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Items: 1 to 20 of 465

1.

Identification of Genes Associated with Hirschsprung Disease, Based on Whole-genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development.

Tang CS, Li P, Lai FP, Fu AX, Lau ST, So MT, Lui KN, Li Z, Zhuang X, Yu M, Liu X, Ngo ND, Miao X, Zhang X, Yi B, Tang S, Sun X, Zhang F, Liu H, Liu Q, Zhang R, Wang H, Huang L, Dong X, Tou J, Cheah KS, Yang W, Yuan Z, Yip KY, Sham PC, Tam PK, Garcia-Barcelo MM, Ngan ES.

Gastroenterology. 2018 Sep 11. pii: S0016-5085(18)34965-5. doi: 10.1053/j.gastro.2018.09.012. [Epub ahead of print]

PMID:
30217742
2.

Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density.

Zhou X, Cheung CL, Karasugi T, Karppinen J, Samartzis D, Hsu YH, Mak TS, Song YQ, Chiba K, Kawaguchi Y, Li Y, Chan D, Cheung KM, Ikegawa S, Cheah KS, Sham PC.

Front Genet. 2018 Aug 3;9:267. doi: 10.3389/fgene.2018.00267. eCollection 2018.

3.

A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia.

Li M, Jiang L, Mak TSH, Kwan JSH, Xue C, Chen P, Leung HC, Cui L, Li T, Sham PC.

Bioinformatics. 2018 Aug 7. doi: 10.1093/bioinformatics/bty682. [Epub ahead of print]

PMID:
30101339
4.

Exploring shared genetic bases and causal relationships of schizophrenia and bipolar disorder with 28 cardiovascular and metabolic traits.

So HC, Chau KL, Ao FK, Mo CH, Sham PC.

Psychol Med. 2018 Jul 26:1-13. doi: 10.1017/S0033291718001812. [Epub ahead of print]

PMID:
30045777
5.

Coverage and diagnostic yield of Whole Exome Sequencing for the Evaluation of Cases with Dilated and Hypertrophic Cardiomyopathy.

Mak TSH, Lee YK, Tang CS, Hai JSH, Ran X, Sham PC, Tse HF.

Sci Rep. 2018 Jul 18;8(1):10846. doi: 10.1038/s41598-018-29263-3.

6.

Gabrb2-knockout mice displayed schizophrenia-like and comorbid phenotypes with interneuron-astrocyte-microglia dysregulation.

Yeung RK, Xiang ZH, Tsang SY, Li R, Ho TYC, Li Q, Hui CK, Sham PC, Qiao MQ, Xue H.

Transl Psychiatry. 2018 Jul 17;8(1):128. doi: 10.1038/s41398-018-0176-9.

7.

Chemotherapy-Induced Cognitive Impairment Is Associated with Cytokine Dysregulation and Disruptions in Neuroplasticity.

Shi DD, Huang YH, Lai CSW, Dong CM, Ho LC, Wu EX, Li Q, Wang XM, Chung SK, Sham PC, Zhang ZJ.

Mol Neurobiol. 2018 Jul 14. doi: 10.1007/s12035-018-1224-4. [Epub ahead of print]

PMID:
30008071
8.

Age at first birth in women is genetically associated with increased risk of schizophrenia.

Ni G, Gratten J, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium.

Sci Rep. 2018 Jul 5;8(1):10168. doi: 10.1038/s41598-018-28160-z.

9.

Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet.

Basil P, Li Q, Gui H, Hui TCK, Ling VHM, Wong CCY, Mill J, McAlonan GM, Sham PC.

Transl Psychiatry. 2018 Jul 2;8(1):125. doi: 10.1038/s41398-018-0167-x.

10.

Tractography-based classification in distinguishing patients with first-episode schizophrenia from healthy individuals.

Deng Y, Hung KSY, Lui SSY, Chui WWH, Lee JCW, Wang Y, Li Z, Mak HKF, Sham PC, Chan RCK, Cheung EFC.

Prog Neuropsychopharmacol Biol Psychiatry. 2018 Jun 20;88:66-73. doi: 10.1016/j.pnpbp.2018.06.010. [Epub ahead of print]

PMID:
29935206
11.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium. Electronic address: douglas.ruderfer@vanderbilt.edu; Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium.

Cell. 2018 Jun 14;173(7):1705-1715.e16. doi: 10.1016/j.cell.2018.05.046.

PMID:
29906448
12.

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.

Wong JKL, Gui H, Kwok M, Ng PW, Lui CHT, Baum L, Sham PC, Kwan P, Cherny SS.

Neurol Genet. 2018 Jun 11;4(3):e245. doi: 10.1212/NXG.0000000000000245. eCollection 2018 Jun.

13.

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.

Huang D, Yi X, Zhang S, Zheng Z, Wang P, Xuan C, Sham PC, Wang J, Li MJ.

Nucleic Acids Res. 2018 Jul 2;46(W1):W114-W120. doi: 10.1093/nar/gky407.

14.

Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood.

Ni G, Moser G; Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray NR, Lee SH.

Am J Hum Genet. 2018 Jun 7;102(6):1185-1194. doi: 10.1016/j.ajhg.2018.03.021. Epub 2018 May 10.

15.

Influenza vaccine effectiveness in hospitalised Hong Kong children: Feasibility of estimates from routine surveillance data.

Yeung KHT, Chan KCC, Chan PKS, Lam DSY, Sham PCO, Yau YS, Chan WH, Chiu WK, Ng KL, Ng DKK, Chan IMC, Nelson EAS.

Vaccine. 2018 Jun 7;36(24):3477-3485. doi: 10.1016/j.vaccine.2018.04.081. Epub 2018 May 5.

16.

A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues.

Ying D, Li MJ, Sham PC, Li M.

Bioinformatics. 2018 Sep 15;34(18):3145-3150. doi: 10.1093/bioinformatics/bty318.

PMID:
29718103
17.

Early onset of disc degeneration in SM/J mice is associated with changes in ion transport systems and fibrotic events.

Zhang Y, Xiong C, Kudelko M, Li Y, Wang C, Wong YL, Tam V, Rai MF, Cheverud J, Lawson HA, Sandell L, Chan WCW, Cheah KSE, Sham PC, Chan D.

Matrix Biol. 2018 Sep;70:123-139. doi: 10.1016/j.matbio.2018.03.024. Epub 2018 Apr 9.

PMID:
29649547
18.

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing.

Tang CS, Zhuang X, Lam WY, Ngan ES, Hsu JS, Michelle YU, Man-Ting SO, Cherny SS, Ngo ND, Sham PC, Tam PK, Garcia-Barcelo MM.

Eur J Hum Genet. 2018 Jun;26(6):818-826. doi: 10.1038/s41431-018-0129-z. Epub 2018 Feb 26.

PMID:
29483666
19.

Evaluation of tools for highly variable gene discovery from single-cell RNA-seq data.

Yip SH, Sham PC, Wang J.

Brief Bioinform. 2018 Feb 21. doi: 10.1093/bib/bby011. [Epub ahead of print]

PMID:
29481632
20.

Mutations in Hnrnpa1 cause congenital heart defects.

Yu Z, Tang PL, Wang J, Bao S, Shieh JT, Leung AW, Zhang Z, Gao F, Wong SY, Hui AL, Gao Y, Dung N, Zhang ZG, Fan Y, Zhou X, Zhang Y, Wong DS, Sham PC, Azhar A, Kwok PY, Tam PP, Lian Q, Cheah KS, Wang B, Song YQ.

JCI Insight. 2018 Jan 25;3(2). pii: 98555. doi: 10.1172/jci.insight.98555. [Epub ahead of print]

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