Jiang Z, Tang H, Ventura M, Cardone MF, Marques-Bonet T, She X, Pevzner P, Eichler EE. (2007). Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution. Nat Genet Nov;39(11):1361-1368 (7 Oct 2007).
Blog Archives
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes and epilepsy
Mefford HC, Clauin S, Sharp AJ, Moller RS, Ullmann R, Kapur R, Pinkel D, Cooper GM, Ventura M, Ropers HH, Tommerup N, Eichler EE, Bellanne-Chantelot C. (2007). Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes and epilepsy. Am J Hum Genet Nov;81(5):1057-1069 (26 Sept 2007).
Optimal design of oligonucleotide microarrays for measurement of DNA copy-number
Sharp AJ, Itsara A, Cheng Z, Alkan C, Schwartz S, Eichler EE. (2007). Optimal design of oligonucleotide microarrays for measurement of DNA copy-number. Hum Mol Genet
Nov;16(22):2770-2779 (28 Aug 2007).
Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21
Lyle R, Prandini P, Osoegawa K, ten Hallers B, Humphray S, Zhu B, Eyras E, Castelo R, Bird CP, Gagos S, Scott C, Cox A, Deutsch S, Ucla C, Cruts M, Dahoun S, She X, Bena F, Wang SY, Van Broeckhoven C, Eichler EE, Guigo R, Rogers J, de Jong PJ, Reymond A, Antonarakis SE. (2007). Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21. Genome Res Nov;17(11):1690-1696
Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data
Alkan C, Ventura M, Archidiacono N, Rocchi M, Sahinalp CS, Eichler EE. (2007). Organization and evolution of primate centromeric DNA from whole-genome shotgun sequence data. PLOS Comput Biol Sep;3(9):e181 (28 Sept 2007).
Mutational and selective effects on copy-number variants in the human genome
Cooper GM, Nickerson DA, Eichler EE. (2007). Mutational and selective effects on copy-number variants in the human genome. Nat Genet Jul;39(7 Suppl):S22-S29 (27 June 2007).
Challenges and standards in integrating surveys of structural variation
Scherer SW, Lee C, Birney E, Altshuler DM, Eichler EE, Carter NP, Hurles ME, Feuk L. (2007). Challenges and standards in integrating surveys of structural variation. Nat Genet
Jul;39(7 Suppl):S7-S15 (27 June 2007).
Completing the map of human genetic variation
Eichler EE, Nickerson DA, Altshuler D, Bowcock AM, Brooks LD, Carter NP, Church DM, Felsenfeld A, Guyer M, Lee C, Lupski JR, Mullikin JC, Pritchard JK, Sebat J, Sherry ST, Smith D, Valle D, Waterston RH. (2007). Completing the map of human genetic variation. Nature May;447(7141):161-165 (10 May 2007).
Population stratification of a common APOBEC gene deletion polymorphism
Kidd JM, Newman TL, Tüzün E, Kaul R, Eichler EE. (2007). Population stratification of a common APOBEC gene deletion polymorphism. PLoS Genet Apr;3(4):e63.
Evolutionary formation of new centromeres in macaque
Ventura M, Antonacci F, Cardone MF, Stanyon R, D’Addabbo P, Cellamare A, Sprague LJ, Eichler EE, Archidiacono N, Rocchi M. (2007). Evolutionary formation of new centromeres in macaque. Science Apr;316(5822):243-246.
Evolutionary and biomedical insights from the rhesus macaque genome
Rhesus Macaque Genome Sequencing and Analysis Consortium, (12 authors), Eichler EE, (162 authors), Zwieq AS. (2007). Evolutionary and biomedical insights from the rhesus macaque genome. Science Apr;316(5822):222-234.
Characterization of a recurrent 15q24 microdeletion syndrome
Sharp AJ, Selzer RR, Veltman JA, Gimelli S, Gimelli G, Striano P, Coppola A, Regan R, Price SM, Knoers NV, Eis PS, Brunner HG, Hennekam RC, Knight SJ, de Vries BB, Zuffardi O, Eichler EE. (2007). Characterization of a recurrent 15q24 microdeletion syndrome. Hum Mol Genet Mar;16(5):567-572 (14 Mar 2007).
