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Tim Wiltshire
Tim Wiltshire
Associate Professor, Eshelman School of Pharmacy, University of North Carolina
Verified email at unc.edu - Homepage
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Cited by
Year
A gene atlas of the mouse and human protein-encoding transcriptomes
AI Su, T Wiltshire, S Batalov, H Lapp, KA Ching, D Block, J Zhang, ...
Proceedings of the National Academy of Sciences 101 (16), 6062-6067, 2004
41422004
Large-scale analysis of the human and mouse transcriptomes
AI Su, MP Cooke, KA Ching, Y Hakak, JR Walker, T Wiltshire, AP Orth, ...
Proceedings of the National Academy of Sciences 99 (7), 4465-4470, 2002
18052002
The Collaborative Cross, a community resource for the genetic analysis of complex traits
Nature genetics 36 (11), 1133-1137, 2004
11592004
Melanopsin is required for non-image-forming photic responses in blind mice
S Panda, I Provencio, DC Tu, SS Pires, MD Rollag, AM Castrucci, ...
Science 301 (5632), 525-527, 2003
8692003
The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9
K Tabeta, K Hoebe, EM Janssen, X Du, P Georgel, K Crozat, S Mudd, ...
Nature immunology 7 (2), 156-164, 2006
7882006
Expression analysis of G Protein-Coupled Receptors in mouse macrophages
JE Lattin, K Schroder, AI Su, JR Walker, J Zhang, T Wiltshire, K Saijo, ...
Immunome research 4, 1-13, 2008
4902008
Uncovering regulatory pathways that affect hematopoietic stem cell function using'genetical genomics'
L Bystrykh, E Weersing, B Dontje, S Sutton, MT Pletcher, T Wiltshire, AI Su, ...
Nature genetics 37 (3), 225-232, 2005
4762005
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
DE Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, ...
Nature genetics 22 (2), 196-198, 1999
4701999
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin
ES Moreira, TJ Wiltshire, G Faulkner, A Nilforoushan, M Vainzof, ...
Nature genetics 24 (2), 163-166, 2000
4272000
c-Myb and p300 regulate hematopoietic stem cell proliferation and differentiation
ML Sandberg, SE Sutton, MT Pletcher, T Wiltshire, LM Tarantino, ...
Developmental cell 8 (2), 153-166, 2005
3202005
Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse
T Wiltshire, MT Pletcher, S Batalov, SW Barnes, LM Tarantino, MP Cooke, ...
Proceedings of the National Academy of Sciences 100 (6), 3380-3385, 2003
2732003
Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse
MT Pletcher, P McClurg, S Batalov, AI Su, SW Barnes, E Lagler, ...
PLoS biology 2 (12), e393, 2004
2662004
Genetical genomics: spotlight on QTL hotspots
R Breitling, Y Li, BM Tesson, J Fu, C Wu, T Wiltshire, A Gerrits, ...
PLoS genetics 4 (10), e1000232, 2008
2472008
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function
M Schwander, A Sczaniecka, N Grillet, JS Bailey, M Avenarius, ...
Journal of Neuroscience 27 (9), 2163-2175, 2007
1892007
Marked interindividual variability in the response to selective inhibitors of cyclooxygenase-2
S Fries, T Grosser, TS Price, JA Lawson, S Kapoor, S DeMarco, ...
Gastroenterology 130 (1), 55-64, 2006
1622006
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans
N Grillet, M Schwander, MS Hildebrand, A Sczaniecka, A Kolatkar, ...
The American Journal of Human Genetics 85 (3), 328-337, 2009
1582009
Induced premature G2/M-phase transition in pachytene spermatocytes includes events unique to meiosis
T Wiltshire, C Park, KA Caldwell, MA Handel
Developmental biology 169 (2), 557-567, 1995
1441995
A novel approach to investigate tissue-specific trinucleotide repeat instability
JM Lee, J Zhang, AI Su, JR Walker, T Wiltshire, K Kang, E Dragileva, ...
BMC systems biology 4, 1-16, 2010
1312010
Gene set enrichment in eQTL data identifies novel annotations and pathway regulators
C Wu, DL Delano, N Mitro, SV Su, J Janes, P McClurg, S Batalov, ...
PLoS genetics 4 (5), e1000070, 2008
1192008
A common and unstable copy number variant is associated with differences in Glo1 expression and anxiety-like behavior
R Williams IV, JE Lim, B Harr, C Wing, R Walters, MG Distler, M Teschke, ...
PloS one 4 (3), e4649, 2009
1182009
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