Lai C - Search Results

1

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP. Maestrini E, et al. Among authors: lai c. Am J Med Genet. 1999 Oct 15;88(5):492-6. doi: 10.1002/(sici)1096-8628(19991015)88:5<492::aid-ajmg11>3.0.co;2-x. Am J Med Genet. 1999. PMID: 10490705

2

FOXP2 is not a major susceptibility gene for autism or specific language impairment.

Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium. Newbury DF, et al. Among authors: lai cs. Am J Hum Genet. 2002 May;70(5):1318-27. doi: 10.1086/339931. Epub 2002 Mar 13. Am J Hum Genet. 2002. PMID: 11894222 Free PMC article.

3

Deciphering the genetic basis of speech and language disorders.

Fisher SE, Lai CS, Monaco AP. Fisher SE, et al. Annu Rev Neurosci. 2003;26:57-80. doi: 10.1146/annurev.neuro.26.041002.131144. Epub 2003 Jan 8. Annu Rev Neurosci. 2003. PMID: 12524432 Review.

4

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Levy ER, Hodgson S, Fox M, Jeremiah S, Povey S, Jamison DC, Green ED, Vargha-Khadem F, Monaco AP. Lai CS, et al. Am J Hum Genet. 2000 Aug;67(2):357-68. doi: 10.1086/303011. Epub 2000 Jul 5. Am J Hum Genet. 2000. PMID: 10880297 Free PMC article.

5

A forkhead-domain gene is mutated in a severe speech and language disorder.

Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. Lai CS, et al. Nature. 2001 Oct 4;413(6855):519-23. doi: 10.1038/35097076. Nature. 2001. PMID: 11586359

6

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

MacDermot KD, Bonora E, Sykes N, Coupe AM, Lai CS, Vernes SC, Vargha-Khadem F, McKenzie F, Smith RL, Monaco AP, Fisher SE. MacDermot KD, et al. Among authors: lai cs. Am J Hum Genet. 2005 Jun;76(6):1074-80. doi: 10.1086/430841. Epub 2005 Apr 22. Am J Hum Genet. 2005. PMID: 15877281 Free PMC article.

7

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Paracchini S, Thomas A, Castro S, Lai C, Paramasivam M, Wang Y, Keating BJ, Taylor JM, Hacking DF, Scerri T, Francks C, Richardson AJ, Wade-Martins R, Stein JF, Knight JC, Copp AJ, Loturco J, Monaco AP. Paracchini S, et al. Among authors: lai c. Hum Mol Genet. 2006 May 15;15(10):1659-66. doi: 10.1093/hmg/ddl089. Epub 2006 Apr 6. Hum Mol Genet. 2006. PMID: 16600991

8

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

Lai CS, Gerrelli D, Monaco AP, Fisher SE, Copp AJ. Lai CS, et al. Brain. 2003 Nov;126(Pt 11):2455-62. doi: 10.1093/brain/awg247. Epub 2003 Jul 22. Brain. 2003. PMID: 12876151

9

Molecular evolution of FOXP2, a gene involved in speech and language.

Enard W, Przeworski M, Fisher SE, Lai CS, Wiebe V, Kitano T, Monaco AP, Pääbo S. Enard W, et al. Nature. 2002 Aug 22;418(6900):869-72. doi: 10.1038/nature01025. Epub 2002 Aug 14. Nature. 2002. PMID: 12192408

10

Bisoprolol in Patients With Chronic Obstructive Pulmonary Disease.

Hsu CK, Lai CC. Hsu CK, et al. Among authors: lai cc. JAMA. 2024 Nov 18. doi: 10.1001/jama.2024.20747. Online ahead of print. JAMA. 2024. PMID: 39556337 No abstract available.

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