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Christine P. Diggle

Observed names: C. P. Diggle, C.P. Diggle, CHRISTINE P. DIGGLE, CP Diggle, Christine Diggle, Christine P Diggle, Christine P. Diggle, Diggle, Christine P.
Observed institutions: University of Leeds, Cancer Research UK, St James's University Hospital, University of York, University of Birmingham, The University of Texas Southwestern Medical Center
ORCID: 0000-0001-6861-359X
Observed ORCID: 0000-0001-6861-359X
OpenAlex ID: A5088081783
Correction: Corrigendum: Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome
2013 · Miguel A. Lanaspa, Takuji Ishimoto, et al. · Nature Communications · 796
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High-fat and high-sucrose (western) diet induces steatohepatitis that is dependent on fructokinase
2013 · Takuji Ishimoto, Miguel A. Lanaspa, et al. · Hepatology · 331
Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy
2008 · Sandeep Uppal, Christine P Diggle, et al. · Nature Genetics · 331
Opposing effects of fructokinase C and A isoforms on fructose-induced metabolic syndrome in mice
2012 · Takuji Ishimoto, Miguel A. Lanaspa, et al. · Proceedings of the National Academy of Sciences · 298
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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte
2011 · David A. Parry, Clare V. Logan, et al. · The American Journal of Human Genetics · 249
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Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome
2013 · Miguel A. Lanaspa, Takuji Ishimoto, et al. · Nature Communications · 247
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Ketohexokinase: Expression and Localization of the Principal Fructose-metabolizing Enzyme
2009 · Christine P. Diggle, Michael Shires, et al. · Journal of Histochemistry & Cytochemistry · 194
Role of PPAR γ and EGFR signalling in the urothelial terminal differentiation programme
2004 · Claire L. Varley, Jens Stahlschmidt, et al. · Journal of Cell Science · 175
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CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
2014 · Rim Hjeij, Alexandros Onoufriadis, et al. · The American Journal of Human Genetics · 173
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Endogenous Fructose Production and Fructokinase Activation Mediate Renal Injury in Diabetic Nephropathy
2014 · Miguel A. Lanaspa, Takuji Ishimoto, et al. · Journal of the American Society of Nephrology · 167
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
2011 · Clare V Logan, Barbara Lucke, et al. · Nature Genetics · 117
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
2012 · Christine P. Diggle, David A. Parry, et al. · Human Mutation · 97
In vitro studies on the relationship between polyunsaturated fatty acids and cancer: tumour or tissue specific effects?
2002 · Christine P Diggle · Progress in Lipid Research · 84
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy
2016 · Christine P. Diggle, Stacey J. Sukoff Rizzo, et al. · The American Journal of Human Genetics · 82
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Malignant hyperthermia, environmental heat stress, and intracellular calcium dysregulation in a mouse model expressing the p.G2435R variant of RYR1
2018 · J.R. Lopez, V. Kaura, et al. · British Journal of Anaesthesia · 71
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Properties of the Purified, Recombinant, NADP(H)‐Binding Domain III of the Proton‐Translocating Nicotinamide Nucleotide Transhydrogenase from Rhodospirillum Rubrum
1996 · Christine Diggle, Tania Bizouarn, et al. · European Journal of Biochemistry · 71
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Properties of the Soluble Polypeptide of the Proton-Translocating Transhydrogenase from Rhodospirillum rubrum Obtained by Expression in Escherichia coli
1995 · Christine Diggle, Mike Mutton, et al. · European Journal of Biochemistry · 70
HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus
2014 · Christine P. Diggle, Daniel J. Moore, et al. · PLoS Genetics · 67
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Mutations in GPAA1 , Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia
2017 · Thi Tuyet Mai Nguyen, Yoshiko Murakami, et al. · The American Journal of Human Genetics · 64
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Both isoforms of ketohexokinase are dispensable for normal growth and development
2010 · C. P. Diggle, M. Shires, et al. · Physiological Genomics · 55
Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy
2010 · Christine P. Diggle, Ian M. Carr, et al. · Lara D. Veeken · 54
A novel RyR1-selective inhibitor prevents and rescues sudden death in mouse models of malignant hyperthermia and heat stroke
2021 · Toshiko Yamazawa, Takuya Kobayashi, et al. · Nature Communications · 52
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Simple Detection of Germline Microsatellite Instability for Diagnosis of Constitutional Mismatch Repair Cancer Syndrome
2013 · Danielle Ingham, Christine P. Diggle, et al. · Human Mutation · 50
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Conformational Dynamics of a Mobile Loop in the NAD(H)‐Binding Subunit of Proton‐Translocating Transhydrogenases from Rhodospirillum Rubrum and Escherichia Coli
1995 · Christine Diggle, Nick P. J. Cotton, et al. · European Journal of Biochemistry · 43
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Development of a rapid, small-scale DNA repair assay for use on clinical samples
2003 · C. P. Diggle · Nucleic Acids Research · 42
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Works count: 57
Citation count: 4,346
H-index: 31
I10-index: 38
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