Related references
Note: Only part of the references are listed.Adapting ACMG/AMP sequence variant classification guidelines for single-gene copy number variants
Tracy Brandt et al.
GENETICS IN MEDICINE (2020)
Novel ZP1 pathogenic variants identified in an infertile patient and a successful live birth following ICSI treatment
Kun Chu et al.
CLINICAL GENETICS (2020)
Borderline form of empty follicle syndrome treated with a novel dual trigger method combined with delayed oocyte retrieval: A case report
Xian-Ling Cao et al.
World Journal of Clinical Cases (2020)
Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect
Ozlem Okutman et al.
GENES (2020)
A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS)
Qianhua Xu et al.
MOLECULAR GENETICS & GENOMIC MEDICINE (2020)
Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome
Mohan Liu et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2020)
Heterozygous mutations in ZP1 and ZP3 cause formation disorder of ZP and female infertility in human
Qiqi Cao et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2020)
Novel mutations inZP1andZP2cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
Geng Luo et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2020)
Novel mutations inLHCGR(luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome
Zhihua Zhang et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2020)
ZP2 pathogenic variants cause in vitro fertilization failure and female infertility
Can Dai et al.
GENETICS IN MEDICINE (2019)
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation
Zhou Zhou et al.
HUMAN GENETICS (2019)
Novel mutation in the ZP1 gene and clinical implications
Ping Yuan et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2019)
Compound heterozygous ZP1 mutations cause empty follicle syndrome in infertile sisters
Ling Sun et al.
HUMAN MUTATION (2019)
A borderline form of empty follicle syndrome treated with a double-trigger of gonadotropin-releasing hormone agonist and human chorionic gonadotropin A case report
Jingyan Song et al.
MEDICINE (2019)
Molecular basis of egg coat cross-linking sheds light on ZP1-associated female infertility
Kaoru Nishimura et al.
NATURE COMMUNICATIONS (2019)
Novel homozygous nonsense mutations in LHCGR lead to empty follicle syndrome and 46, XY disorder of sex development
C. Chen et al.
HUMAN REPRODUCTION (2018)
Infertility due to Lack of Zona Pellucida Caused by a Compound Heterozygous Mutation in ZP1 Gene
Zheng Zhang et al.
REPRODUCTIVE AND DEVELOPMENTAL MEDICINE (2018)
Novel zona pellucida gene variants identified in patients with oocyte anomalies
Ping Yang et al.
FERTILITY AND STERILITY (2017)
Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility
Wenqiang Liu et al.
HUMAN GENETICS (2017)
Genetic evidence of 'genuine' empty follicle syndrome: a novel effective mutation in the LHCGR gene and review of the literature
Ping Yuan et al.
HUMAN REPRODUCTION (2017)
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility
Tailai Chen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
A common 'aggregation-prone' interface possibly participates in the self-assembly of human zona pellucida proteins
Nikolaos N. Louros et al.
FEBS LETTERS (2016)
Dual trigger for final oocyte maturation improves the oocyte retrieval rate of suboptimal responders to gonadotropin-releasing hormone agonist
Xuefeng Lu et al.
FERTILITY AND STERILITY (2016)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
Mutant ZP1 in Familial Infertility
Hua-Lin Huang et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration
Helga Thorvaldsdottir et al.
BRIEFINGS IN BIOINFORMATICS (2013)
Empty follicle syndrome: successful treatment in a recurrent case and review of the literature
R. Beck-Fruchter et al.
HUMAN REPRODUCTION (2012)
Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome
Kemal O. Yariz et al.
FERTILITY AND STERILITY (2011)
The prevalence of genuine empty follicle syndrome
Tolga B. Mesen et al.
FERTILITY AND STERILITY (2011)
Human Sperm Binding Is Mediated by the Sialyl-Lewisx Oligosaccharide on the Zona Pellucida
Poh-Choo Pang et al.
SCIENCE (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Kai Wang et al.
NUCLEIC ACIDS RESEARCH (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Empty follicle syndrome: the reality of a controversial syndrome, a systematic review
Tania Luisa Stevensan et al.
FERTILITY AND STERILITY (2008)
Zona pellucida glycoproteins
Paul M. Wassarman
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
A faster circular binary segmentation algorithm for the analysis of array CGH data
E. S. Venkatraman et al.
BIOINFORMATICS (2007)
Three-dimensional structure of the zona pellucida at ovulation
Giuseppe Familiari et al.
MICROSCOPY RESEARCH AND TECHNIQUE (2006)
Cracking the egg:: increased complexity in the zona pellucida
SJ Conner et al.
HUMAN REPRODUCTION (2005)
Intercellular communication in the mammalian ovary: Oocytes carry the conversation
MM Matzuk et al.
SCIENCE (2002)
A profile of fertilization in mammals
PM Wassarman et al.
NATURE CELL BIOLOGY (2001)
Empty follicle syndrome: evidence for recurrence
TG Zreik et al.
HUMAN REPRODUCTION (2000)
Borderline form of empty follicle syndrome: is it really an entity?
AZ Isik et al.
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY (2000)