Turic DE - Search Results

1

A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability.

Plomin R, Turic DM, Hill L, Turic DE, Stephens M, Williams J, Owen MJ, O'Donovan MC. Plomin R, et al. Among authors: turic de. Mol Psychiatry. 2004 Jun;9(6):582-6. doi: 10.1038/sj.mp.4001441. Mol Psychiatry. 2004. PMID: 14981524

2

Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease.

Hamilton G, Samedi F, Knight J, Archer N, Foy C, Walter S, Turic D, Jehu L, Moore P, Hollingworth P, O'Donovan MC, Williams J, Owen MJ, Lovestone S, Powell JF. Hamilton G, et al. Neurosci Lett. 2006 Jun 19;401(1-2):77-80. doi: 10.1016/j.neulet.2006.03.021. Epub 2006 Mar 29. Neurosci Lett. 2006. PMID: 16574322

3

DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children.

Fisher PJ, Turic D, Williams NM, McGuffin P, Asherson P, Ball D, Craig I, Eley T, Hill L, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Plomin R, Owen MJ. Fisher PJ, et al. Hum Mol Genet. 1999 May;8(5):915-22. doi: 10.1093/hmg/8.5.915. Hum Mol Genet. 1999. PMID: 10196382

4

DNA pooling and dense marker maps: a systematic search for genes for cognitive ability.

Hill L, Craig IW, Asherson P, Ball D, Eley T, Ninomiya T, Fisher PJ, Turic D, McGuffin P, Owen MJ, Chorney K, Chorney MJ, Benbow CP, Lubinski D, Thompson LA, Plomin R. Hill L, et al. Neuroreport. 1999 Mar 17;10(4):843-8. doi: 10.1097/00001756-199903170-00032. Neuroreport. 1999. PMID: 10208558

5

Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder.

Speight G, Turic D, Austin J, Hoogendoorn B, Cardno AG, Jones L, Murphy KC, Sanders R, McCarthy G, Jones I, McCandless F, McGuffin P, Craddock N, Owen MJ, Buckland P, O'Donovan MC. Speight G, et al. Mol Psychiatry. 2000 May;5(3):327-31. doi: 10.1038/sj.mp.4000717. Mol Psychiatry. 2000. PMID: 10889538

6

No association between apolipoprotein E polymorphisms and general cognitive ability in children.

Turic D, Fisher PJ, Plomin R, Owen MJ. Turic D, et al. Neurosci Lett. 2001 Feb 16;299(1-2):97-100. doi: 10.1016/s0304-3940(00)01789-4. Neurosci Lett. 2001. PMID: 11166947

7

A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups.

Plomin R, Hill L, Craig IW, McGuffin P, Purcell S, Sham P, Lubinski D, Thompson LA, Fisher PJ, Turic D, Owen MJ. Plomin R, et al. Behav Genet. 2001 Nov;31(6):497-509. doi: 10.1023/a:1013385125887. Behav Genet. 2001. PMID: 11838529

8

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Turic D, et al. Mol Psychiatry. 2003 Feb;8(2):176-85. doi: 10.1038/sj.mp.4001216. Mol Psychiatry. 2003. PMID: 12610650

9

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

Turic D, Langley K, Mills S, Stephens M, Lawson D, Govan C, Williams N, Van Den Bree M, Craddock N, Kent L, Owen M, O'Donovan M, Thapar A. Turic D, et al. Mol Psychiatry. 2004 Feb;9(2):169-73. doi: 10.1038/sj.mp.4001387. Mol Psychiatry. 2004. PMID: 14966475

10

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q.

Morris DW, Robinson L, Turic D, Duke M, Webb V, Milham C, Hopkin E, Pound K, Fernando S, Easton M, Hamshere M, Williams N, McGuffin P, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Morris DW, et al. Hum Mol Genet. 2000 Mar 22;9(5):843-8. doi: 10.1093/hmg/9.5.843. Hum Mol Genet. 2000. PMID: 10749993

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