Clare Neuwirth - Concepedia

Author

Clare Neuwirth

Also Known As

C K Neuwirth, C Neuwirth, C. K. Y. Neuwirth, C. Neuwirth, Clare K. Neuwirth, Clare K. Y. Neuwirth, Clare K.Y. Neuwirth, Clare Neuwirth

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Hammersmith Hospital Imperial College London Medical Research Council University College London NIHR Imperial Biomedical Research Centre

About

Clare Neuwirth is an author at Hammersmith Hospital specializing in medicine, atherosclerosis, and cardiovascular disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	882
2	Public Health	10	10	618
3	Health Sciences	2	2	55
4	Cell Biology	2	2	141
5	Diabetes	2	2	88

Clare Neuwirth

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Familial Hypercholesterolaemia Regression Study: a randomised trial of low-density-lipoprotein apheresis G. R. Thompson, Vincent Maher, Y. Kitano, The Lancet ObesityMetabolic SyndromeFamily MedicineLipid DisorderCardiovascular Disease	1995	245
Severe Hypercholesterolemia in Four British Families With the D374Y Mutation in the PCSK9 Gene R.P. Naoumova, Isabella Tosi, Dilip Patel, Arteriosclerosis Thrombosis and Vascular Biology	2005	179
Evidence for effect of mutant PCSK9 on apolipoprotein B secretion as the cause of unusually severe dominant hypercholesterolaemia Xi‐Ming Sun, Emily R. Eden, Isabella Tosi, Human Molecular Genetics	2005	146
Decreased production of low density lipoprotein by atorvastatin after apheresis in homozygous familial hypercholesterolemia A. David Marais, R.P. Naoumova, Jean Firth, Journal of Lipid Research	1997	125
Reperfusion Hemorrhage Following Acute Myocardial Infarction: Assessment with T2* Mapping and Effect on Measuring the Area at Risk Declan P. O’Regan, Rizwan Ahmed, Narayan Karunanithy, Radiology ThrombosisPercutaneous Coronary InterventionReperfusion HemorrhageCardiovascular DiseaseAtherosclerosis	2009	96
Genetic defects causing familial hypercholesterolaemia: Identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid Clinic Isabella Tosi, Paola Toledo-Leiva, Clare Neuwirth, Atherosclerosis Lipid DisorderGenetic DisorderFamilial HypercholesterolaemiaGeneticsInherited Metabolic Disease	2006	83
Assessment of severe reperfusion injury with T2* cardiac MRI in patients with acute myocardial infarction Declan P. O’Regan, Ben Ariff, Clare Neuwirth, Heart	2010	82
Prolonged inhibition of cholesterol synthesis explains the efficacy of atorvastatin R.P. Naoumova, Shannon E. Dunn, Loukianos Rallidis, Journal of Lipid Research	1997	80
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemia Jana Vandrovcová, Ellen Thomas, Santosh S. Atanur, Genetics in Medicine	2013	77
Restoration of LDL receptor function in cells from patients with autosomal recessive hypercholesterolemia by retroviral expression of ARH1 Emily R. Eden, Dilipkumar Patel, Xi‐Ming Sun, Journal of Clinical Investigation Familial HypercholesterolemiaAutoimmune DiseaseGenetic DisorderGeneticsImmunology	2002	75

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