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Results: 1 to 20 of 549

1.

Plasma lipidomics analysis finds long chain cholesteryl esters to be associated with Alzheimer's disease.

Proitsi P, Kim M, Whiley L, Pritchard M, Leung R, Soininen H, Kloszewska I, Mecocci P, Tsolaki M, Vellas B, Sham P, Lovestone S, Powell JF, Dobson RJ, Legido-Quigley C.

Transl Psychiatry. 2015 Jan 13;5:e494. doi: 10.1038/tp.2014.127.

PMID:
25585166
[PubMed - in process]
2.

Correction for kwok et Al., genomic diversity of epstein-barr virus genomes isolated from primary nasopharyngeal carcinoma biopsy samples.

Kwok H, Wu CW, Palser AL, Kellam P, Sham PC, Kwong DL, Chiang AK.

J Virol. 2015 Jan 1;89(1):886. doi: 10.1128/JVI.03005-14. Epub 2014 Dec 16. No abstract available.

PMID:
25516607
[PubMed - in process]
3.

Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort.

Toulopoulou T, van Haren N, Zhang X, Sham PC, Cherny SS, Campbell DD, Picchioni M, Murray R, Boomsma DI, Pol HH, Brouwer R, Schnack H, Fañanás L, Sauer H, Nenadic I, Weisbrod M, Cannon TD, Kahn RS.

Mol Psychiatry. 2014 Dec 2. doi: 10.1038/mp.2014.152. [Epub ahead of print]

PMID:
25450228
[PubMed - as supplied by publisher]
4.

MGAS: a powerful tool for multivariate gene-based genome-wide association analysis.

Van der Sluis S, Dolan CV, Li J, Song Y, Sham P, Posthuma D, Li M.

Bioinformatics. 2014 Nov 26. pii: btu783. [Epub ahead of print]

PMID:
25431328
[PubMed - as supplied by publisher]
Free Article
5.

The p.Ser267Phe variant in SLC10A1 is associated with resistance to chronic hepatitis B.

Peng L, Zhao Q, Li Q, Li M, Li C, Xu T, Jing X, Zhu X, Wang Y, Li F, Liu R, Zhong C, Pan Q, Zeng B, Liao Q, Hu B, Hu ZX, Huang YS, Sham P, Liu J, Xu S, Wang J, Gao ZL, Wang Y.

Hepatology. 2014 Nov 21. doi: 10.1002/hep.27608. [Epub ahead of print]

PMID:
25418280
[PubMed - as supplied by publisher]
6.

Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family.

Cheng J, Zhou X, Lu Y, Chen J, Han B, Zhu Y, Liu L, Choy KW, Han D, Sham PC, Zhang MQ, Zhang X, Yuan H.

Ann Hum Genet. 2014 Sep 17. doi: 10.1111/ahg.12084. [Epub ahead of print]

PMID:
25227905
[PubMed - as supplied by publisher]
7.

Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis.

Proitsi P, Lupton MK, Velayudhan L, Newhouse S, Fogh I, Tsolaki M, Daniilidou M, Pritchard M, Kloszewska I, Soininen H, Mecocci P, Vellas B; Alzheimer's Disease Neuroimaging Initiative, Williams J; GERAD1 Consortium, Stewart R, Sham P, Lovestone S, Powell JF.

PLoS Med. 2014 Sep 16;11(9):e1001713. doi: 10.1371/journal.pmed.1001713. eCollection 2014 Sep.

PMID:
25226301
[PubMed - in process]
Free PMC Article
8.

Prenatal maternal immune activation causes epigenetic differences in adolescent mouse brain.

Basil P, Li Q, Dempster EL, Mill J, Sham PC, Wong CC, McAlonan GM.

Transl Psychiatry. 2014 Sep 2;4:e434. doi: 10.1038/tp.2014.80.

PMID:
25180573
[PubMed - in process]
Free PMC Article
9.

Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease.

Proitsi P, Lupton MK, Velayudhan L, Hunter G, Newhouse S, Lin K, Fogh I, Tsolaki M, Daniilidou M, Pritchard M, Craig D, Todd S, Johnston JA, McGuinness B, Kloszewska I, Soininen H, Mecocci P, Vellas B, Passmore PA, Sims R, Williams J, Brayne C; Alzheimer's Disease Neuroimaging Initiative; GERAD1 Consortium, Stewart R, Sham P, Lovestone S, Powell JF.

Neurobiol Aging. 2014 Dec;35(12):2883.e3-2883.e10. doi: 10.1016/j.neurobiolaging.2014.07.023. Epub 2014 Jul 24.

PMID:
25150574
[PubMed - in process]
10.

Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.

Zhang Y, Zhang J, Yang J, Wang Y, Zhang L, Zuo X, Sun L, Pan HF, Hirankarn N, Wang T, Chen R, Ying D, Zeng S, Shen JJ, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, Wong SN, Lee KW, Ho MH, Lee PP, Chung BH, Chong CY, Wong RW, Mok MY, Wong WH, Tong KL, Tse NK, Li XP, Avihingsanon Y, Rianthavorn P, Deekajorndej T, Suphapeetiporn K, Shotelersuk V, Ying SK, Fung SK, Lai WM, Wong CM, Ng IO, Garcia-Barcelo MM, Cherny SS, Tam PK, Sham PC, Yang S, Ye DQ, Cui Y, Zhang XJ, Lau YL, Yang W.

Hum Mol Genet. 2015 Jan 1;24(1):274-84. doi: 10.1093/hmg/ddu429. Epub 2014 Aug 22.

PMID:
25149475
[PubMed - in process]
11.

PMCA4 (ATP2B4) mutation in familial spastic paraplegia.

Li M, Ho PW, Pang SY, Tse ZH, Kung MH, Sham PC, Ho SL.

PLoS One. 2014 Aug 13;9(8):e104790. doi: 10.1371/journal.pone.0104790. eCollection 2014.

PMID:
25119969
[PubMed - in process]
Free PMC Article
12.

Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels.

Kwan JS, Hsu YH, Cheung CL, Dupuis J, Saint-Pierre A, Eriksson J, Handelman SK, Aragaki A, Karasik D, Pramstaller PP, Kooperberg C, Lacroix AZ, Larson MG, Lau KS, Lorentzon M, Pichler I, Sham PC, Taliun D, Vandenput L, Kiel DP, Hicks AA, Jackson RD, Ohlsson C, Benjamin EJ, Kung AW.

Hum Mol Genet. 2014 Dec 15;23(24):6684-93. doi: 10.1093/hmg/ddu386. Epub 2014 Jul 30.

PMID:
25080503
[PubMed - in process]
13.

MRI predicts remission at 1 year in first-episode schizophrenia in females with larger striato-thalamic volumes.

Fung G, Cheung C, Chen E, Lam C, Chiu C, Law CW, Leung MK, Deng M, Cheung V, Qi L, Nailin Y, Tai KS, Yip L, Suckling J, Sham P, McAlonan G, Chua SE.

Neuropsychobiology. 2014;69(4):243-8. doi: 10.1159/000358837. Epub 2014 Jun 27.

PMID:
24993979
[PubMed - in process]
14.

Genomic diversity of Epstein-Barr virus genomes isolated from primary nasopharyngeal carcinoma biopsy samples.

Kwok H, Wu CW, Palser AL, Kellam P, Sham PC, Kwong DL, Chiang AK.

J Virol. 2014 Sep;88(18):10662-72. doi: 10.1128/JVI.01665-14. Epub 2014 Jul 2.

PMID:
24991008
[PubMed - indexed for MEDLINE]
15.

Targeted next-generation sequencing on hirschsprung disease: a pilot study exploits DNA pooling.

Gui H, Bao JY, Tang CS, So MT, Ngo DN, Tran AQ, Bui DH, Pham DH, Nguyen TL, Tong A, Lok S, Sham PC, Tam PK, Cherny SS, Garcia-Barcelo MM.

Ann Hum Genet. 2014 Sep;78(5):381-7. doi: 10.1111/ahg.12076. Epub 2014 Jun 20.

PMID:
24947032
[PubMed - in process]
16.

Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.

Li MJ, Yan B, Sham PC, Wang J.

Brief Bioinform. 2014 Jun 10. pii: bbu018. [Epub ahead of print]

PMID:
24916300
[PubMed - as supplied by publisher]
17.

Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study.

Gui H, Jiang CQ, Cherny SS, Sham PC, Xu L, Liu B, Jin YL, Zhu T, Zhang WS, Thomas GN, Cheng KK, Lam TH.

Neurobiol Aging. 2014 Oct;35(10):2422.e3-8. doi: 10.1016/j.neurobiolaging.2014.04.022. Epub 2014 Apr 30.

PMID:
24863667
[PubMed - in process]
18.

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations.

European Network of National Networks studying Gene-Environment Interactions in Schizophrenia (EU-GEI), van Os J, Rutten BP, Myin-Germeys I, Delespaul P, Viechtbauer W, van Zelst C, Bruggeman R, Reininghaus U, Morgan C, Murray RM, Di Forti M, McGuire P, Valmaggia LR, Kempton MJ, Gayer-Anderson C, Hubbard K, Beards S, Stilo SA, Onyejiaka A, Bourque F, Modinos G, Tognin S, Calem M, O'Donovan MC, Owen MJ, Holmans P, Williams N, Craddock N, Richards A, Humphreys I, Meyer-Lindenberg A, Leweke FM, Tost H, Akdeniz C, Rohleder C, Bumb JM, Schwarz E, Alptekin K, Üçok A, Saka MC, Atbaşoğlu EC, Gülöksüz S, Gumus-Akay G, Cihan B, Karadağ H, Soygür H, Cankurtaran EŞ, Ulusoy S, Akdede B, Binbay T, Ayer A, Noyan H, Karadayı G, Akturan E, Ulaş H, Arango C, Parellada M, Bernardo M, Sanjuán J, Bobes J, Arrojo M, Santos JL, Cuadrado P, Rodríguez Solano JJ, Carracedo A, García Bernardo E, Roldán L, López G, Cabrera B, Cruz S, Díaz Mesa EM, Pouso M, Jiménez E, Sánchez T, Rapado M, González E, Martínez C, Sánchez E, Olmeda MS, de Haan L, Velthorst E, van der Gaag M, Selten JP, van Dam D, van der Ven E, van der Meer F, Messchaert E, Kraan T, Burger N, Leboyer M, Szoke A, Schürhoff F, Llorca PM, Jamain S, Tortelli A, Frijda F, Vilain J, Galliot AM, Baudin G, Ferchiou A, Richard JR, Bulzacka E, Charpeaud T, Tronche AM, De Hert M, van Winkel R, Decoster J, Derom C, Thiery E, Stefanis NC, Sachs G, Aschauer H, Lasser I, Winklbaur B, Schlögelhofer M, Riecher-Rössler A, Borgwardt S, Walter A, Harrisberger F, Smieskova R, Rapp C, Ittig S, Soguel-dit-Piquard F, Studerus E, Klosterkötter J, Ruhrmann S, Paruch J, Julkowski D, Hilboll D, Sham PC, Cherny SS, Chen EY, Campbell DD, Li M, Romeo-Casabona CM, Emaldi Cirión A, Urruela Mora A, Jones P, Kirkbride J, Cannon M, Rujescu D, Tarricone I, Berardi D, Bonora E, Seri M, Marcacci T, Chiri L, Chierzi F, Storbini V, Braca M, Minenna MG, Donegani I, Fioritti A, La Barbera D, La Cascia CE, Mulè A, Sideli L, Sartorio R, Ferraro L, Tripoli G, Seminerio F, Marinaro AM, McGorry P, Nelson B, Amminger GP, Pantelis C, Menezes PR, Del-Ben CM, Gallo Tenan SH, Shuhama R, Ruggeri M, Tosato S, Lasalvia A, Bonetto C, Ira E, Nordentoft M, Krebs MO, Barrantes-Vidal N, Cristóbal P, Kwapil TR, Brietzke E, Bressan RA, Gadelha A, Maric NP, Andric S, Mihaljevic M, Mirjanic T.

Schizophr Bull. 2014 Jul;40(4):729-36. doi: 10.1093/schbul/sbu069. Epub 2014 May 24.

PMID:
24860087
[PubMed - in process]
19.

Adiponectin gene variants and the risk of coronary heart disease: a 16-year longitudinal study.

Cheung CY, Hui EY, Cheung BM, Woo YC, Xu A, Fong CH, Ong KL, Yeung CY, Janus ED, Tse HF, Sham PC, Lam KS.

Eur J Endocrinol. 2014 Jul;171(1):107-15. doi: 10.1530/EJE-14-0079. Epub 2014 Apr 23.

PMID:
24760538
[PubMed - indexed for MEDLINE]
20.

Statistical power and significance testing in large-scale genetic studies.

Sham PC, Purcell SM.

Nat Rev Genet. 2014 May;15(5):335-46. doi: 10.1038/nrg3706. Review.

PMID:
24739678
[PubMed - indexed for MEDLINE]

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