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Items: 1 to 50 of 66

1.

Rediscovering the value of families for psychiatric genetics research.

Glahn DC, Nimgaonkar VL, Raventós H, Contreras J, McIntosh AM, Thomson PA, Jablensky A, McCarthy NS, Charlesworth JC, Blackburn NB, Peralta JM, Knowles EEM, Mathias SR, Ament SA, McMahon FJ, Gur RC, Bucan M, Curran JE, Almasy L, Gur RE, Blangero J.

Mol Psychiatry. 2018 Jun 28. doi: 10.1038/s41380-018-0073-x. [Epub ahead of print]

PMID:
29955165
2.

DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders.

Ryan NM, Lihm J, Kramer M, McCarthy S, Morris SW, Arnau-Soler A, Davies G, Duff B, Ghiban E, Hayward C, Deary IJ, Blackwood DHR, Lawrie SM, McIntosh AM, Evans KL, Porteous DJ, McCombie WR, Thomson PA.

Mol Psychiatry. 2018 Jun 7. doi: 10.1038/s41380-018-0087-4. [Epub ahead of print]

PMID:
29880880
3.

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, Blackwood DRH, Bryois J, Buttenschøn HN, Bybjerg-Grauholm J, Cai N, Castelao E, Christensen JH, Clarke TK, Coleman JIR, Colodro-Conde L, Couvy-Duchesne B, Craddock N, Crawford GE, Crowley CA, Dashti HS, Davies G, Deary IJ, Degenhardt F, Derks EM, Direk N, Dolan CV, Dunn EC, Eley TC, Eriksson N, Escott-Price V, Kiadeh FHF, Finucane HK, Forstner AJ, Frank J, Gaspar HA, Gill M, Giusti-Rodríguez P, Goes FS, Gordon SD, Grove J, Hall LS, Hannon E, Hansen CS, Hansen TF, Herms S, Hickie IB, Hoffmann P, Homuth G, Horn C, Hottenga JJ, Hougaard DM, Hu M, Hyde CL, Ising M, Jansen R, Jin F, Jorgenson E, Knowles JA, Kohane IS, Kraft J, Kretzschmar WW, Krogh J, Kutalik Z, Lane JM, Li Y, Li Y, Lind PA, Liu X, Lu L, MacIntyre DJ, MacKinnon DF, Maier RM, Maier W, Marchini J, Mbarek H, McGrath P, McGuffin P, Medland SE, Mehta D, Middeldorp CM, Mihailov E, Milaneschi Y, Milani L, Mill J, Mondimore FM, Montgomery GW, Mostafavi S, Mullins N, Nauck M, Ng B, Nivard MG, Nyholt DR, O'Reilly PF, Oskarsson H, Owen MJ, Painter JN, Pedersen CB, Pedersen MG, Peterson RE, Pettersson E, Peyrot WJ, Pistis G, Posthuma D, Purcell SM, Quiroz JA, Qvist P, Rice JP, Riley BP, Rivera M, Saeed Mirza S, Saxena R, Schoevers R, Schulte EC, Shen L, Shi J, Shyn SI, Sigurdsson E, Sinnamon GBC, Smit JH, Smith DJ, Stefansson H, Steinberg S, Stockmeier CA, Streit F, Strohmaier J, Tansey KE, Teismann H, Teumer A, Thompson W, Thomson PA, Thorgeirsson TE, Tian C, Traylor M, Treutlein J, Trubetskoy V, Uitterlinden AG, Umbricht D, Van der Auwera S, van Hemert AM, Viktorin A, Visscher PM, Wang Y, Webb BT, Weinsheimer SM, Wellmann J, Willemsen G, Witt SH, Wu Y, Xi HS, Yang J, Zhang F; eQTLGen; 23andMe, Arolt V, Baune BT, Berger K, Boomsma DI, Cichon S, Dannlowski U, de Geus ECJ, DePaulo JR, Domenici E, Domschke K, Esko T, Grabe HJ, Hamilton SP, Hayward C, Heath AC, Hinds DA, Kendler KS, Kloiber S, Lewis G, Li QS, Lucae S, Madden PFA, Magnusson PK, Martin NG, McIntosh AM, Metspalu A, Mors O, Mortensen PB, Müller-Myhsok B, Nordentoft M, Nöthen MM, O'Donovan MC, Paciga SA, Pedersen NL, Penninx BWJH, Perlis RH, Porteous DJ, Potash JB, Preisig M, Rietschel M, Schaefer C, Schulze TG, Smoller JW, Stefansson K, Tiemeier H, Uher R, Völzke H, Weissman MM, Werge T, Winslow AR, Lewis CM, Levinson DF, Breen G, Børglum AD, Sullivan PF; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.

Nat Genet. 2018 May;50(5):668-681. doi: 10.1038/s41588-018-0090-3. Epub 2018 Apr 26.

PMID:
29700475
4.

Altered DNA methylation associated with a translocation linked to major mental illness.

McCartney DL, Walker RM, Morris SW, Anderson SM, Duff BJ, Marioni RE, Millar JK, McCarthy SE, Ryan NM, Lawrie SM, Watson AR, Blackwood DHR, Thomson PA, McIntosh AM, McCombie WR, Porteous DJ, Evans KL.

NPJ Schizophr. 2018 Mar 19;4(1):5. doi: 10.1038/s41537-018-0047-7.

5.

Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank.

Hall LS, Adams MJ, Arnau-Soler A, Clarke TK, Howard DM, Zeng Y, Davies G, Hagenaars SP, Maria Fernandez-Pujals A, Gibson J, Wigmore EM, Boutin TS, Hayward C, Scotland G; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Porteous DJ, Deary IJ, Thomson PA, Haley CS, McIntosh AM.

Transl Psychiatry. 2018 Jan 10;8(1):9. doi: 10.1038/s41398-017-0034-1.

6.

Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank.

Howard DM, Hall LS, Hafferty JD, Zeng Y, Adams MJ, Clarke TK, Porteous DJ, Nagy R, Hayward C, Smith BH, Murray AD, Ryan NM, Evans KL, Haley CS, Deary IJ, Thomson PA, McIntosh AM.

Transl Psychiatry. 2017 Nov 30;7(11):1263. doi: 10.1038/s41398-017-0010-9.

7.

Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank.

Howard DM, Adams MJ, Clarke TK, Wigmore EM, Zeng Y, Hagenaars SP, Lyall DM, Thomson PA, Evans KL, Porteous DJ, Nagy R, Hayward C, Haley CS, Smith BH, Murray AD, Batty GD, Deary IJ, McIntosh AM.

Wellcome Open Res. 2017 Aug 10;2:61. doi: 10.12688/wellcomeopenres.12171.1. eCollection 2017.

8.

Do regional brain volumes and major depressive disorder share genetic architecture? A study of Generation Scotland (n=19 762), UK Biobank (n=24 048) and the English Longitudinal Study of Ageing (n=5766).

Wigmore EM, Clarke TK, Howard DM, Adams MJ, Hall LS, Zeng Y, Gibson J, Davies G, Fernandez-Pujals AM, Thomson PA, Hayward C, Smith BH, Hocking LJ, Padmanabhan S, Deary IJ, Porteous DJ, Nicodemus KK, McIntosh AM.

Transl Psychiatry. 2017 Aug 15;7(8):e1205. doi: 10.1038/tp.2017.148.

9.

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Teng S, Thomson PA, McCarthy S, Kramer M, Muller S, Lihm J, Morris S, Soares DC, Hennah W, Harris S, Camargo LM, Malkov V, McIntosh AM, Millar JK, Blackwood DH, Evans KL, Deary IJ, Porteous DJ, McCombie WR.

Mol Psychiatry. 2018 May;23(5):1270-1277. doi: 10.1038/mp.2017.115. Epub 2017 Jun 20.

10.

Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.

Zeng Y, Navarro P, Shirali M, Howard DM, Adams MJ, Hall LS, Clarke TK, Thomson PA, Smith BH, Murray A, Padmanabhan S, Hayward C, Boutin T, MacIntyre DJ, Lewis CM, Wray NR, Mehta D, Penninx BWJH, Milaneschi Y, Baune BT, Air T, Hottenga JJ, Mbarek H, Castelao E, Pistis G, Schulze TG, Streit F, Forstner AJ, Byrne EM, Martin NG, Breen G, Müller-Myhsok B, Lucae S, Kloiber S, Domenici E; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Deary IJ, Porteous DJ, Haley CS, McIntosh AM.

Biol Psychiatry. 2017 Sep 1;82(5):312-321. doi: 10.1016/j.biopsych.2016.12.012. Epub 2016 Dec 16.

11.

Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression.

Zeng Y, Navarro P, Xia C, Amador C, Fernandez-Pujals AM, Thomson PA, Campbell A, Nagy R, Clarke TK, Hafferty JD, Smith BH, Hocking LJ, Padmanabhan S, Hayward C, MacIntyre DJ, Porteous DJ, Haley CS, McIntosh AM.

EBioMedicine. 2016 Dec;14:161-167. doi: 10.1016/j.ebiom.2016.11.003. Epub 2016 Nov 4.

12.

Balanced translocation linked to psychiatric disorder, glutamate, and cortical structure/function.

Thomson PA, Duff B, Blackwood DH, Romaniuk L, Watson A, Whalley HC, Li X, Dauvermann MR, Moorhead TW, Bois C, Ryan NM, Redpath H, Hall L, Morris SW, van Beek EJ, Roberts N, Porteous DJ, St Clair D, Whitcher B, Dunlop J, Brandon NJ, Hughes ZA, Hall J, McIntosh A, Lawrie SM.

NPJ Schizophr. 2016 Aug 10;2:16024. doi: 10.1038/npjschz.2016.24. eCollection 2016.

13.

Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort.

Clarke TK, Obsteter J, Hall LS, Hayward C, Thomson PA, Smith BH, Padmanabhan S, Hocking LJ, Deary IJ, Porteous DJ, McIntosh AM.

Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):227-234. doi: 10.1002/ajmg.b.32478. Epub 2016 Aug 2.

14.

A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder.

Zeng Y, Navarro P, Fernandez-Pujals AM, Hall LS, Clarke TK, Thomson PA, Smith BH, Hocking LJ, Padmanabhan S, Hayward C, MacIntyre DJ, Wray NR; Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Deary IJ, Porteous DJ, Haley CS, McIntosh AM.

Biol Psychiatry. 2017 Feb 15;81(4):336-346. doi: 10.1016/j.biopsych.2016.04.017. Epub 2016 May 2.

15.

Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort.

Clarke TK, Smith AH, Gelernter J, Kranzler HR, Farrer LA, Hall LS, Fernandez-Pujals AM, MacIntyre DJ, Smith BH, Hocking LJ, Padmanabhan S, Hayward C, Thomson PA, Porteous DJ, Deary IJ, McIntosh AM.

Addict Biol. 2016 Mar;21(2):469-80. doi: 10.1111/adb.12245. Epub 2015 Apr 10.

16.

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.

Clarke TK, Lupton MK, Fernandez-Pujals AM, Starr J, Davies G, Cox S, Pattie A, Liewald DC, Hall LS, MacIntyre DJ, Smith BH, Hocking LJ, Padmanabhan S, Thomson PA, Hayward C, Hansell NK, Montgomery GW, Medland SE, Martin NG, Wright MJ, Porteous DJ, Deary IJ, McIntosh AM.

Mol Psychiatry. 2016 Mar;21(3):419-25. doi: 10.1038/mp.2015.12. Epub 2015 Mar 10.

17.

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.

Rannikmäe K, Davies G, Thomson PA, Bevan S, Devan WJ, Falcone GJ, Traylor M, Anderson CD, Battey TW, Radmanesh F, Deka R, Woo JG, Martin LJ, Jimenez-Conde J, Selim M, Brown DL, Silliman SL, Kidwell CS, Montaner J, Langefeld CD, Slowik A, Hansen BM, Lindgren AG, Meschia JF, Fornage M, Bis JC, Debette S, Ikram MA, Longstreth WT, Schmidt R, Zhang CR, Yang Q, Sharma P, Kittner SJ, Mitchell BD, Holliday EG, Levi CR, Attia J, Rothwell PM, Poole DL, Boncoraglio GB, Psaty BM, Malik R, Rost N, Worrall BB, Dichgans M, Van Agtmael T, Woo D, Markus HS, Seshadri S, Rosand J, Sudlow CL; METASTROKE Consortium; CHARGE WMH Group; ISGC ICH GWAS Study Collaboration; WMH in Ischemic Stroke GWAS Study Collaboration; International Stroke Genetics Consortium.

Neurology. 2015 Mar 3;84(9):918-26. doi: 10.1212/WNL.0000000000001309. Epub 2015 Feb 4.

18.

Expression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia.

Rampino A, Walker RM, Torrance HS, Anderson SM, Fazio L, Di Giorgio A, Taurisano P, Gelao B, Romano R, Masellis R, Ursini G, Caforio G, Blasi G, Millar JK, Porteous DJ, Thomson PA, Bertolino A, Evans KL.

PLoS One. 2014 Jun 18;9(6):e99892. doi: 10.1371/journal.pone.0099892. eCollection 2014.

19.

DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan.

Porteous DJ, Thomson PA, Millar JK, Evans KL, Hennah W, Soares DC, McCarthy S, McCombie WR, Clapcote SJ, Korth C, Brandon NJ, Sawa A, Kamiya A, Roder JC, Lawrie SM, McIntosh AM, St Clair D, Blackwood DH.

Mol Psychiatry. 2014 Feb;19(2):141-3. doi: 10.1038/mp.2013.160. No abstract available.

20.

Use of product listing agreements by Canadian provincial drug benefit plans.

Morgan SG, Friesen MK, Thomson PA, Daw JR.

Healthc Policy. 2013 May;8(4):45-55.

21.

Canadian policy makers' views on pharmaceutical reimbursement contracts involving confidential discounts from drug manufacturers.

Morgan SG, Thomson PA, Daw JR, Friesen MK.

Health Policy. 2013 Oct;112(3):248-54. doi: 10.1016/j.healthpol.2013.05.022. Epub 2013 Jun 25.

22.

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.

Thomson PA, Parla JS, McRae AF, Kramer M, Ramakrishnan K, Yao J, Soares DC, McCarthy S, Morris SW, Cardone L, Cass S, Ghiban E, Hennah W, Evans KL, Rebolini D, Millar JK, Harris SE, Starr JM, MacIntyre DJ; Generation Scotland, McIntosh AM, Watson JD, Deary IJ, Visscher PM, Blackwood DH, McCombie WR, Porteous DJ.

Mol Psychiatry. 2014 Jun;19(6):668-75. doi: 10.1038/mp.2013.68. Epub 2013 Jun 4.

23.

DISC1 genetics, biology and psychiatric illness.

Thomson PA, Malavasi EL, Grünewald E, Soares DC, Borkowska M, Millar JK.

Front Biol (Beijing). 2013 Feb 1;8(1):1-31.

24.

Here today, gone tomorrow: the issue attention cycle and national print media coverage of prescription drug financing in Canada.

Daw JR, Morgan SG, Thomson PA, Law MR.

Health Policy. 2013 Apr;110(1):67-75. doi: 10.1016/j.healthpol.2013.01.006. Epub 2013 Feb 16.

PMID:
23419420
25.

Inter-jurisdictional cooperation on pharmaceutical product listing agreements: views from Canadian provinces.

Morgan SG, Thomson PA, Daw JR, Friesen MK.

BMC Health Serv Res. 2013 Jan 31;13:34. doi: 10.1186/1472-6963-13-34.

26.

Genetic copy number variation and general cognitive ability.

MacLeod AK, Davies G, Payton A, Tenesa A, Harris SE, Liewald D, Ke X, Luciano M, Lopez LM, Gow AJ, Corley J, Redmond P, McNeill G, Pickles A, Ollier W, Horan M, Starr JM, Pendleton N, Thomson PA, Porteous DJ, Deary IJ.

PLoS One. 2012;7(12):e37385. doi: 10.1371/journal.pone.0037385. Epub 2012 Dec 26.

27.

White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.

Sprooten E, Fleming KM, Thomson PA, Bastin ME, Whalley HC, Hall J, Sussmann JE, McKirdy J, Blackwood D, Lawrie SM, McIntosh AM.

Psychiatry Res. 2013 Apr 30;206(2-3):223-31. doi: 10.1016/j.psychres.2012.11.002. Epub 2012 Dec 4.

PMID:
23218918
28.

Association of DISC1 variants with age of onset in a population-based sample of recurrent major depression.

Thomson PA, MacIntyre DJ, Hamilton G, Dominiczak A, Smith BH, Morris A, Evans KL, Porteous DJ.

Mol Psychiatry. 2013 Jul;18(7):745-7. doi: 10.1038/mp.2012.117. Epub 2012 Aug 7. No abstract available.

PMID:
22869032
29.

Developmental expression of orphan G protein-coupled receptor 50 in the mouse brain.

Grünewald E, Tew KD, Porteous DJ, Thomson PA.

ACS Chem Neurosci. 2012 Jun 20;3(6):459-72. doi: 10.1021/cn300008p. Epub 2012 Apr 15.

30.

Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression.

McIntosh AM, Simen AA, Evans KL, Hall J, Macintyre DJ, Blackwood D, Morris AD, Smith BH, Dominiczak A, Porteous D, Deary HI, Thomson PA.

Front Genet. 2012 Jul 2;3:116. doi: 10.3389/fgene.2012.00116. eCollection 2012.

31.

The DISC1 promoter: characterization and regulation by FOXP2.

Walker RM, Hill AE, Newman AC, Hamilton G, Torrance HS, Anderson SM, Ogawa F, Derizioti P, Nicod J, Vernes SC, Fisher SE, Thomson PA, Porteous DJ, Evans KL.

Hum Mol Genet. 2012 Jul 1;21(13):2862-72. doi: 10.1093/hmg/dds111. Epub 2012 Mar 20.

PMID:
22434823
32.

Alzheimer's disease risk factor complement receptor 1 is associated with depression.

Hamilton G, Evans KL, Macintyre DJ, Deary IJ, Dominiczak A, Smith BH, Morris AD, Porteous DJ, Thomson PA.

Neurosci Lett. 2012 Feb 21;510(1):6-9. doi: 10.1016/j.neulet.2011.12.059. Epub 2012 Jan 8.

PMID:
22244847
33.

PKA phosphorylation of NDE1 is DISC1/PDE4 dependent and modulates its interaction with LIS1 and NDEL1.

Bradshaw NJ, Soares DC, Carlyle BC, Ogawa F, Davidson-Smith H, Christie S, Mackie S, Thomson PA, Porteous DJ, Millar JK.

J Neurosci. 2011 Jun 15;31(24):9043-54. doi: 10.1523/JNEUROSCI.5410-10.2011.

34.

The effects of DISC1 risk variants on brain activation in controls, patients with bipolar disorder and patients with schizophrenia.

Chakirova G, Whalley HC, Thomson PA, Hennah W, Moorhead TW, Welch KA, Giles S, Hall J, Johnstone EC, Lawrie SM, Porteous DJ, Brown VJ, McIntosh AM.

Psychiatry Res. 2011 Apr 30;192(1):20-8. doi: 10.1016/j.pscychresns.2011.01.015. Epub 2011 Mar 3.

PMID:
21376542
35.

Synaptic modulators Nrxn1 and Nrxn3 are disregulated in a Disc1 mouse model of schizophrenia.

Brown SM, Clapcote SJ, Millar JK, Torrance HS, Anderson SM, Walker R, Rampino A, Roder JC, Thomson PA, Porteous DJ, Evans KL.

Mol Psychiatry. 2011 Jun;16(6):585-7. doi: 10.1038/mp.2010.134. Epub 2011 Feb 15. No abstract available. Erratum in: Mol Psychiatry. 2012 Apr;17(4):469.

PMID:
21321563
36.

DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder?

Boxall R, Porteous DJ, Thomson PA.

PLoS One. 2011 Jan 26;6(1):e16263. doi: 10.1371/journal.pone.0016263.

37.

DISC1 in schizophrenia: genetic mouse models and human genomic imaging.

Johnstone M, Thomson PA, Hall J, McIntosh AM, Lawrie SM, Porteous DJ.

Schizophr Bull. 2011 Jan;37(1):14-20. doi: 10.1093/schbul/sbq135. Epub 2010 Dec 13. Review.

38.

Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder.

Walker RM, Christoforou A, Thomson PA, McGhee KA, Maclean A, Mühleisen TW, Strohmaier J, Nieratschker V, Nöthen MM, Rietschel M, Cichon S, Morris SW, Jilani O, Stclair D, Blackwood DH, Muir WJ, Porteous DJ, Evans KL.

Neurosci Lett. 2010 Jun 30;478(1):9-13. doi: 10.1016/j.neulet.2010.04.056. Epub 2010 May 7.

PMID:
20435087
39.

Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.

Macintyre DJ, McGhee KA, Maclean AW, Afzal M, Briffa K, Henry B, Thomson PA, Muir WJ, Blackwood DH.

Neurosci Lett. 2010 May 21;475(3):169-73. doi: 10.1016/j.neulet.2010.03.072. Epub 2010 Apr 3.

PMID:
20371266
40.

Convergence of linkage, association and GWAS findings for a candidate region for bipolar disorder and schizophrenia on chromosome 4p.

Christoforou A, McGhee KA, Morris SW, Thomson PA, Anderson S, McLean A, Torrance HS, Le Hellard S, Pickard BS, StClair D, Muir WJ, Blackwood DH, Porteous DJ, Evans KL.

Mol Psychiatry. 2011 Mar;16(3):240-2. doi: 10.1038/mp.2010.25. Epub 2010 Mar 30. No abstract available.

PMID:
20351716
41.

Variation in DISC1 is associated with anxiety, depression and emotional stability in elderly women.

Harris SE, Hennah W, Thomson PA, Luciano M, Starr JM, Porteous DJ, Deary IJ.

Mol Psychiatry. 2010 Mar;15(3):232-4. doi: 10.1038/mp.2009.88. No abstract available.

PMID:
20168324
42.

GPR50 interacts with neuronal NOGO-A and affects neurite outgrowth.

Grünewald E, Kinnell HL, Porteous DJ, Thomson PA.

Mol Cell Neurosci. 2009 Dec;42(4):363-71. doi: 10.1016/j.mcn.2009.08.007. Epub 2009 Aug 21.

PMID:
19699797
43.

The infusion illusion.

Targownik LE, Thomson PA.

Am J Gastroenterol. 2008 Dec;103(12):3019-21. doi: 10.1111/j.1572-0241.2008.02164.x. Epub 2008 Oct 3.

PMID:
18853974
44.

Interacting haplotypes at the NPAS3 locus alter risk of schizophrenia and bipolar disorder.

Pickard BS, Christoforou A, Thomson PA, Fawkes A, Evans KL, Morris SW, Porteous DJ, Blackwood DH, Muir WJ.

Mol Psychiatry. 2009 Sep;14(9):874-84. doi: 10.1038/mp.2008.24. Epub 2008 Mar 4.

PMID:
18317462
45.

Association analysis of the chromosome 4p15-p16 candidate region for bipolar disorder and schizophrenia.

Christoforou A, Le Hellard S, Thomson PA, Morris SW, Tenesa A, Pickard BS, Wray NR, Muir WJ, Blackwood DH, Porteous DJ, Evans KL.

Mol Psychiatry. 2007 Nov;12(11):1011-25. Epub 2007 Apr 24.

PMID:
17457313
46.

Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1.

Blackwood DH, Pickard BJ, Thomson PA, Evans KL, Porteous DJ, Muir WJ.

Neurotox Res. 2007 Jan;11(1):73-83.

PMID:
17449450
47.

The PDE4B gene confers sex-specific protection against schizophrenia.

Pickard BS, Thomson PA, Christoforou A, Evans KL, Morris SW, Porteous DJ, Blackwood DH, Muir WJ.

Psychiatr Genet. 2007 Jun;17(3):129-33.

PMID:
17417055
48.

Gastroprotective strategies among NSAID users: guidelines for appropriate use in chronic illness.

Targownik LE, Thomson PA.

Can Fam Physician. 2006 Sep;52(9):1100-5. Review.

49.

A neuregulin 1 variant associated with abnormal cortical function and psychotic symptoms.

Hall J, Whalley HC, Job DE, Baig BJ, McIntosh AM, Evans KL, Thomson PA, Porteous DJ, Cunningham-Owens DG, Johnstone EC, Lawrie SM.

Nat Neurosci. 2006 Dec;9(12):1477-8. Epub 2006 Oct 29.

PMID:
17072305
50.

Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorder.

Le Hellard S, Lee AJ, Underwood S, Thomson PA, Morris SW, Torrance HS, Anderson SM, Adams RR, Navarro P, Christoforou A, Houlihan LM, Detera-Wadleigh S, Owen MJ, Asherson P, Muir WJ, Blackwood DH, Wray NR, Porteous DJ, Evans KL.

Biol Psychiatry. 2007 Mar 15;61(6):797-805. Epub 2006 Sep 25.

PMID:
16996484

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