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Genetics

D-Index
65
Citations
21590
World Ranking
2667
National Ranking
339

Overview

Anthony J. Brookes is affiliated with the University of Leicester in the United Kingdom.

Their research intersectsthe fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a focus on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Cancer Research, and Economics and Econometrics.

The main topics in their work include:

  • Genomics and Rare Diseases
  • Ethics in Clinical Research
  • Cancer Genomics and Diagnostics
  • Genomic variations and chromosomal abnormalities
  • Health Systems, Economic Evaluations, Quality of Life
  • Dementia and Cognitive Impairment Research
  • Bioinformatics and Genomic Networks

Recent publications by Anthony J. Brookes include:

  • GA4GH: International policies and standards for data sharing across genomic research and healthcare, 2021, Cell Genomics
  • The sputum microbiome is distinct between COPD and health, independent of smoking history, 2020, Respiratory Research
  • Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases, 2021, European Journal of Human Genetics
  • The Data Use Ontology to streamline responsible access to human biomedical datasets, 2021, Cell Genomics
  • Beacon v2 and Beacon networks: A "lingua franca" for federated data discovery in biomedical genomics, and beyond, 2022, Human Mutation

Frequent co-authors collaborating with Anthony J. Brookes include:

  • Colin Veal
  • Spencer Gibson
  • Sergi Beltrán
  • Steven Laurie
  • Greg Warren

Anthony J. Brookes has published multiple articles in the following venues:

  • European Journal of Human Genetics
  • Faculty of 1000 Research Ltd
  • Nature Medicine
  • Cell Genomics
  • Frontiers in Neurology

Best Publications

  • Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

    R. Sherrington;E. I. Rogaev;Y. Liang;E. A. Rogaeva

  • The essence of SNPs.

    Anthony J. Brookes

  • A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

    Ludmila Prokunina;Casimiro Castillejo-López;Fredrik Öberg;Iva Gunnarsson

  • The BioMart community portal: an innovative alternative to large, centralized data repositories

    Damian Smedley;Syed Haider;Steffen Durinck;Luca Pandini

  • The Matchmaker Exchange: a platform for rare disease gene discovery

    Anthony A. Philippakis;Anthony A. Philippakis;Anthony A. Philippakis;Danielle R. Azzariti;Sergi Beltran;Anthony J. Brookes

  • Dynamic allele-specific hybridization

    W. Mathias Howell;Magnus Jobs;Ulf Gyllensten;Anthony J. Brookes

  • International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.

    Kym M. Boycott;Ana Rath;Jessica X. Chong;Taila Hartley

  • Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones

    Tadashi Imanishi;Takeshi Itoh;Yutaka Suzuki;Claire O'Donovan

  • MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

    Maria Swanberg;Olle Lidman;Leonid Padyukov;Per Eriksson

  • Targeted enrichment of genomic DNA regions for next generation sequencing

    Florian Mertes;Abdou ElSharawy;Sascha Sauer;Joop M.L.M. van Helvoort

  • Systems medicine and integrated care to combat chronic noncommunicable diseases

    Jean Bousquet;Josep M. Anto;Peter J. Sterk;Ian M. Adcock

  • Splinkerettes—improved vectorettes for greater efficiency in PCR walking

    Rebecca S. Devon;David J. Porteous;Anthony J. Brookes

  • Complex SNP-related sequence variation in segmental genome duplications.

    David Fredman;Stefan J White;Susanna Potter;Evan E Eichler

  • Point Mutations (Thr240Arg and Ala311Stop) in theParkinGene

    Nobutaka Hattori;Hiroto Matsumine;Shuichi Asakawa;Tohru Kitada;Tohru Kitada

  • Robust and Accurate Single Nucleotide Polymorphism Genotyping by Dynamic Allele-Specific Hybridization (DASH): Design Criteria and Assay Validation

    Jonathan A. Prince;Lars Feuk;W. Mathias Howell;Magnus Jobs

  • The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease

    Tudor Groza;Sebastian Köhler;Dawid Moldenhauer;Nicole Vasilevsky

  • Prepublication data sharing.

    E Birney;T J Hudson;Green

  • SNP association studies in Alzheimer's disease highlight problems for complex disease analysis

    Tesfai Emahazion;Lars Feuk;Magnus Jobs;Sarah L. Sawyer

  • Single nucleotide polymorphisms in the proximal promoter region of the adiponectin (APM1) gene are associated with type 2 diabetes in Swedish Caucasians

    Harvest F. Gu;Adili Abulaiti;Claes Göran Östenson;Keith Humphreys

  • GWAS Central: a comprehensive resource for the comparison and interrogation of genome-wide association studies

    Tim Beck;Robert K Hastings;Sirisha Gollapudi;Robert C Free

Frequent Co-Authors

Kaj Blennow
Kaj Blennow University of Gothenburg
David J. Porteous
David J. Porteous University of Edinburgh
Pui-Yan Kwok
Pui-Yan Kwok University of California, San Francisco
Niels Andreasen
Niels Andreasen Karolinska University Hospital
Barend Mons
Barend Mons Leiden University Medical Center
Stephen J. Chanock
Stephen J. Chanock National Institutes of Health
Bartha Maria Knoppers
Bartha Maria Knoppers McGill University Health Centre
Paul Flicek
Paul Flicek The Jackson Laboratory
Pieter Jelle Visser
Pieter Jelle Visser Amsterdam University Medical Centers
Lars Feuk
Lars Feuk Uppsala University

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