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Author Details
Full Name
David J Adams
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
1980
Papers
379
H Index
78
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36219477
Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma.
J Pathol
2023
37635261
Cross-species oncogenomics offers insight into human muscle-invasive bladder cancer.
Genome Biol
2023
37957154
Knockout or inhibition of USP30 protects dopaminergic neurons in a Parkinson's disease mouse model.
Nat Commun
2023
37550943
Breathing in danger: how particulate matter pollution is putting the public at risk of lung cancer<sup>â¿ </sup>.
J Pathol
2023
38057330
Saturation genome editing of DDX3X clarifies pathogenicity of germline and somatic variation.
Nat Commun
2023
37394429
An Atlas of Variant Effects to understand the genome at nucleotide resolution.
Genome Biol
2023
37256941
FIRRM/C1orf112 mediates resolution of homologous recombination intermediates in response to DNA interstrand crosslinks.
Sci Adv
2023
37373578
The Promise of Single-Cell RNA Sequencing to Redefine the Understanding of Crohn's Disease Fibrosis Mechanisms.
J Clin Med
2023
37395714
Acetaldehyde and defective mismatch repair increase colonic tumours in a Lynch syndrome model with Aldh1b1 inactivation.
Dis Model Mech
2023
36890003
Targeting synthetic lethal paralogs in cancer.
Trends Cancer
2023
36876055
Association of germline variants in telomere maintenance genes (<i>POT1, TERF2IP, ACD,</i> and <i>TERT</i>) with spitzoid morphology in familial melanoma: A multi-center case series.
JAAD Int
2023
36539277
Population-based analysis of <i>POT1</i> variants in a cutaneous melanoma case-control cohort.
J Med Genet
2023
36711784
IFI207, a young and fast-evolving antiviral factor, stabilizes STING.
bioRxiv
2023
36637239
Prolidase Deficiency Causes Spontaneous T Cell Activation and Lupus-like Autoimmunity.
J Immunol
2023
36793076
Towards a clinically-based common coordinate framework for the human gut cell atlas: the gut models.
BMC Med Inform Decis Mak
2023
36259947
Identifying the Transcriptional Drivers of Metastasis Embedded within Localized Melanoma.
Cancer Discov
2023
34197659
Molecular pathology of skin adnexal tumours.
Histopathology
2022
35581257
Author Correction: Tumour gene expression signature in primary melanoma predicts long-term outcomes.
Nat Commun
2022
35764636
SHLD1 is dispensable for 53BP1-dependent V(D)J recombination but critical for productive class switch recombination.
Nat Commun
2022
35365791
Identification of gut microbial species linked with disease variability in a widely used mouse model of colitis.
Nat Microbiol
2022
35460607
Germline MBD4 deficiency causes a multi-tumor predisposition syndrome.
Am J Hum Genet
2022
35394069
'Know thyself' - host factors influencing cancer response to immune checkpoint inhibitors.
J Pathol
2022
35357426
Defining novel causal SNPs and linked phenotypes at melanoma-associated loci.
Hum Mol Genet
2022
36292683
Robust Genetic Analysis of the X-Linked Anophthalmic (<i>Ie</i>) Mouse.
Genes (Basel)
2022
36388765
Uncovering novel mutational signatures by <i>de novo</i> extraction with SigProfilerExtractor.
Cell Genom
2022
36112789
Transposon Mutagenesis Reveals RBMS3 Silencing as a Promoter of Malignant Progression of BRAFV600E-Driven Lung Tumorigenesis.
Cancer Res
2022
35073853
The MITRE trial protocol: a study to evaluate the microbiome as a biomarker of efficacy and toxicity in cancer patients receiving immune checkpoint inhibitor therapy.
BMC Cancer
2022
35051265
CRLF3 plays a key role in the final stage of platelet genesis and is a potential therapeutic target for thrombocythemia.
Blood
2022
35296311
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
BMC Biol
2022
34958502
Primary de-differentiated, trans-differentiated and undifferentiated melanomas: overview of the clinicopathological, immunohistochemical and molecular spectrum.
Histopathology
2022
35322020
eIF6 rebinding dynamically couples ribosome maturation and translation.
Nat Commun
2022
34791067
Variant Library Annotation Tool (VaLiAnT): an oligonucleotide library design and annotation tool for saturation genome editing and other deep mutational scanning experiments.
Bioinformatics
2022
32330367
Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease.
Pigment Cell Melanoma Res
2021
33602918
Tumour gene expression signature in primary melanoma predicts long-term outcomes.
Nat Commun
2021
33545064
Melanoma models for the next generation of therapies.
Cancer Cell
2021
33597266
Epitope spreading toward wild-type melanocyte-lineage antigens rescues suboptimal immune checkpoint blockade responses.
Sci Transl Med
2021
33764464
Mutagenic mechanisms of cancer-associated DNA polymerase ϵ alleles.
Nucleic Acids Res
2021
33761966
Unraveling the cartography of the cancer ecosystem.
Genome Biol
2021
33758365
CRISPR activation screen in mice identifies novel membrane proteins enhancing pulmonary metastatic colonisation.
Commun Biol
2021
33731925
Identification of bacteria-derived HLA-bound peptides in melanoma.
Nature
2021
33637726
Combinatorial CRISPR screen identifies fitness effects of gene paralogues.
Nat Commun
2021
33500573
Cancer research needs a better map.
Nature
2021
33931647
Cut-like homeobox 1 (CUX1) tumor suppressor gene haploinsufficiency induces apoptosis evasion to sustain myeloid leukemia.
Nat Commun
2021
33722351
Editorial overview: The most difficult of years in cancer research.
Curr Opin Genet Dev
2021
34529939
Cooperation between melanoma cell states promotes metastasis through heterotypic cluster formation.
Dev Cell
2021
34529928
Comprehensive prediction of robust synthetic lethality between paralog pairs in cancer cell lines.
Cell Syst
2021
34543445
Ethanol-induced formation of colorectal tumours and precursors in a mouse model of Lynch syndrome.
J Pathol
2021
34651586
Combined presentation and immunogenicity analysis reveals a recurrent RAS.Q61K neoantigen in melanoma.
J Clin Invest
2021
33963380
Membrane protein regulators of melanoma pulmonary colonization identified using a CRISPRa screen and spontaneous metastasis assay in mice.
G3 (Bethesda)
2021
34155350
The clinicopathologic spectrum and genomic landscape of de-/trans-differentiated melanoma.
Mod Pathol
2021
1 - 50 of 379
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Alexander Kamb
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Stephen H Friend
University of Oxford
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1978
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Sean Davis
Johns Hopkins School of Medicine, National Cancer Institute, Princeton University, University of Colorado Anschutz Medical Campus, University of Pittsburgh, University of Washington
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1974
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European Bioinformatics Institute
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Jacqueline K White
Wellcome Trust Sanger Institute
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Allan Bradley
The Wellcome Trust Sanger Institute
Co-authored papers
24
Jos Jonkers
Oncode Institute, Netherlands Cancer Institute
Co-authored papers
19
Lodewyk F A Wessels
University Medical Centre Mannheim, University of Heidelberg
Co-authored papers
19
Natasha A Karp
Wellcome Sanger Institute
Co-authored papers
18
Jonathan Flint
Center for Neurobehavioral Genetics
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17
Stephen P Jackson
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12
Paul Flicek
European Bioinformatics Institute
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Steve D M Brown
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
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Jeroen de Ridder
Center for Molecular Medicine, University Medical Center Utrecht
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10
Jane Rogers
The Wellcome Trust Sanger Institute
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9
Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Co-authored papers
9
Nicholas K Hayward
QIMR Berghofer Medical Research Institute
Co-authored papers
9
Ultan McDermott
Wellcome Sanger Institute
Co-authored papers
8
Richard Mott
Co-authored papers
8
Sara Wells
Mary Lyon Centre at Medical Research Council
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8
Martin Hrab?? de Angelis
German Center for Diabetes Research (DZD e.V.)
Co-authored papers
8
David A Rizzieri
Duke University Medical Center
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8
Ann-Marie Mallon
The Turing Institute
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7
Tim Hubbard
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7
J??r??mie Nsengimana
Population Health Sciences Institute, Newcastle University
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Monica J Justice
The Hospital for Sick Children
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Valerie Gailus-Durner
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David A Largaespada
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Peter J Campbell
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