Martin Farrall - Genetic Mutations

Author Information

Martin Farrall is a prominent figure in the field of Genetics, affiliated with the Wellcome Centre for Human Genetics at the University of Oxford in Oxford, UK. His work primarily focuses on understanding genetic determinants and their implications in various health conditions, notably within the realm of cardiovascular genetics. Martin Farrall’s contributions to the field are recognized globally, as evidenced by his extensive publication record and significant citation metrics.

Research Contributions

Martin Farrall has made substantial contributions to the field of genetics, particularly in understanding heritability and genetic determinants of cardiovascular-related conditions. His research includes exploring the genetic underpinnings of hypertrophic cardiomyopathy, congenital heart disease, and coronary disease risk, especially in individuals with type 2 diabetes. His work often employs family-based GWAS analyses and other sophisticated genetic modeling techniques to uncover insights into these conditions. Additionally, he has contributed to methodological advancements in meta-analysis, providing tools to explore heterogeneity in genetic studies.

Aliases

Martin Farrall is also known by several aliases in academic publications, including M Farrall, M G Farrall, and M. Farrall.

Publication and Citation Metrics

Metric Value
Total Citation Count 65,427
h-index 108
Total Paper Count 430

Publications:

DOI: 10.1093/hmg/ddab002

Year: 2021

DOI: 10.1161/circ.144.suppl_1.11789

Year: 2021

DOI: 10.1101/2021.04.19.21255650

Year: 2021

DOI: 10.1038/s41588-020-00764-0

Year: 2021

DOI: 10.1002/gepi.22434

Year: 2021

DOI:

Year: 2020

DOI:

Year: 2020

DOI: 10.1161/CIRCGEN.119.002783

Year: 2020

DOI: 10.1038/s41598-020-71354-7

Year: 2020

DOI: 10.1136/jmedgenet-2020-106922

Year: 2020

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