Yi He - Publications

Exome-based preconception carrier testing for consanguineous couples in China.

Journal: Prenatal diagnosis

Published: May 17, 2021

Recurrent Wilms tumor in a Chinese family caused by a novel WT1 variant inherited from a mosaic parent.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: August 28, 2020

Co-occurrence of two rare genetic diseases: A potential pitfall for prenatal diagnosis in successive pregnancies.

Journal: Prenatal diagnosis

Published: April 03, 2020

Prenatal genetic diagnosis of cardiac rhabdomyoma: A single-center experience.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: January 29, 2020

Early prenatal detection of triploidy: a 9-year experience in mainland China.

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: December 20, 2019

Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management.

Journal: Prenatal diagnosis

Published: September 21, 2019

Carnitine palmitoyltransferase II deficiency in a prenatal case with polycystic kidney disease-like phenotype.

Journal: Congenital anomalies

Published: August 01, 2019

A prenatal case of osteogenesis imperfecta diagnosed with next-generation sequencing.

Journal: Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology

Published: March 21, 2017