Yuanyuan U. Xiao

Taishan North Road #173
Deyang, 618000, China

Last Updated: 09/26/2026

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Found 65 publications

Development and Evaluation of a Novel Microhaplotype Panel for DNA Mixture and Kinship Analysis.

Development and Evaluation of a Novel Microhaplotype Panel for DNA Mixture and Kinship Analysis.

Journal: Electrophoresis

Published: December 26, 2025

Kinship Inferences for Second-Degree Relatives With a Combination of STRs and Microhaplotypes.

Kinship Inferences for Second-Degree Relatives With a Combination of STRs and Microhaplotypes.

Journal: Electrophoresis

Published: August 28, 2025

Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK-Related Disorders.

Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK-Related Disorders.

Journal: Prenatal diagnosis

Published: August 28, 2025

From decline to rebound: a 25-year Joinpoint analysis of tuberculosis mortality in the United States, 1999-2023.

From decline to rebound: a 25-year Joinpoint analysis of tuberculosis mortality in the United States, 1999-2023.

Journal: BMC infectious diseases

Published: August 19, 2025

Fetal Phenotype and Diagnosis of Treacher Collins Syndrome Due to a Novel POLR1D Variant.

Fetal Phenotype and Diagnosis of Treacher Collins Syndrome Due to a Novel POLR1D Variant.

Journal: Prenatal diagnosis

Published: August 19, 2025

A Novel Homozygous Frameshift Variant in the FLVCR1 Gene Is Associated With Prenatal Microcephaly, Multiple Brain Structural Anomalies, and Abnormal Foot Posture.

A Novel Homozygous Frameshift Variant in the FLVCR1 Gene Is Associated With Prenatal Microcephaly, Multiple Brain Structural Anomalies, and Abnormal Foot Posture.

Journal: Prenatal diagnosis

Published: July 23, 2025

Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese Families.

Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese Families.

Journal: Genetic testing and molecular biomarkers

Published: April 29, 2025

Genetic diagnosis and prenatal diagnosis of patients with cystic kidney disease in Southwest China.

Genetic diagnosis and prenatal diagnosis of patients with cystic kidney disease in Southwest China.

Journal: BMC nephrology

Published: April 09, 2025

Prenatal Phenotype of a Heterozygous Missense CHD4 Variant in a Fetus With Widened Cerebral Subarachnoid Space, Increased Head Circumference and Polyhydramnios.

Prenatal Phenotype of a Heterozygous Missense CHD4 Variant in a Fetus With Widened Cerebral Subarachnoid Space, Increased Head Circumference and Polyhydramnios.

Journal: Prenatal diagnosis

Published: March 28, 2025

Targeted exome sequencing for molecular diagnosis of pediatric Alport syndrome in Southwest China.

Targeted exome sequencing for molecular diagnosis of pediatric Alport syndrome in Southwest China.

Journal: Frontiers in genetics

Published: February 21, 2025

Ibuprofen exposure interferes with the mitochondrial dynamics processes and affects lipid metabolism in the yellowstripe goby (Mugilogobius chulae).

Ibuprofen exposure interferes with the mitochondrial dynamics processes and affects lipid metabolism in the yellowstripe goby (Mugilogobius chulae).

Journal: Aquatic toxicology (Amsterdam, Netherlands)

Published: January 22, 2025

Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing.

Corrigendum: Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing.

Journal: Frontiers in genetics

Published: January 06, 2025

Showing 1-12 of 65

Last Updated: 09/26/2026