Mathew T. Pletcher
Mathew T. Pletcher
Rare Disease Research Unit, Pfizer
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Cited by
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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
TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer
M Kuramochi, H Fukuhara, T Nobukuni, T Kanbe, T Maruyama, HP Ghosh, ...
Nature genetics 27 (4), 427-430, 2001
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RKC Yuen, D Merico, M Bookman, JL Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
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
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
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome
P Kahlem, M Sultan, R Herwig, M Steinfath, D Balzereit, B Eppens, ...
Genome research 14 (7), 1258-1267, 2004
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
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
Genome-wide characteristics of de novo mutations in autism
RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ...
NPJ genomic medicine 1 (1), 1-10, 2016
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
Global disruption of the cerebellar transcriptome in a Down syndrome mouse model
NG Saran, MT Pletcher, JAE Natale, Y Cheng, RH Reeves
Human molecular genetics 12 (16), 2013-2019, 2003
Histopathologic characterization of the BTBR mouse model of autistic-like behavior reveals selective changes in neurodevelopmental proteins and adult hippocampal neurogenesis
DT Stephenson, SM O'Neill, S Narayan, A Tiwari, E Arnold, HD Samaroo, ...
Molecular autism 2 (1), 1-22, 2011
Genetic regulation of behavioral and neuronal responses to fluoxetine
BH Miller, LE Schultz, A Gulati, MD Cameron, MT Pletcher
Neuropsychopharmacology 33 (6), 1312-1322, 2008
Inositol (1, 4, 5) trisphosphate 3 kinase B controls positive selection of T cells and modulates Erk activity
BG Wen, MT Pletcher, M Warashina, SH Choe, N Ziaee, T Wiltshire, ...
Proceedings of the National Academy of Sciences 101 (15), 5604-5609, 2004
Phenotypic characterization of a genetically diverse panel of mice for behavioral despair and anxiety
BH Miller, LE Schultz, A Gulati, AI Su, MT Pletcher
PloS one 5 (12), e14458, 2010
Comparative analysis of haplotype association mapping algorithms
P McClurg, MT Pletcher, T Wiltshire, AI Su
BMC bioinformatics 7 (1), 1-15, 2006
The Tribolium decapentaplegic gene is similar in sequence, structure, and expression to the Drosophila dpp gene
J Sanchez-Salazar, MT Pletcher, RL Bennett, SJ Brown, TJ Dandamudi, ...
Development genes and evolution 206 (4), 237-246, 1996
Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse
LH Pinto, MH Vitaterna, K Shimomura, SM Siepka, V Balannik, ...
Visual neuroscience 24 (1), 111-123, 2007
Comparative genomic sequence analysis of the human chromosome 21 Down syndrome critical region
A Toyoda, H Noguchi, TD Taylor, T Ito, MT Pletcher, Y Sakaki, RH Reeves, ...
Genome research 12 (9), 1323-1332, 2002
Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21
MT Pletcher, T Wiltshire, DE Cabin, M Villanueva, RH Reeves
Genomics 74 (1), 45-54, 2001
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