D.N. Cooper
Impact in
- Genetics top 0.01%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 0.05%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
Papers in
- Genetics 252
- Genomics and Rare Diseases 133
- Genomic variations and chromosomal abnormalities 96
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- RNA and protein synthesis mechanisms 73
- RNA modifications and cancer 56
- Genomics and Phylogenetic Studies 45
- Co-authors
- Michael Krawczak (70 shared papers)Peter D. Stenson (68 shared papers)Matthew E. Mort (69 shared papers)Edward V. Ball (25 shared papers)S H Barondes (12 shared papers)Jana Marie Schwarz (3 shared papers)Markus Schuelke (3 shared papers)Dominik Seelow (3 shared papers)
- Journals
- Human Genetics (103 papers)Human Mutation (83 papers)Human Genomics (27 papers)Nucleic Acids Research (24 papers)Proceedings of the National Academy of Sciences (11 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
D.N. Cooper
632 papers receiving 70.2k citations
D.N. Cooper's Hit Papers
Peers
Comparison fields: 5 of 223
- Genetics 24.6k
- Molecular Biology 32.9k
- Cancer Research 5.6k
- Hematology 4.0k
- Immunology 5.8k
Countries citing papers authored by D.N. Cooper
This map shows the geographic impact of D.N. Cooper'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 D.N. Cooper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D.N. Cooper more than expected).
Fields of papers citing papers by D.N. Cooper
This network shows the impact of papers produced by D.N. Cooper. 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 D.N. Cooper. The network helps show where D.N. Cooper may publish in the future.
Co-authors
The 25 scholars most cited alongside D.N. Cooper, 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 652 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12574 |
| 2 | Analysis of protein-coding genetic variation in 60,706 humans Hit paper breakdown → | 2016 | 7751 |
| 3 | MutationTaster2: mutation prediction for the deep-sequencing age Hit paper breakdown → | 2014 | 2970 |
| 4 | Genome sequence of the Brown Norway rat yields insights into mammalian evolution Hit paper breakdown → | 2004 | 1679 |
| 5 | Human Gene Mutation Database (HGMD®): 2003 update Hit paper breakdown → | 2003 | 1498 |
| 6 | Galectins. Structure and function of a large family of animal lectins. Hit paper breakdown → | 1994 | 1337 |
| 7 | The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences Hit paper breakdown → | 1992 | 1161 |
| 8 | The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine Hit paper breakdown → | 2013 | 1095 |
| 9 | Evolutionary and Biomedical Insights from the Rhesus Macaque Genome Hit paper breakdown → | 2007 | 1081 |
| 10 | The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies Hit paper breakdown → | 2017 | 1065 |
| 11 | Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models Hit paper breakdown → | 2012 | 1038 |
| 12 | A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes Hit paper breakdown → | 2012 | 923 |
| 13 | The CpG dinucleotide and human genetic disease Hit paper breakdown → | 1988 | 825 |
| 14 | The yak genome and adaptation to life at high altitude Hit paper breakdown → | 2012 | 743 |
| 15 | The Human Gene Mutation Database: 2008 update Hit paper breakdown → | 2009 | 710 |
| 16 | Classification of human epithelia and their neoplasms using monoclonal antibodies to keratins: strategies, applications, and limitations. Hit paper breakdown → | 1985 | 676 |
| 17 | Automated inference of molecular mechanisms of disease from amino acid substitutions Hit paper breakdown → | 2009 | 668 |
| 18 | M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity Hit paper breakdown → | 2016 | 627 |
| 19 | Insights into hominid evolution from the gorilla genome sequence Hit paper breakdown → | 2012 | 534 |
| 20 | Gene expression across mammalian organ development Hit paper breakdown → | 2019 | 519 |
About D.N. Cooper
D.N. Cooper is a scholar working on Genetics, Molecular Biology, Hematology, Cancer Research and Neurology, having authored 652 papers that have together received 72.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (133 papers), Genomic variations and chromosomal abnormalities (96 papers), RNA and protein synthesis mechanisms (73 papers), Blood Coagulation and Thrombosis Mechanisms (61 papers), RNA modifications and cancer (56 papers), Neurofibromatosis and Schwannoma Cases (47 papers), Chromosomal and Genetic Variations (45 papers) and Genomics and Phylogenetic Studies (45 papers). The work is most often cited by research in Genetics (24.6k citations), Molecular Biology (32.9k citations), Cancer Research (5.6k citations), Hematology (4.0k citations) and Immunology (5.8k citations). D.N. Cooper has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Michael Krawczak, Peter D. Stenson, Matthew E. Mort, Edward V. Ball, S H Barondes, Jana Marie Schwarz, Markus Schuelke, Dominik Seelow, Andrew D. Phillips and Nadia A Chuzhanova. Their work appears in journals such as Human Genetics, Human Mutation, Human Genomics, Nucleic Acids Research and Proceedings of the National Academy of Sciences.
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.