17
results
for author:"Gregory S.G."
in Literature Citations
| Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis. McCauley J.L., Zuvich R.L., Bradford Y., Kenealy S.J., Schnetz-Boutaud N., Gregory S.G., Hauser S.L., Oksenberg J.R., Mortlock D.P., Pericak-Vance M.A. et al. Genes Immun. 10:624-630(2009) · Mapped (79) |
| Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis. Crosslin D.R., Shah S.H., Nelson S.C., Haynes C.S., Connelly J.J., Gadson S., Goldschmidt-Clermont P.J., Vance J.M., Rose J., Granger C.B. et al. Hum. Genet. 125:217-229(2009) · Mapped (4) |
| Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis. Shah S.H., Freedman N.J., Zhang L., Crosslin D.R., Stone D.H., Haynes C., Johnson J., Nelson S., Wang L., Connelly J.J. et al. PLoS Genet. 5:e1000318-e1000318(2009) · Mapped (2) |
| Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease. Wang L., Hauser E.R., Shah S.H., Seo D., Sivashanmugam P., Exum S.T., Gregory S.G., Granger C.B., Haines J.L., Jones C.J. et al. Ann. Hum. Genet. 72:443-453(2008) · Mapped (3) |
| Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets. Sutton B.S., Crosslin D.R., Shah S.H., Nelson S.C., Bassil A., Hale A.B., Haynes C., Goldschmidt-Clermont P.J., Vance J.M., Seo D. et al. Hum. Mol. Genet. 17:1318-1328(2008) · Mapped (4) |
| Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Gregory S.G., Schmidt S., Seth P., Oksenberg J.R., Hart J., Prokop A., Caillier S.J., Ban M., Goris A., Barcellos L.F. et al. |
| Risk alleles for multiple sclerosis identified by a genomewide study. International Multiple Sclerosis Genetics Consortium N. Engl. J. Med. 357:851-862(2007) · Mapped (21) |
| Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease. Wang L., Hauser E.R., Shah S.H., Pericak-Vance M.A., Haynes C., Crosslin D., Harris M. II, Nelson S., Hale A.B., Granger C.B. et al. Am. J. Hum. Genet. 80:650-663(2007) · UniProtKB (1) · Mapped (3) |
| A second major histocompatibility complex susceptibility locus for multiple sclerosis. Yeo T.W., De Jager P.L., Gregory S.G., Barcellos L.F., Walton A., Goris A., Fenoglio C., Ban M., Taylor C.J., Goodman R.S. et al. Ann. Neurol. 61:228-236(2007) · Mapped (828) |
| GATA2 is associated with familial early-onset coronary artery disease. Connelly J.J., Wang T., Cox J.E., Haynes C., Wang L., Shah S.H., Crosslin D.R., Hale A.B., Nelson S., Crossman D.C. et al. PLoS Genet. 2:e139-e139(2006) · Mapped (2) |
| Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis. Schmidt S., Pericak-Vance M.A., Sawcer S., Barcellos L.F., Hart J., Sims J., Prokop A.M., van der Walt J., DeLoa C., Lincoln R.R. et al. Genes Immun. 7:384-392(2006) · Mapped (6) |
| The DNA sequence and biological annotation of human chromosome 1. Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A. et al. Nature 441:315-321(2006) · UniProtKB (2,550) |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,194) |
| Organization of the MASP2 locus and its expression profile in mouse and rat. Stover C.M., Lynch N.J., Hanson S.J., Windbichler M., Gregory S.G., Schwaeble W.J. |
| Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P. Hoffman H.M., Gregory S.G., Mueller J.L., Tresierras M., Broide D.H., Wanderer A.A., Kolodner R.D. |
| A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation. McMullan T.W., Crolla J.A., Gregory S.G., Carter N.P., Cooper R.A., Howell G.R., Robinson D.O. |
| A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. Schutte B.C., Bjork B.C., Coppage K.B., Malik M.I., Gregory S.G., Scott D.J., Brentzell L.M., Watanabe Y., Dixon M.J., Murray J.C. Genome Res. 10:81-94(2000) · UniProtKB (1) |
