Maternal NLRP7 and C6orf221 variants are not a common risk factor for androgenetic moles, triploidy and recurrent miscarriage

Mutations inNLRP7are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles

(2012) Peter H Dixon et al.   JOURNAL OF MEDICAL GENETICS

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

Aneuploidy in the Human Cleavage Stage Embryo

(2011) A. Mantzouratou et al.   CYTOGENETIC AND GENOME RESEARCH

NLRP7, a Nucleotide Oligomerization Domain-like Receptor Protein, Is Required for Normal Cytokine Secretion and Co-localizes with Golgi and the Microtubule-organizing Center

(2011) Christiane Messaed et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage

(2011) C. Messaed et al.   JOURNAL OF MEDICAL GENETICS

The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes

(2011) JianHua Qian et al.   MOLECULAR HUMAN REPRODUCTION

Recurrent triploid and dispermic conceptions in patients with NLRP7 mutations

(2011) R. Slim et al.   PLACENTA

The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

(2010) DK Bourque et al.   CLINICAL GENETICS

Genetic variation within the hypothalamus-pituitary-ovarian axis in women with recurrent miscarriage

(2010) Courtney W. Hanna et al.   HUMAN REPRODUCTION

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

HomozygousNLRP7mutations in a Moroccan woman with recurrent reproductive failure

(2009)   CLINICAL GENETICS

Genetic and Epigenetic Analysis of Recurrent Hydatidiform Mole

(2009) Bruce E. Hayward et al.   HUMAN MUTATION

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region

(2009) C M Wang et al.   JOURNAL OF MEDICAL GENETICS

Role of Filia, a maternal effect gene, in maintaining euploidy during cleavage-stage mouse embryogenesis

(2009) P. Zheng et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

NLRP7 mutations in women with diploid androgenetic and triploid moles: a proposed mechanism for mole formation

(2008) Catherine Deveault et al.   HUMAN MOLECULAR GENETICS