Sarah Hunt

118.1k total citations · 3 hit papers
55 papers, 8.2k citations indexed

About

Sarah Hunt is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sarah Hunt has authored 55 papers receiving a total of 8.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 24 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Sarah Hunt's work include Genomics and Rare Diseases (17 papers), Genetic Associations and Epidemiology (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Sarah Hunt is often cited by papers focused on Genomics and Rare Diseases (17 papers), Genetic Associations and Epidemiology (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Sarah Hunt collaborates with scholars based in United Kingdom, United States and Netherlands. Sarah Hunt's co-authors include Fiona Cunningham, Paul Flicek, Anja Thormann, William McLaren, Laurent Gil, Graham R. S. Ritchie, Harpreet Singh Riat, Panos Deloukas, David Bentley and Peter Donnelly and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Sarah Hunt

53 papers receiving 8.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Ensembl Variant Effect Predictor

2016 4.0k citations William McLaren, Laurent Gil et al. Genome biology profile →
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

2004 707 citations Sarah Hunt, Panos Deloukas et al. profile →
Ensembl variation resources

2018 309 citations Sarah Hunt, William McLaren et al. profile →

Peers

Countries citing papers authored by Sarah Hunt

Since Specialization

Citations

This map shows the geographic impact of Sarah Hunt'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 Hunt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Hunt more than expected).

Fields of papers citing papers by Sarah Hunt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah Hunt. 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 Hunt. The network helps show where Sarah Hunt may publish in the future.

Co-authorship network of co-authors of Sarah Hunt

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Hunt. A scholar is included among the top collaborators of Sarah Hunt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sarah Hunt. Sarah Hunt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Curating genomic disease-gene relationships with Gene2Phenotype (G2P) 2024 ·Genome Medicine ·(unknown), Morad Ansari, (unknown), Sarah Hunt, Elena Cibrián–Uhalte, (unknown), (unknown), Caroline F. Wright, Helen V. Firth	2
2	EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders 2023 ·Journal of Medical Genetics ·Eva Lenassi, Ana Carolina de Carvalho, Anja Thormann, (unknown), Gavin Arno, Tracy Fletcher, (unknown), Javier Ferreiros, Sarah Hunt, Patrick Short, Panagiotis I. Sergouniotis, Michel Michaelides, Andrew R. Webster, Fiona Cunningham, Simon Ramsden, Dalia Kasperavičiūtė, David Fitzpatrick, Graeme C. Black, Jamie M. Ellingford	3
3	Scripting Analyses of Genomes in Ensembl Plants 2022 ·Methods in molecular biology ·Bruno Contreras‐Moreira, Guy Naamati, (unknown), James E. Allen, Sarah Hunt, Matthieu Muffato, Astrid Gall, Paul Flicek	12
4	The European Variation Archive: a FAIR resource of genomic variation for all species 2021 ·Nucleic Acids Research ·Timothée Cezard, Fiona Cunningham, Sarah Hunt, (unknown), Nitin Kumar, Gary Saunders, (unknown), (unknown), Kirill Tsukanov, (unknown), Paul Flicek, Helen Parkinson, Thomas Keane	62
5	Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP 2019 ·Nature Communications ·Anja Thormann, Mihail Halachev, William McLaren, David Moore, Victoria Svinti, Archie Campbell, Shona M. Kerr, Marc Tischkowitz, Sarah Hunt, Malcolm G. Dunlop, Matthew E. Hurles, Caroline F. Wright, Helen V. Firth, Fiona Cunningham, David Fitzpatrick	53
6	The Ensembl Variant Effect Predictor breakdown → 2016 ·Genome biology ·William McLaren, Laurent Gil, Sarah Hunt, Harpreet Singh Riat, Graham R. S. Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham	4020
7	Validation of the OMNI RPE Seven Day Exertional Recall Questionnaire 2013 ·Research Quarterly for Exercise and Sport ·Mark A. Schafer, Robert J. Robertson, (unknown), Michael Gallagher, Sarah Hunt, Fredric L. Goss, Deborah J. Aaron	0
8	The Agilent Technologies' SureSelect™ All Exon Product Portfolio: High Performance Target Enrichment System for Human and Mouse Exome Sequencing on Illumina and SOLiD Platforms 2011 ·Journal of Biomolecular Techniques JBT ·A. Giuffre, Carlos Pabón-Peña, Ben J. Novak, (unknown), (unknown), (unknown), Micah Hamady, (unknown), (unknown), Sarah Hunt, Scott Happe, David J. Roberts, Emily M LeProust, Harini Ravi	1
9	The GENCODE exome: sequencing the complete human exome 2011 ·European Journal of Human Genetics ·(unknown), Felix Kokocinski, (unknown), Carol Scott, Priit Palta, Eleanor Drury, Christopher J. Joyce, Emily M LeProust, Jennifer Harrow, Sarah Hunt, (unknown), Daniel J. Turner, Tim Hubbard, Aarno Palotie	43
10	A Genome-wide Survey of the Prevalence and Evolutionary Forces Acting on Human Nonsense SNPs 2009 ·The American Journal of Human Genetics ·Bryndís Yngvadóttir, Yali Xue, Steve Searle, Sarah Hunt, Marcos Delgado, Jonathan J. Morrison, Pamela Whittaker, Panos Deloukas, Chris Tyler‐Smith	59
11	Concurrent Muscle Hurt and Perceived Exertion of Children during Resistance Exercise 2009 ·Medicine & Science in Sports & Exercise ·Robert J. Robertson, Fredric L. Goss, Deborah J. Aaron, Elizabeth F. Nagle, Michael Gallagher, Irene Kane, (unknown), Mark A. Schafer, Sarah Hunt	14
12	Haplotype‐based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1–DQA1–DQB1 haplotype 2009 ·Diabetes Obesity and Metabolism ·Ralph McGinnis, William McLaren, (unknown), Pamela Whittaker, Sarah Hunt, Panos Deloukas	3
13	The portability of tagSNPs across populations: A worldwide survey 2006 ·Genome Research ·Anna González‐Neira, Xiayi Ke, Óscar Lao, Francesc Calafell, Arcadi Navarro, David Comas, Howard M. Cann, Suzannah Bumpstead, Jilur Ghori, Sarah Hunt, Panos Deloukas, Ian Dunham, Lon R. Cardon, Jaume Bertranpetit	73
14	Genome-Wide Associations of Gene Expression Variation in Humans 2005 ·PLoS Genetics ·Barbara E. Stranger, Matthew S. Forrest, Andrew G. Clark, (unknown), Samuel Deutsch, Robert Lyle, Sarah Hunt, (unknown), Stylianos E. Antonarakis, Simon Tavaré, Panos Deloukas, Emmanouil T. Dermitzakis	382
15	Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants 2005 ·Genome Research ·Robert Lawrence, David M. Evans, (unknown), Xiayi Ke, Sarah Hunt, Marta Paolucci, Jiannis Ragoussis, Panos Deloukas, David Bentley, Lon R. Cardon	22
16	A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization 2004 ·Genome Research ·Yeun‐Jun Chung, Jos Jonkers, (unknown), Heike Fiegler, Sean Humphray, Carol Scott, Sarah Hunt, (unknown), Ichiko Nishijima, Arno Velds, Henne Holstege, (unknown), Allan Bradley	88
17	Linkage Disequilibrium Mapping via Cladistic Analysis of Single-Nucleotide Polymorphism Haplotypes 2004 ·The American Journal of Human Genetics ·Caroline Durrant, Krina T. Zondervan, Lon R. Cardon, Sarah Hunt, Panos Deloukas, Andrew P. Morris	153
18	Utilisation of erythrocyte 6-thioguanine metabolite levels to optimise azathioprine therapy in patients with inflammatory bowel disease 2001 ·Gut ·Carmen Cuffari, Sarah Hunt, T. M. Bayless	232
19	A SNP Resource for Human Chromosome 22: Extracting Dense Clusters of SNPs From the Genomic Sequence 2001 ·Genome Research ·Elisabeth Dawson, Yuan Chen, Sarah Hunt, Luc J Smink, Adrienne Hunt, (unknown), (unknown), Suzannah Bumpstead, Richard Bruskiewich, Pak C. Sham, (unknown), Mark D. Adams, Kazuhiko Kawasaki, Nobuyoshi Shimizu, Satoshi Minoshima, Bruce A. Roe, David Bentley, Ian Dunham	59
20	Enhanced bioavailability of azathioprine compared to 6‐mercaptopurine therapy in inflammatory bowel disease: correlation with treatment efficacy 2000 ·Alimentary Pharmacology & Therapeutics ·Carmelo Cuffari, Sarah Hunt, T. M. Bayless	72

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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