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Adam P Giess

Effects of control interventions on Clostridium difficile infection in England: an observational study
2017 · Kate E Dingle, Xavier Didelot, et al. · The Lancet Infectious Diseases · 328
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Nested Russian Doll-Like Genetic Mobility Drives Rapid Dissemination of the Carbapenem Resistance Gene bla KPC
2016 · Anna E. Sheppard, Nicole Stoesser, et al. · Antimicrobial Agents and Chemotherapy · 298
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Substitution mutational signatures in whole-genome–sequenced cancers in the UK population
2022 · Andrea Degasperi, Xueqing Zou, et al. · Science · 283
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes
2022 · Wei Wei, Katherine R. Schon, et al. · Nature · 250
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Assessment of Mycobacterium tuberculosis transmission in Oxfordshire, UK, 2007–12, with whole pathogen genome sequences: an observational study
2014 · Timothy M Walker, Maeve K Lalor, et al. · The Lancet Respiratory Medicine · 223
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Origins and impact of extrachromosomal DNA
2024 · Chris Bailey, Oriol Pich, et al. · Nature · 184
A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage
2021 · Xueqing Zou, Gene Ching Chiek Koh, et al. · Nature Cancer · 160
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Klebsiella pneumoniae Carbapenemase (KPC)-Producing K. pneumoniae at a Single Institution: Insights into Endemicity from Whole-Genome Sequencing
2015 · Amy J. Mathers, Nicole Stoesser, et al. · Antimicrobial Agents and Chemotherapy · 148
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Genome Sequencing of an Extended Series of NDM-Producing Klebsiella pneumoniae Isolates from Neonatal Infections in a Nepali Hospital Characterizes the Extent of Community- versus Hospital-Associated Transmission in an Endemic Setting
2014 · N. Stoesser, A. Giess, et al. · Antimicrobial Agents and Chemotherapy · 131
Maternal colonization with Streptococcus agalactiae and associated stillbirth and neonatal disease in coastal Kenya
2016 · Anna C. Seale, Angela C. Koech, et al. · Nature Microbiology · 118
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Ongoing chromothripsis underpins osteosarcoma genome complexity and clonal evolution
2025 · Jose Espejo Valle-Inclan, Solange De Noon, et al. · Cell · 97
Extensive Within-Host Diversity in Fecally Carried Extended-Spectrum-Beta-Lactamase-Producing Escherichia coli Isolates: Implications for Transmission Analyses
2015 · N. Stoesser, A. E. Sheppard, et al. · Journal of Clinical Microbiology · 86
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Signatures of TOP1 transcription-associated mutagenesis in cancer and germline
2022 · Martin A. M. Reijns, David A. Parry, et al. · Nature · 83
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Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features
2022 · Pauline Robbe, Kate E. Ridout, et al. · Nature Genetics · 76
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Cdc14 phosphatase promotes segregation of telomeres through repression of RNA polymerase II transcription
2011 · Andres Clemente-Blanco, Nicholas Sen, et al. · Nature Cell Biology · 72
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Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders
2021 · Charlie Rowlands, Huw B. Thomas, et al. · Scientific Reports · 66
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Spectrum of mutational signatures in T-cell lymphoma reveals a key role for UV radiation in cutaneous T-cell lymphoma
2021 · Christine L. Jones, Andrea Degasperi, et al. · Scientific Reports · 65
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Genome sequencing reveals underdiagnosis of primary ciliary dyskinesia in bronchiectasis
2022 · Amelia Shoemark, Helen Griffin, et al. · European Respiratory Journal · 64
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
2022 · Nadine Spielmann, Gregor Miller, et al. · Nature Cardiovascular Research · 63
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REPARATION: ribosome profiling assisted (re-)annotation of bacterial genomes
2017 · Elvis Ndah, Veronique Jonckheere, et al. · Nucleic Acids Research · 63
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Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
2023 · Helena Martins Custodio, Lisa M Clayton, et al. · Brain · 62
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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy
2020 · David A. Parry, Carol-Anne Martin, et al. · Genetics in Medicine · 57
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An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy
2020 · Alistair T Pagnamenta, Rauan Kaiyrzhanov, et al. · Brain · 55
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Dynamics of MDR Enterobacter cloacae outbreaks in a neonatal unit in Nepal: insights using wider sampling frames and next-generation sequencing
2015 · N. Stoesser, A. E. Sheppard, et al. · Journal of Antimicrobial Chemotherapy · 51
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An intermediate-effect size variant in UMOD confers risk for chronic kidney disease
2022 · Eric Olinger, Céline Schaeffer, et al. · Proceedings of the National Academy of Sciences · 49
Works count: 99
Citation count: 4,373
H-index: 37
I10-index: 63
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