Publications by Dr Emma Watson - ePrints

Newcastle Authors	Title	Year
Dr Steven Hardy Dr Emma Watson Sila Hopton Professor Robert Taylor	Pigmentary retinopathy, rod–cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNALys (m.8340G>A) gene variant	2017
Dr Emma Watson Dr Langping He Professor Robert Taylor	POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonism	2017
Dr Peter Kullar Professor Robert Taylor Dr Charlotte Alston Dr Emma Watson Professor Patrick Chinnery et al.	The frequency of the m.1555A > G (MTRNR1) variant in UK patients with suspected mitochondrial deafness	2016
Dr Lyndsey Butterworth Dr Laura Irving Dr Charlotte Alston Dr Emma Watson Professor Bobby McFarland et al.	Preimplantation genetic diagnosis for mitochondrial DNA disease	2014
Dr Emma Watson Professor Robert Taylor	MTO1 Mutations are Associated with Hypertrophic Cardiomyopathy and Lactic Acidosis and Cause Respiratory Chain Deficiency in Humans and Yeast	2013