Richard A. Lewis - Concepedia

Author

Richard A. Lewis

Also Known As

Froni, Hua Ling, Julian A. Martínez-Agosto, L. Ma, Lewis, Richard, Lewis, Richard A, Lewis, Richard A., Nirav Malani, R A Lewis, R Lewis

205

Publications

8.3K

Citations

H-Index

154

Concepts

All Affiliations

Novartis (Switzerland)University of California, Santa Barbara Baylor College of Medicine University of California San Diego Novartis Institutes for BioMedical Research

About

Richard A. Lewis is an author at Novartis (Switzerland) specializing in medicine, drug discovery, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	33	3.4K
2	Engineering	18	22	1.2K
3	Natural Sciences	16	16	1.2K
4	Business	1	1	21
5	Allergy	1	1	98

Richard A. Lewis

Publications

6.7K

Citations

H-Index

Page 1

	Year	Citations
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Cell Genome InstabilityLinking Renal CiliopathiesCep164 MutationsGeneticsGenomic Mechanism	2012	390
Lessons in Molecular Recognition: The Effects of Ligand and Protein Flexibility on Molecular Docking Accuracy Jon A. Erickson, Mehran Jalaie, D. H. Robertson, Journal of Medicinal Chemistry	2003	386
Community assessment to advance computational prediction of cancer drug combinations in a pharmacogenomic screen Michael P. Menden, Dennis Wang, Mike J. Mason, Nature Communications	2019	350
Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis Su Kyoung Kim, Asako Shindo, Tae Joo Park, Science Developmental BiologyXenopus EmbryosCell DivisionMedicineCell Interaction	2010	349
Association Between Osteosarcoma and Deleterious Mutations in the RECQL4 Gene in Rothmund-Thomson Syndrome Liangliang Wang, Anu Gannavarapu, Claudia A. Kozinetz, JNCI Journal of the National Cancer Institute	2003	337
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies Melanie M. Sohocki, Stephen P. Daiger, Sara J. Bowne, Human Mutation	2000	331
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome Nicholas Katsanis, Philip L. Beales, Michael O. Woods, Nature Genetics Mendelian DisorderOphthalmologyMkks Cause ObesityGenetic DisorderInherited Metabolic Disease	2000	321
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy Edgar A. Otto, Toby W. Hurd, Rannar Airik, Nature Genetics Ocular DiseaseRetinaOphthalmologyMedicinePathology	2010	318
Synthesis, Pharmacological Characterization, and Molecular Modeling of Heterobicyclic Amino Acids Related to (+)-2-Aminobicyclo[3.1.0]hexane- 2,6-dicarboxylic Acid (LY354740): Identification of Two New Potent, Selective, and Systemically Active Agonists for Group II Metabotropic Glutamate Receptors James A. Monn, Matthew J. Valli, Steven M. Massey, Journal of Medicinal Chemistry Active AgonistsMglu ReceptorsPharmacotherapyChemical BiologyPharmaceutical Chemistry	1999	286
Prediction of multivariate time series by autoregressive model fitting Richard A. Lewis, Gregory C. Reinsel Journal of Multivariate Analysis Forecasting MethodologyPredictive AnalyticsAutoregressive Model FittingForecastingNonlinear Time Series	1985	267

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