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Eva G. Álvarez

University College London · ES
Area of research
Cancer Research · Pathology and Forensic Medicine
Research interest
Research interests include Cancer Genomics and Diagnostics, Genetic factors in colorectal cancer, Research Data Management Practices, and Genomics and Phylogenetic Studies.
h-index
28
citations
16,947
works
84
NIH funding
primary concept
Biology
email

Recent publications

Author Correction: Pan-cancer analysis of whole genomes
Nature 2023cited by 13position: middledoi
Author Correction: The repertoire of mutational signatures in human cancer
Nature 2023cited by 9position: middledoi
Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Nature Genetics 2023cited by 4position: middledoi
Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers
Nature Genetics 2023cited by 2position: middledoi
Author Correction: The landscape of viral associations in human cancers
Nature Genetics 2023cited by 1position: middledoi
Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Nature Genetics 2023cited by 1position: middledoi
Author Correction: A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
Nature Communications 2022cited by 2position: middledoi
Author Correction: Divergent mutational processes distinguish hypoxic and normoxic tumours
Nature Communications 2022cited by 1position: middledoi
Author Correction: Genomic footprints of activated telomere maintenance mechanisms in cancer
Nature Communications 2022cited by 0position: middledoi
Author Correction: High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations
Nature Communications 2022cited by 0position: middledoi
Author Correction: Inferring structural variant cancer cell fraction
Nature Communications 2022cited by 0position: middledoi
Author Correction: Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig
Nature Communications 2022cited by 0position: middledoi
Aberrant integration of Hepatitis B virus DNA promotes major restructuring of human hepatocellular carcinoma genome architecture
Nature Communications 2021cited by 55position: firstdoi
The repertoire of mutational signatures in human cancer
Nature 2020cited by 3,686position: middledoi
Pan-cancer analysis of whole genomes
Nature 2020cited by 3,258position: middledoi
Patterns of somatic structural variation in human cancer genomes
Nature 2020cited by 979position: middledoi
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Nature Genetics 2020cited by 765position: middledoi
Comprehensive molecular characterization of mitochondrial genomes in human cancers
Nature Genetics 2020cited by 507position: middledoi
The landscape of viral associations in human cancers
Nature Genetics 2020cited by 398position: middledoi
Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Nature Genetics 2020cited by 305position: middledoi
A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns
Nature Communications 2020cited by 235position: middledoi
Divergent mutational processes distinguish hypoxic and normoxic tumours
Nature Communications 2020cited by 142position: middledoi
Sex differences in oncogenic mutational processes
Nature Communications 2020cited by 125position: middledoi
High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations
Nature Communications 2020cited by 75position: middledoi
Inferring structural variant cancer cell fraction
Nature Communications 2020cited by 56position: middledoi
Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig
Nature Communications 2020cited by 50position: middledoi
Publisher Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Nature Genetics 2020cited by 13position: middledoi
Germline determinants of the somatic mutation landscape in 2,642 cancer genomes
bioRxiv (Cold Spring Harbor Laboratory) 2017cited by 26position: middledoi
Pan-cancer analysis of whole genomes reveals driver rearrangements promoted by LINE-1 retrotransposition in human tumours
bioRxiv (Cold Spring Harbor Laboratory) 2017cited by 18position: middledoi

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Frequent collaborators

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