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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1948 1
1953 2
1988 1
1989 1
1990 1
1991 5
1992 1
1994 1
2002 2
2004 1
2005 1
2006 2
2010 2
2011 2
2013 1
2024 0

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24 results

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Page 1
CACNA1C (rs1006737) is associated with schizophrenia.
Nyegaard M, Demontis D, Foldager L, Hedemand A, Flint TJ, Sørensen KM, Andersen PS, Nordentoft M, Werge T, Pedersen CB, Hougaard DM, Mortensen PB, Mors O, Børglum AD. Nyegaard M, et al. Among authors: flint tj. Mol Psychiatry. 2010 Feb;15(2):119-21. doi: 10.1038/mp.2009.69. Mol Psychiatry. 2010. PMID: 20098439 No abstract available.
Linkage analysis of spinal muscular atrophy.
Daniels RJ, Thomas NH, MacKinnon RN, Lehner T, Ott J, Flint TJ, Dubowitz V, Ignatius J, Donner M, Zerres K, et al. Daniels RJ, et al. Among authors: flint tj. Genomics. 1992 Feb;12(2):335-9. doi: 10.1016/0888-7543(92)90382-3. Genomics. 1992. PMID: 1346777
Genotype prediction in the fragile X syndrome.
Hirst MC, Nakahori Y, Knight SJ, Schwartz C, Thibodeau SN, Roche A, Flint TJ, Connor JM, Fryns JP, Davies KE. Hirst MC, et al. Among authors: flint tj. J Med Genet. 1991 Dec;28(12):824-9. doi: 10.1136/jmg.28.12.824. J Med Genet. 1991. PMID: 1757957 Free PMC article.
Molecular heterogeneity of the fragile X syndrome.
Nakahori Y, Knight SJ, Holland J, Schwartz C, Roche A, Tarleton J, Wong S, Flint TJ, Froster-Iskenius U, Bentley D, et al. Nakahori Y, et al. Among authors: flint tj. Nucleic Acids Res. 1991 Aug 25;19(16):4355-9. doi: 10.1093/nar/19.16.4355. Nucleic Acids Res. 1991. PMID: 1886762 Free PMC article.
An association study of suicide and candidate genes in the serotonergic system.
Buttenschøn HN, Flint TJ, Foldager L, Qin P, Christoffersen S, Hansen NF, Kristensen IB, Mortensen PB, Børglum AD, Mors O. Buttenschøn HN, et al. Among authors: flint tj. J Affect Disord. 2013 Jun;148(2-3):291-8. doi: 10.1016/j.jad.2012.12.011. Epub 2013 Jan 11. J Affect Disord. 2013. PMID: 23313272
Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes.
Pers TH, Hansen NT, Lage K, Koefoed P, Dworzynski P, Miller ML, Flint TJ, Mellerup E, Dam H, Andreassen OA, Djurovic S, Melle I, Børglum AD, Werge T, Purcell S, Ferreira MA, Kouskoumvekaki I, Workman CT, Hansen T, Mors O, Brunak S. Pers TH, et al. Among authors: flint tj. Genet Epidemiol. 2011 Jul;35(5):318-32. doi: 10.1002/gepi.20580. Epub 2011 Apr 11. Genet Epidemiol. 2011. PMID: 21484861
Support for a bipolar affective disorder susceptibility locus on chromosome 12q24.3.
Buttenschøn HN, Foldager L, Flint TJ, Olsen IM, Deleuran T, Nyegaard M, Hansen MM, Kallunki P, Christensen KV, Blackwood DH, Muir WJ, Straarup SE, Als TD, Nordentoft M, Børglum AD, Mors O. Buttenschøn HN, et al. Among authors: flint tj. Psychiatr Genet. 2010 Jun;20(3):93-101. doi: 10.1097/YPG.0b013e32833a2066. Psychiatr Genet. 2010. PMID: 20410851
Association of GRIN1 and GRIN2A-D with schizophrenia and genetic interaction with maternal herpes simplex virus-2 infection affecting disease risk.
Demontis D, Nyegaard M, Buttenschøn HN, Hedemand A, Pedersen CB, Grove J, Flint TJ, Nordentoft M, Werge T, Hougaard DM, Sørensen KM, Yolken RH, Mors O, Børglum AD, Mortensen PB. Demontis D, et al. Among authors: flint tj. Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):913-22. doi: 10.1002/ajmg.b.31234. Epub 2011 Sep 14. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21919190
24 results