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Showing 1 - 12 of 16 for “Genetic Signatures”

All Results (16)Article (16)

Article

[Expert consensus on the diagnosis, exclusion, and follow-up for newborns with positive genetic screening results by next-generation sequencing (2026 Edition)].

Research record from Zhonghua Yi Xue Yi Chuan Xue Za Zhi, 2026-09-01. PMID 42663019.

Article

Direct quantitative PCR detects genetic biomarkers of antileishmanial drug resistance in clinical samples from dogs with leishmaniosis.

Research record from BMC Vet Res, 2026-07-07. PMID 42410421.

Article

Droplet digital PCR as a first-line detection tool in the genetic diagnosis of vascular anomalies.

Research record from Hum Mol Genet, 2026-10-01. PMID 42900767.

Article

From Genomic Diagnosis to Personalized RNA Medicine: Advances in Next-Generation Sequencing and N-of-1 Antisense Oligonucleotide Therapies for Rare Genetic Diseases.

Research record from Genes (Basel), 2026-03-15. PMID 41898852.

Article

Genetic and Clinical Features in TP53-Mutated Patients With Myelodysplastic Neoplasms: A Retrospective Study Based on Next-Generation Sequencing Data.

Research record from Cancer Rep (Hoboken), 2026-06-01. PMID 42213496.

Article

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Research record from Clin Genet, 2026-09-15. PMID 42742065.

Article

Genetic yield of next-generation sequencing for detecting monogenic familial hypercholesterolemia in uzbek patients with coronary artery disease.

Research record from PLoS One, 2026-07-09. PMID 42424361.

Article

Identification of genetic variants associated with monogenic autoinflammatory diseases in patients with Still's disease using next-generation sequencing.

Research record from Immunol Res, 2026-10-01. PMID 42821198.

Article

Integrating deep-exome sequencing and droplet digital PCR for genetic diagnosis of 142 patients with somatic overgrowth and vascular malformation.

Research record from J Med Genet, 2026-10-12. PMID 42864007.

Article

Investigating Genetic Risk to Oxaliplatin-Induced Sinusoidal Obstruction Syndrome in Colorectal Cancer Through Routinely Available Next-Generation Sequencing Data.

Research record from Mod Pathol, 2026-03-03. PMID 41786212.

Article

Nanoparticle-enriched mass spectrometry proteomics in British South Asians identifies links between genetic variants, plasma protein levels and disease risk.

Research record from Nat Genet, 2026-07-24. PMID 42498778.

Article

Next-Generation Sequencing to Identify Genetic Causes of Chinese Patients Affected With Non-retinal Developmental Eye Disorders.

Research record from Hum Mutat, 2026-10-16. PMID 42891061.

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