Tim Wiltshire - Concepedia

Author

Tim Wiltshire

Genomics Institute of the Novartis Research Foundation ORCID

Also Known As

Bailey, Janice S., Cao, Yanguang, Gonzalez, Ricardo D., Gregory E Crawford, Havener, Tammy M., Heather Patisaul, Lee, Jong-Min, Linda A Toth, McLeod, Howard L., Meloto, Carolina B.

157

Publications

13.5K

Citations

H-Index

182

Concepts

All Affiliations

Genomics Institute of the Novartis Research Foundation University of North Carolina at Chapel Hill Scripps Research Institute Johns Hopkins University Johns Hopkins Medicine

About

Tim Wiltshire is an author at Genomics Institute of the Novartis Research Foundation specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	43	7.7K
2	Natural Sciences	7	7	511
3	Health Sciences	3	3	327
4	Engineering	2	2	3.5K
5	Arts	1	1	97

Tim Wiltshire

Publications

12.1K

Citations

H-Index

Page 1

	Year	Citations
A gene atlas of the mouse and human protein-encoding transcriptomes Andrew I. Su, Tim Wiltshire, Serge Batalov, Proceedings of the National Academy of Sciences EngineeringGeneticsTranscriptomics TechnologyGene CharacterizationMolecular Genetics	2004	3.5K
Large-scale analysis of the human and mouse transcriptomes Andrew I. Su, M. Cooke, Keith A. Ching, Proceedings of the National Academy of Sciences	2002	1.5K
The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9 Koichi Tabeta, Kasper Hoebe, Edith M. Janssen, Nature Immunology Toll-like ReceptorsAutoimmune DiseaseUnc93b1 Mutation 3DInnate Immune SystemImmunology	2006	708
Melanopsin Is Required for Non-Image-Forming Photic Responses in Blind Mice Satchidananda Panda, Ignacio Provencio, Daniel C. Tu, Science	2003	705
Expression analysis of G Protein-Coupled Receptors in mouse macrophages Jane Lattin, Kate Schroder, Andrew I. Su, Immunome Research	2008	438
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly Deeann Wallis, Erich Roessler, Ute Hehr, Nature Genetics Developmental BiologyGenetic DisorderGeneticsAutophagyMolecular Genetics	1999	427
Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics' Leonid Bystrykh, Ellen Weersing, Bert Dontje, Nature Genetics Regulatory PathwaysMedicineGeneticsStem Cell MobilizationStem Cell Research	2005	381
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin Eloísa S. Moreira, Tim Wiltshire, Georgine Faulkner, Nature Genetics Skeletal MuscleGenetic DisorderGeneticsSarcomeric Protein TelethoninSystems Biology	2000	333
c-Myb and p300 Regulate Hematopoietic Stem Cell Proliferation and Differentiation Mark L. Sandberg, Susan Sutton, Mathew T. Pletcher, Developmental Cell Hematological MalignancyDevelopmental BiologyMedicineStem Cell MobilizationHematology	2005	272
Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse Tim Wiltshire, Mathew T. Pletcher, Serge Batalov, Proceedings of the National Academy of Sciences BiologyDisease SusceptibilityPhenotypic VariationLinkage DisequilibriumGenotype-phenotype Association	2003	229

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