Jialing Yu

Hangzhou, 311215, China

Last Updated: 09/26/2026

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Found 12 publications

Application of polygenic risk score-based comprehensive breast cancer risk assessment in preimplantation embryo selection for a BRCA1 mutation carrier

Application of polygenic risk score-based comprehensive breast cancer risk assessment in preimplantation embryo selection for a BRCA1 mutation carrier

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: June 01, 2026

Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.

Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathy.

Journal: Human molecular genetics

Published: November 29, 2022

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.

Journal: Investigative ophthalmology & visual science

Published: June 22, 2021

Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone

Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: January 05, 2020

Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation

Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: January 05, 2020

Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes

Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes

Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Published: January 05, 2020

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

Journal: The Journal of clinical investigation

Published: November 14, 2019

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.

Journal: Human molecular genetics

Published: September 08, 2018

Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinoma.

Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinoma.

Journal: Oncotarget

Published: May 19, 2017

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function.

Journal: Molecular and cellular biology

Published: April 21, 2016

Aminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagy.

Aminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagy.

Journal: PloS one

Published: June 26, 2014

Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells.

Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells.

Journal: Mitochondrion

Published: July 21, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026