Author

Katherine Yates

University of Cambridge

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Allan LawrieiD· 1 shared Andrea OlschewskiiD· 1 shared Andrew J. PeacockiD· 1 shared Anton Vonk NoordegraafiD· 1 shared Arjan C. HouwelingiD· 1 shared Barbara Girerd· 1 shared Bin LiuiD· 1 shared Carmen Treacy· 1 shared

Activity by Year

2018-2018 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Allan LawrieORCID

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1 paper

Recent·Most cited

Identification of novel rare sequence variation underlying heritable pulmonary arterial hypertension

Stefan Gräf, Matthias Haimel, Marta Bleda, Charaka Hadinnapola, Laura Southgate, Wei Li, Joshua Hodgson, Bin Liu, Richard M. Salmon, Mark R. Southwood, Rajiv D. Machado, Jennifer M. Martin, Carmen Treacy, Katherine Yates, Louise C. Daugherty, , Nicholas W. Morrell

This study identifies novel rare genetic variants associated with heritable pulmonary arterial hypertension through whole genome sequencing of cases and controls.

Nature Communications · Apr 11, 2018Peer-reviewedGenetics