Francks C - Search Results

1

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Chen XS, Reader RH, Hoischen A, Veltman JA, Simpson NH, Francks C, Newbury DF, Fisher SE. Chen XS, et al. Among authors: francks c. Sci Rep. 2017 Apr 25;7:46105. doi: 10.1038/srep46105. Sci Rep. 2017. PMID: 28440294 Free PMC article.

2

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. 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.

3

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: francks c. Behav Genet. 2001 Mar;31(2):219-30. doi: 10.1023/a:1010209629021. Behav Genet. 2001. PMID: 11545538

4

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: francks c. Nat Genet. 2002 Jan;30(1):86-91. doi: 10.1038/ng792. Epub 2001 Dec 17. Nat Genet. 2002. PMID: 11743577

5

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. 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.

6

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. Psychiatr Genet. 2002 Mar;12(1):35-41. doi: 10.1097/00041444-200203000-00005. Psychiatr Genet. 2002. PMID: 11901358

7

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.

Fisher SE, Francks C, McCracken JT, McGough JJ, Marlow AJ, MacPhie IL, Newbury DF, Crawford LR, Palmer CG, Woodward JA, Del'Homme M, Cantwell DP, Nelson SF, Monaco AP, Smalley SL. Fisher SE, et al. Among authors: francks c. Am J Hum Genet. 2002 May;70(5):1183-96. doi: 10.1086/340112. Epub 2002 Mar 28. Am J Hum Genet. 2002. PMID: 11923911 Free PMC article.

8

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.

Smalley SL, Kustanovich V, Minassian SL, Stone JL, Ogdie MN, McGough JJ, McCracken JT, MacPhie IL, Francks C, Fisher SE, Cantor RM, Monaco AP, Nelson SF. Smalley SL, et al. Among authors: francks c. Am J Hum Genet. 2002 Oct;71(4):959-63. doi: 10.1086/342732. Epub 2002 Aug 14. Am J Hum Genet. 2002. PMID: 12187510 Free PMC article.

9

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

Marlow AJ, Fisher SE, Francks C, MacPhie IL, Cherny SS, Richardson AJ, Talcott JB, Stein JF, Monaco AP, Cardon LR. Marlow AJ, et al. Among authors: francks c. Am J Hum Genet. 2003 Mar;72(3):561-70. doi: 10.1086/368201. Epub 2003 Feb 13. Am J Hum Genet. 2003. PMID: 12587094 Free PMC article.

10

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.

Ogdie MN, Macphie IL, Minassian SL, Yang M, Fisher SE, Francks C, Cantor RM, McCracken JT, McGough JJ, Nelson SF, Monaco AP, Smalley SL. Ogdie MN, et al. Among authors: francks c. Am J Hum Genet. 2003 May;72(5):1268-79. doi: 10.1086/375139. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687500 Free PMC article.

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