Shunyao Liao
Chengdu, China
Last Updated: 09/26/2026
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Found 10 publications
Whole-exome sequencing of de novo genetic variants in a Chinese family with a sporadic case of congenital nonsyndromic hearing loss.
Journal: F1000Research
Published: August 18, 2021
DNA demethylation facilitates the specific transcription of the mouse X-linked Tsga8 gene in round spermatids†.
Journal: Biology of reproduction
Published: June 08, 2018
Heterogeneous impact of type 2 diabetes mellitus-related genetic variants on gestational glycemic traits: review and future research needs.
Journal: Molecular genetics and genomics : MGG
Published: May 02, 2018
Novel compound heterozygous mutations of ALDH1A3 contribute to anophthalmia in a non-consanguineous Chinese family.
Journal: Genetics and molecular biology
Published: May 10, 2016
The Impact of Genetic Variants for Different Physiological Characterization of Type 2 Diabetes Loci on Gestational Insulin Signaling in Nondiabetic Pregnant Chinese Women.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: April 17, 2015
Association of variants in CDKN2A/2B and CDKAL1 genes with gestational insulin sensitivity and disposition in pregnant Han Chinese women.
Journal: Journal of diabetes investigation
Published: August 23, 2014
Familial multinodular goiter syndrome with papillary thyroid carcinomas: mutational analysis of the associated genes in 5 cases from 1 Chinese family.
Journal: BMC endocrine disorders
Published: June 04, 2013
Association of genetic variants of melatonin receptor 1B with gestational plasma glucose level and risk of glucose intolerance in pregnant Chinese women.
Journal: PloS one
Published: January 11, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026