Sarah Edkins

55.8k citations

23 papers · 1.7k indexed · h-index 17

Impact in

Cancer Research top 5%
- Cancer Genomics and Diagnostics
Oncology top 5%
- Colorectal Cancer Treatments and Studies

Papers in

Genetics 10
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 4
Microbiology 2

Co-authors: Michael R. Stratton Sarah O’Meara P. Andrew Futreal Graham R. Bignell Richard Wooster Chris Greenman Helen Davies Thomas Santarius
Journals: The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (2 papers)Journal of Comparative Pathology (1 paper)British Journal of Cancer (1 paper)Bioinformatics (1 paper)
Partner nations: United Kingdom Brazil United States

In The Last Decade

Sarah Edkins

23 papers receiving 1.7k citations

Peers

Countries citing papers authored by Sarah Edkins

Since Specialization

Citations

This map shows the geographic impact of Sarah Edkins's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sarah Edkins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Edkins more than expected).

Fields of papers citing papers by Sarah Edkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah Edkins. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sarah Edkins. The network helps show where Sarah Edkins may publish in the future.

Co-authors

The 25 scholars most cited alongside Sarah Edkins, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sarah Edkins Line = papers co-authored together Sarah Edkins links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Gene filtering strategies for machine learning guided biomarker discovery using neonatal sepsis RNA-seq data Frontiers in Genetics ·Edward Parkinson, Federico Liberatore, William J. Watkins, Robert Andrews, Sarah Edkins, Julie Hibbert, Tobias Strunk, Andrew Currie, Peter Ghazal	2023	3
2	Distinctive Features of Orbital Adipose Tissue (OAT) in Graves’ Orbitopathy International Journal of Molecular Sciences ·Lei Zhang, Anna Evans, Chris von Ruhland, Mohd Shazli Draman, Sarah Edkins, Amy E. Vincent, Rolando Berlinguer‐Palmini, Aled Rees, Anjana Haridas, Dan Morris, Andrew R. Tee, Marian Ludgate, Douglass M. Turnbull, Fredrik Karpe, Colin Dayan	2020	11
3	Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia Stem Cell Reports ·Juan Bautista Menendez-Gonzalez, Milica Vukovic, Ali Abdelfattah, Lubaid Saleh, Alhomidi Almotiri, Leigh-anne Thomas, Aloña Agirre‐Lizaso, Aleksandra Azevedo, Ana Catarina Menezes, Giusy Tornillo, Sarah Edkins, Kay Kong, Peter Giles, Fernando Anjos‐Afonso, Alex Tonks, Ashleigh S. Boyd, Kamil R. Kranc, Neil P. Rodrigues	2019	55
4	An Evaluation of Different Target Enrichment Methods in Pooled Sequencing Designs for Complex Disease Association Studies PLoS ONE ·Aaron Day-Williams, Kirsten McLay, Eleanor Drury, Sarah Edkins, Alison J. Coffey, Aarno Palotie, Eleftheria Zeggini	2011	10
5	GLO1—A novel amplified gene in human cancer Genes Chromosomes and Cancer ·Thomas Santarius, Graham R. Bignell, Chris Greenman, Sara Widaa, Lina Chen, Claire Mahoney, Adam P. Butler, Sarah Edkins, Sahar Waris, Paul J. Thornalley, P. Andrew Futreal, Michael R. Stratton	2010	90
6	Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation European Journal of Human Genetics ·Sinitdhorn Rujirabanjerd, John W. Nelson, Patrick Tarpey, Anna Hackett, Sarah Edkins, F. Lucy Raymond, Charles E. Schwartz, Gillian Turner, Shigeki Iwase, Yang Shi, P. Andrew Futreal, Michael R. Stratton, Jozef Gécz	2009	50
7	PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data Biostatistics ·Chris Greenman, Graham R. Bignell, Adam P. Butler, Sarah Edkins, Jonathan Hinton, David Beare, S. Swamy, Thomas Santarius, Lina Chen, Sara Widaa, P. Andrew Futreal, Michael R. Stratton	2009	135
8	LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition British Journal of Cancer ·Claire Mahoney, Bhudipa Choudhury, Helen Davies, Sarah Edkins, Chris Greenman, Gijs van Haaften, Tatiana Mironenko, Thomas Santarius, Claire Stevens, Michael R. Stratton, P. Andrew Futreal	2009	96
9	Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation The American Journal of Human Genetics ·Florence Molinari, François Foulquier, Patrick Tarpey, Willy Morelle, Sarah Boissel, Jon W. Teague, Sarah Edkins, P. Andrew Futreal, Michael R. Stratton, Gillian Turner, Gert Matthijs, Jozef Gécz, Arnold Münnich, Laurence Colleaux	2008	110
10	Oligosaccharyltransferase subunits mutations in non-syndromic mental retardation European Journal of Human Genetics ·Florence Molinari, S. Romano, François Foulquier, Willy Morelle, Pascale de Lonlay, PS Tarpey, J. Teague, Sarah Edkins, PA Futreal, Stratton, M Partington, G. Turner, Gert Matthijs, Jozef Gécz, Arnold Münnich, Laurence Colleaux	2007	4
11	Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution Genome Research ·Graham R. Bignell, Thomas Santarius, Jessica C. Pole, Adam P. Butler, Janet Perry, Erin Pleasance, Chris Greenman, Andrew Menzies, Sheila Taylor, Sarah Edkins, Peter J. Campbell, Michael A. Quail, Bob Plumb, Lucy Matthews, Kirsten McLay, Paul A. Edwards, Jane Rogers, Richard Wooster, P. Andrew Futreal, Michael R. Stratton	2007	143
12	A novel Gln358Glu mutation in ectodysplasin A associated with X‐linked dominant incisor hypodontia American Journal of Medical Genetics Part A ·Patrick Tarpey, Trevor J. Pemberton, David W. Stockton, Parimal Das, Vasiliki Ninis, Sarah Edkins, P. Andrew Futreal, Richard Wooster, Sushanth Kamath, Rabindra Nayak, Michael R. Stratton, Pragna I. Patel	2007	42
13	High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison Genomics ·Helen Davies, Ed Dicks, Philip Stephens, Charles Cox, Jon W. Teague, Chris Greenman, Graham R. Bignell, Sarah O’Meara, Sarah Edkins, Adrian G. Parker, Claire Stevens, Andrew Menzies, Matthew J. Blow, Bill Bottomley, Mark Dronsfield, P. Andrew Futreal, Michael R. Stratton, Richard Wooster	2006	32
14	Recurrent KRAS codon 146 mutations in human colorectal cancer Cancer Biology & Therapy ·Sarah Edkins, Sarah O’Meara	2006	183
15	Mutations in the RSK2(RPS6KA3) gene cause Coffin–Lowry syndrome and nonsyndromic X‐linked mental retardation Clinical Genetics ·Michael Field, Patrick Tarpey, J Boyle, Sarah Edkins, Judith Goodship, Ying Luo, Jennifer A. Moon, Jon W. Teague, MR Stratton, PA Futreal, Richard Wooster, FL Raymond, Gillian Turner	2006	21
16	A survey of homozygous deletions in human cancer genomes Proceedings of the National Academy of Sciences ·Charles Cox, Graham R. Bignell, Chris Greenman, Arne Stabenau, William Warren, Philip Stephens, Helen Davies, Stephen M. Watt, Jon W. Teague, Sarah Edkins, Ewan Birney, Douglas F. Easton, Richard Wooster, P. Andrew Futreal, Michael R. Stratton	2005	69
17	The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21 The American Journal of Human Genetics ·Nazneen Rahman, Melanie Dunstan, M. Dawn Teare, Sandra Hanks, Sarah Edkins, Jaime Hughes, Graham R. Bignell, Grazia M.S. Mancini, Wim J. Kleijer, Mary Ellen Campbell, Gökhan Keser, Carol M. Black, Nigel Williams, Laura Arbour, Matthew L. Warman, Andrea Superti‐Furga, P. Andrew Futreal, F. Michael Pope	2002	58
18	Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia. PubMed ·Siu Tsan Yuen, Helen Davies, Tsun Leung Chan, Judy Ho, Graham R. Bignell, Charles Cox, Philip Stephens, Sarah Edkins, Wendy Tsui, Annie S Y Chan, P. Andrew Futreal, Michael R. Stratton, Richard Wooster, Suet Yi Leung	2002	359
19	The Gene for Cherubism Maps to Chromosome 4p16.3 The American Journal of Human Genetics ·Jonathan Mangion, Nazneen Rahman, Sarah Edkins, Rita Barfoot, Trang Thi Thu Nguyen, Ásgeir Sigurðsson, John Townend, David Fitzpatrick, Adrienne M. Flanagan, Michael R. Stratton	1999	115
20	A Gene for Lymphedema-Distichiasis Maps to 16q24.3 The American Journal of Human Genetics ·Jonathan Mangion, Nazneen Rahman, Sahar Mansour, Glen Brice, Jane L. Rosbotham, Anne H. Child, Victoria A. Murday, Peter Mortimer, Rita Barfoot, A Sigurdsson, Sarah Edkins, M. Sarfarazi, K G Burnand, Alison Evans, T. O. NUNAN, Michael R. Stratton, Steve Jeffery	1999	64

About Sarah Edkins

Sarah Edkins is a scholar working on Genetics, Microbiology, Oral Surgery, Pathology and Forensic Medicine and Molecular Biology, having authored 23 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (5 papers), Genomics and Phylogenetic Studies (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (3 papers), Glycosylation and Glycoproteins Research (3 papers), Cancer Genomics and Diagnostics (3 papers) and Gene expression and cancer classification (3 papers). The work is most often cited by research in Cancer Research (380 citations), Oncology (570 citations), Pathology and Forensic Medicine (365 citations), Oral Surgery (131 citations) and Molecular Biology (989 citations). Sarah Edkins has collaborated with scholars based in United Kingdom, Brazil and United States. Frequent co-authors include Michael R. Stratton, Sarah O’Meara, P. Andrew Futreal, Graham R. Bignell, Richard Wooster, Chris Greenman, Helen Davies, Thomas Santarius, Philip Stephens and Charles Cox. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Journal of Comparative Pathology, British Journal of Cancer and Bioinformatics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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