Philip A. Wilkinson - Concepedia

Author

Philip A. Wilkinson

University College London

Also Known As

P A WILKINSON, P A Wilkinson, P Wilkinson, P. A. Wilkinson, P.A. Wilkinson, Philip A. Wilkinson, Philip Wilkinson

Publications

509

Citations

H-Index

Concepts

All Affiliations

University College London St George's, University of London The Royal Free Hospital Royal London Hospital Roland Hill (United Kingdom)

About

Philip A. Wilkinson is an author at University College London specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	391
2	Social Sciences	2	2	198
3	Health Sciences	1	1	34
4	Epidemiology	1	1	34
5	Hepatology	1	1	34

Philip A. Wilkinson

Publications

440

Citations

H-Index

Page 1

	Year	Citations
Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration Maria K. Tsaousidou, Karim Ouahchi, Thomas T. Warner, The American Journal of Human Genetics Neurodegenerative DiseasesMolecular NeuroscienceOxysterolMotor-neuron DegenerationDegenerative Disease	2008	182
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia Philip A. Wilkinson Brain Mitochondrial Protein ParapleginMitochondrial FunctionMitochondrial BiogenesisMedicineGenetics	2004	92
A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia Philip A. Wilkinson, Andrew H. Crosby, Caria E. Turner, Neurology Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic Epidemiology	2003	36
Occurrence of an abnormal lipoprotein in patients with liver disease A. Ross, G. M. Murphy, Philip A. Wilkinson, Gut PathologyHyperlipidemiaFatty Liver DiseaseCirrhosisMetabolic Syndrome	1970	34
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia Philip A. Wilkinson, Paul Hart, Harshad B. Patel, Journal of the Neurological Sciences Rare DiseasesMendelian DisorderSpg3a MutationGenetic DisorderGenetics	2003	31
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (<i>DNCHC1</i>) and familial motor neuron disorders Azlina Ahmad‐Annuar, Paresh Shah, Majid Hafezparast, Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders	2003	27
Four novel <i>SPG3A/atlastin </i>mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra‐familial variability in age of onset and complex phenotype Steve Bevan, Caroline Vance, P. Renwick, Clinical Genetics	2009	22
NEUROSCHISTOSOMIASIS PRESENTING AS BRAINSTEM ENCEPHALITIS Michael J. Devine, Philip A. Wilkinson, J.F. Doherty, Neurology NeuropsychologyNeurological DisorderUnited KingdomBrain LesionCommon Neurological Disorders	2008	16

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