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Genetics
UK
2024
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Genetics and Molecular Biology
UK
2024

D-Index & Metrics

Genetics

D-Index
128
Citations
115736
World Ranking
268
National Ranking
50

Medicine

D-Index
125
Citations
104766
World Ranking
3005
National Ranking
306

Research.com Recognitions

  • 2024 - Research.com Genetics in United Kingdom Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in United Kingdom Leader Award
  • 2023 - Research.com Genetics in United Kingdom Leader Award

Overview

David Neil Cooper is affiliated with Cardiff University in the United Kingdom. Their research primarily focuses on Biochemistry, Genetics, and Molecular Biology, with significant contributions in Medicine. The main subfields of their work include Molecular Biology, Genetics, Surgery, Cancer Research, and Oncology.

Cooper's research covers a range of topics, notably:

  • Genomics and Rare Diseases
  • Pancreatitis Pathology and Treatment
  • RNA and protein synthesis mechanisms
  • Genomics and Phylogenetic Studies
  • Pancreatic and Hepatic Oncology Research
  • RNA modifications and cancer
  • Gastrointestinal disorders and treatments

Their publication record includes frequent appearances in the following venues:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Human Genetics
  • Nature Communications
  • Human Mutation
  • Proceedings of the National Academy of Sciences

Cooper has contributed to several recent papers, including:

  • Inferring the molecular and phenotypic impact of amino acid variants with MutPred2, 2020, Nature Communications
  • The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting, 2020, Human Genetics
  • NextDenovo: an efficient error correction and accurate assembly tool for noisy long reads, 2024, Genome Biology
  • MutationTaster2021, 2021, Nucleic Acids Research
  • Phylogenomic analyses provide insights into primate evolution, 2023, Science

Frequent co-authors in Cooper's work include:

  • Peter D. Stenson
  • Jian-Min Chen
  • Claude Férec
  • Emmanuelle Masson
  • Yuval Itan

In addition to articles, Cooper has authored several books published by Garland Science eBooks, such as:

  • Human Gene Evolution, 2024
  • Functional Analysis of the Human Genome, 2020
  • Gene Therapy, 2020

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Analysis of protein-coding genetic variation in 60,706 humans

    Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • MutationTaster2: mutation prediction for the deep-sequencing age

    Jana Marie Schwarz;David Neil Cooper;Markus Schuelke;Dominik Seelow

  • Genome sequence of the Brown Norway rat yields insights into mammalian evolution

    Richard A. Gibbs;George M. Weinstock;Michael L. Metzker;Donna M. Muzny

  • Human Gene Mutation Database (HGMD): 2003 update.

    Peter Daniel Stenson;Edward Vincent Ball;Matthew Edwin Mort;Andrew David Phillips

  • A massive phytoplankton bloom induced by an ecosystem-scale iron fertilization experiment in the equatorial Pacific Ocean

    Kenneth H. Coale;Kenneth S. Johnson;Kenneth S. Johnson;Steve E. Fitzwater;R. Michael Gordon

  • The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences.

    Michael Krawczak;Jochen Reiss;David Neil Cooper

  • Encyclopedia of life sciences

    Yixian Zheng;Cheryl Tickle;Roland Jansson;Hildegard Kehrer-Sawatzki

  • Evolutionary and biomedical insights from the rhesus macaque genome

    Richard A. Gibbs;Jeffrey Rogers

  • The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies

    Peter D. Stenson;Matthew Mort;Edward V. Ball;Katy Evans

  • A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

    Daniel G. MacArthur;Daniel G. MacArthur;Suganthi Balasubramanian;Adam Frankish;Ni Huang

  • The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

    Peter D. Stenson;Matthew Mort;Edward V. Ball;Katy Shaw

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models.

    Hashem A. Shihab;Julian Gough;David Neil Cooper;Peter Daniel Stenson

  • The Human Gene Mutation Database: 2008 update

    Peter Daniel Stenson;Matthew Mort;Edward Ball;Katy Howells

  • The CpG dinucleotide and human genetic disease

    David Neil Cooper;Hagop Youssoufian

  • The yak genome and adaptation to life at high altitude

    Qiang Qiu;Guojie Zhang;Tao Ma;Wubin Qian

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • The human gene mutation database

    David Neil Cooper;Edward V. Ball;Michael Krawczak

Frequent Co-Authors

Jian-Min Chen
Jian-Min Chen University of Western Brittany
Matthew Mort
Matthew Mort Cardiff University
Michael Krawczak
Michael Krawczak Kiel University
Peter D. Stenson
Peter D. Stenson Cardiff University
Nadia Chuzhanova
Nadia Chuzhanova Nottingham Trent University
Claude Férec
Claude Férec University of Western Brittany
Hildegard Kehrer-Sawatzki
Hildegard Kehrer-Sawatzki University of Ulm
Meena Upadhyaya
Meena Upadhyaya Cardiff University
Kenneth K. Kidd
Kenneth K. Kidd Yale University
Anne M. Bowcock
Anne M. Bowcock Icahn School of Medicine at Mount Sinai

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