Mathew T. Pletcher
Affiliations: | Human Genetics | Johns Hopkins University School of Medicine, Baltimore, MD, United States |
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"Mathew Pletcher"Parents
Sign in to add mentor| Roger H. Reeves | grad student | 1997-2002 | Johns Hopkins | |
| (Genetic basis of Down syndrome: Physical, comparative, and molecular analysis of chromosome 21.) | ||||
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Publications
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| C Yuen RK, Merico D, Bookman M, et al. (2017) Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder. Nature Neuroscience |
| Jeong S, Patel N, Edlund CK, et al. (2015) Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension. Investigative Ophthalmology & Visual Science. 56: 2737-48 |
| Miller BH, Schultz LE, Long BC, et al. (2010) Quantitative trait locus analysis identifies Gabra3 as a regulator of behavioral despair in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 21: 247-57 |
| Hayes KR, Young BM, Pletcher MT. (2009) Expression quantitative trait loci mapping identifies new genetic models of glutathione S-transferase variation. Drug Metabolism and Disposition: the Biological Fate of Chemicals. 37: 1269-76 |
| Sussan TE, Pletcher MT, Murakami Y, et al. (2005) Tumor suppressor in lung cancer 1 (TSLC1) alters tumorigenic growth properties and gene expression Molecular Cancer. 4 |
| Bystrykh L, Weersing E, Dontje B, et al. (2005) Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'. Nature Genetics. 37: 225-32 |
| Pletcher M, Wiltshire T. (2004) Can we find the genes involved in complex traits? Genome Biology. 5: 347 |
| Kahlem P, Sultan M, Herwig R, et al. (2004) Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome. Genome Research. 14: 1258-67 |
| Saran NG, Pletcher MT, Natale JE, et al. (2003) Global disruption of the cerebellar transcriptome in a Down syndrome mouse model. Human Molecular Genetics. 12: 2013-9 |
| Villanueva MP, Aiyer AR, Muller S, et al. (2002) Genetic and comparative mapping of genes dysregulated in mouse hearts lacking the Hand2 transcription factor gene Genomics. 80: 593-600 |