1 - 25 of
40
results
for author:"Myers R.M."
in Literature Citations
| Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Scott L.J., Muglia P., Kong X.Q., Guan W., Flickinger M., Upmanyu R., Tozzi F., Li J.Z., Burmeister M., Absher D. et al. Proc. Natl. Acad. Sci. U.S.A. 106:7501-7506(2009) · Mapped (12) |
| Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder. Rollins B., Martin M.V., Sequeira P.A., Moon E.A., Morgan L.Z., Watson S.J., Schatzberg A., Akil H., Myers R.M., Jones E.G. et al. PLoS ONE 4:e4913-e4913(2009) · Mapped (4) |
| Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects. McGowan K.A., Li J.Z., Park C.Y., Beaudry V., Tabor H.K., Sabnis A.J., Zhang W., Fuchs H., de Angelis M.H., Myers R.M. et al. Nat. Genet. 40:963-970(2008) · Mapped (18) |
| Multiple transcription start sites for FOXP2 with varying cellular specificities. Schroeder D.I., Myers R.M. Gene 413:42-48(2008) · Mapped (12) |
| Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction. Knowles J.W., Wang H., Itakura H., Southwick A., Myers R.M., Iribarren C., Fortmann S.P., Go A.S., Quertermous T., Hlatky M.A. Am. Heart J. 154:1052-1058(2007) · Mapped (18) |
| Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease. Hlatky M.A., Ashley E., Quertermous T., Boothroyd D.B., Ridker P., Southwick A., Myers R.M., Iribarren C., Fortmann S.P., Go A.S. Am. Heart J. 154:1043-1051(2007) · Mapped (21) |
| Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease. Hlatky M.A., Quertermous T., Boothroyd D.B., Priest J.R., Glassford A.J., Myers R.M., Fortmann S.P., Iribarren C., Tabor H.K., Assimes T.L. et al. Am. Heart J. 154:1035-1042(2007) · Mapped (35) |
| The ets-related transcription factor GABP directs bidirectional transcription. Collins P.J., Kobayashi Y., Nguyen L., Trinklein N.D., Myers R.M. PLoS Genet. 3:e208-e208(2007) · Mapped (5) |
| A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease. Assimes T.L., Knowles J.W., Priest J.R., Basu A., Borchert A., Volcik K.A., Grove M.L., Tabor H.K., Southwick A., Tabibiazar R. et al. Atherosclerosis 198:136-144(2008) · Mapped (7) |
| Genome-wide mapping of in vivo protein-DNA interactions. Johnson D.S., Mortazavi A., Myers R.M., Wold B. Science 316:1497-1502(2007) · Mapped (4) |
| Serum response factor binding sites differ in three human cell types. Cooper S.J., Trinklein N.D., Nguyen L., Myers R.M. Genome Res. 17:136-144(2007) · Mapped (3) |
| Wild-type huntingtin participates in protein trafficking between the Golgi and the extracellular space. Strehlow A.N., Li J.Z., Myers R.M. Hum. Mol. Genet. 16:391-409(2007) · Mapped (3) |
| Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels. Carlson C.S., Aldred S.F., Lee P.K., Tracy R.P., Schwartz S.M., Rieder M., Liu K., Williams O.D., Iribarren C., Lewis E.C. et al. Am. J. Hum. Genet. 77:64-77(2005) · Mapped (3) |
| Generation and annotation of the DNA sequences of human chromosomes 2 and 4. Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M. et al. Nature 434:724-731(2005) · UniProtKB (4,275) |
| Widespread parallel evolution in sticklebacks by repeated fixation of Ectodysplasin alleles. Colosimo P.F., Hosemann K.E., Balabhadra S., Villarreal G. Jr., Dickson M., Grimwood J., Schmutz J., Myers R.M., Schluter D., Kingsley D.M. Science 307:1928-1933(2005) · UniProtKB (4) |
| The sequence and analysis of duplication-rich human chromosome 16. Martin J., Han C., Gordon L.A., Terry A., Prabhakar S., She X., Xie G., Hellsten U., Chan Y.M., Altherr M. et al. Nature 432:988-994(2004) · UniProtKB (638) |
| The DNA sequence and comparative analysis of human chromosome 5. Schmutz J., Martin J., Terry A., Couronne O., Grimwood J., Lowry S., Gordon L.A., Scott D., Xie G., Huang W. et al. Nature 431:268-274(2004) · UniProtKB (616) |
| The DNA sequence and biology of human chromosome 19. Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M. et al. Nature 428:529-535(2004) · UniProtKB (1,180) |
| Lack of evidence for an association between WNT2 and RELN polymorphisms and autism. Li J., Nguyen L., Gleason C., Lotspeich L., Spiker D., Risch N., Myers R.M. Am. J. Med. Genet. B Neuropsychiatr. Genet. 126B:51-57(2004) · Mapped (8) |
| Selective disruption of lysosomes in HeLa cells triggers apoptosis mediated by cleavage of Bid by multiple papain-like lysosomal cathepsins. Cirman T., Oresic K., Mazovec G.D., Turk V., Reed J.C., Myers R.M., Salvesen G.S., Turk B. J. Biol. Chem. 279:3578-3587(2004) · Mapped (7) |
| Apoptosis caused by cathepsins does not require Bid signaling in an in vivo model of progressive myoclonus epilepsy (EPM1). Houseweart M.K., Vilaythong A., Yin X.M., Turk B., Noebels J.L., Myers R.M. Cell Death Differ. 10:1329-1335(2003) · Mapped (2) |
| Neuropathological changes in a mouse model of progressive myoclonus epilepsy: cystatin B deficiency and Unverricht-Lundborg disease. Shannon P., Pennacchio L.A., Houseweart M.K., Minassian B.A., Myers R.M. J. Neuropathol. Exp. Neurol. 61:1085-1091(2002) · Mapped (1) |
| Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg R.L., Feingold E.A., Grouse L.H., Derge J.G., Klausner R.D., Collins F.S., Wagner L., Shenmen C.M., Schuler G.D., Altschul S.F. et al. Proc. Natl. Acad. Sci. U.S.A. 99:16899-16903(2002) · UniProtKB (500) · Mapped (7,383) |
| Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families. Li J., Tabor H.K., Nguyen L., Gleason C., Lotspeich L.J., Spiker D., Risch N., Myers R.M. Am. J. Med. Genet. 114:24-30(2002) · Mapped (8) |
| Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes. Lieuallen K., Pennacchio L.A., Park M., Myers R.M., Lennon G.G. Hum. Mol. Genet. 10:1867-1871(2001) · Mapped (1) |
