Associated Papers
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
27512948 (PubMed )
Supplement: PATH-240-315-s015.xlsx › Table_S2
Pharmacogenetic analysis of advanced non-small-cell lung cancer patients treated with first-line paclitaxel and carboplatin chemotherapy.
Park HS et al.
Pharmacogenetics and Genomics, 2016
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
26110913 (PubMed )
Supplement: HUMU-36-903-s001.zip › humu22825-sup-0007-Table_S10.xlsx › Sheet1
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A0CT-01A.domain
Large-scale profiling and identification of potential regulatory mechanisms for allelic gene expression in colorectal cancer cells.
Lee RD et al.
Gene, 2013
Association of HK2 and NCK2 with normal tension glaucoma in the Japanese population.
Shi D et al.
Plos One, 2013
SNP-based large-scale identification of allele-specific gene expression in human B cells.
Song MY et al.
Gene, 2012
Glucose metabolism gene polymorphisms and clinical outcome in pancreatic cancer.
Dong X et al.
Cancer, 2011
Candidate gene association study in type 2 diabetes indicates a role for genes involved in beta-cell function as well as insulin action.
Barroso I et al.
Plos Biology, 2003
14551916 (PubMed )
Supplement: pbio.0000020.st001.xls › Sheet1
Functional consequences of naturally occurring variants of human hexokinase II.
Malkki M et al.
Diabetologia, 1998
Variant sequences of the Hexokinase II gene in familial NIDDM.
Taylor RW et al.
Diabetologia, 1996
Identification of the aminoacid polymorphisms in hexokinase II in Japanese subjects.
Shimada F et al.
Diabetologia, 1996
Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity.
Lehto M et al.
Diabetologia, 1995
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