Caroline F. Wright

12.0k total citations · 1 hit paper
77 papers, 3.3k citations indexed

About

Caroline F. Wright is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Caroline F. Wright has authored 77 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Genetics, 25 papers in Molecular Biology and 14 papers in Cancer Research. Recurrent topics in Caroline F. Wright's work include Genomics and Rare Diseases (44 papers), Genomic variations and chromosomal abnormalities (28 papers) and Cancer Genomics and Diagnostics (14 papers). Caroline F. Wright is often cited by papers focused on Genomics and Rare Diseases (44 papers), Genomic variations and chromosomal abnormalities (28 papers) and Cancer Genomics and Diagnostics (14 papers). Caroline F. Wright collaborates with scholars based in United Kingdom, United States and Australia. Caroline F. Wright's co-authors include Helen V. Firth, David Fitzpatrick, Jane Clarke, Matthew E. Hurles, H. Burton, Christopher M. Dobson, Sarah A. Teichmann, Eugene Bragin, Jeremy F. McRae and Alison Hall and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

Caroline F. Wright

72 papers receiving 3.2k 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.

Paediatric genomics: diagnosing rare disease in children

2018 343 citations Caroline F. Wright, David Fitzpatrick et al. profile →

Peers

Countries citing papers authored by Caroline F. Wright

Since Specialization

Citations

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

Fields of papers citing papers by Caroline F. Wright

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Caroline F. Wright. 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 Caroline F. Wright. The network helps show where Caroline F. Wright may publish in the future.

Co-authorship network of co-authors of Caroline F. Wright

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline F. Wright. A scholar is included among the top collaborators of Caroline F. Wright 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 Caroline F. Wright. Caroline F. Wright is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	What do we mean by actionability? Examining a key criterion in genomic prenatal and newborn screening 2025 ·Genetics in Medicine ·(unknown), (unknown), (unknown), Leigh Jackson, Caroline F. Wright	0
2	Genetic modifiers of rare variants in monogenic developmental disorder loci 2024 ·Nature Genetics ·(unknown), Robin N. Beaumont, Andrew R. Wood, Michael N. Weedon, Caroline F. Wright	11
3	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
4	Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders 2024 ·Scientific Reports ·Emilie M. Wigdor, Kaitlin E. Samocha, Ruth Y. Eberhardt, V. Kartik Chundru, Helen V. Firth, Caroline F. Wright, Matthew E. Hurles, Hilary C. Martin	0
5	Evaluating the use of paralogous protein domains to increase data availability for missense variant classification 2023 ·Genome Medicine ·Adam C. Gunning, Caroline F. Wright	0
6	Estimating diagnostic noise in panel-based genomic analysis 2022 ·Genetics in Medicine ·Robin N. Beaumont, Caroline F. Wright	9
7	IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disorders 2022 ·Human Genetics and Genomics Advances ·Stuart Aitken, Helen V. Firth, Caroline F. Wright, Matthew E. Hurles, David Fitzpatrick, Colin A. Semple	1
8	Reduced penetrance of MODY-associated HNF1A/HNF4A variants but not GCK variants in clinically unselected cohorts 2022 ·The American Journal of Human Genetics ·Uyenlinh L. Mirshahi, Kevin Colclough, Caroline F. Wright, Andrew R. Wood, Robin N. Beaumont, Jessica Tyrrell, Thomas W. Laver, Richard C. Stahl, Alicia Golden, (unknown), (unknown), Andrew T. Hattersley, David J. Carey, Michael N. Weedon, Kashyap Patel	42
9	Common genetic variants with fetal effects on birth weight are enriched for proximity to genes implicated in rare developmental disorders 2021 ·Human Molecular Genetics ·Robin N. Beaumont, (unknown), Rachel M. Freathy, Caroline F. Wright	1
10	Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation 2021 ·BMJ ·(unknown), Leigh Jackson, (unknown), (unknown), Jessica Tyrrell, Andrew T. Hattersley, Caroline F. Wright	29
11	Assessing performance of pathogenicity predictors using clinically relevant variant datasets 2020 ·Journal of Medical Genetics ·Adam C. Gunning, (unknown), James Fasham, Andrew H. Crosby, Sian Ellard, Emma L. Baple, Caroline F. Wright	69
12	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
13	Common genetic variants contribute to risk of rare severe neurodevelopmental disorders 2018 ·Nature ·Mari Niemi, Hilary C. Martin, Daniel L Rice, Giuseppe Gallone, Scott D. Gordon, Martin Kelemen, Kerrie McAloney, Jeremy F. McRae, Elizabeth J. Radford, Sui Yu, Jozef Gécz, Nicholas G. Martin, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles, Jeffrey C. Barrett	184
14	Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders 2018 ·Genetics in Medicine ·Caroline F. Wright, Jeremy F. McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas Fitzgerald, (unknown), Elena Prigmore, Diana Rajan, Jenny Lord, Alejandro Sifrim, Rosemary E. Kelsell, Michael Parker, Jeffrey C. Barrett, Matthew E. Hurles, David Fitzpatrick, Helen V. Firth	193
15	De novo mutations in regulatory elements in neurodevelopmental disorders 2018 ·Nature ·Patrick Short, Jeremy F. McRae, Giuseppe Gallone, Alejandro Sifrim, Hyejung Won, Daniel H. Geschwind, Caroline F. Wright, Helen V. Firth, David Fitzpatrick, Jeffrey C. Barrett, Matthew E. Hurles	128
16	Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research 2015 ·European Journal of Human Genetics ·(unknown), Anna Middleton, Katherine I. Morley, Eugene Bragin, Helen V. Firth, Matthew E. Hurles, Caroline F. Wright, Michael Parker	142
17	Costs and Benefits of Mutational Robustness in RNA Viruses 2014 ·Cell Reports ·Adi Stern, Simone Bianco, Ming Te Yeh, Caroline F. Wright, Kristin Butcher, Chao Tang, Rasmus Nielsen, Raul Andino	40
18	Policy challenges of clinical genome sequencing 2013 ·BMJ ·Caroline F. Wright, Anna Middleton, H. Burton, Fiona Cunningham, Steve E. Humphries, Jane A. Hurst, Ewan Birney, (unknown)	37
19	Deciphering Developmental Disorders 2012 ·Journal of Medical Genetics ·Caroline F. Wright, Helen V. Firth, Diana L. Fitzpatrick, (unknown), Michael W. Parker, (unknown), (unknown)	32
20	Informatics and clinical genome sequencing: opening the black box 2012 ·Genetics in Medicine ·Sowmiya Moorthie, Alison Hall, Caroline F. Wright	24

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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