Publications by Dr Andrew Morris - ePrints

Browsing publications by Dr Andrew Morris.

Newcastle Authors	Title	Year
Dr Andrew Morris Dr Richard Martin	Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing	2017
Dr Monika Olahova Dr Steven Hardy Dr John Yarham William Wilson Dr Charlotte Alston et al.	LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population	2015
Dr Monika Olahova Dr Charlotte Alston Jess Houghton Dr Langping He Dr Andrew Morris et al.	A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency	2015
Dr Elizabeth Jones Dr Andrew Morris	Mosaic structural variation in children with developmental disorders	2015
Professor Robert Taylor Dr Angela Pyle Dr Helen Griffin Dr Jennifer Duff Dr Langping He et al.	Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies	2014
Professor Bobby McFarland Dr Andrew Morris Professor Robert Taylor	SURF1 deficiency: a multi-centre natural history study	2013
Dr Charlotte Alston Dr Andrew Morris Emeritus Professor Doug Turnbull Professor Bobby McFarland Professor Robert Taylor et al.	Maternally inherited mitochondrial DNA disease in consanguineous families	2011
Anna Butterworth Dr Andrew Morris Professor Robert Taylor	Mitochondrial DNA depletion syndrome due to mutations in the MPV17 gene	2011
Dr Helen Tuppen Dr Vanessa Hogan Dr Langping He Dr Mazhor Aldosary Dr Gabriele Saretzki et al.	The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families	2010
Professor Bobby McFarland Dr Helen Tuppen Dr Andrew Morris Dr Anita Devlin Professor Robert Taylor et al.	Recurrent mutations in the NDUFS2 gene causing isolated complex I deficiency in skeletal muscle	2009
Dr Helen Tuppen Professor Bobby McFarland Professor Robert Taylor Dr Andrew Morris	The Biochemical and Molecular Genetic Aetiology of Leigh Syndrome	2009
Dr Martin Ward Platt Dr Andrew Morris	Hypothesis: proposals for the management of a neonate at risk of hyperammonaemia due to a urea cycle disorder	2008
Joanna Stewart Dr Angela Pyle Emeritus Professor Mike Sir Michael Rawlins Professor Gavin Hudson Dr Andrew Morris et al.	Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children.	2008
Dr Morteza Pourfarzam Emeritus Professor Doug Turnbull Dr Andrew Morris	ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency	2007
Dr Andrew Morris Rachel Appleton Professor Robert Taylor Emeritus Professor Doug Turnbull	Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy	2007
Professor Bobby McFarland Professor Patrick Chinnery Dr Andrew Schaefer Dr Andrew Morris Sharon Foster et al.	Homoplasmy, heteroplasmy, and mitochondrial dystonia	2007
Professor Robert Taylor Dr Margaret Johnson Professor Zofia Chrzanowska-Lightowlers Dr Andrew Morris Emeritus Professor Doug Turnbull et al.	A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome	2004
Dr Anita Devlin Dr Anil Gholkar OBE Helen Fernandes Dr Vankateswara Ramesh Dr Andrew Morris et al.	Cerebral edema associated with betaine treatment in classical homocystinuria	2004
Dr Morteza Pourfarzam Dr Andrew Morris Dr Raul Dias	Lipid-storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late-onset multiple acyl-CoA dehydrogenation deficiency	2004
Dr Andrew Morris Dr Sally Lynch	Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome	2004
Dr Andrew Morris Emeritus Professor Doug Turnbull Dr Morteza Pourfarzam	Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency	2003
Professor Robert Taylor Dr Andrew Morris Dr Michael Hutchinson Emeritus Professor Doug Turnbull	Leigh disease associated with a novel mitochondrial DNA ND5 mutation	2002
Dr Andrew Morris	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Clinical presentation and follow-up of 50 patients	2002
Professor Bobby McFarland Kim Clark Dr Andrew Morris Professor Robert Taylor Dr Sheila MacPhail et al.	Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation	2002
Dr Katherine Eastham Dr Jonathan Wyllie Dr Sally Lynch Dr Andrew Morris	ARC syndrome: An expanding range of phenotypes	2001
Dr Andrew Morris	Mutation spectrum in patients with fructose-1,6-bisphosphatase deficiency	2001
Dr Andrew Morris Dr Simon Baudouin Dr Michael Snow	Renal tubular acidosis and hypophosphataemia after treatment with nucleoside reverse transcriptase inhibitors	2001
Dr Andrew Morris Professor Robert Lightowlers	Can paternal mtDNA be inherited?	2000
Dr Andrew Morris	Improving the outcome for fatty acid oxidation disorders	2000
Dr Andrew Morris	Inborn errors of metabolism around time of birth	2000
Dr Andrew Morris Professor Timothy Cheetham	Infantile hypophosphatasia: disappointing results of treatment	2000
Dr Andrew Morris Professor Robert Lightowlers	Mitochondrial DNA recombination	2000
Dr Andrew Morris	Neonatal screening for inborn errors of metabolism	2000
Dr Andrew Morris	Changes in serum phenylalanine after overnight fasts in youngsters with phenylketonuria	1999
Dr Andrew Morris	Glutaric aciduria and suspected child abuse	1999
Dr Andrew Morris	HIV nucleoside analogues: new adverse effects on mitochondria?	1999
Dr Andrew Morris	Mitochondrial depletion syndrome is expressed in amniotic fluid cell cultures	1999
Dr Andrew Morris	Mitochondrial respiratory chain disorders and the liver	1999
Dr Andrew Morris	Novel mutations in patients with fructose-1,6-bisphosphatase deficiency	1999
Dr Andrew Morris Emeritus Professor Robert Perry Dr Paul Griffiths Professor Alastair Burt Emeritus Professor Doug Turnbull et al.	Respiratory chain dysfunction in progressive neuronal degeneration of childhood with liver disease	1996