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Items: 1 to 20 of 236

1.

Next-generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2.

Maksemous N, Roy B, Smith RA, Griffiths LR.

Mol Genet Genomic Med. 2016 Jan 20;4(2):211-22. doi: 10.1002/mgg3.196. eCollection 2016 Mar.

2.

Data defining markers of human neural stem cell lineage potential.

Oikari LE, Okolicsanyi RK, Griffiths LR, Haupt LM.

Data Brief. 2016 Feb 19;7:206-15. doi: 10.1016/j.dib.2016.02.030. eCollection 2016 Jun.

3.

Blood gene expression studies in migraine: Potential and caveats.

Gerring Z, Rodriguez-Acevedo AJ, Powell JE, Griffiths LR, Montgomery GW, Nyholt DR.

Cephalalgia. 2016 Jun;36(7):669-78. doi: 10.1177/0333102416628463. Epub 2016 Feb 9. Review.

PMID:
26862113
4.

Cell surface heparan sulfate proteoglycans as novel markers of human neural stem cell fate determination.

Oikari LE, Okolicsanyi RK, Qin A, Yu C, Griffiths LR, Haupt LM.

Stem Cell Res. 2016 Jan;16(1):92-104. doi: 10.1016/j.scr.2015.12.011. Epub 2015 Dec 17.

5.

Evaluation of a 7-Gene Genetic Profile for Athletic Endurance Phenotype in Ironman Championship Triathletes.

Grealy R, Herruer J, Smith CL, Hiller D, Haseler LJ, Griffiths LR.

PLoS One. 2015 Dec 30;10(12):e0145171. doi: 10.1371/journal.pone.0145171. eCollection 2015.

6.

Ratios of T-cell immune effectors and checkpoint molecules as prognostic biomarkers in diffuse large B-cell lymphoma: a population-based study.

Keane C, Vari F, Hertzberg M, Cao KA, Green MR, Han E, Seymour JF, Hicks RJ, Gill D, Crooks P, Gould C, Jones K, Griffiths LR, Talaulikar D, Jain S, Tobin J, Gandhi MK.

Lancet Haematol. 2015 Oct;2(10):e445-55. doi: 10.1016/S2352-3026(15)00150-7. Epub 2015 Oct 1.

PMID:
26686046
7.

The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-Analysis.

Au A, Griffiths LR, Cheng KK, Wee Kooi C, Irene L, Keat Wei L.

Sci Rep. 2015 Dec 15;5:18224. doi: 10.1038/srep18224.

8.

Genetic and epigenetic variants in the MTHFR gene are not associated with non-Hodgkin lymphoma.

Bradshaw G, Sutherland HG, Camilleri ET, Lea RA, Haupt LM, Griffiths LR.

Meta Gene. 2015 Oct 22;6:91-5. doi: 10.1016/j.mgene.2015.09.004. eCollection 2015 Dec.

9.

Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate.

Benton MC, Lea RA, Macartney-Coxson D, Bellis C, Carless MA, Curran JE, Hanna M, Eccles D, Chambers GK, Blangero J, Griffiths LR.

BMC Genet. 2015 Dec 2;16:136. doi: 10.1186/s12863-015-0291-z.

10.

Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility.

Chacon-Cortes D, Smith RA, Haupt LM, Lea RA, Youl PH, Griffiths LR.

BMC Med Genet. 2015 Nov 17;16:107. doi: 10.1186/s12881-015-0248-0.

11.

Association of the microRNA-Single Nucleotide Polymorphism rs2910164 in miR146a with sporadic breast cancer susceptibility: A case control study.

Upadhyaya A, Smith RA, Chacon-Cortes D, Revêchon G, Bellis C, Lea RA, Haupt LM, Chambers SK, Youl PH, Griffiths LR.

Gene. 2016 Jan 15;576(1 Pt 2):256-60. doi: 10.1016/j.gene.2015.10.019. Epub 2015 Oct 18.

PMID:
26476291
12.

A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers.

Benton MC, Lea RA, Macartney-Coxson D, Hanna M, Eccles DA, Carless MA, Chambers GK, Bellis C, Goring HH, Curran JE, Harper JL, Gibson G, Blangero J, Griffiths LR.

PLoS Genet. 2015 Oct 16;11(10):e1005593. doi: 10.1371/journal.pgen.1005593. eCollection 2015 Oct.

13.

Erratum to: 'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture.

Benton MC, Stuart S, Bellis C, Macartney-Coxson D, Eccles D, Curran JE, Chambers G, Blangero J, Lea RA, Griffiths LR.

Investig Genet. 2015 Oct 7;6:12. doi: 10.1186/s13323-015-0029-8. eCollection 2015.

14.

Human Mesenchymal Stem Cells Retain Multilineage Differentiation Capacity Including Neural Marker Expression after Extended In Vitro Expansion.

Okolicsanyi RK, Camilleri ET, Oikari LE, Yu C, Cool SM, van Wijnen AJ, Griffiths LR, Haupt LM.

PLoS One. 2015 Sep 10;10(9):e0137255. doi: 10.1371/journal.pone.0137255. eCollection 2015.

15.

Common polygenic variation contributes to risk of migraine in the Norfolk Island population.

Rodriguez-Acevedo AJ, Ferreira MA, Benton MC, Carless MA, Goring HH, Curran JE, Blangero J, Lea RA, Griffiths LR.

Hum Genet. 2015 Oct;134(10):1079-87. doi: 10.1007/s00439-015-1587-9. Epub 2015 Jul 29.

PMID:
26220684
16.

Clinical Relevance of MTHFR, eNOS, ACE, and ApoE Gene Polymorphisms and Serum Vitamin Profile among Malay Patients with Ischemic Stroke.

Wei LK, Au A, Menon S, Gan SH, Griffiths LR.

J Stroke Cerebrovasc Dis. 2015 Sep;24(9):2017-25. doi: 10.1016/j.jstrokecerebrovasdis.2015.04.011. Epub 2015 Jul 15.

PMID:
26187788
17.

Directional dominance on stature and cognition in diverse human populations.

Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stančáková A, Faul JD, Zhao W, Bartz TM, Concas MP, Franceschini N, Enroth S, Vitart V, Trompet S, Guo X, Chasman DI, O'Connel JR, Corre T, Nongmaithem SS, Chen Y, Mangino M, Ruggiero D, Traglia M, Farmaki AE, Kacprowski T, Bjonnes A, van der Spek A, Wu Y, Giri AK, Yanek LR, Wang L, Hofer E, Rietveld CA, McLeod O, Cornelis MC, Pattaro C, Verweij N, Baumbach C, Abdellaoui A, Warren HR, Vuckovic D, Mei H, Bouchard C, Perry JR, Cappellani S, Mirza SS, Benton MC, Broeckel U, Medland SE, Lind PA, Malerba G, Drong A, Yengo L, Bielak LF, Zhi D, van der Most PJ, Shriner D, Mägi R, Hemani G, Karaderi T, Wang Z, Liu T, Demuth I, Zhao JH, Meng W, Lataniotis L, van der Laan SW, Bradfield JP, Wood AR, Bonnefond A, Ahluwalia TS, Hall LM, Salvi E, Yazar S, Carstensen L, de Haan HG, Abney M, Afzal U, Allison MA, Amin N, Asselbergs FW, Bakker SJ, Barr RG, Baumeister SE, Benjamin DJ, Bergmann S, Boerwinkle E, Bottinger EP, Campbell A, Chakravarti A, Chan Y, Chanock SJ, Chen C, Chen YD, Collins FS, Connell J, Correa A, Cupples LA, Smith GD, Davies G, Dörr M, Ehret G, Ellis SB, Feenstra B, Feitosa MF, Ford I, Fox CS, Frayling TM, Friedrich N, Geller F, Scotland G, Gillham-Nasenya I, Gottesman O, Graff M, Grodstein F, Gu C, Haley C, Hammond CJ, Harris SE, Harris TB, Hastie ND, Heard-Costa NL, Heikkilä K, Hocking LJ, Homuth G, Hottenga JJ, Huang J, Huffman JE, Hysi PG, Ikram MA, Ingelsson E, Joensuu A, Johansson Å, Jousilahti P, Jukema JW, Kähönen M, Kamatani Y, Kanoni S, Kerr SM, Khan NM, Koellinger P, Koistinen HA, Kooner MK, Kubo M, Kuusisto J, Lahti J, Launer LJ, Lea RA, Lehne B, Lehtimäki T, Liewald DC, Lind L, Loh M, Lokki ML, London SJ, Loomis SJ, Loukola A, Lu Y, Lumley T, Lundqvist A, Männistö S, Marques-Vidal P, Masciullo C, Matchan A, Mathias RA, Matsuda K, Meigs JB, Meisinger C, Meitinger T, Menni C, Mentch FD, Mihailov E, Milani L, Montasser ME, Montgomery GW, Morrison A, Myers RH, Nadukuru R, Navarro P, Nelis M, Nieminen MS, Nolte IM, O'Connor GT, Ogunniyi A, Padmanabhan S, Palmas WR, Pankow JS, Patarcic I, Pavani F, Peyser PA, Pietilainen K, Poulter N, Prokopenko I, Ralhan S, Redmond P, Rich SS, Rissanen H, Robino A, Rose LM, Rose R, Sala C, Salako B, Salomaa V, Sarin AP, Saxena R, Schmidt H, Scott LJ, Scott WR, Sennblad B, Seshadri S, Sever P, Shrestha S, Smith BH, Smith JA, Soranzo N, Sotoodehnia N, Southam L, Stanton AV, Stathopoulou MG, Strauch K, Strawbridge RJ, Suderman MJ, Tandon N, Tang ST, Taylor KD, Tayo BO, Töglhofer AM, Tomaszewski M, Tšernikova N, Tuomilehto J, Uitterlinden AG, Vaidya D, van Hylckama Vlieg A, van Setten J, Vasankari T, Vedantam S, Vlachopoulou E, Vozzi D, Vuoksimaa E, Waldenberger M, Ware EB, Wentworth-Shields W, Whitfield JB, Wild S, Willemsen G, Yajnik CS, Yao J, Zaza G, Zhu X; BioBank Japan Project, Salem RM, Melbye M, Bisgaard H, Samani NJ, Cusi D, Mackey DA, Cooper RS, Froguel P, Pasterkamp G, Grant SF, Hakonarson H, Ferrucci L, Scott RA, Morris AD, Palmer CN, Dedoussis G, Deloukas P, Bertram L, Lindenberger U, Berndt SI, Lindgren CM, Timpson NJ, Tönjes A, Munroe PB, Sørensen TI, Rotimi CN, Arnett DK, Oldehinkel AJ, Kardia SL, Balkau B, Gambaro G, Morris AP, Eriksson JG, Wright MJ, Martin NG, Hunt SC, Starr JM, Deary IJ, Griffiths LR, Tiemeier H, Pirastu N, Kaprio J, Wareham NJ, Pérusse L, Wilson JG, Girotto G, Caulfield MJ, Raitakari O, Boomsma DI, Gieger C, van der Harst P, Hicks AA, Kraft P, Sinisalo J, Knekt P, Johannesson M, Magnusson PK, Hamsten A, Schmidt R, Borecki IB, Vartiainen E, Becker DM, Bharadwaj D, Mohlke KL, Boehnke M, van Duijn CM, Sanghera DK, Teumer A, Zeggini E, Metspalu A, Gasparini P, Ulivi S, Ober C, Toniolo D, Rudan I, Porteous DJ, Ciullo M, Spector TD, Hayward C, Dupuis J, Loos RJ, Wright AF, Chandak GR, Vollenweider P, Shuldiner AR, Ridker PM, Rotter JI, Sattar N, Gyllensten U, North KE, Pirastu M, Psaty BM, Weir DR, Laakso M, Gudnason V, Takahashi A, Chambers JC, Kooner JS, Strachan DP, Campbell H, Hirschhorn JN, Perola M, Polašek O, Wilson JF.

Nature. 2015 Jul 23;523(7561):459-62. doi: 10.1038/nature14618. Epub 2015 Jul 1.

18.

Methylenetetrahydrofolate Reductase CpG Islands: Epigenotyping.

Wei LK, Sutherland H, Au A, Camilleri E, Haupt LM, Gan SH, Griffiths LR.

J Clin Lab Anal. 2015 Jun 25. doi: 10.1002/jcla.21860. [Epub ahead of print]

PMID:
26109141
19.

Case-control study of ADARB1 and ADARB2 gene variants in migraine.

Gasparini CF, Sutherland HG, Maher B, Rodriguez-Acevedo AJ, Khlifi E, Haupt LM, Griffiths LR.

J Headache Pain. 2015;16:511. doi: 10.1186/s10194-015-0511-y. Epub 2015 Apr 3.

20.

A potential epigenetic marker mediating serum folate and vitamin B12 levels contributes to the risk of ischemic stroke.

Wei LK, Sutherland H, Au A, Camilleri E, Haupt LM, Gan SH, Griffiths LR.

Biomed Res Int. 2015;2015:167976. doi: 10.1155/2015/167976. Epub 2015 Feb 1.

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