Yanping X. Lu

28 Fuxing Road
Beijing, 100853, China

Last Updated: 09/26/2026

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Found 24 publications

Expression and prognosis of NR3C1 in uterine corpus endometrial carcinoma based on multiple datasets.

Expression and prognosis of NR3C1 in uterine corpus endometrial carcinoma based on multiple datasets.

Journal: Discover oncology
Published: October 22, 2024

Tailoring monogenic disease carrier screening panels for Chinese populations: The importance of considering regional differences.

Tailoring monogenic disease carrier screening panels for Chinese populations: The importance of considering regional differences.

Journal: European journal of medical genetics
Published: October 18, 2024

A bearing fault diagnosis method based on hybrid artificial intelligence models.

A bearing fault diagnosis method based on hybrid artificial intelligence models.

Journal: PloS one
Published: October 03, 2024

Expert consensus over genetic counseling for carrier screening of Spinal muscular atrophy

Expert consensus over genetic counseling for carrier screening of Spinal muscular atrophy

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 31, 2024

Expert consensus on the genetic counseling for Dystrophinopathies

Expert consensus on the genetic counseling for Dystrophinopathies

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 31, 2024

Two cases of spontaneous rupture of the uterine artery in the perinatal period: A case report.

Two cases of spontaneous rupture of the uterine artery in the perinatal period: A case report.

Journal: Medicine
Published: June 19, 2023

Application of expanded noninvasive prenatal test in prenatal diagnosis of fetuses with increased nuchal translucency.

Application of expanded noninvasive prenatal test in prenatal diagnosis of fetuses with increased nuchal translucency.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: October 15, 2021

Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield.

Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield.

Journal: Prenatal diagnosis
Published: September 09, 2020

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.

Simultaneous detection of fetal aneuploidy, de novo FGFR3 mutations and paternally derived β-thalassemia by a novel method of noninvasive prenatal testing.

Journal: Prenatal diagnosis
Published: August 07, 2020

Whole-exome sequencing identified two novel mutations of DYNC2LI1 in fetal skeletal ciliopathy.

Whole-exome sequencing identified two novel mutations of DYNC2LI1 in fetal skeletal ciliopathy.

Journal: Molecular genetics & genomic medicine
Published: May 17, 2020

Two novel TCTN2 mutations cause Meckel-Gruber syndrome.

Two novel TCTN2 mutations cause Meckel-Gruber syndrome.

Journal: Journal of human genetics
Published: March 02, 2020

Two novel mutations of COL1A1 in fetal genetic skeletal dysplasia of Chinese.

Two novel mutations of COL1A1 in fetal genetic skeletal dysplasia of Chinese.

Journal: Molecular genetics & genomic medicine
Published: August 20, 2019
Showing 1-12 of 24

Last Updated: 09/26/2026