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Page 1
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO, Raubeson MJ, Song Y, Yasuno K, Ho WS, Bilguvar K, Glessner J, Chu SH, Leckman JF, King RA, Gilbert DL, Heiman GA, Tischfield JA, Hoekstra PJ, Devlin B, Hakonarson H, Mane SM, Günel M, State MW. Fernandez TV, et al. Among authors: gunel m. Biol Psychiatry. 2012 Mar 1;71(5):392-402. doi: 10.1016/j.biopsych.2011.09.034. Epub 2011 Dec 14. Biol Psychiatry. 2012. PMID: 22169095 Free PMC article.
Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.
State MW, Greally JM, Cuker A, Bowers PN, Henegariu O, Morgan TM, Gunel M, DiLuna M, King RA, Nelson C, Donovan A, Anderson GM, Leckman JF, Hawkins T, Pauls DL, Lifton RP, Ward DC. State MW, et al. Among authors: gunel m. Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4684-9. doi: 10.1073/pnas.0730775100. Epub 2003 Apr 7. Proc Natl Acad Sci U S A. 2003. PMID: 12682296 Free PMC article.
Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13.
Nahed BV, Seker A, Guclu B, Ozturk AK, Finberg K, Hawkins AA, DiLuna ML, State M, Lifton RP, Gunel M. Nahed BV, et al. Among authors: gunel m. Am J Hum Genet. 2005 Jan;76(1):172-9. doi: 10.1086/426953. Epub 2004 Nov 11. Am J Hum Genet. 2005. PMID: 15540160 Free PMC article.
Sequence variants in SLITRK1 are associated with Tourette's syndrome.
Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS 4th, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW. Abelson JF, et al. Among authors: gunel m. Science. 2005 Oct 14;310(5746):317-20. doi: 10.1126/science.1116502. Science. 2005. PMID: 16224024
Genetics of intracranial aneurysms.
Nahed BV, Bydon M, Ozturk AK, Bilguvar K, Bayrakli F, Gunel M. Nahed BV, et al. Among authors: gunel m. Neurosurgery. 2007 Feb;60(2):213-25; discussion 225-6. doi: 10.1227/01.NEU.0000249270.18698.BB. Neurosurgery. 2007. PMID: 17290171 Review.
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW. Bakkaloglu B, et al. Among authors: gunel m. Am J Hum Genet. 2008 Jan;82(1):165-73. doi: 10.1016/j.ajhg.2007.09.017. Am J Hum Genet. 2008. PMID: 18179895 Free PMC article.
255 results