Fisher SE - Search Results

1

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.

Doust C, Fontanillas P, Eising E, Gordon SD, Wang Z, Alagöz G, Molz B; 23andMe Research Team; Quantitative Trait Working Group of the GenLang Consortium; Pourcain BS, Francks C, Marioni RE, Zhao J, Paracchini S, Talcott JB, Monaco AP, Stein JF, Gruen JR, Olson RK, Willcutt EG, DeFries JC, Pennington BF, Smith SD, Wright MJ, Martin NG, Auton A, Bates TC, Fisher SE, Luciano M. Doust C, et al. Among authors: fisher se. Nat Genet. 2023 Mar;55(3):520. doi: 10.1038/s41588-023-01336-8. Nat Genet. 2023. PMID: 36823321 Free PMC article. No abstract available.

2

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

3

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.

4

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.

5

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.

6

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

7

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

8

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, Monaco AP. Fisher SE, et al. Nat Genet. 2002 Jan;30(1):86-91. doi: 10.1038/ng792. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743577

9

A genomewide linkage screen for relative hand skill in sibling pairs.

Francks C, Fisher SE, MacPhie IL, Richardson AJ, Marlow AJ, Stein JF, Monaco AP. Francks C, et al. Among authors: fisher se. Am J Hum Genet. 2002 Mar;70(3):800-5. doi: 10.1086/339249. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774074 Free PMC article.

10

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: fisher se. 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.

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