Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray

Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis.

Nature genetics·2026

Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction.

Nature genetics·2026

KCNA2 variants cause dilated cardiomyopathy, obesity and sleep apnea through RAC-ERK pathway.

EMBO molecular medicine·2026

Meta-analysis of genome-wide association studies of food allergy and IgE sensitization.

The Journal of allergy and clinical immunology·2026

Genome-wide association study identifies ABCG1 as a susceptibility locus for tick-borne encephalitis.

iScience·2025

The European BestAgeing Study on microRNA candidates reveals distinct signatures with diagnostic and prognostic potential in cardiovascular disease.

BMC medicine·2025

Distinguishing Acute Myocardial Infarction from Other Forms of Cardiac Injury with the Cardiac Troponin Long-T ITC Complex and High-Sensitivity Troponin I and T in Patients with Suspected Acute Coronary Syndrome: MERITnI Substudy.

Clinical chemistry·2026

Biological Variation of Adrenal-Related Endocrine Biomarkers Used for Investigation of Secondary Hypertension.

Clinical chemistry·2026

Enriching Microbial Cell-Free DNA in Clinical Metagenomics Using Epigenetic Filters.

Clinical chemistry·2026

APOB to Estimated APOB Ratio for Screening for the APOE2 Genotype.

Clinical chemistry·2026

Highly Accurate Sequencing Methods for Low-Frequency Variant Detection.

Clinical chemistry·2026

Prognostic Value of Cardiac Myosin Binding Protein C in the General Population: The Akershus Cardiac Examination 1950 Study.

Clinical chemistry·2026

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

Frontiers in genetics·2026

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

Journal of molecular endocrinology·2026

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Neuroimage. Reports·2026

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

iScience·2026

Structural variants contribute substantially to complex trait heritability.

Research square·2026

Related Experiment Videos

Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray

Related Concept Videos

Multi-ancestry genome-wide association analyses provide insights into the genetic basis of Hashimoto's thyroiditis.

Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction.

KCNA2 variants cause dilated cardiomyopathy, obesity and sleep apnea through RAC-ERK pathway.

Meta-analysis of genome-wide association studies of food allergy and IgE sensitization.

Genome-wide association study identifies ABCG1 as a susceptibility locus for tick-borne encephalitis.

The European BestAgeing Study on microRNA candidates reveals distinct signatures with diagnostic and prognostic potential in cardiovascular disease.

Distinguishing Acute Myocardial Infarction from Other Forms of Cardiac Injury with the Cardiac Troponin Long-T ITC Complex and High-Sensitivity Troponin I and T in Patients with Suspected Acute Coronary Syndrome: MERITnI Substudy.

Biological Variation of Adrenal-Related Endocrine Biomarkers Used for Investigation of Secondary Hypertension.

Enriching Microbial Cell-Free DNA in Clinical Metagenomics Using Epigenetic Filters.

APOB to Estimated APOB Ratio for Screening for the APOE2 Genotype.

Highly Accurate Sequencing Methods for Low-Frequency Variant Detection.

Prognostic Value of Cardiac Myosin Binding Protein C in the General Population: The Akershus Cardiac Examination 1950 Study.

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

Structural variants contribute substantially to complex trait heritability.

Related Experiment Videos

Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray

Related Concept Videos

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