Monaco AP - Search Results

1

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.

Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, St Pourcain B, Brandler W, Honbolygó F, Tóth D, Csépe V, Huguet G, Morris AP, Hulslander J, Willcutt EG, DeFries JC, Olson RK, Smith SD, Pennington BF, Vaessen A, Maurer U, Lyytinen H, Peyrard-Janvid M, Leppänen PHT, Brandeis D, Bonte M, Stein JF, Talcott JB, Fauchereau F, Wilcke A, Francks C, Bourgeron T, Monaco AP, Ramus F, Landerl K, Kere J, Scerri TS, Paracchini S, Fisher SE, Schumacher J, Nöthen MM, Müller-Myhsok B, Schulte-Körne G. Gialluisi A, et al. Among authors: monaco ap. Transl Psychiatry. 2019 Feb 11;9(1):77. doi: 10.1038/s41398-019-0402-0. Transl Psychiatry. 2019. PMID: 30741946 Free PMC article.

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. Among authors: monaco ap. 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. Among authors: monaco ap. 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. Among authors: monaco ap. 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: monaco ap. 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: monaco ap. 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: monaco ap. 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. Among authors: monaco ap. 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: monaco ap. 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

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

Francks C, Fisher SE, Olson RK, Pennington BF, Smith SD, DeFries JC, Monaco AP. Francks C, et al. Among authors: monaco ap. Psychiatr Genet. 2002 Mar;12(1):35-41. doi: 10.1097/00041444-200203000-00005. Psychiatr Genet. 2002. PMID: 11901358

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