A view of Neandertal genetic diversity

Light Dark Matter Search with 7.8 Tonne-Year of Ionization-Only Data in XENONnT.

Physical review letters·2026

Challenging Spontaneous Quantum Collapse with the XENONnT Dark Matter Detector.

Physical review letters·2026

The slow component of oxygen uptake of insulated muscular groups measured with NIRS during intermittent isometric contractions in humans.

Physiological reports·2026

Cardiopulmonary and skeletal muscle strategies underlying exhaustive exercise in adults with glycogen storage disease type III.

Physiological reports·2026

WIMP Dark Matter Search Using a 3.1 Tonne-Year Exposure of the XENONnT Experiment.

Physical review letters·2025

Half-Life and Precision Shape Measurement of the 2νββ Decay of ^{130}Te.

Physical review letters·2025

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Nature genetics·2026

Distinguishing different psychiatric disorders using DDx-PRS.

Nature genetics·2026

Adaptive evolution of polyploid crops.

Nature genetics·2026

Rare variant effect estimation and polygenic risk prediction.

Nature genetics·2026

Spatial analysis of head and neck cancer identifies two ecosystems with distinct modes of epithelial-to-mesenchymal transition.

Nature genetics·2026

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

Nature genetics·2026

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Related Experiment Videos

A view of Neandertal genetic diversity

Related Concept Videos

Light Dark Matter Search with 7.8 Tonne-Year of Ionization-Only Data in XENONnT.

Challenging Spontaneous Quantum Collapse with the XENONnT Dark Matter Detector.

The slow component of oxygen uptake of insulated muscular groups measured with NIRS during intermittent isometric contractions in humans.

Cardiopulmonary and skeletal muscle strategies underlying exhaustive exercise in adults with glycogen storage disease type III.

WIMP Dark Matter Search Using a 3.1 Tonne-Year Exposure of the XENONnT Experiment.

Half-Life and Precision Shape Measurement of the 2νββ Decay of ^{130}Te.

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Distinguishing different psychiatric disorders using DDx-PRS.

Adaptive evolution of polyploid crops.

Rare variant effect estimation and polygenic risk prediction.

Spatial analysis of head and neck cancer identifies two ecosystems with distinct modes of epithelial-to-mesenchymal transition.

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

Related Experiment Videos

A view of Neandertal genetic diversity

Related Concept Videos

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