 |
Eric D. Green, M.D., Ph.D.
Selected Publications
Bouffard G.G., Idol J.I., Braden V.V., Iyer L.M., Cunningham A.F., Weintraub L.A., Touchman J.W., Mohr-Tidwell R.M., Peluso D.C., Fulton R.S., Ueltzen M.S., Weissenbach J., Magness C.L., Green E.D. A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kb. Genome Res, 7:673-692. 1997. [PubMed]
Everett L.A., Glaser B., Beck J.C., Idol J.R., Buchs A., Heyman M., Adawi F., Hazani E., Nassir E., Baxevanis A., Sheffield V.C., Green E.D. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat Genet, 17:411-422. 1997. [PubMed]
Everett L.A., Belyantseva I.A., Noben-Trauth K., Cantos R., Chen A., Thakkar S.I., Hoogstraten-Miller S.L., Kachar B., Wu D.K., Green E.D. Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. Hum Mol Genet, 10:153-161. 2001. [PubMed]
- Video clips displaying the vestibular phenotype in Pds-/- mice
DeSilva U., Elnitski L., Idol J.R., Doyle J.L., Gan W., Thomas J.W., Schwartz S., Dietrich N.L., Beckstrom-Sternberg S.M., McDowell J.C., Blakesley R.W., Bouffard G.G., Thomas P.J., Touchman J.W., Miller W., Green E.D.. Generation and comparative analysis of ~3.3 mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome. Genome Res, 12(1):3-15. 2002. [PubMed]
Thomas J.W., Prasad A.B., Summers T.J., Lee-Lin S-Q., Maduro V.V.B., Idol J.R., Ryan J.F., Thomas P.J., McDowell J.C., and Green E.D.: Parallel construction of orthologous sequence-ready clone contig maps in multiple species. Genome Research, 12:1277-1285. 2002. [PubMed]
Antonellis A., Ellsworth R.E., Sambuughin N., Puls I., Abel A., Lee-Lin S-Q., Jordanova A., Kremensky I., Christodoulou K., Middleton L.T., Sivakumar K., Ionasescu V., Funalot B., Vance J.M., Goldfarb L.G., Fischbeck K.H., and Green E.D. Glycyl tRNA synthetade mutations in Charcot-Marie-Tooth Disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet, 72:1293-1299. 2003. [PubMed]
Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K., Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Cordes M., Du H., Sun H., Edwards J., Bradshaw-Cordum H., Ali J., Andrews S., Isak A., VanBrunt A., Nguyen C., Du F., Lamar B., Courtney L., Kalicki J., Ozersky P., Bielicki L., Scott K., Holmes A., Harkins R., Harris A., Strong C.M., Hou S., Tomlinson C, Dauphin-Kohlberg S, Kozlowicz-Reilly A., Leonard S., Rohlfing T., Rock S.M., Tin-Wollam A-M., Abbott A., Minx P., Maupin R., Strowmatt C., Latreille P., Miller N., Johnson D., Murray J., Woessner J.P., Wendl M.C., Yang S-P., Schultz B.R., Wallis J.W., Spieth J., Bieri T.A., Nelson J.O., Berkowicz N., Wohldmann P.E., Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Bedell J.A., Mardis E.R., Clifton S.W., Chissoe S.L., Marra M.A., Raymond C., Haugen E., Gillett W., Zhou Y., James R., Phelps K., Iadanoto S., Bubb K., Simms E., Levy R., Clendenning J., Kaul R., Kent W.J., Furey T.S., Baertsch R.A., Brent M.R., Keibler E., Flicek P., Bork P., Suyama M., Bailey J.A., Portnoy M.E., Torrents D., Chinwalla A.T., Gish W.R., Eddy S.R., McPherson J.D., Olson M.V., Eichler E.E., Green E.D., Waterston R.H., and Wilson R.K. The DNA sequence of human chromosome 7. Nature, 424:157-164. 2003. [PubMed]
Thomas JW, Touchman JW, Blakesley RW, Bouffard GG, Beckstrom-Sternberg SM, Margulies EH, Blanchette M, Siepel AC, Thomas PJ, McDowell JC, Maskeri B, Hansen NF, Schwartz MS, Weber RJ, Kent WJ, Karolchik D, Bruen TC, Bevan R, Cutler DJ, Schwartz S, Elnitski L, Idol JR, Prasad AB, Lee-Lin S-Q, Maduro VVB, Summers TJ, Portnoy ME, Dietrich NL, Akhter N, Ayele K, Benjamin B, Cariaga K, Brinkley CP, Brooks SY, Granite S, Guan X, Gupta J, Haghighi P, Ho S-L, Huang MC, Karlins E, Laric PL, Legaspi R, Lim MJ, Maduro QL, Masiello CA, Mastrian SD, McCloskey JC, Pearson R, Stantripop S, Tiongson EE, Tran JT, Tsurgeon C, Vogt JL, Walker MA, Wetherby KD, Wiggins LS, Young AC, Zhang L-H, Osoegawa K, Zhu B, Zhao B, Shu CL, De Jong PJ, Lawrence CE, Smit AF, Chakravarti A, Haussler C, Green P, Miller W, and Green ED. Comparative analyses of multi-species sequences from targeted genomic regions. Nature, 424:788-793. 2003. [PubMed]
Thomas J.W., NISC Comparative Sequencing Program, and Green E.D. Comparative sequence analysis of a single-gene conserved segment in mouse and human. Mammalian Genome, 14:673-678. 2003. [PubMed]
Margulies E.H., Blanchette M., NISC Comparative Sequencing Program, Haussler D., and Green E.D.. Identification and characterization of multi-species conserved sequences. Genome Research, 14:673-678. 2003. [PubMed]
Blakesley R.W., Hansen N.F., Mullikin J.C., Thomas P.J., McDowell J.C., Maskeri B., Young A.C., Benjamin B., Brooks S.Y., Coleman B.I., Gupta J., Ho S-L., Karlins E.M., Maduro Q.L., Stantripop S., Tsurgeon C., Vogt J.L., Walker M.A., Masiello C.A., Guan X., NISC Comparative Sequencing Program, Bouffard G.G., Green E.D. An intermediate grade of finished genomic sequence suitable for comparative analyses. Genome Research, 14:2235-2244. 2004. [PubMed]
Margulies E.H., NISC Comparative Sequencing Program, Maduro V.V.B., Thomas P.J., Tomkins J.P., Amemiya C.T., Luo M., Green E.D. Comparative sequencing provides insights about the structure and conservation of marsupial and monotreme genomes. Proc Natl Acad Sci USA, 102:3354-3359. 2005. [PubMed]
Margulies, E.H., Vinson J.P., NISC Comparative Sequencing Program, Miller W,
Jaffe, D.B., Lindblad-Toh, K, Chang, J.L., Green, E.D., Lander, E.S., Mullikin, J.C., and
Clamp, M. An initial strategy for the systematic identification of
functional elements in the human genome by low-redundancy comparative
sequencing. Proc Natl Acad Sci USA, 102:4795-4800. 2005. [PubMed]
Schueler, M.G., Dunn, J.M., Bird, C.P., Ross, M.T., Viggiano, L., NISC Comparative
Sequencing Program, Rocchi, M., Willard, H.F., and Green, E.D. Progressive
proximal expansion of the primate X chromosome centromere. Proc Natl Acad
Sci USA, 102:10563-10568. 2005. [PubMed]
Margulies, E.H., Chen, C.W., and Green, E.D. Differences between pair-wise and
multi-sequence alignment methods affect vertebrate genome comparisons.
Trends Genet, 22:187-193. 2006. [PubMed]
Antonellis, A., Lee-Lin, S.-Q., Wasterlain, A., Leo, P., Quezado, M., Goldfarb, L.G., Myung, K., Burgess, S., Fischbeck, K.H., and Green, E.D.
Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons. J Neurosci, 26:10397-406.
2006. [PubMed]
Hurle, B., Swanson, W., NISC Comparative Sequencing Program, and Green,
E.D. Comparative sequence analyses reveal rapid and divergent evolutionary
changes of the WFDC locus in the primate lineage. Genome Res, 17:276-286. 2007. [PubMed]
The ENCODE Project Consortium. Identification and analysis of functional
elements in 1% of the human genome by the ENCODE pilot project. Nature,
447:799-816. 2007. [PubMed]
Margulies, E.H., Cooper, G.M., Asimenos, G., Thomas, D.J., Dewey, C.N.,
Siepel, A., Birney, E., Keefe, D., Schwartz, A.S., Hou, M., Taylor, J.,
Nikolaev, S., Montoya-Burgos, J.I., Loytynoja, A., Whelen, S., Pardi, F.,
Massingham, T., Brown, J.B., Bickel, P., Holmes, I., Mullikin, J.C.,
Ureta-Vidal, A., Paten, B., Stone, E.A., Rosenbloom, K.R., Kent, W.J., NISC
Comparative Sequencing Program, Bayor College of Medicine Human Genome
Sequencing Center, Washington University Genome Sequencing Center, Broad
Institute, UCSC Genome Brower Team, British Columbia Cancer Agency Genome
Sciences Center, Antonarakis, S.E., Batzoglou, S., Goldman, N., Hardison,
R., Haussler, D., Miller, W., Pachter, L., Green, E.D., and Sidow, A.
Analyses of deep mammalian sequence alignments and constraint predictions
for 1% of the human genome. Genome Res, 17:760-774. 2007. [PubMed]
Books
Green, E.D., Birren, B., Klapholz, S., Myers, R.M., and Hieter, P., eds. Genome Analysis: A Laboratory Manual (Volumes 1-4). Cold Spring Harbor Laboratory Press, NY: Cold Spring Harbor Laboratory, 1997.
Last Reviewed: July 23, 2008
|
|
Copyright
Print Version