Associated Papers
Clinical exome sequencing identifies novel gene variants associated with ischemic stroke in the Saudi Tabuk population.
Hamadi A et al.
Frontiers in Human Neuroscience, 2025
Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma.
Patiño-García A et al.
Ebiomedicine, 2024
38484556 (PubMed )
Supplement: mmc1.xlsx › Supp_Table_2
Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.
Valentine H et al.
Cancer Research Communications, 2022
36643868 (PubMed )
Supplement: crc-22-0245-s07.xlsx › Variants_All_Exonic.exclude_ncR
Exome Sequencing Data Analysis and a Case-Control Study in Mexican Population Reveals Lipid Trait Associations of New and Known Genetic Variants in Dyslipidemia-Associated Loci.
Jurado-Camacho PA et al.
Frontiers in Genetics, 2022
35669185 (PubMed )
Supplement: Table2.XLSX › Hoja1
Population History and Gene Divergence in Native Mexicans Inferred from 76 Human Exomes.
Ávila-Arcos MC et al.
Molecular Biology and Evolution, 2020
31848607 (PubMed )
Supplement: msz282-supplementary_data.zip › msz282-Suppl_Data › Table_S14.xlsx › Table_S14
Dissecting the Mutational Landscape of Cutaneous Melanoma: An Omic Analysis Based on Patients from Greece.
Kontogianni G et al.
Cancers, 2018
29596374 (PubMed )
Supplement: cancers-10-00096-s001.zip › Table_S1.xlsx › S1
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T2
Coding-sequence variants are associated with blood lipid levels in 14,473 Chinese.
Lu X et al.
Human Molecular Genetics, 2016
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.
Lamina C et al.
Human Molecular Genetics, 2016
Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution.
Patel AP et al.
Atherosclerosis, 2016
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk.
Holmen OL et al.
Nature Genetics, 2014
24633158 (PubMed )
Supplement: NIHMS570373-supplement-1.pdf
Medullary amyloidosis associated with apolipoprotein A-IV deposition.
Sethi S et al.
Kidney International, 2012
Select a paper to view details