Associated Papers
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
33907296 (PubMed )
Supplement: 42003_2021_2024_MOESM11_ESM.xlsx › Supplementary_Data_8
An enhanced workflow for variant interpretation in UniProtKB/Swiss-Prot improves consistency and reuse in ClinVar.
Famiglietti ML et al.
Database : the Journal of Biological Databases and Curation, 2019
30937429 (PubMed )
Supplement: famiglietti_supplementarytables1_rev_baz040.xlsx › common
Characterization of DNA variants in the human kinome in breast cancer.
Agarwal D et al.
Scientific Reports, 2015
26420498 (PubMed )
Supplement: srep14736-s3.xls › HFI_Unique
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
Karageorgos I et al.
Human Genomics, 2015
26092435 (PubMed )
Supplement: 40246_2015_34_MOESM1_ESM.xlsx › FamilyB
Genetic variants and risk of cervical cancer: epidemiological evidence, meta-analysis and research review.
Zhang X et al.
Bjog : an International Journal of Obstetrics and Gynaecology, 2014
A single nucleotide polymorphism in EXO1 gene is associated with cervical cancer susceptibility in Chinese patients.
Luo X et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society, 2012
Exome sequencing of only seven Qataris identifies potentially deleterious variants in the Qatari population.
Rodriguez-Flores JL et al.
Plos One, 2012
Association between the CDC6 G1321A polymorphism and the risk of cervical cancer.
Xiong XD et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society, 2010
A novel polymorphism in CDC6 is associated with the decline in lung function of ex-smokers in COPD.
Takabatake N et al.
Biochemical and Biophysical Research Communications, 2009
Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
Webb EL et al.
Human Molecular Genetics, 2006
Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins.
Savas S et al.
Proteins, 2005
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