Andrew M. Schaefer - Concepedia

Author

Andrew M. Schaefer

Also Known As

A SCHAEFER, A Schaefer, A. M. Schaefer, A. Schaefer, A.M. Schaefer, Andrew M. Schaefer, Andrew G. Schaefer, Andrew Hattersley, Andrew M Schaefer, Andrew M. Schaefer

125

Publications

7.8K

Citations

H-Index

Concepts

All Affiliations

Newcastle University Wellcome Centre for Mitochondrial Research Royal Victoria Infirmary Newcastle upon Tyne Hospitals NHS Foundation Trust University College London

About

Andrew M. Schaefer is an author at Newcastle University specializing in medicine, mitochondrial function, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	1.6K
2	Health Sciences	3	3	436
3	Public Health	2	2	141
4	Arts	1	1	11
5	Natural Sciences	1	1	23

Andrew M. Schaefer

Publications

5.8K

Citations

H-Index

Page 1

	Year	Citations
Prevalence of nuclear and mitochondrial <scp>DNA</scp> mutations related to adult mitochondrial disease Gráinne S. Gorman, Andrew M. Schaefer, Yi Shiau Ng, Annals of Neurology	2015	915
Prevalence of mitochondrial DNA disease in adults Andrew M. Schaefer, Robert McFarland, Emma L. Blakely, Annals of Neurology	2007	578
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance Gavin Hudson, Patrizia Amati‐Bonneau, Emma L. Blakely, Brain	2007	416
mt <scp>DNA</scp> heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease John P. Grady, Sarah J. Pickett, Yi Shiau Ng, EMBO Molecular Medicine	2018	277
Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions Tanja Taivassalo, Justin L. Gardner, Robert W. Taylor, Brain GeneticsEndurance TrainingStrength TrainingExercise RehabilitationMitochondrial Myopathy	2006	220
Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans Jack J. Collier, Claire Guissart, Monika Oláhová, New England Journal of Medicine	2021	185
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
Resistance training in patients with single, large-scale deletions of mitochondrial DNA Jane Murphy, Emma L. Blakely, Andrew M. Schaefer, Brain Mature Skeletal MuscleMuscle FunctionGeneticsMolecular BiologyMolecular Genetics	2008	165
Mitochondrial disease in adults: A scale to monitor progression and treatment Andrew M. Schaefer, C. Phoenix, Joanna L. Elson, Neurology Mitochondrial MyopathyTranslational MedicineDisease ProgressionMitochondrial FunctionMitochondrial Dynamic	2006	161
Mutations of <i>ANT1</i> , <i>Twinkle</i> , and <i>POLG1</i> in sporadic progressive external ophthalmoplegia (PEO) A. Agostino, Lorella Valletta, Patrick F. Chinnery, Neurology BiologyOcular DiseaseMendelian DisorderOphthalmologyPolg1 Genes	2003	152

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