Matthew Lyon - Concepedia

Author

Matthew Lyon

University of Southampton ORCID

Also Known As

Lyon, MS, Lyon, Matthew, Lyon, Matthew S, M LYON, M Lyon, Matt Lyon, Matthew Lyon, Matthew S. Lyon

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

University of Southampton University of Bristol NIHR Bristol Biomedical Research Centre Wessex Regional Genetics Laboratory National Institute for Health Research

About

Matthew Lyon is an author at University of Southampton specializing in medicine, bioinformatics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	1K
2	Engineering	2	2	947
3	Public Health	2	2	239
4	Education	1	1	206
5	Health Sciences	1	1	67

Matthew Lyon

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
The MRC IEU OpenGWAS data infrastructure Ben Elsworth, Matthew Lyon, Tessa Alexander, Cluster ComputingEngineeringGeneticsGenetic EpidemiologyAbstract Data	2020	931
Collagen (<i>COL4A</i>) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis Christine Gast, Reuben J. Pengelly, Matthew Lyon, Nephrology Dialysis Transplantation	2015	242
The variant call format provides efficient and robust storage of GWAS summary statistics Matthew Lyon, Shea J. Andrews, Benjamin Elsworth, Genome biology	2021	235
Dairying, diseases and the evolution of lactase persistence in Europe Richard P. Evershed, George Davey Smith, Mélanie Roffet‐Salque, Nature NutritionAnimal NutritionAnimal ScienceLactase PersistenceLivestock Production	2022	206
Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance Htoo A. Wai, Jenny Lord, Matthew Lyon, Genetics in Medicine	2020	178
Evaluation of methods to detect CALR mutations in myeloproliferative neoplasms Amy V. Jones, Daniel Ward, Matthew Lyon, Leukemia Research Hematological MalignancySomatic VariantMedicineHematologyCalr Mutations	2014	67
The variant call format provides efficient and robust storage of GWAS summary statistics Matthew Lyon, Shea J. Andrews, Benjamin Elsworth, Variant Call FormatGeneticsGenomicsHigh Throughput SequencingGenome-wide Association Studies	2020	33
Systematic screening of <i>FBN1</i> gene unclassified missense variants for splice abnormalities DO Robinson, Feng Lin, Matthew Lyon, Clinical Genetics EngineeringGeneticsRna SplicingPathologyMolecular Genetics	2011	16

Page 1