D.N. Cooper
Impact in
- Genetics top 0.01%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Forensic and Genetic Research
- Genomic variations and chromosomal abnormalities
- Clinical Biochemistry top 0.1%
Papers in
- Genetics 296
- Genomics and Rare Diseases 173
- Genomic variations and chromosomal abnormalities 76
- Genetic Associations and Epidemiology 65
- Hematology 83
- Blood Coagulation and Thrombosis Mechanisms 55
- Co-authors
- Michael Krawczak (77 shared papers)Peter D. Stenson (71 shared papers)Matthew E. Mort (70 shared papers)Edward V. Ball (25 shared papers)Dominik Seelow (3 shared papers)Jana Marie Schwarz (3 shared papers)Markus Schuelke (3 shared papers)Andrew D. Phillips (11 shared papers)
- Journals
- Human Genetics (104 papers)Human Mutation (83 papers)Human Genomics (28 papers)Nucleic Acids Research (23 papers)The American Journal of Human Genetics (11 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
D.N. Cooper
582 papers receiving 65.3k citations
D.N. Cooper's Hit Papers
Peers
Comparison fields: 5 of 203
- Genetics 27.6k
- Clinical Biochemistry 1.3k
- Hematology 3.5k
- Molecular Biology 16.1k
- Neurology 3k
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 601 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 | 12887 |
| 2 | Analysis of protein-coding genetic variation in 60,706 humans Hit paper breakdown → | 2016 | 7891 |
| 3 | MutationTaster2: mutation prediction for the deep-sequencing age Hit paper breakdown → | 2014 | 2991 |
| 4 | Genome sequence of the Brown Norway rat yields insights into mammalian evolution Hit paper breakdown → | 2004 | 1680 |
| 5 | Human Gene Mutation Database (HGMD®): 2003 update Hit paper breakdown → | 2003 | 1504 |
| 6 | The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences Hit paper breakdown → | 1992 | 1135 |
| 7 | 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 | 1104 |
| 8 | Evolutionary and Biomedical Insights from the Rhesus Macaque Genome Hit paper breakdown → | 2007 | 1096 |
| 9 | 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 | 1073 |
| 10 | Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models Hit paper breakdown → | 2012 | 1047 |
| 11 | A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes Hit paper breakdown → | 2012 | 937 |
| 12 | The CpG dinucleotide and human genetic disease Hit paper breakdown → | 1988 | 817 |
| 13 | The yak genome and adaptation to life at high altitude Hit paper breakdown → | 2012 | 747 |
| 14 | The Human Gene Mutation Database: 2008 update Hit paper breakdown → | 2009 | 712 |
| 15 | Automated inference of molecular mechanisms of disease from amino acid substitutions Hit paper breakdown → | 2009 | 672 |
| 16 | M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity Hit paper breakdown → | 2016 | 642 |
| 17 | Inferring the molecular and phenotypic impact of amino acid variants with MutPred2 Hit paper breakdown → | 2020 | 554 |
| 18 | Insights into hominid evolution from the gorilla genome sequence Hit paper breakdown → | 2012 | 541 |
| 19 | Gene expression across mammalian organ development Hit paper breakdown → | 2019 | 537 |
| 20 | An integrative approach to predicting the functional effects of non-coding and coding sequence variation Hit paper breakdown → | 2015 | 521 |
About D.N. Cooper
D.N. Cooper is a scholar working on Genetics, Hematology, Neurology, Molecular Biology and Cancer Research, having authored 601 papers that have together received 66.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (173 papers), Genomic variations and chromosomal abnormalities (76 papers), Genetic Associations and Epidemiology (65 papers), Blood Coagulation and Thrombosis Mechanisms (55 papers), Neurofibromatosis and Schwannoma Cases (51 papers), Genomics and Phylogenetic Studies (33 papers), Chromosomal and Genetic Variations (32 papers) and Pancreatitis Pathology and Treatment (31 papers). The work is most often cited by research in Genetics (27.6k citations), Clinical Biochemistry (1.3k citations), Hematology (3.5k citations), Molecular Biology (16.1k citations) and Neurology (3k citations). D.N. Cooper has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Michael Krawczak, Peter D. Stenson, Matthew E. Mort, Edward V. Ball, Dominik Seelow, Jana Marie Schwarz, Markus Schuelke, Andrew D. Phillips, Nadia A Chuzhanova and Hildegard Kehrer‐Sawatzki. Their work appears in journals such as Human Genetics, Human Mutation, Human Genomics, 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.