A functional copy number variation in the WWOX gene is associated with lung cancer risk in Chinese

A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer

(2012) Bin Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Germline copy number variations and cancer predisposition

(2012) Ana Cristina Victorino Krepischi et al.   Future Oncology

Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population

(2012) Jing Dong et al.   NATURE GENETICS

Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform

(2011) Jeanette E Eckel-Passow et al.   BMC BIOINFORMATICS

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

(2011) Liming Huang et al.   CARCINOGENESIS

A functional polymorphism at microRNA-629-binding site in the 3′-untranslated region of NBS1 gene confers an increased risk of lung cancer in Southern and Eastern Chinese population

(2011) Lei Yang et al.   CARCINOGENESIS

p73 tumor suppressor protein: A close relative of p53 not only in structure but also in anti-cancer approach?

(2011) Joanna Zawacka-Pankau et al.   CELL CYCLE

A gender-specific association of CNV at 6p21.3 with NPC susceptibility

(2011) K.-P. Tse et al.   HUMAN MOLECULAR GENETICS

The polymorphism and haplotypes of PIN1 gene are associated with the risk of lung cancer in southern and eastern chinese populations

(2011) Jiachun Lu et al.   HUMAN MUTATION

Evidences that the polymorphism Pro-282-Ala within the tumor suppressor gene WWOX is a new risk factor for differentiated thyroid carcinoma

(2011) Lisa Cancemi et al.   INTERNATIONAL JOURNAL OF CANCER

Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability

(2010) Feng Zhang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-Wide Catalogue of Chromosomal Aberrations in Barrett's Esophagus and Esophageal Adenocarcinoma: A High-Density Single Nucleotide Polymorphism Array Analysis

(2010) J. Gu et al.   Cancer Prevention Research

A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum

(2010) K. M. Walsh et al.   ENDOCRINE-RELATED CANCER

WWOX tumour suppressor gene polymorphisms and ovarian cancer pathology and prognosis

(2010) Adam J.W. Paige et al.   EUROPEAN JOURNAL OF CANCER

WWOXgene and gene product: tumor suppression through specific protein interactions

(2010) Zaidoun Salah et al.   Future Oncology

Missing heritability and strategies for finding the underlying causes of complex disease

(2010) Evan E. Eichler et al.   NATURE REVIEWS GENETICS

WWOX Gene Expression Abolishes Ovarian Cancer Tumorigenicity In vivo and Decreases Attachment to Fibronectin via Integrin  3

(2009) C. Gourley et al.   CANCER RESEARCH

A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: An integrated genomics approach reveals a wide gene dosage effect

(2009) Luca Agnelli et al.   GENES CHROMOSOMES & CANCER

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

(2008) Iuliana Ionita-Laza et al.   GENOMICS

Genome-wide linkage scan for prostate cancer susceptibility from the university of michigan prostate cancer genetics project: Suggestive evidence for linkage at 16q23

(2008) Ethan M. Lange et al.   PROSTATE