A. A. M. Morris - Concepedia

Author

A. A. M. Morris

University College London

Also Known As

A A M MORRIS, A A M Morris, A A Morris, A Morris, A. A. M. Morris, A. A. Morris, A. Morris, A.A.M. Morris

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University College London Newcastle University Great Ormond Street Hospital Royal Victoria Infirmary Sheffield Children's Hospital

About

A. A. M. Morris is an author at University College London specializing in medicine, pathology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	341
2	Health Sciences	2	2	121
3	Natural Sciences	1	1	103
4	Public Health	1	1	16
5	Social Sciences	1	1	13

A. A. M. Morris

Publications

906

Citations

H-Index

Page 1

	Year	Citations
Deficiency of respiratory chain complex I is a common cause of leigh disease A. A. M. Morris, James V. Leonard, Garry K. Brown, Annals of Neurology	1996	120
Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeography Heriberto Pfeiffer, B. Brinkmann, J. Hühne, International Journal of Legal Medicine Genetic DiversityDna BarcodingGenetic TestingPhylogeneticsMolecular Ecology	1999	103
Glutaric aciduria and suspected child abuse A. A. M. Morris, Georg F. Hoffmann, E. R. Naughten, Archives of Disease in Childhood Neurological DisorderSuspected Child AbuseBrain InjuryNeurologyNeuropathology	1999	73
Homoplasmy, heteroplasmy, and mitochondrial dystonia Robert McFarland, Patrick F. Chinnery, Emma L. Blakely, Neurology	2007	73
MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA Robert W. Taylor, Patrick F. Chinnery, Faye Haldane, Annals of Neurology	1996	68
Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease. A. A. M. Morris, A Thekekara, Z. Wilks, Archives of Disease in Childhood	1996	61
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency S. E. Olpin, Amal Afifi, S. Clark, Journal of Inherited Metabolic Disease	2003	52
A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype A. A. M. Morris, S. E. Olpin, M. Brivet, The Journal of Pediatrics Carnitine-acylcarnitine Translocase Deficiency	1998	50
Biotinidase Deficiency: a Treatable Leukoencephalopathy Susanne Grünewald, M. P. Champion, J V Leonard, Neuropediatrics Neurological DisorderHematologyPediatricsExperimental PathologyPathology	2004	48
Novel <i>POLG1</i> mutations associated with neuromuscular and liver phenotypes in adults and children Joanna D. Stewart, Stephen Tennant, Heather Powell, Journal of Medical Genetics	2009	46

Page 1