Author

Celina Whalley

University of BirminghamORCID 0000-0001-7183-5388Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 5 Research Focus:differential expression· 4 Assay:DNA methylation· 3 Research Focus:gene regulatory network inference· 3 Organism:human· 3 Assay:whole-genome sequencing· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Andrew David BeggsiD· 4 shared Aleksandar J DimovskiiD· 1 shared Alexander J. GarviniD· 1 shared Andrea SottorivaiD· 1 shared Andreas J GruberiD· 1 shared Andrés Dacal Rivas· 1 shared Andrew BlakeiD· 1 shared Andrew Warwick RobertsiD· 1 shared

Activity by Year

2017-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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4 shared papersDevelopmental Biology

Andrew David BeggsORCID

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5 papers

Recent·Most cited

Developmental BiologyDevelopmental CellPeer-reviewedJan 1, 2023

The miR-430 locus with extreme promoter density is a transcription body organizer, which facilitates long range regulation in zygotic genome activation

Yavor Hadzhiev, Lucy Wheatley, Ledean Cooper…·Ferenc Müller

The paper identifies a high-density miR-430 promoter cluster that forms a transcription body, enabling early gene activation during the minor wave of zygotic genome activation in zebrafish.

43 citationstop 4%

zebrafishwhole-genome sequencing

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Molecular BiologybioRxivPreprintMar 20, 2022

RAD52 underlies the synthetic-lethal relationship between BRCA1/2 and 53BP1 deficiencies and DNA polymerase theta loss.

Katarzyna Starowicz, George E. Ronson, Elizabeth J. Anthony…·Joanna R. Morris

The paper identifies RAD52 as the mediator of synthetic-lethal interactions between BRCA1/2, 53BP1 deficiencies, and DNA polymerase theta loss in murine cells.

1 citation

mousestatistical model

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GeneticsbioRxivPreprintApr 27, 2021

Germline loss-of-function variants in the base-excision repair gene MBD4 cause a Mendelian recessive syndrome of adenomatous colorectal polyposis and acute myeloid leukaemia

Claire Palles, Edward Chew, Judith E. Grolleman…·Richarda M. de Voer

3 citations

humanDNA methylation

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Genetic & Genomic MedicineEpigenomesPeer-reviewedFeb 19, 2021

Ultra-low DNA input into whole genome methylation assays and detection of oncogenic methylation & copy number variants in circulating tumour DNA

Celina Whalley, Karl F.B. Payne, Enric Domingo…·Andrew David Beggs

This study demonstrates that the Illumina Infinium HD methylation assay can reliably detect methylation and copy number variants in low-input DNA samples, including circulating tumour DNA.

13 citations

humanDNA methylation

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GenomicsbioRxivPreprintMar 6, 2017

Whole genome methylation analysis of non-dysplastic Barretts oesophagus that progresses to invasive cancer

MP Dilworth, Tom Nieto, JD Stockton…·Andrew David Beggs

The paper identifies methylation markers that distinguish non-dysplastic Barrett's oesophagus patients who progress to cancer from those that do not.

DOI 10.1101/114298

humanDNA methylation

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