Keya Tong

Chongqing Key Laboratory Of Human Embryo Engineering And Precision Medicine
Chongqing, 400016, China

Last Updated: 09/26/2026

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Found 10 publications

Identification of the homozygous truncating mutation in CNTD1 as a novel genetic cause of diminished ovarian reserve.

Identification of the homozygous truncating mutation in CNTD1 as a novel genetic cause of diminished ovarian reserve.

Journal: Genes & diseases

Published: June 03, 2025

Carrier screening and prenatal diagnosis for Spinal muscular atrophy in 17 926 women of reproductive age in Chongqing

Carrier screening and prenatal diagnosis for Spinal muscular atrophy in 17 926 women of reproductive age in Chongqing

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 11, 2025

Are the number of nucleolar precursor body and size of pronuclear correlated with embryo development and ploidy status in 1PN zygotes?: an analysis through the time-lapse monitoring and pre-implantation genetic testing.

Are the number of nucleolar precursor body and size of pronuclear correlated with embryo development and ploidy status in 1PN zygotes?: an analysis through the time-lapse monitoring and pre-implantation genetic testing.

Journal: Zygote (Cambridge, England)

Published: December 13, 2024

ChromInst: a multicentre evaluation of robustness in aneuploidy and structural rearrangement testing.

ChromInst: a multicentre evaluation of robustness in aneuploidy and structural rearrangement testing.

Journal: Journal of translational medicine

Published: November 28, 2024

Identification of the novel homozygous whole exon deletion in MEI1 underlying azoospermia and embryonic arrest in one consanguineous family.

Identification of the novel homozygous whole exon deletion in MEI1 underlying azoospermia and embryonic arrest in one consanguineous family.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: November 10, 2024

Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida.

Novel variants in ZP1, ZP2 and ZP3 associated with empty follicle syndrome and abnormal zona pellucida.

Journal: Reproductive biomedicine online

Published: August 10, 2022

Genetic screening and analysis of TUBB8 variants in females seeking ART.

Genetic screening and analysis of TUBB8 variants in females seeking ART.

Journal: Reproductive biomedicine online

Published: June 20, 2022

Identification and characterization of a novel homozygous splice site variant of PATL2 causing female infertility due to oocyte germinal vesicle arrest.

Identification and characterization of a novel homozygous splice site variant of PATL2 causing female infertility due to oocyte germinal vesicle arrest.

Journal: Frontiers in genetics

Published: June 12, 2022

Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China.

Clinical Utility of Medical Exome Sequencing: Expanded Carrier Screening for Patients Seeking Assisted Reproductive Technology in China.

Journal: Frontiers in genetics

Published: May 13, 2022

Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1.

Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozygous Mutations of MKS1.

Journal: Frontiers in genetics

Published: December 27, 2021

Showing 1-10 of 10

Last Updated: 09/26/2026