| 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 | 4183 | 2004 |
| 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 | 1827 | 2002 |
| The Collaborative Cross, a community resource for the genetic analysis of complex traits Nature genetics 36 (11), 1133-1137, 2004 | 1206 | 2004 |
| 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 | 890 | 2003 |
| 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 | 809 | 2006 |
| 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 | 501 | 2008 |
| 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 | 473 | 2005 |
| 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 | 473 | 1999 |
| 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 | 433 | 2000 |
| 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 | 328 | 2005 |
| 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 | 274 | 2003 |
| 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 | 266 | 2004 |
| 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 | 252 | 2008 |
| 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 | 204 | 2007 |
| 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 | 168 | 2006 |
| 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 | 163 | 2009 |
| 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 | 149 | 2010 |
| 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 | 144 | 1995 |
| 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 | 121 | 2009 |
| 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 | 120 | 2008 |
