Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure

Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations

(2020) Lin Zhao et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest

(2019) Jian Mu et al.   JOURNAL OF MEDICAL GENETICS

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility

(2019) Ling Wu et al.   JOURNAL OF HUMAN GENETICS

Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest

(2019) Wenjing Wang et al.   JOURNAL OF MEDICAL GENETICS

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles

(2018) JianHua Qian et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family

(2018) M Ben Khelifa et al.   HUMAN REPRODUCTION

The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients

(2018) Ngoc Minh Phuong Nguyen et al.   MODERN PATHOLOGY

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest

(2018) Xueqian Wang et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Clinical and genetic-epigenetic aspects of recurrent hydatidiform mole: A review of literature

(2018) Najmeh Moein-Vaziri et al.   Taiwanese Journal of Obstetrics & Gynecology

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

(2018) Ngoc Minh Phuong Nguyen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

(2018) Biaobang Chen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Hydatidiform moles among patients with incomplete abortion in Mwanza City, North western Tanzania

(2016) Bernard Kitange et al.   African Health Sciences

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest

(2016) Yao Xu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The subcortical maternal complex: multiple functions for one biological structure?

(2016) D. Bebbere et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Mutations inTUBB8cause a multiplicity of phenotypes in human oocytes and early embryos

(2016) Ruizhi Feng et al.   JOURNAL OF MEDICAL GENETICS

Zygotic Genome Activation During the Maternal-to-Zygotic Transition

(2014) Miler T. Lee et al.   Annual Review of Cell and Developmental Biology

Identification of a human subcortical maternal complex

(2014) K. Zhu et al.   MOLECULAR HUMAN REPRODUCTION

Prevalence of infertility in the United States as estimated by the current duration approach and a traditional constructed approach

(2013) Marie E. Thoma et al.   FERTILITY AND STERILITY

Recurrent implantation failure: definition and management

(2013) C. Coughlan et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

(2011) David A. Parry et al.   AMERICAN JOURNAL OF HUMAN GENETICS

International Committee for Monitoring Assisted Reproductive Technology (ICMART) and the World Health Organization (WHO) revised glossary of ART terminology, 2009∗

(2009) F. Zegers-Hochschild et al.   FERTILITY AND STERILITY