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34
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for author:"Eichler E."
in Literature Citations
| Personalized copy number and segmental duplication maps using next-generation sequencing. Alkan C., Kidd J.M., Marques-Bonet T., Aksay G., Antonacci F., Hormozdiari F., Kitzman J.O., Baker C., Malig M., Mutlu O. et al. Nat. Genet. 41:1061-1067(2009) · Mapped (6) |
| Programmed loss of millions of base pairs from a vertebrate genome. Smith J.J., Antonacci F., Eichler E.E., Amemiya C.T. Proc. Natl. Acad. Sci. U.S.A. 106:11212-11217(2009) · UniProtKB (1) |
| Lineage-specific biology revealed by a finished genome assembly of the mouse. Church D.M., Goodstadt L., Hillier L.W., Zody M.C., Goldstein S., She X., Bult C.J., Agarwala R., Cherry J.L., DiCuccio M. et al. PLoS Biol. 7:E1000112-E1000112(2009) · UniProtKB (2,534) |
| Death and resurrection of the human IRGM gene. Bekpen C., Marques-Bonet T., Alkan C., Antonacci F., Leogrande M.B., Ventura M., Kidd J.M., Siswara P., Howard J.C., Eichler E.E. PLoS Genet. 5:e1000403-e1000403(2009) · UniProtKB (12) · Mapped (1) |
| Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis. de Cid R., Riveira-Munoz E., Zeeuwen P.L., Robarge J., Liao W., Dannhauser E.N., Giardina E., Stuart P.E., Nair R., Helms C. et al. Nat. Genet. 41:211-215(2009) · Mapped (373) |
| Evolutionary toggling of the MAPT 17q21.31 inversion region. Zody M.C., Jiang Z., Fung H.C., Antonacci F., Hillier L.W., Cardone M.F., Graves T.A., Kidd J.M., Cheng Z., Abouelleil A. et al. Nat. Genet. 40:1076-1083(2008) · Mapped (5) |
| Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Landsverk M.L., Ruzzo E.K., Mefford H.C., Buysse K., Buchan J.G., Eichler E.E., Petty E.M., Peterson E.A., Knutzen D.M., Barnett K. et al. Hum. Mol. Genet. 18:1200-1208(2009) · Mapped (5) |
| 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Helbig I., Mefford H.C., Sharp A.J., Guipponi M., Fichera M., Franke A., Muhle H., de Kovel C., Baker C., von Spiczak S. et al. Nat. Genet. 41:160-162(2009) · Mapped (15) |
| Population stratification of a common APOBEC gene deletion polymorphism. Kidd J.M., Newman T.L., Tuzun E., Kaul R., Eichler E.E. PLoS Genet. 3:e63-e63(2007) · Mapped (2) |
| Analysis of the DNA sequence and duplication history of human chromosome 15. Zody M.C., Garber M., Sharpe T., Young S.K., Rowen L., O'Neill K., Whittaker C.A., Kamal M., Chang J.L., Cuomo C.A. et al. Nature 440:671-675(2006) · UniProtKB (463) |
| Human chromosome 11 DNA sequence and analysis including novel gene identification. Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W. et al. Nature 440:497-500(2006) · UniProtKB (945) |
| 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) |
| 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) |
| Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution. Hillier L.W., Miller W., Birney E., Warren W., Hardison R.C., Ponting C.P., Bork P., Burt D.W., Groenen M.A.M., Delany M.E. et al. Nature 432:695-716(2004) · UniProtKB (10) |
| 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) |
| Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Gibbs R.A., Weinstock G.M., Metzker M.L., Muzny D.M., Sodergren E.J., Scherer S., Scott G., Steffen D., Worley K.C., Burch P.E. et al. |
| Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons. Chai J.-H., Locke D.P., Greally J.M., Knoll J.H.M., Ohta T., Dunai J., Yavor A., Eichler E.E., Nicholls R.D. Am. J. Hum. Genet. 73:898-925(2003) · UniProtKB (7) · Mapped (13) |
| The DNA sequence of human chromosome 7. 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. et al. Nature 424:157-164(2003) · UniProtKB (1) |
| The DNA sequence of human chromosome 7. 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. et al. Nature 424:157-164(2003) · UniProtKB (2,635) |
| Genomic sequence and transcriptional profile of the boundary between pericentromeric satellites and genes on human chromosome arm 10p. Guy J., Hearn T., Crosier M., Mudge J., Viggiano L., Koczan D., Thiesen H.-J., Bailey J.A., Horvath J.E., Eichler E.E. et al. Genome Res. 13:159-172(2003) · UniProtKB (7) |
| Divergent origins and concerted expansion of two segmental duplications on chromosome 16. Eichler E.E., Johnson M.E., Alkan C., Tuzun E., Sahinalp C., Misceo D., Archidiacono N., Rocchi M. J. Hered. 92:462-468(2001) · UniProtKB (1) |
| A cascade of complex subtelomeric duplications during the evolution of the hominoid and Old World monkey genomes. van Geel M., Eichler E.E., Beck A.F., Shan Z., Haaf T., van der Maarel S.M., Frants R.R., de Jong P.J. Am. J. Hum. Genet. 70:269-278(2002) · UniProtKB (4) · Mapped (1) |
| Positive selection of a gene family during the emergence of humans and African apes. Johnson M.E., Viggiano L., Bailey J.A., Abdul-Rauf M., Goodwin G., Rocchi M., Eichler E.E. Nature 413:514-519(2001) · UniProtKB (93) |
| Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q. Loftus B.J., Kim U.-J., Sneddon V.P., Kalush F., Brandon R., Fuhrmann J., Mason T., Crosby M.L., Barnstead M., Cronin L. et al. Genomics 60:295-308(1999) · UniProtKB (70) |
