Haplotype diversity of two Y-chromosomal SNPs in Chinese populations

[Influencing factors of nutritional anemia in children and adolescents aged 6-17 years in China].

Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi·2025

Methylation Mesa define functional regulatory elements for targeted gene activation.

Research square·2024

Dual-faced SH3BGRL: oncogenic in mice, tumor suppressive in humans.

Oncogene·2015

Effect of IL-18 gene promoter polymorphisms on prostate cancer occurrence and prognosis in Han Chinese population.

Genetics and molecular research : GMR·2013

Plasma ghrelin levels and weight loss in Chinese Uygur patients with chronic obstructive pulmonary disease.

The Journal of international medical research·2008

Performance evaluation of a scent transfer unit for sampling of explosives and their residues to investigate nuisance alerts.

Journal of forensic sciences·2026

Defining overkill homicide through quantitative criteria: Evidence from a retrospective forensic study over a 34-year period in a Tunisian forensic center.

Journal of forensic sciences·2026

Recording living and postmortem friction ridge patterns using image processing and a fiber-optic-inspired total internal reflection method.

Journal of forensic sciences·2026

Reading between the lesions: Recognizing intent in pediatric burn injuries.

Journal of forensic sciences·2026

Dura mater-preserving technique for fetal brain extraction after intrauterine death with prolonged retention.

Journal of forensic sciences·2026

Field validation of blow fly age estimation methods for determining time of placement of human remains in Tennessee, USA.

Journal of forensic sciences·2026

Genetic covariance between plant biparental populations: concept and estimation.

Heredity·2026

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

iScience·2026

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Journal of equine science·2026

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Frontiers in medicine·2026

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

EBioMedicine·2026

Cross-Ethnic Replication of Intersectin-1 as a Parkinson's Disease Susceptibility Gene in a Large Chinese Cohort.

Movement disorders : official journal of the Movement Disorder Society·2026

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Haplotype diversity of two Y-chromosomal SNPs in Chinese populations

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[Influencing factors of nutritional anemia in children and adolescents aged 6-17 years in China].

Methylation Mesa define functional regulatory elements for targeted gene activation.

Dual-faced SH3BGRL: oncogenic in mice, tumor suppressive in humans.

Effect of IL-18 gene promoter polymorphisms on prostate cancer occurrence and prognosis in Han Chinese population.

Plasma ghrelin levels and weight loss in Chinese Uygur patients with chronic obstructive pulmonary disease.

Performance evaluation of a scent transfer unit for sampling of explosives and their residues to investigate nuisance alerts.

Defining overkill homicide through quantitative criteria: Evidence from a retrospective forensic study over a 34-year period in a Tunisian forensic center.

Recording living and postmortem friction ridge patterns using image processing and a fiber-optic-inspired total internal reflection method.

Reading between the lesions: Recognizing intent in pediatric burn injuries.

Dura mater-preserving technique for fetal brain extraction after intrauterine death with prolonged retention.

Field validation of blow fly age estimation methods for determining time of placement of human remains in Tennessee, USA.

Genetic covariance between plant biparental populations: concept and estimation.

T2T-CHM13 reference genome reduces mapping bias and enhances alignment accuracy at disease-associated variants.

Genome-wide exploration of coat color-associated loci in Hokkaido Native Horses, with a novel locus implicated in the roan phenotype.

Diagnostic limitations of routine low-coverage CNV-seq in detecting mosaic paternal uniparental disomy in Beckwith-Wiedemann syndrome: a case report.

Cataract GWAS meta-analysis and multi-omics Mendelian randomisation inform disease mechanisms and candidate target prioritisation.

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Haplotype diversity of two Y-chromosomal SNPs in Chinese populations

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