bonthron (2 shared papers)Alexander F. Markham (2 shared papers)Ricardo Godoy (4 shared papers)Sandeep Uppal (2 shared papers)Philip Helliwell (1 shared paper)Colin W. G. Fishwick (1 shared paper)
Journals
Nature Genetics (3 papers)Journal of Medical Genetics (3 papers)Human Ecology (2 papers)Bulletin of Indonesian Economic Studies (2 papers)Human Mutation (1 paper)
Partner nations
United KingdomUnited StatesItaly

In The Last Decade

Christopher P. A. Bennett

24 papers receiving 1.8k citations

Christopher P. A. Bennett's Hit Papers

Evidence for 28 genetic disorders discovered by combining healthcare and research data 2020 · 402 citations
4020+2+4Years since publication100200300400
What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

  1. 2020 Nature

Peers

Christopher P. A. Bennett
Comparison fields: 5 of 108
  • Genetics 1.1k
  • Rheumatology 253
  • Molecular Biology 908
  • Pathology and Forensic Medicine 158
  • Pediatrics, Perinatology and Child Health 156
Replace Dustin Baldridge with:
Dustin Baldridge United States
Yline Capri France
Virginia K. Proud United States
Sérgio Bernardo de Sousa Portugal
Patricia G. Wheeler United States
Fatema Alzahrani Saudi Arabia
Dicky J. J. Halley Netherlands
Thessa Kroes Australia
Thatjana Gardeitchik Netherlands
Markus Zweier Switzerland
Christopher P. A. Bennett relative to Dustin Baldridge United States Dustin Baldridge's profile →
Citations per field
00.5×1.5×2.1×
Dustin Baldridge · 1×
Citations per year

Countries citing papers authored by Christopher P. A. Bennett

Since Specialization
Citations

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

Fields of papers citing papers by Christopher P. A. Bennett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher P. A. Bennett. 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 Christopher P. A. Bennett. The network helps show where Christopher P. A. Bennett may publish in the future.

Co-authors

The 25 scholars most cited alongside Christopher P. A. Bennett, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Christopher P. A. Bennett Line = papers co-authored together Christopher P. A. Bennett links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Evidence for 28 genetic disorders discovered by combining healthcare and research data
Nature ·Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, Zhancheng Zhang, Kevin J. Arvai, Ruth Y. Eberhardt, Giuseppe Gallone, Stefan H. Lelieveld
Hit paper breakdown →		2020402
2
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
Nature Genetics ·Sandeep Uppal, Christine P. Diggle, Ian Carr, Colin W. G. Fishwick, Mushtaq Ahmed, Gamal H Ibrahim, Philip Helliwell, Anna Latos‐Bieleńska
2008246
3
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Nature Genetics ·Ursula M. Smith, Mark B. Consugar, Louise J. Tee, Brandy M McKee, Esther N. Maina, Shelly L. Whelan, Neil V. Morgan, Erin Goranson
2006240
4
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan
Nature Genetics ·Tony Roscioli, Erik‐Jan Kamsteeg, Karen Buysse, Isabelle Maystadt, Jeroen van Reeuwijk, Christa van den Elzen, Ellen van Beusekom, Moniek Riemersma
2012185
5
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
European Journal of Human Genetics ·Siddharth Banka, Ratna Veeramachaneni, William Reardon, Emma Howard, Sancha Bunstone, Nicola Ragge, Michael James Parker, Yanick Joseph Crow
2011139
6
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism
Journal of Medical Genetics ·Morad Ansari, Gemma Poke, Quentin R. V. Ferry, Kathleen A. Williamson, Roland Christopher Lochore Aldridge, Alison M. Meynert, Hemant Bengani, Cheng Yee Chan
2014134
7
Spectrum ofMKS1andMKS3mutations in Meckel syndrome: a genotype-phenotype correlation
Human Mutation ·Rana Khaddour, Ursula M. Smith, Lekbir Baala, Jéléna Martinovic, Davina Clavering, Rizwana Shaffiq, Catherine Ozilou, Andrew R. Cullinane
200780
8
Evolutionarily Assembled cis-Regulatory Module at a Human Ciliopathy Locus
Science ·Jeong Ho Lee, Jennifer L. Silhavy, Ji Eun Lee, Lihadh Al‐Gazali, Sophie Thomas, Erica E. Davis, Stephanie L. Bielas, Kiley J. Hill
201278
9
Early-onset Lafora body disease
Brain ·Julie Turnbull, Jean-Marie Girard, Hannes Lohi, Elayne M. Chan, Peixiang Wang, Erica Tiberia, Salah Omer, Mushtaq Ahmed
201266
10
Mutations in GPAA1 , Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
The American Journal of Human Genetics ·Thi Tuyet Mai Nguyen, Yoshiko Murakami, Eamonn G. Sheridan, Sophie Ehresmann, Justine Rousseau, Anik St‐Denis, Guoliang Chai, Norbert Fonya Ajeawung
201756
11
HACE1 deficiency causes an autosomal recessive neurodevelopmental syndrome
Journal of Medical Genetics ·Ronja Hollstein, David A.D. Parry, Lisa Nalbach, Clare V. Logan, Tim Matthias Strom, Verity L. Hartill, Ian Carr, Georg Christoph Korenke
201542
12
The contribution of X-linked coding variation to severe developmental disorders
Nature Communications ·Hilary C. Martin, Eugene J. Gardner, Kaitlin E. Samocha, Joanna Kaplanis, Nadia A. Akawi, Alejandro Sifrim, Ruth Y. Eberhardt, Ana Lisa Taylor Tavares
202142
13
Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain
Journal of Medical Genetics ·Stella Zhang, Saghira Malik Sharif, Ya‐Chun Chen, Enza Maria Valente, Mushtaq Ahmed, Eamonn G. Sheridan, Christopher P. A. Bennett, Geoffrey C. Woods
201633
14
Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene
Human Genetics ·Sharon D. Whatley, Andrew Roberts, David H. Llewellyn, Christopher P. A. Bennett, Christine Garrett, George H. Elder
200025
15
Diversification among coffee smallholders in the highlands of South Sumatra, Indonesia
Human Ecology ·Ricardo Godoy, Christopher P. A. Bennett
198823
16
Duplication involving band 4q32 with minimal clinical effect
American Journal of Medical Genetics ·Edna L. Maltby, I C Barnes, Christopher P. A. Bennett
199921
17
Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
Journal of Investigative Dermatology ·Neil Vincent Whittock, Louise Izatt, Anúska Mann, Tessa Homfray, Christopher P. A. Bennett, Sahar Mansour, Jane A. Hurst, Alan E Fryer
200318
18
Early Repolarization Syndrome; Mechanistic Theories and Clinical Correlates
Frontiers in Physiology ·Ben N. Mercer, Gordon A. Begg, Stephen P Page, Christopher P. A. Bennett, Muzahir Hassan Tayebjee, Saagar Mahida
201617
19
The economics of monocropping and intercropping by smallholders: The case of coconuts in Indonesia
Human Ecology ·Ricardo Godoy, Christopher P. A. Bennett
199113
20
Further delineation of phenotypic spectrum of SCN2A ‐related disorder
American Journal of Medical Genetics Part A ·Ruth E. Richardson, Diana Baralle, Christopher P. A. Bennett, Tracy Ann Briggs, Emilia K. Bijlsma, Jill Clayton‐Smith, Panayiotis Constantinou, Nicola C. Foulds
20217

About Christopher P. A. Bennett

Christopher P. A. Bennett is a scholar working on Genetics, Molecular Biology, Rheumatology, Strategy and Management and Cell Biology, having authored 26 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic and Kidney Cyst Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers), Global trade, sustainability, and social impact (2 papers), Lysosomal Storage Disorders Research (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (1.1k citations), Rheumatology (253 citations), Molecular Biology (908 citations), Pathology and Forensic Medicine (158 citations) and Pediatrics, Perinatology and Child Health (156 citations). Christopher P. A. Bennett has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Mushtaq Ahmed, Ian Carr, David T. Bonthron, Alexander F. Markham, Ricardo Godoy, Sandeep Uppal, Philip Helliwell, Colin W. G. Fishwick, S.E.V. Phillips and Anna Latos‐Bieleńska. Their work appears in journals such as Nature Genetics, Journal of Medical Genetics, Human Ecology, Bulletin of Indonesian Economic Studies and Human Mutation.

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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