Guoling L. You

Shanghai, China

Last Updated: 09/26/2026

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Found 26 publications

Identification of novel genes involved in pediatric congenital heart disease using trio-based whole genome sequencing.

Identification of novel genes involved in pediatric congenital heart disease using trio-based whole genome sequencing.

Journal: Science bulletin

Published: November 27, 2025

Combined hearing screening and genetic screening of deafness among Sanya newborns in Hainan Province.

Combined hearing screening and genetic screening of deafness among Sanya newborns in Hainan Province.

Journal: International journal of pediatric otorhinolaryngology

Published: March 19, 2025

Simultaneous quantification and pharmacokinetics of vincristine and its major metabolite M1 in Chinese pediatric ALL patients by LC-MS/MS.

Simultaneous quantification and pharmacokinetics of vincristine and its major metabolite M1 in Chinese pediatric ALL patients by LC-MS/MS.

Journal: Journal of pharmaceutical and biomedical analysis

Published: May 05, 2023

Novel dominant-negative FOXJ1 mutation in a family with heterotaxy plus mouse model.

Novel dominant-negative FOXJ1 mutation in a family with heterotaxy plus mouse model.

Journal: Translational pediatrics

Published: January 13, 2023

Corrigendum to "Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene" [Stem Cell Res. 56 (2021) 102517].

Corrigendum to "Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene" [Stem Cell Res. 56 (2021) 102517].

Journal: Stem cell research

Published: May 23, 2022

Molecular Spectrum, Ethnic and Geographical Distribution of Thalassemia in the Southern Area of Hainan, China.

Molecular Spectrum, Ethnic and Geographical Distribution of Thalassemia in the Southern Area of Hainan, China.

Journal: Frontiers in pediatrics

Published: March 11, 2022

Correction to: ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells.

Correction to: ARE/SUZ12 dual specifically-regulated adenoviral TK/GCV system for CML blast crisis cells.

Journal: Journal of experimental & clinical cancer research : CR

Published: February 10, 2022

Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene.

Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene.

Journal: Stem cell research

Published: April 07, 2021

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients.

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients.

Journal: eLife

Published: February 12, 2021

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing.

Identification of the genetic basis of sporadic polydactyly in China by targeted sequencing.

Journal: Computational and structural biotechnology journal

Published: December 17, 2020

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle.

Journal: BMC medical genomics

Published: December 14, 2020

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families.

Nonframeshifting indel variations in polyalanine repeat of HOXD13 gene underlies hereditary limb malformation for two Chinese families.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: August 03, 2020

Showing 1-12 of 26

Last Updated: 09/26/2026