Matthew Traylor

21.1k citations

55 papers · 2.3k indexed · 1 hit paper · h-index 25

Neurology top 5%
- Cerebrovascular and genetic disorders 7
- Neurological diseases and metabolism 4
Neurology top 5%
- Cerebrovascular and genetic disorders 7
- Neurological diseases and metabolism 4
Genetics top 5%
- Genetic Associations and Epidemiology 23
Rheumatology top 5%
- Folate and B Vitamins Research 5
Cardiology and Cardiovascular Medicine top 5%
Molecular Biology
- RNA regulation and disease 7
- Bioinformatics and Genomic Networks 5
Surgery
- Lipoproteins and Cardiovascular Health 5
Cancer Research
- Cancer-related molecular mechanisms research 5

Co-authors: Hugh S. Markus Martin Dichgans Susanna C. Larsson Rainer Malik Cathie Sudlow Loes C.A. Rutten‐Jacobs Cathryn M. Lewis Stephen Burgess
Cited by: Neurology Genetics Rheumatology
Journals: Stroke (15 papers)Neurology (4 papers)PLoS ONE (4 papers)
Partner nations: United Kingdom United States Germany

In The Last Decade

Matthew Traylor

54 papers receiving 2.3k citations

Hit Papers

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Peers

Countries citing papers authored by Matthew Traylor

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Traylor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Matthew Traylor, 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 Matthew Traylor Line = papers co-authored together Matthew Traylor links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Interpretable machine learning leverages proteomics to improve cardiovascular disease risk prediction and biomarker identification Communications Medicine ·Héctor Climente-González,Min Oh,Urszula Chajewska,Roya Hosseini,Sudipto Mukherjee,Wei Gan,Matthew Traylor,Sile Hu,Ghazaleh Fatemifar,Jonas Ghouse,Naresh Babu,Erik Vernet,Nils Koelling,Liang Du,Robin Abraham,Chuan Li,Joanna M. M. Howson	2025	2
2	Systematic Mendelian randomization using the human plasma proteome to discover potential therapeutic targets for stroke Nature Communications ·Lingyan Chen,James E. Peters,Bram P. Prins,Elodie Persyn,Matthew Traylor,Praveen Surendran,Savita Karthikeyan,Ekaterina Yonova-Doing,Emanuele Di Angelantonio,David J. Roberts,Nicholas A. Watkins,Willem H. Ouwehand,John Danesh,Cathryn M. Lewis,Paola G. Bronson,Hugh S. Markus,Stephen Burgess,Adam S. Butterworth,Joanna M. M. Howson	2022	59
3	The Histone Deacetylase 9 Stroke-Risk Variant Promotes Apoptosis and Inflammation in a Human iPSC-Derived Smooth Muscle Cells Model Frontiers in Cardiovascular Medicine ·Alessandra Granata,Vivek V. Jasti,Felipe Serrano,James D. Cooper,Matthew Traylor,Sanjay Sinha,Hugh S. Markus	2022	8
4	Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities Brain ·Rainer Malik,Nathalie Beaufort,Amanda Baldessar,Benno Gesierich,Marios K. Georgakis,Kristiina Rannikmäe,Amy Ferguson,Christof Haffner,Matthew Traylor,Michael Ehrmann,Cathie Sudlow,Martin Dichgans	2021	16
5	Hypertension genetics past, present and future applications Journal of Internal Medicine ·junyue zhang,元彦祝田,Choi 최은주Eun Ju,Matthew Traylor,Claudia Cabrera,Patricia B. Munroe	2021	31
6	The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare Genome Medicine ·Ken B. Hanscombe,Elodie Persyn,Matthew Traylor,Kylie P. Glanville,Mark Hamer,Jonathan R. I. Coleman,Cathryn M. Lewis	2021	27
7	Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants Nature Communications ·Elodie Persyn,Ken B. Hanscombe,Joanna M. M. Howson,Cathryn M. Lewis,Matthew Traylor,Hugh S. Markus	2020	112
8	Proceedings of the 25th International Stroke Genetics Consortium Workshop: Cambridge, UK Neurology Genetics ·Jemma C. Hopewell,Matthew Traylor,Hugh S. Markus	2020	1
9	Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226) Neurology ·Matthew Traylor,Daniel J. Tozer,Iain D. Croall,Zhao Rongan,Ch. Marcher,Giorgio B. Boncoraglio,Martin Dichgans,Robin Lemmens,Jonathan Rosand,Natalia S. Rost,Peter M. Rothwell,Cathie Sudlow,Vincent Thijs,Loes C.A. Rutten‐Jacobs,Hugh S. Markus	2019	58
10	ukbtools: An R package to manage and query UK Biobank data PLoS ONE ·Ken B. Hanscombe,Jonathan R. I. Coleman,Matthew Traylor,Cathryn M. Lewis	2019	33
11	Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases PLoS ONE ·Matthew Traylor,Rachel Knevel,Jing Cui,John Taylor,J.A. San Martín,Philip G. Conaghan,Andrew P. Cope,Charles Curtis,Paul Emery,Stephen Newhouse,Hamel Patel,Sophia Steer,Peter K. Gregersen,Nancy A. Shadick,Michael E. Weinblatt,Annette H M van der Helm–van Mil,Jennifer H. Barrett,Ann W Morgan,Cathryn M. Lewis,Ian C. Scott	2019	12
12	Do Cerebral Small Vessel Disease and Multiple Sclerosis Share Common Mechanisms of White Matter Injury? Stroke ·Robin Brown,Matthew Traylor,Stephen Burgess,Stephen Sawcer,Hugh S. Markus	2019	14
13	How common are single gene mutations as a cause for lacunar stroke? Neurology ·Rhea Tan,Matthew Traylor,Karyn Mégy,Daniel Duarte,Sri V. V. Deevi,Olga Shamardina,Rutendo Mapeta,Willem H. Ouwehand,Stefan Gräf,Kate Downes,Hugh S. Markus	2019	29
14	Genetic risk, incident stroke, and the benefits of adhering to a healthy lifestyle: cohort study of 306 473 UK Biobank participantsbreakdown → BMJ ·Loes C.A. Rutten‐Jacobs,Susanna C. Larsson,Rainer Malik,Kristiina Rannikmäe,Cathie Sudlow,Martin Dichgans,Hugh S. Markus,Matthew Traylor	2018	221
15	Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia Stroke ·Loes C.A. Rutten‐Jacobs,Daniel J. Tozer,Marco Duering,Yuko Yoshida-Ichikawa,Martin Dichgans,Hugh S. Markus,Matthew Traylor	2018	54
16	Serum 25-Hydroxyvitamin D Concentrations and Ischemic Stroke and Its Subtypes Stroke ·Susanna C. Larsson,Matthew Traylor,Aniket Mishra,Joanna M. M. Howson,Karl Michaëlsson,Hugh S. Markus	2018	24
17	Genome‐wide meta‐analysis identifies 3 novel loci associated with stroke Annals of Neurology ·Rainer Malik,Kristiina Rannikmäe,Matthew Traylor,Marios K. Georgakis,Muralidharan Sargurupremraj,Hugh S. Markus,Jemma C. Hopewell,Stéphanie Debette,Cathie Sudlow,Martin Dichgans	2018	53
18	Association of MTHFR genotype with lacunar stroke supports causal role for homocysteine International Journal of Stroke ·宏一長岡,Matthew Traylor,Vincent Thijs,Cathie Sudlow,Peter M. Rothwell,Giorgio B. Boncoraglio,Martin Dichgans,Christopher Levi,Steve Bevan,Пилилян Елена Константиновна	2015	1
19	Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke Stroke ·Ken B. Hanscombe,Matthew Traylor,Pirro G. Hysi,Steve Bevan,Martin Dichgans,Peter M. Rothwell,Bradford B. Worrall,Sudha Seshadri,Cathie Sudlow,Frances M. K. Williams,Hugh S. Markus,Cathryn M. Lewis	2015	15
20	Association of the novel single-nucleotide polymorphism which increases oxidized low-density lipoprotein levels with cerebrovascular disease events Atherosclerosis ·Kari-Matti Mäkelä,Matthew Traylor,Niku Oksala,Marcus E. Kleber,Ilkka Seppälä,Leo‐Pekka Lyytikäinen,Jussi Hernesniemi,Mika Kähönen,Steve Bevan,Peter M. Rothwell,Cathie Sudlow,Martin Dichgans,Graciela Delgado,Tanja B. Grammer,Hubert Scharnagl,Hugh S. Markus,Winfried März,Terho Lehtimäki	2014	13

About Matthew Traylor

Matthew Traylor is a scholar working on Genetics, Rheumatology, Neurology, Neurology and Cancer Research, having authored 55 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (23 papers), RNA regulation and disease (7 papers), Cerebrovascular and genetic disorders (7 papers), Lipoproteins and Cardiovascular Health (5 papers), Cancer-related molecular mechanisms research (5 papers), Bioinformatics and Genomic Networks (5 papers), Folate and B Vitamins Research (5 papers) and Neurological diseases and metabolism (4 papers). The work is most often cited by research in Neurology (296 citations), Neurology (400 citations), Genetics (645 citations), Rheumatology (272 citations) and Cardiology and Cardiovascular Medicine (350 citations). Matthew Traylor has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Hugh S. Markus, Martin Dichgans, Susanna C. Larsson, Rainer Malik, Cathie Sudlow, Loes C.A. Rutten‐Jacobs, Cathryn M. Lewis, Stephen Burgess, Hugh S. Markus and Kristiina Rannikmäe. Their work appears in journals such as Stroke, Neurology, PLoS ONE, Brain and Neurology Genetics.

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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