P. Sharp

1.8k citations

41 papers · 1.6k · h-index 25

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Biochemistry top 2%
- Lipid metabolism and biosynthesis

Papers in

Molecular Biology 28
- Peroxisome Proliferator-Activated Receptors 27
- RNA regulation and disease 3
Physiology 20
- Adipose Tissue and Metabolism 11
- Lysosomal Storage Disorders Research 8

Co-authors: A. Poulos (21 shared papers)David W. Johnson (12 shared papers)A.J. Fellenberg (8 shared papers)Harmeet Singh (7 shared papers)M.J. Whiting (1 shared paper)Phillip D. Whitfield (4 shared papers)Peter J. Meikle (4 shared papers)Barbara C. Paton (6 shared papers)
Journals: Biochemical Journal (5 papers)Molecular Genetics and Metabolism (4 papers)European Journal of Pediatrics (3 papers)Prenatal Diagnosis (3 papers)Clinical Genetics (3 papers)
Partner nations: Australia United States Canada

In The Last Decade

P. Sharp

41 papers receiving 1.5k citations

Peers

Countries citing papers authored by P. Sharp

Since Specialization

Citations

This map shows the geographic impact of P. Sharp'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 P. Sharp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. Sharp more than expected).

Fields of papers citing papers by P. Sharp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. Sharp. 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 P. Sharp. The network helps show where P. Sharp may publish in the future.

Co-authors

The 25 scholars most cited alongside P. Sharp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P. Sharp Line = papers co-authored together P. Sharp links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 41 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome? Clinical Genetics ·A. Poulos, P. Sharp, M.J. Whiting	1984	116
2	Pex13Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype Molecular and Cellular Biology ·Megan Maxwell, Jonas Björkman, Tam Nguyen, P. Sharp, John Finnie, Carol Paterson, Ian D. Tonks, Barbara C. Paton, Graham F. Kay, Denis I. Crane	2003	93
3	The occurrence of polyenoic fatty acids with greater than 22 carbon atoms in mammalian spermatozoa Biochemical Journal ·A. Poulos, P. Sharp, David W. Johnson, I. White, A.J. Fellenberg	1986	87
4	Simple mass spectrometric differentiation of then-3,n-6 andn-9 series of methylene interrupted polyenoic acids Journal of Mass Spectrometry ·A.J. Fellenberg, David W. Johnson, A. Poulos, P. Sharp	1987	73
5	The occurrence of polyenoic very long chain fatty acids with greater than 32 carbon atoms in molecular species of phosphatidylcholine in normal and peroxisome-deficient (Zellweger's syndrome) brain Biochemical Journal ·A. Poulos, P. Sharp, David W. Johnson, Christopher J. Easton	1988	67
6	Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction European Journal of Pediatrics ·A. Poulos, P. Sharp, A.J. Fellenberg, David W. Johnson	1988	65
7	Cerebro-hepato-renal (Zellweger) syndrome, adrenoleukodystrophy, and Refsum's disease: Plasma changes and skin fibroblast phytanic acid oxidase Human Genetics ·A. Poulos, P. Sharp, A.J. Fellenberg, David M. Danks	1985	63
8	Detection of a homologous series of C26-C38 polyenoic fatty acids in the brain of patients without peroxisomes (Zellweger's syndrome) Biochemical Journal ·A. Poulos, P. Sharp, Harmeet Singh, David W. Johnson, A.J. Fellenberg, A.C. Pollard	1986	63
9	Very long chain fatty acids in X‐linked adrenoleukodystrophy brain after treatment with Lorenzo's oil Annals of Neurology ·Alfred Poulos, Robert A. Gibson, P. Sharp, K. Beckman, Padraic G Rattan‐Smith	1994	62
10	Human Mucopolysaccharidosis IIID Journal of Neuropathology & Experimental Neurology ·M. Z. Jones, Joseph Alroy, Joseph C. Rutledge, John W. Taylor, Ellsworth C. Alvord, Jennifer R. Toone, Derek A. Applegarth, John J. Hopwood, Ehud Skutelsky, Christopher J. Ianelli, David A. Thorley‐Lawson, CYNTHIA MITCHELL-HERPOLSHEIMER, A. García Arias, P. Sharp, R. Wendell Evans, David Sillence, Kevin Cavanagh	1997	62
11	Accumulation and defective β‐oxidation of very long chain fatty acids in Zellweger's syndrome, adrenoleukodystrophy and Refsum's disease variants Clinical Genetics ·A. Poulos, Harmeet Singh, Barbara C. Paton, P. Sharp, Nicholas Derwas	1986	56
12	Formic acid is a product of the α-oxidation of fatty acids by human skin fibroblasts: deficiency of formic acid production in peroxisome-deficient fibroblasts Biochemical Journal ·A. Poulos, P. Sharp, Harmeet Singh, David W. Johnson, W.F. Carey, Christopher J. Easton	1993	56
13	PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress Disease Models & Mechanisms ·Crı́stian Müller, Tam Nguyen, Barbara Ahlemeyer, Mallika Meshram, Nishreen Santrampurwala, Siyu Cao, P. Sharp, Pamela B. Fietz, Eveline Baumgart‐Vogt, Denis I. Crane	2010	55
14	Urinary Lipid Profiling for the Identification of Fabry Hemizygotes and Heterozygotes Clinical Chemistry ·Maria Fuller, P. Sharp, Tina Rozaklis, Phillip D. Whitfield, David Blacklock, John J. Hopwood, Peter J. Meikle	2005	54
15	Rhizomelic chondrodysplasia punctata: Clinical, pathologic, and biochemical findings in two patients The Journal of Pediatrics ·A. Poulos, L. J. Sheffield, P. Sharp, Geoffrey Sherwood, David W. Johnson, K. Beckman, A.J. Fellenberg, J. E. Wraith, C. W. Chow, S. Usher, Harmeet Singh	1988	52
16	Molecular Species of Phosphatidylcholine Containing Very Long Chain Fatty Acids in Human Brain: Enrichment in X‐Linked Adrenoleukodystrophy Brain and Diseases of Peroxisome Biogenesis Brain Journal of Neurochemistry ·P. Sharp, David W. Johnson, A. Poulos	1991	51
17	Quantification of galactosylsphingosine in the twitcher mouse using electrospray ionization-tandem mass spectrometry Journal of Lipid Research ·Phillip D. Whitfield, P. Sharp, Rosanne M. Taylor, Peter J. Meikle	2001	47
18	Correlation among Genotype, Phenotype, and Biochemical Markers in Gaucher Disease: Implications for the Prediction of Disease Severity Molecular Genetics and Metabolism ·Phillip D. Whitfield, Paul V. Nelson, P. Sharp, Colleen Bindloss, Caroline Dean, Elaine M. Ravenscroft, B. A. Fong, (unknown), John J. Hopwood, Peter J. Meikle	2002	47
19	Plasma and skin fibroblast C ₂₆ fatty acids in infantile Refsum's disease Neurology ·A. Poulos, P. Sharp	1984	47
20	Characterization of Urinary Sulfatides in Metachromatic Leukodystrophy Using Electrospray Ionization-Tandem Mass Spectrometry Molecular Genetics and Metabolism ·Phillip D. Whitfield, P. Sharp, David W. Johnson, Paul V. Nelson, Peter J. Meikle	2001	46

About P. Sharp

P. Sharp is a scholar working on Molecular Biology, Physiology, Clinical Biochemistry, Nutrition and Dietetics and Biochemistry, having authored 41 papers that have together received 1.6k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (27 papers), Metabolism and Genetic Disorders (18 papers), Adipose Tissue and Metabolism (11 papers), Lysosomal Storage Disorders Research (8 papers), Lipid metabolism and biosynthesis (4 papers), Vitamin K Research Studies (3 papers), RNA regulation and disease (3 papers) and Folate and B Vitamins Research (2 papers). The work is most often cited by research in Clinical Biochemistry (518 citations), Biochemistry (198 citations), Physiology (554 citations), Molecular Biology (1.1k citations) and Physiology (57 citations). P. Sharp has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include A. Poulos, David W. Johnson, A.J. Fellenberg, Harmeet Singh, M.J. Whiting, Phillip D. Whitfield, Peter J. Meikle, Barbara C. Paton, Christopher J. Easton and K. Beckman. Their work appears in journals such as Biochemical Journal, Molecular Genetics and Metabolism, European Journal of Pediatrics, Prenatal Diagnosis and Clinical Genetics.

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.

Explore authors with similar magnitude of impact

P. Sharp

Impact in

Papers in i

In The Last Decade

P. Sharp

Peers

Countries citing papers authored by P. Sharp

Fields of papers citing papers by P. Sharp

All Works

About P. Sharp

Explore authors with similar magnitude of impact

Papers in