Janet Perry - Concepedia

Author

Janet Perry

Northwick Park Hospital ORCID

Also Known As

J D Perry, J PERRY, J Perry, J. D. PERRY, J. D. Perry, J. Perry, J.D Perry, J.D. Perry, Janet PERRY, Janet Perry

153

Publications

10.6K

Citations

H-Index

114

Concepts

All Affiliations

Northwick Park Hospital Royal London Hospital Wellcome Sanger Institute Queen Mary University of London Institute of Cancer Research

About

Janet Perry is an author at Northwick Park Hospital specializing in medicine, metabolism, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	27	46	7.1K
2	Health Sciences	14	17	896
3	Public Health	9	9	343
4	Engineering	2	2	277
5	Natural Sciences	2	2	136

Janet Perry

Publications

9.8K

Citations

H-Index

Page 1

	Year	Citations
Patterns of somatic mutation in human cancer genomes Christopher Greenman, Philip Stephens, Raffaella Smith, Nature Somatic MutationSomatic VariantGeneticsMedicineEpigenetics	2007	3.1K
Intragenic ERBB2 kinase mutations in tumours Philip Stephens, Chris Hunter, Graham R. Bignell, Nature Tumor BiologyReceptor Tyrosine KinaseCancer GeneticsMedicineCell Biology	2004	785
Somatic Mutations of the Protein Kinase Gene Family in Human Lung Cancer Helen Davies, Chris Hunter, Raffaella Smith, Cancer Research	2005	466
Mutation analysis of 24 known cancer genes in the NCI-60 cell line set Ogechi Ikediobi, Helen Davies, Graham R. Bignell, Molecular Cancer Therapeutics	2006	439
A Hypermutation Phenotype and Somatic <i>MSH6</i> Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy Chris Hunter, Raffaella Smith, Daniel P. Cahill, Cancer Research	2006	428
A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer Philip Stephens, Sarah Edkins, Helen Davies, Nature Genetics Gene Family IdentifiesBreast OncologySomatic VariantSomatic MutationsTumor Heterogeneity	2005	333
Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells Andrea Pellagatti, Mario Cazzola, Aristoteles Giagounidis, Leukemia Developmental BiologyBone Marrow FailureMedicineStem Cell MobilizationHematology	2010	286
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Patrick Tarpey, F. Lucy Raymond, Lam Son Nguyen, Nature Genetics Developmental BiologyGenetic DisorderGeneticsPsychiatric GeneticsNonsyndromic Mental Retardation	2007	284
Intra-articular triamcinolone hexacetonide in knee osteoarthritis: factors influencing the clinical response. Karl Gaffney, Joanna Ledingham, Janet Perry Annals of the Rheumatic Diseases	1995	245
Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor Patrick Tarpey, F. Lucy Raymond, Sarah O’Meara, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsFragile X SpectrumNeuroscience	2007	223

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