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Research 751–780 of 1000+
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Chronic overlapping pain conditions and nociplastic pain
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- The Enticing Path of miR Therapeutics: Difficult but Not without Prospects
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- A genetically informed brain atlas for enhancing brain imaging genomics
- Characterisation of Four New Genes in the Ovine KAP19 Family
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Genetic Variants and Protective Immunity against SARS-CoV-2
- The potential impact of melanosomal pH and metabolism on melanoma
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Improving human forensics through advances in genetics, genomics and molecular biology
- Epigenetics of Colorectal Cancer
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- 4 Vitamin D resistance
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Rizatriptan benzoate-loaded dissolving microneedle patch for management of acute migraine therapy
- Past, Present and Future Perspectives of Forensic Genetics