Fisher SE - Search Results

1

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, Baird G, Paracchini S, Fisher SE, Newbury DF; SLI Consortium. Simpson NH, et al. Among authors: fisher se. Dev Med Child Neurol. 2014 Apr;56(4):346-53. doi: 10.1111/dmcn.12294. Epub 2013 Oct 9. Dev Med Child Neurol. 2014. PMID: 24117048 Free PMC article.

2

High-resolution comparative mapping of the proximal region of the mouse X chromosome.

Blair HJ, Ho M, Monaco AP, Fisher S, Craig IW, Boyd Y. Blair HJ, et al. Genomics. 1995 Jul 20;28(2):305-10. doi: 10.1006/geno.1995.1146. Genomics. 1995. PMID: 8530041

3

Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.

Fisher SE, Hatchwell E, Chand A, Ockenden N, Monaco AP, Craig IW. Fisher SE, et al. Genomics. 1995 Sep 20;29(2):496-502. doi: 10.1006/geno.1995.9976. Genomics. 1995. PMID: 8666400

4

Localisation of a gene implicated in a severe speech and language disorder.

Fisher SE, Vargha-Khadem F, Watkins KE, Monaco AP, Pembrey ME. Fisher SE, et al. Nat Genet. 1998 Feb;18(2):168-70. doi: 10.1038/ng0298-168. Nat Genet. 1998. PMID: 9462748

5

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.

Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, Richardson AJ, Weeks DE, Stein JF, Monaco AP. Fisher SE, et al. Am J Hum Genet. 1999 Jan;64(1):146-56. doi: 10.1086/302190. Am J Hum Genet. 1999. PMID: 9915953 Free PMC article.

6

A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).

Fisher SE, Stein JF, Monaco AP. Fisher SE, et al. Eur Child Adolesc Psychiatry. 1999;8 Suppl 3:47-51. doi: 10.1007/pl00010694. Eur Child Adolesc Psychiatry. 1999. PMID: 10638370 Review.

7

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. Among authors: fisher se. 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.

8

A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.

Francks C, Fisher SE, Marlow AJ, Richardson AJ, Stein JF, Monaco AP. Francks C, et al. Among authors: fisher se. Prostaglandins Leukot Essent Fatty Acids. 2000 Jul-Aug;63(1-2):27-31. doi: 10.1054/plef.2000.0187. Prostaglandins Leukot Essent Fatty Acids. 2000. PMID: 10970709 Review.

9

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.

Marlow AJ, Fisher SE, Richardson AJ, Francks C, Talcott JB, Monaco AP, Stein JF, Cardon LR. Marlow AJ, et al. Among authors: fisher se. Behav Genet. 2001 Mar;31(2):219-30. doi: 10.1023/a:1010209629021. Behav Genet. 2001. PMID: 11545538

10

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. Among authors: fisher se. Nature. 2001 Oct 4;413(6855):519-23. doi: 10.1038/35097076. Nature. 2001. PMID: 11586359

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