Yalin Luo

1037 Luoyu Road
Wuhan, 430074, China

Last Updated: 09/26/2026

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Found 11 publications

Ultrahigh-Surface Area Hierarchically Porous Carbon Derived From Sweet Potato Extraction Residue-Syrup for High Performance Supercapacitor.

Ultrahigh-Surface Area Hierarchically Porous Carbon Derived From Sweet Potato Extraction Residue-Syrup for High Performance Supercapacitor.

Journal: Chemistry, an Asian journal

Published: December 31, 2024

GBF1 deficiency causes cataracts in human and mouse.

GBF1 deficiency causes cataracts in human and mouse.

Journal: Human genetics

Published: April 26, 2024

A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family.

A novel mutation in the GALC gene causes Krabbe disease accompanied with extensive Mongolian spots in a consanguineous family.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 08, 2023

A novel homozygous mutation in ACTL7A leads to male infertility.

A novel homozygous mutation in ACTL7A leads to male infertility.

Journal: Molecular genetics and genomics : MGG

Published: September 13, 2022

Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.

Juvenile-Onset Kufs Disease in a Chinese Consanguineous Family due to CLN6 Mutation.

Journal: Neuro-degenerative diseases

Published: December 18, 2021

Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.

Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: August 20, 2021

Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility.

Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: August 16, 2021

Novel mutations in ZP2 and ZP3 cause female infertility in three patients.

Novel mutations in ZP2 and ZP3 cause female infertility in three patients.

Journal: Journal of assisted reproduction and genetics

Published: June 20, 2021

TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure.

TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: December 22, 2020

A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.

A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.

Journal: American journal of medical genetics. Part A

Published: December 09, 2020

A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.

A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.

Journal: Journal of assisted reproduction and genetics

Published: March 19, 2020

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Last Updated: 09/26/2026