Sarah Dwyer

5.1k total citations
22 papers, 1.2k citations indexed

About

Sarah Dwyer is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Sarah Dwyer has authored 22 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in Sarah Dwyer's work include Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Sarah Dwyer is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Sarah Dwyer collaborates with scholars based in United Kingdom, United States and Australia. Sarah Dwyer's co-authors include Michael O’Donovan, Hywel Williams, Michael J. Owen, Valentina Moskvina, Nigel Williams, Nadine Norton, Stanley Zammit, George Kirov, Marian L. Hamshere and Anna Preece and has published in prestigious journals such as Gut, Journal of Allergy and Clinical Immunology and Human Molecular Genetics.

In The Last Decade

Sarah Dwyer

21 papers receiving 1.1k citations

Peers

Countries citing papers authored by Sarah Dwyer

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Dwyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Dwyer

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Dwyer. A scholar is included among the top collaborators of Sarah Dwyer 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 Dwyer. Sarah Dwyer 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	Improved AAV9-based gene therapy design for SURF1-related Leigh syndrome with minimal toxicity 2025 ·Molecular Therapy — Methods & Clinical Development ·(unknown), (unknown), Henry N. Higgs, Yuhui Hu, Sarah Dwyer, Steven J. Gray	0
2	Genomic analysis defines distinct pancreatic and neuronal subtypes of lung carcinoid 2024 ·The Journal of Pathology ·(unknown), Saffron A.G. Willis‐Owen, Amit Kumar Mandal, Anca Năstase, Sarah Dwyer, Cecilia Brambilla, (unknown), (unknown), Sanjay Popat, Robert Eveleigh, (unknown), Eric Lim, Andrew G. Nicholson, G.M. Lathrop, William Cookson, Miriam F. Moffatt	1
3	Enhanced bacterial cancer therapy delivering therapeutic RNA interference of c-Myc 2024 ·Cell & Bioscience ·Jason S. Williams, (unknown), (unknown), (unknown), (unknown), Cleo Bonnet, (unknown), (unknown), Trevor Hay, Tianqi Wang, Claire Morgan, Sarah Dwyer, (unknown), Catherine Hogan, Matthew J. Smalley, Lee Parry, Paul Dyson	4
4	Endoscopic full-thickness resection of well-differentiated T2 neuroendocrine tumors in the duodenal bulb: a case series 2022 ·VideoGIE ·Sarah Dwyer, Shaffer Mok	3
5	Comparison of mortality risk in patients with cirrhosis and COVID-19 compared with patients with cirrhosis alone and COVID-19 alone: multicentre matched cohort 2020 ·Gut ·Jasmohan S. Bajaj, Guadalupe García–Tsao, Scott W. Biggins, Patrick S. Kamath, Florence Wong, Sara McGeorge, Jawaid Shaw, (unknown), (unknown), Andrew Fagan, Randolph de la Rosa Rodríguez, (unknown), Amy Olofson, Vanessa Weir, (unknown), Sarah Dwyer, K. Rajender Reddy	150
6	Bacterial microbiota of the upper respiratory tract and childhood asthma 2016 ·Journal of Allergy and Clinical Immunology ·Martin Depner, Markus Ege, Michael J. Cox, Sarah Dwyer, Alan W. Walker, (unknown), Jon Genuneit, Elisabeth Horak, Charlotte Braun‐Fahrländer, Hanna Danielewicz, Raina M. Maier, Miriam F. Moffatt, William Cookson, Dick Heederik, Erika von Mutius, Antje Legatzki	145
7	Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation 2015 ·Psychiatric Genetics ·Liam Carroll, (unknown), (unknown), Hywel Williams, Sarah Dwyer, James Walters, George Kirov, Michael O’Donovan, Michael J. Owen	43
8	The ENCODE project: implications for psychiatric genetics 2013 ·Molecular Psychiatry ·David H. Kavanagh, Sarah Dwyer, Michael O’Donovan, Michael J. Owen	18
9	A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents 2013 ·Schizophrenia Bulletin ·Stanley Zammit, Marian L. Hamshere, Sarah Dwyer, (unknown), Nicholas J. Timpson, Valentina Moskvina, Alexander Richards, David M. Evans, Glyn Lewis, Peter B. Jones, Michael J. Owen, Michael O’Donovan	61
10	Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis‐acting regulation of mRNA expression in adult human brain 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Hywel Williams, Valentina Moskvina, (unknown), Sarah Dwyer, Giancarlo Russo, Michael J. Owen, Michael O’Donovan	12
11	Analysis of neurogranin (NRGN) in schizophrenia 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), Deborah A. Knight, Hywel Williams, Sarah Dwyer, Alexander Richards, George Kirov, Michael O’Donovan, Michael J. Owen	13
12	No evidence that rare coding variants inZNF804Aconfer risk of schizophrenia 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Sarah Dwyer, Hywel Williams, Peter Holmans, Valentina Moskvina, Nicholas Craddock, Michael J. Owen, Michael O’Donovan	17
13	Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries 2010 ·Human Molecular Genetics ·Hywel Williams, Nick Craddock, Giancarlo Russo, Marian L. Hamshere, Valentina Moskvina, Sarah Dwyer, Richard L. Smith, Eric D. Green, Detelina Grozeva, Peter Holmans, M J Owen, Michael O’Donovan	132
14	Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high‐resolution melting analysis 2009 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Sarah Dwyer, Liam Carroll, Kiran K. Mantripragada, Mike Owen, Michael O’Donovan, Nigel Williams	11
15	Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia 2007 ·Schizophrenia Research ·Hywel Williams, Nadine Norton, T Peirce, Sarah Dwyer, Nigel Williams, Valentina Moskvina, Michael J. Owen, Michael O’Donovan	15
16	Association analysis of AKT1 and schizophrenia in a UK case control sample 2007 ·Schizophrenia Research ·Nadine Norton, Hywel Williams, Sarah Dwyer, Liam Carroll, (unknown), Valentina Moskvina, Ricardo Segurado, Ivan Nikolov, Nigel Williams, Masashi Ikeda, Nakao Iwata, Michael J. Owen, Michael O’Donovan	48
17	Variation at the DAOA/G30 Locus Influences Susceptibility to Major Mood Episodes but Not Psychosis in Schizophrenia and Bipolar Disorder 2006 ·Archives of General Psychiatry ·Nigel Williams, Elaine Green, Stuart MacGregor, Sarah Dwyer, Nadine Norton, Hywel Williams, Rachel Raybould, Detelina Grozeva, Marian L. Hamshere, Stanley Zammit, Lisa Jones, Alastair G. Cardno, George Kirov, Ian Jones, Michael O’Donovan, Michael J. Owen, Nick Craddock	99
18	No evidence for association between polymorphisms in GRM3and schizophrenia 2005 ·BMC Psychiatry ·Nadine Norton, Hywel Williams, Sarah Dwyer, Dobril Ivanov, Anna Preece, Amy Gerrish, Nigel Williams, (unknown), Stanley Zammit, Michael O’Donovan, Michael J. Owen	43
19	Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia 2005 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Nadine Norton, Valentina Moskvina, Derek W. Morris, Nicholas J. Bray, Stanley Zammit, Nigel Williams, Hywel Williams, Anna Preece, Sarah Dwyer, (unknown), Gillian Spurlock, George Kirov, Paul R. Buckland, John L. Waddington, Michael Gill, Aiden Corvin, Michael J. Owen, Michael O’Donovan	140
20	Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1) 2004 ·Archives of General Psychiatry ·Nigel Williams, Anna Preece, Derek W. Morris, Gillian Spurlock, Nicholas J. Bray, M.F.C. Stephens, Nadine Norton, Hywel Williams, Mathew Clement, Sarah Dwyer, Catherine Curran, (unknown), Valentina Moskvina, John L. Waddington, Michael Gill, Aiden Corvin, Stanley Zammit, George Kirov, Michael J. Owen, Michael O’Donovan	156

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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