Andrew A.M. Morris - Concepedia

Author

Andrew A.M. Morris

Also Known As

A. A. M. Morris, ANDREW MORRIS, Andrew A M Morris, Andrew A. M. Morris, Andrew A.M. Morris, Andrew AM Morris, Andrew Morris, Myositis Genetics Scientific Interest Group

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Newcastle University Wellcome Centre for Mitochondrial Research Royal Victoria Infirmary Aarhus University Hospital Helmholtz Zentrum München

About

Andrew A.M. Morris is an author at Newcastle University specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1.2K
2	Natural Sciences	6	6	680
3	Biochemistry	4	4	593
4	Allergy	1	1	57
5	Biology	1	1	172

Andrew A.M. Morris

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency Rikke Katrine Jentoft Olsen, S. E. Olpin, Brage Storstein Andresen, Brain Metabolic DisorderGeneticsMolecular BiologyHyperlipidemiaMolecular Genetics	2007	326
Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis, The American Journal of Human Genetics Genetic DiseasesDisease PhenotypeGenetic DeterminantGenetic DisorderGenetics	1999	300
<i>IDH2</i> Mutations in Patients with <scp>d</scp> -2-Hydroxyglutaric Aciduria Martijn Kranendijk, Eduard A. Struys, Emile Van Schaftingen, Science UrologySomatic VariantAldehyde DehydrogenaseBiochemistryGenetic Disorder	2010	192
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation Robert McFarland, Kim M. Clark, Andrew A.M. Morris, Nature Genetics BiologyMitochondrial FunctionMultiple Neonatal DeathsNatural SciencesGenetics	2002	172
<i>LRPPRC</i>mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population Monika Oláhová, Steven Hardy, Julie Hall, Brain	2015	105
Leigh disease associated with a novel mitochondrial DNA ND5 mutation Robert W. Taylor, Andrew A.M. Morris, Michael Hutchinson, European Journal of Human Genetics Mendelian DisorderMitochondrial FunctionGenetic DisorderNatural SciencesGenetics	2002	93
Analysis of mutant DNA polymerase γ in patients with mitochondrial DNA depletion Jan‐Willem Taanman, Shamima Rahman, Alistair T. Pagnamenta, Human Mutation	2008	60
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain Andrew A.M. Morris, Robert W. Taylor, Mark A. Birch‐Machin, Pediatric Nephrology Complex IiiRespiratory ChainAllergyNeonatal Fanconi Syndrome	1995	57
A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency Monika Oláhová, Tobias B. Haack, Charlotte L. Alston, European Journal of Human Genetics GeneticsPet100 MutationGenetic EpidemiologyPathologyMolecular Biology	2014	38
The cDNA sequence of the flavoprotein subunit of human heart succinate dehydrogenase Andrew A.M. Morris, L. Farnsworth, Brian A.C. Ackrell, Biochimica et Biophysica Acta (BBA) - Bioenergetics BiosynthesisCellular EnzymologyBiochemistryNatural SciencesGenetics	1994	37

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