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209 results

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Page 1
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: wigler m. 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.
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. Among authors: wigler m. Science. 2007 Apr 20;316(5823):445-9. doi: 10.1126/science.1138659. Epub 2007 Mar 15. Science. 2007. PMID: 17363630 Free PMC article.
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: wigler m. 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 Free 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: wigler m. 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.
Rates of contributory de novo mutation in high and low-risk autism families.
Yoon S, Munoz A, Yamrom B, Lee YH, Andrews P, Marks S, Wang Z, Reeves C, Winterkorn L, Krieger AM, Buja A, Pradhan K, Ronemus M, Baldwin KK, Levy D, Wigler M, Iossifov I. Yoon S, et al. Among authors: wigler m. Commun Biol. 2021 Sep 1;4(1):1026. doi: 10.1038/s42003-021-02533-z. Commun Biol. 2021. PMID: 34471188 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. Among authors: wigler m. Science. 2004 Jul 23;305(5683):525-8. doi: 10.1126/science.1098918. Science. 2004. PMID: 15273396
Rare de novo germline copy-number variation in testicular cancer.
Stadler ZK, Esposito D, Shah S, Vijai J, Yamrom B, Levy D, Lee YH, Kendall J, Leotta A, Ronemus M, Hansen N, Sarrel K, Rau-Murthy R, Schrader K, Kauff N, Klein RJ, Lipkin SM, Murali R, Robson M, Sheinfeld J, Feldman D, Bosl G, Norton L, Wigler M, Offit K. Stadler ZK, et al. Among authors: wigler m. Am J Hum Genet. 2012 Aug 10;91(2):379-83. doi: 10.1016/j.ajhg.2012.06.019. Epub 2012 Aug 2. Am J Hum Genet. 2012. PMID: 22863192 Free PMC article.
209 results