Yinan Ma

Beijing, China

Last Updated: 09/26/2026

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Found 26 publications

Carrier rates for recessive monogenic diseases in the Chinese Han population: a systematic review.

Carrier rates for recessive monogenic diseases in the Chinese Han population: a systematic review.

Journal: Human genomics

Published: October 26, 2025

A Novel Fetal Intracranial Measurement Contributing to the Differential Diagnosis of Fetal Microcephaly.

A Novel Fetal Intracranial Measurement Contributing to the Differential Diagnosis of Fetal Microcephaly.

Journal: Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine

Published: September 08, 2025

EC-Less High-Entropy Electrolytes Enabling High-Safety and Durable Ni-Rich Lithium-Ion Batteries.

EC-Less High-Entropy Electrolytes Enabling High-Safety and Durable Ni-Rich Lithium-Ion Batteries.

Journal: Small (Weinheim an der Bergstrasse, Germany)

Published: August 17, 2025

Relationship between prenatal ultrasound signs and genetic abnormalities for fetal malformations of cortical development.

Relationship between prenatal ultrasound signs and genetic abnormalities for fetal malformations of cortical development.

Journal: Ultraschall in der Medizin (Stuttgart, Germany : 1980)

Published: December 19, 2024

A de novo novel variant in the MT-TD gene is associated with prominent extra-neurologic manifestations.

A de novo novel variant in the MT-TD gene is associated with prominent extra-neurologic manifestations.

Journal: Clinical genetics

Published: May 25, 2024

Retrospective analysis of the prognostic factors of fetal corpus callosum dysplasia.

Retrospective analysis of the prognostic factors of fetal corpus callosum dysplasia.

Journal: BMC pregnancy and childbirth

Published: October 14, 2023

Inconsistencies between prenatal diagnostic and genetic testing laboratories on variant validation of rare monogenic diseases.

Inconsistencies between prenatal diagnostic and genetic testing laboratories on variant validation of rare monogenic diseases.

Journal: Prenatal diagnosis

Published: September 26, 2023

Case report: mitochondrial diabetes mellitus in a Chinese family due to m.3243A>G.

Case report: mitochondrial diabetes mellitus in a Chinese family due to m.3243A>G.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: February 04, 2023

Reasons and Resolutions for Inconsistent Variant Interpretation.

Reasons and Resolutions for Inconsistent Variant Interpretation.

Journal: Human mutation

Published: December 01, 2022

Correlation of Phenotype-Genotype and Protein Structure in RYR1-Related Myopathy.

Correlation of Phenotype-Genotype and Protein Structure in RYR1-Related Myopathy.

Journal: Frontiers in neurology

Published: February 06, 2022

Spectrum peak detection algorithm based on trend accumulation without base deduction

Spectrum peak detection algorithm based on trend accumulation without base deduction

Journal: Se pu = Chinese journal of chromatography

Published: July 06, 2021

Genetic analysis and prenatal diagnosis of 76 Chinese families with X-linked adrenoleukodystrophy.

Genetic analysis and prenatal diagnosis of 76 Chinese families with X-linked adrenoleukodystrophy.

Journal: Molecular genetics & genomic medicine

Published: June 20, 2021

Showing 1-12 of 26

Last Updated: 09/26/2026