Sancha Martin - Concepedia

Author

Sancha Martin

Also Known As

Amber L. Johns, Davies, Helen R, I Martincorena, Iigo Martincorena, Inigo Martincorena, Iñigo Martincorena, Jeffrey Marks, John W. M. Martens, Luke Marsden, Marco A. Marra

160

Publications

49K

Citations

H-Index

Concepts

All Affiliations

Wellcome Sanger Institute University of Cambridge Oslo University Hospital Dana-Farber Cancer Institute Centre Léon Bérard

About

Sancha Martin is an author at Wellcome Sanger Institute specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	17	12.7K
2	Cell Biology	3	3	1.2K
3	Engineering	1	1	1.7K
4	Health Sciences	1	1	815
5	Natural Sciences	1	1	166

Sancha Martin

Publications

23.4K

Citations

H-Index

Page 1

	Year	Citations
The zebrafish reference genome sequence and its relationship to the human genome Kerstin Howe, Matthew D. Clark, Carlos Torroja, Nature	2013	5K
Pan-cancer analysis of whole genomes Lauri A. Aaltonen, Federico Abascal, Adam Abeshouse, Nature	2020	3.1K
Landscape of somatic mutations in 560 breast cancer whole-genome sequences Serena Nik‐Zainal, Helen Davies, Johan Staaf, Nature Somatic VariantSomatic MutationsTumor HeterogeneityMedicineGenetics	2016	2.3K
Mutational Processes Molding the Genomes of 21 Breast Cancers Serena Nik‐Zainal, Ludmil B. Alexandrov, David C. Wedge, Cell Somatic VariantTumor HeterogeneityGeneticsMutational ProcessesDna Replication	2012	2K
The landscape of cancer genes and mutational processes in breast cancer Philip J. Stephens, Patrick Tarpey, Helen Davies, Nature Breast OncologyEngineeringSomatic VariantTumor HeterogeneityCancer Genes	2012	1.7K
The Life History of 21 Breast Cancers Serena Nik‐Zainal, Peter Van Loo, David C. Wedge, Cell Tumor BiologyBreast OncologyMedicineEpidemiology Of CancerPathology	2012	1.5K
HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures Helen Davies, Dominik Głodzik, Sandro Morganella, Nature Medicine Genetic DisorderMedicineGeneticsBrca2 DeficiencyPathology	2017	1.1K
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone Sam Behjati, Patrick Tarpey, Nadège Presneau, Nature Genetics Tumor BiologyDistinct H3f3aBone Morphogenic ProteinGiant Cell TumorPathology	2013	836
Subclonal diversification of primary breast cancer revealed by multiregion sequencing Lucy Yates, Moritz Gerstung, Stian Knappskog, Nature Medicine Breast OncologyOncologyTumor HeterogeneityMedicinePathology	2015	815
DNA sequence and analysis of human chromosome 9 Sean Humphray, Karen Oliver, Adrienne Hunt, Nature ChromatinDnaCytogeneticsGeneticsHuman Chromosome 9	2004	654

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