Author

Samantha Farrow

National Health Service

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

Biology Disciplines

Click to filter author papers

Genomics· 3 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:bulk RNA-seq· 4 Research Focus:gene regulatory network inference· 4 Organism:human· 4 Approach:statistical model· 4 Assay:ChIP-seq· 2 Research Focus:differential expression· 2 Assay:DNA methylation· 2 Approach:benchmark study· 1

Frequent Co-Authors

Frances BurdeniD· 4 shared Kate DownesiD· 4 shared Mattia FrontiniiD· 4 shared Laura ClarkeiD· 3 shared Paul FlicekiD· 3 shared Christoph BockiD· 2 shared David RichardsoniD· 2 shared Denis SeyresiD· 2 shared

Activity by Year

2017-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

4 shared papersGenomics

Frances BurdenORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Transcriptional, epigenetic and metabolic signatures in cardiometabolic syndrome defined by extreme phenotypes.

Denis Seyres, Alessandra Cabassi, John J. Lambourne, Frances Burden, Samantha Farrow, Harriet McKinney, Joana Batista, Carly Kempster, Maik Pietzner, Oliver C. Slingsby, Thong Huy Cao, Paulene A. Quinn, Luca Stefanucci, Matthew C. Sims, Karola Rehnström, , Mattia Frontini

The paper identifies molecular and metabolic signatures of cardiometabolic syndrome using extreme phenotype groups and shows changes after bariatric surgery.

Clinical Epigenetics · Mar 12, 2022Peer-reviewedGenomics

Cell type specific novel lincRNAs and circRNAs in the BLUEPRINT haematopoietic transcriptomes atlas.

Luigi Grassi, Osagie G. Izuogu, Natasha Andressa Nogueira Jorge, Denis Seyres, Mariona Bustamante, Frances Burden, Samantha Farrow, Neda Farahi, Fergal J. Martin, Adam Frankish, Jonathan M. Mudge, Myrto A. Kostadima, Romina Petersen, John J. Lambourne, Sophia Rowlston, , Mattia Frontini

The paper identifies novel long non-coding RNAs and circular RNAs in hematopoietic cells using BLUEPRINT consortium data, highlighting their cell type specificity.

bioRxiv · Sep 10, 2019 · PreprintGenomics

Variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility

Stephen B. Watt, Louella J. Vasquez, Klaudia Walter, Alice Mann, Kousik Kundu, Lu Chen, Yan Yan, Simone Ecker, Frances Burden, Samantha Farrow, Ben W. Farr, Valentina Iotchkova, Heather Elding, Daniel G. Mead, Manuel Tardáguila, , Nicole Soranzo

The paper identifies how variation in PU.1 binding and chromatin looping at neutrophil enhancers influences autoimmune disease susceptibility and cell count differences.

bioRxiv · Apr 29, 2019 · PreprintGenetics

Comparative analysis of neutrophil and monocyte epigenomes

Daniel Rico, Joost H.A. Martens, Kate Downes, Enrique Carrillo de Santa Pau, Véra Pancaldi, Alessandra Breschi, David Richardson, Simon Charles Heath, Sadia Saeed, Mattia Frontini, Lu Chen, Stephen B. Watt, Fabian Müller, Laura Clarke, Hindrik H. D. Kerstens, , Hendrik G. Stunnenberg

This study compares the epigenomes of neutrophils and monocytes to identify regulatory elements and chromatin states, revealing differences in enhancer activity and DNA methylation.

bioRxiv · Dec 22, 2017 · PreprintGenomics