Prediction of Potential Cancer-Risk Regions Based on Transcriptome Data: Towards a Comprehensive View

Combined gene expression and proteomic analysis of EGF induced apoptosis in A431 cells suggests multiple pathways trigger apoptosis

(2013) Ibrahim Alanazi et al.   APOPTOSIS

RETRACTED: Common genetic variants in the microRNA biogenesis pathway are associated with malignant peripheral nerve sheath tumor risk in a Chinese population

(2013) Yuxiong Weng et al.   Cancer Epidemiology

Underlying functional genomics of fat deposition in adipose tissue

(2013) Mohammad Reza Bakhtiarizadeh et al.   GENE

Predicting distinct organization of transcription factor binding sites on the promoter regions: a new genome-based approach to expand human embryonic stem cell regulatory network

(2013) Batool Hosseinpour et al.   GENE

MicroRNA-30c inhibits human breast tumour chemotherapy resistance by regulating TWF1 and IL-11

(2013) Jessica Bockhorn et al.   Nature Communications

Duplication 12p and Pallister-Killian syndrome: A case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region

(2012) Kosuke Izumi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Association of the 15q25 and 5p15 Lung Cancer Susceptibility Regions with Gene Expression in Lung Tumor Tissue

(2012) G. Fehringer et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia

(2012) Qing Lan et al.   NATURE GENETICS

Integration of DNA Copy Number Alterations and Transcriptional Expression Analysis in Human Gastric Cancer

(2012) Biao Fan et al.   PLoS One

Protein Interaction Network of Arabidopsis thaliana Female Gametophyte Development Identifies Novel Proteins and Relations

(2012) Batool Hosseinpour et al.   PLoS One

DDX5 Regulates DNA Replication and Is Required for Cell Proliferation in a Subset of Breast Cancer Cells

(2012) Anthony Mazurek et al.   Cancer Discovery

NOTCH1 mutations in CLL associated with trisomy 12

(2011) V. Balatti et al.   BLOOD

Perturbation of 14q32 miRNAs-cMYC gene network in osteosarcoma

(2011) Venugopal Thayanithy et al.   BONE

Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk

(2011) Liming Huang et al.   CARCINOGENESIS

MicroRNA in Prostate, Bladder, and Kidney Cancer: A Systematic Review

(2011) James W.F. Catto et al.   EUROPEAN UROLOGY

Assessment of palindromes as platforms for DNA amplification in breast cancer

(2011) J. Guenthoer et al.   GENOME RESEARCH

Genome-wide linkage scan for prostate cancer susceptibility in Finland: Evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22

(2011) Cheryl D. Cropp et al.   INTERNATIONAL JOURNAL OF CANCER

Chromosome 14q loss defines a molecular subtype of clear-cell renal cell carcinoma associated with poor prognosis

(2011) Federico A Monzon et al.   MODERN PATHOLOGY

Principles for the post-GWAS functional characterization of cancer risk loci

(2011) Matthew L Freedman et al.   NATURE GENETICS

Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations

(2011) Chen Wu et al.   NATURE GENETICS

Discovery of EST-SSRs in Lung Cancer: Tagged ESTs with SSRs Lead to Differential Amino Acid and Protein Expression Patterns in Cancerous Tissues

(2011) Mohammad Reza Bakhtiarizadeh et al.   PLoS One

Amplification of multiple regions of chromosome 12, including 12q13-15, in chronic lymphocytic leukaemia

(2010) Mats Merup et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Germline copy number variations in BRCA1-associated ovarian cancer patients

(2010) Kosuke Yoshihara et al.   GENES CHROMOSOMES & CANCER

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24

(2010) Ellen L Goode et al.   NATURE GENETICS

Common variants at 19p13 are associated with susceptibility to ovarian cancer

(2010) Kelly L Bolton et al.   NATURE GENETICS

Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3

(2010) Zi-Jiang Chen et al.   NATURE GENETICS

Synonymous Polymorphisms at Splicing Regulatory Sites are Associated with CpGs in Neurodegenerative Disease-Related Genes

(2010) Maria Karambataki et al.   NEUROMOLECULAR MEDICINE

Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

(2009) Da Wei Huang et al.   Nature Protocols

Pscan: finding over-represented transcription factor binding site motifs in sequences from co-regulated or co-expressed genes

(2009) Federico Zambelli et al.   NUCLEIC ACIDS RESEARCH

MicroRNA Expression Profiles in Serous Ovarian Carcinoma

(2008) E. J. Nam et al.   CLINICAL CANCER RESEARCH

Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case-control sample

(2008) Clemens Schafmayer et al.   INTERNATIONAL JOURNAL OF CANCER

Identification of a Herpes Simplex Labialis Susceptibility Region on Human Chromosome 21

(2008) Maurine R. Hobbs et al.   JOURNAL OF INFECTIOUS DISEASES

Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21

(2008) Albert Tenesa et al.   NATURE GENETICS

Simultaneous Analysis of All SNPs in Genome-Wide and Re-Sequencing Association Studies

(2008) Clive J. Hoggart et al.   PLoS Genetics