A. A. M. Morris

1.5k total citations
27 papers, 1.0k citations indexed

About

A. A. M. Morris is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, A. A. M. Morris has authored 27 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Clinical Biochemistry, 19 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in A. A. M. Morris's work include Metabolism and Genetic Disorders (23 papers), Mitochondrial Function and Pathology (15 papers) and Diet and metabolism studies (5 papers). A. A. M. Morris is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Mitochondrial Function and Pathology (15 papers) and Diet and metabolism studies (5 papers). A. A. M. Morris collaborates with scholars based in United Kingdom, Germany and Denmark. A. A. M. Morris's co-authors include James V. Leonard, Douglass M. Turnbull, Laurence A. Bindoff, Patrick F. Chinnery, S. E. Olpin, Klaus Eschrich, Peter T. Clayton, Birger Herzog, Heriberto Pfeiffer and Mitchell M. Holland and has published in prestigious journals such as Neurology, Annals of Neurology and The Journal of Pediatrics.

In The Last Decade

A. A. M. Morris

26 papers receiving 1.0k citations

Peers

A. A. M. Morris

PHYSI

GENET

PPCH

Michinori Ito Japan

Diane S. Roe United States

M Tuchman United States

Andrew A. M. Morris United Kingdom

C. Jakobs Netherlands

Jennifer R. Toone Canada

Stephen D. Cederbaum United States

Carla Carducci Italy

V. Barash Israel

Sara Boenzi Italy

Michinori Ito Japan

A. A. M. Morris

483 ×0.8

524 ×1.0

361 ×1.4

PHYSI

119 ×0.9

GENET

190 ×1.7

PPCH

Citations per year, relative to A. A. M. Morris A. A. M. Morris (= 1×) peers Michinori Ito

Countries citing papers authored by A. A. M. Morris

Since Specialization

Citations

This map shows the geographic impact of A. A. M. Morris's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A. A. M. Morris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. A. M. Morris more than expected).

Fields of papers citing papers by A. A. M. Morris

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. A. M. Morris. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A. A. M. Morris. The network helps show where A. A. M. Morris may publish in the future.

Co-authorship network of co-authors of A. A. M. Morris

This figure shows the co-authorship network connecting the top 25 collaborators of A. A. M. Morris. A scholar is included among the top collaborators of A. A. M. Morris based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A. A. M. Morris. A. A. M. Morris is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bala, Paulina, Sacha Ferdinandusse, S. E. Olpin, P Chetcuti, & A. A. M. Morris. (2015). Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency. JIMD Reports. 27. 11–15. 1 indexed citations

Leonard, James V. & A. A. M. Morris. (2011). The investigation and the initial management of children with suspected metabolic disease presenting acutely. Paediatrics and Child Health. 21(2). 51–55. 1 indexed citations

Stewart, Joanna D., Stephen Tennant, Heather Powell, et al.. (2009). Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children. Journal of Medical Genetics. 46(3). 209–214. 39 indexed citations

Grünewald, Susanne, M. P. Champion, J V Leonard, Jutta Schaper, & A. A. M. Morris. (2004). Biotinidase Deficiency: a Treatable Leukoencephalopathy. Neuropediatrics. 35(4). 211–216. 26 indexed citations

Morris, A. A. M.. (2004). Cerebral ketone body metabolism. Journal of Inherited Metabolic Disease. 28(2). 109–121. 235 indexed citations

Russell‐Eggitt, I, et al.. (2003). Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). Ophthalmic Genetics. 24(1). 49–57. 1 indexed citations

Kvittingen, E. A., et al.. (2003). Acute respiratory distress syndrome in long‐chain 3‐hydroxyacyl‐CoA dehydrogenase and mitochondrial trifunctional protein deficiencies. Journal of Inherited Metabolic Disease. 26(6). 537–541. 11 indexed citations

Leonard, James V. & A. A. M. Morris. (2002). Urea cycle disorders. Seminars in Neonatology. 7(1). 27–35. 124 indexed citations

Morris, A. A. M., Georg F. Hoffmann, E. R. Naughten, et al.. (1999). Glutaric aciduria and suspected child abuse. Archives of Disease in Childhood. 80(5). 404–405. 47 indexed citations

10.

Pfeiffer, Heriberto, B. Brinkmann, J. Hühne, et al.. (1999). Expanding the forensic German mitochondrial DNA control region database: genetic diversity as a function of sample size and microgeography. International Journal of Legal Medicine. 112(5). 291–298. 80 indexed citations

11.

Morris, A. A. M., S. E. Olpin, M. Brivet, et al.. (1998). A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype. The Journal of Pediatrics. 132(3). 514–516. 34 indexed citations

12.

Morris, A. A. M., Phillipa J. Lamont, & Peter T. Clayton. (1997). Pearson's syndrome without marrow involvement. Archives of Disease in Childhood. 77(1). 56–57. 11 indexed citations

13.

Morris, A. A. M. & James V. Leonard. (1997). Early recognition of metabolic decompensation. Archives of Disease in Childhood. 76(6). 555–556. 20 indexed citations

14.

Adwani, Satish, B. Whitehead, P Rees, et al.. (1997). Heart Transplantation for Barth Syndrome. Pediatric Cardiology. 18(2). 143–145. 28 indexed citations

15.

Morris, A. A. M., et al.. (1997). Parent-child transmission of infantile cholestasis with lymphoedema (Aagenaes syndrome).. Journal of Medical Genetics. 34(10). 852–853. 5 indexed citations

16.

Taylor, Robert W., Patrick F. Chinnery, Faye Haldane, et al.. (1996). MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA. Annals of Neurology. 40(3). 459–462. 50 indexed citations

17.

Morris, A. A. M., James V. Leonard, Garry K. Brown, et al.. (1996). Deficiency of respiratory chain complex I is a common cause of leigh disease. Annals of Neurology. 40(1). 25–30. 89 indexed citations

18.

Morris, A. A. M., et al.. (1996). Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease.. Archives of Disease in Childhood. 75(2). 115–119. 37 indexed citations

19.

Morris, A. A. M., Margaret Jackson, Laurence A. Bindoff, & Douglass M. Turnbull. (1995). The investigation of mitochondrial respiratory chain disease.. PubMed. 88(4). 217P–222P. 11 indexed citations

20.

Brown, Richard B., et al.. (1989). Adverse effects of antibiotics. Journal of the American Podiatric Medical Association. 79(10). 500–504. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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