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104 results

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Copy-number variants in patients with a strong family history of pancreatic cancer.
Lucito R, Suresh S, Walter K, Pandey A, Lakshmi B, Krasnitz A, Sebat J, Wigler M, Klein AP, Brune K, Palmisano E, Maitra A, Goggins M, Hruban RH. Lucito R, et al. Among authors: sebat j. Cancer Biol Ther. 2007 Oct;6(10):1592-9. doi: 10.4161/cbt.6.10.4725. Epub 2007 Jul 12. Cancer Biol Ther. 2007. PMID: 17912030
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation.
Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M, Rodgers L, Brady A, Sebat J, Troge J, West JA, Rostan S, Nguyen KC, Powers S, Ye KQ, Olshen A, Venkatraman E, Norton L, Wigler M. Lucito R, et al. Among authors: sebat j. Genome Res. 2003 Oct;13(10):2291-305. doi: 10.1101/gr.1349003. Epub 2003 Sep 15. Genome Res. 2003. PMID: 12975311 Free PMC article.
Distribution of short paired duplications in mammalian genomes.
Thomas EE, Srebro N, Sebat J, Navin N, Healy J, Mishra B, Wigler M. Thomas EE, et al. Among authors: sebat j. Proc Natl Acad Sci U S A. 2004 Jul 13;101(28):10349-54. doi: 10.1073/pnas.0403727101. Epub 2004 Jul 6. Proc Natl Acad Sci U S A. 2004. PMID: 15240876 Free PMC article.
Large-scale copy number polymorphism in the human genome.
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P, Månér S, Massa H, Walker M, Chi M, Navin N, Lucito R, Healy J, Hicks J, Ye K, Reiner A, Gilliam TC, Trask B, Patterson N, Zetterberg A, Wigler M. Sebat J, et al. Science. 2004 Jul 23;305(5683):525-8. doi: 10.1126/science.1098918. Science. 2004. PMID: 15273396
PROBER: oligonucleotide FISH probe design software.
Navin N, Grubor V, Hicks J, Leibu E, Thomas E, Troge J, Riggs M, Lundin P, Månér S, Sebat J, Zetterberg A, Wigler M. Navin N, et al. Among authors: sebat j. Bioinformatics. 2006 Oct 1;22(19):2437-8. doi: 10.1093/bioinformatics/btl273. Epub 2006 Jun 1. Bioinformatics. 2006. PMID: 16740623 Free article.
Strong association of de novo copy number mutations with autism.
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M. Sebat J, et al. Science. 2007 Apr 20;316(5823):445-9. doi: 10.1126/science.1138659. Epub 2007 Mar 15. Science. 2007. PMID: 17363630 Free PMC article.
A unified genetic theory for sporadic and inherited autism.
Zhao X, Leotta A, Kustanovich V, Lajonchere C, Geschwind DH, Law K, Law P, Qiu S, Lord C, Sebat J, Ye K, Wigler M. Zhao X, et al. Among authors: sebat j. Proc Natl Acad Sci U S A. 2007 Jul 31;104(31):12831-6. doi: 10.1073/pnas.0705803104. Epub 2007 Jul 25. Proc Natl Acad Sci U S A. 2007. PMID: 17652511 Free PMC article.
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J. Walsh T, et al. Among authors: sebat j. Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27. Science. 2008. PMID: 18369103
104 results