Ian Wilson - Concepedia

Author

Ian Wilson

Also Known As

I Wilson, I. J. Wilson, I. WILSON, I. Wilson, I.J. Wilson, IJ Wilson, Ian J Wilson, Ian J. Wilson, Ian J. Wilson (75492), Ian Wilson

170

Publications

6.5K

Citations

H-Index

119

Concepts

All Affiliations

Newcastle University Wellcome Centre for Mitochondrial Research University of Oxford Newcastle upon Tyne Hospitals NHS Foundation Trust University of Cambridge

About

Ian Wilson is an author at Newcastle University specializing in medicine, genetics, and population genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	18	2.2K
2	Engineering	6	6	187
3	Natural Sciences	6	6	994
4	Public Health	6	6	663
5	Health Sciences	1	1	75

Ian Wilson

Publications

5.6K

Citations

H-Index

Page 1

	Year	Citations
Universal heteroplasmy of human mitochondrial DNA Brendan Payne, Ian Wilson, Patrick Yu‐Wai‐Man, Human Molecular Genetics DnaMitochondrial BiogenesisMitochondrial FunctionPoint Mutation LoadMitochondrial Dna	2012	432
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease Rachel Soemedi, Ian Wilson, Jamie Bentham, The American Journal of Human Genetics	2012	335
Genealogical Inference From Microsatellite Data Ian Wilson, David J. Balding Genetics	1998	278
Inferences from DNA Data: Population Histories, Evolutionary Processes and Forensic Match Probabilities Ian Wilson, Michael E. Weale, David J. Balding Journal of the Royal Statistical Society Series A (Statistics in Society) GeneticsDna AnalysisDna SequencesGenomicsFlexible Class	2003	268
Fatty acid oxidation is required for the respiration and proliferation of malignant glioma cells Hua Lin, Shaan Patel, Valerie Affleck, Neuro-Oncology	2016	254
Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations Brendan Payne, Ian Wilson, Charlotte A Hateley, Nature Genetics Lifespan ExtensionMitochondrial AgingMitochondrial BiogenesisMitochondrial FunctionLongevity	2011	235
A Predominantly Neolithic Origin for European Paternal Lineages Patricia Balaresque, Georgina R. Bowden, Susan M. Adams, PLoS Biology Molecular EcologyPaleolithic ArchaeologyMedicineGeneticsEvolutionary Biology	2010	229
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance Gerald Pfeffer, Gráinne S. Gorman, Helen Griffin, Brain Mitochondrial Dna MaintenanceOcular DiseaseMendelian DisorderMitochondrial BiogenesisOphthalmology	2014	174
The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care Brian T. Wilson, Zornitza Stark, Ruth E. Sutton, Genetics in Medicine	2015	169
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls Rachel Soemedi, Ana Töpf, Ian Wilson, Human Molecular Genetics	2011	162

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