Mengmeng Li

Peking Union Medical College Hospital, Chinese Academy Of Medical Science & Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 15 publications

Xq28 duplication not F8 inversion: integrated genetic reanalysis redefines prenatal carrier diagnosis.

Xq28 duplication not F8 inversion: integrated genetic reanalysis redefines prenatal carrier diagnosis.

Journal: Scientific reports

Published: November 17, 2025

A methodological study on the process of prenatal optical genome mapping: focusing on cell culture and quality control.

A methodological study on the process of prenatal optical genome mapping: focusing on cell culture and quality control.

Journal: Molecular cytogenetics

Published: June 24, 2025

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy.

Incidental Identification of Potentially Affected Individuals Through Expanded Carrier Screening During Preconception or Early Pregnancy.

Journal: Prenatal diagnosis

Published: April 30, 2025

The clinical utility of systematic reporting of secondary findings in prenatal diagnosis.

The clinical utility of systematic reporting of secondary findings in prenatal diagnosis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 02, 2025

The distribution of D4Z4 repeats in China and direct prenatal diagnosis of FSHD by optical genome mapping.

The distribution of D4Z4 repeats in China and direct prenatal diagnosis of FSHD by optical genome mapping.

Journal: Orphanet journal of rare diseases

Published: December 23, 2024

Prenatal diagnosis and pregnancy outcomes of mosaicism detected by CMA-seq.

Prenatal diagnosis and pregnancy outcomes of mosaicism detected by CMA-seq.

Journal: BMC pregnancy and childbirth

Published: September 20, 2024

Optical genome mapping to decipher the chromosomal aberrations in families seeking for preconception genetic counseling.

Optical genome mapping to decipher the chromosomal aberrations in families seeking for preconception genetic counseling.

Journal: Scientific reports

Published: August 31, 2024

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia.

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia.

Journal: Prenatal diagnosis

Published: July 22, 2024

Gene Analysis of Four Families with Severe Peripartum Cardiomyopathy Reveals Known Gene Mutations and Supports the Recent Call for Screening.

Gene Analysis of Four Families with Severe Peripartum Cardiomyopathy Reveals Known Gene Mutations and Supports the Recent Call for Screening.

Journal: Reviews in cardiovascular medicine

Published: March 12, 2024

Prenatal diagnosis of recurrent Kagami-Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review.

Prenatal diagnosis of recurrent Kagami-Ogata syndrome inherited from a mother affected by Temple syndrome: a case report and literature review.

Journal: BMC medical genomics

Published: March 02, 2024

Study of a fetus with confined placental mosaicism for trisomy 2 in conjunct with fetal uniparental disomy and a literature review

Study of a fetus with confined placental mosaicism for trisomy 2 in conjunct with fetal uniparental disomy and a literature review

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

Published: November 23, 2023

Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting.

Contribution of uniparental disomy to fetal growth restriction: a whole-exome sequencing series in a prenatal setting.

Journal: Scientific reports

Published: September 12, 2023

Showing 1-12 of 15

Last Updated: 09/26/2026