A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest

A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review

(2018) Yanwei Sha et al.   BMC Medical Genetics

Point-of-care whole-exome sequencing of idiopathic male infertility

(2018) Khalid A Fakhro et al.   GENETICS IN MEDICINE

A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes

(2017) Moran Gershoni et al.   GENETICS IN MEDICINE

Analysis of protein-coding genetic variation in 60,706 humans

(2016) Monkol Lek et al.   NATURE

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse

(2015) F. Yang et al.   EMBO Molecular Medicine

X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men

(2015) Alexander N. Yatsenko et al.   NEW ENGLAND JOURNAL OF MEDICINE

BioGPS: building your own mash-up of gene annotations and expression profiles

(2015) Chunlei Wu et al.   NUCLEIC ACIDS RESEARCH

A unique view on male infertility around the globe

(2015) Ashok Agarwal et al.   Reproductive Biology and Endocrinology

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

(2015) et al.   SCIENCE

The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease

(2014) Janan T. Eppig et al.   NUCLEIC ACIDS RESEARCH

Reduced selection and accumulation of deleterious mutations in genes exclusively expressed in men

(2014) Moran Gershoni et al.   Nature Communications

Risks of Reproducing with a Genetic Disorder

(2013) Robert Lebel et al.   SEMINARS IN REPRODUCTIVE MEDICINE

MEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombination

(2013) Mengcheng Luo et al.   Nature Communications

MEIOB Targets Single-Strand DNA and Is Necessary for Meiotic Recombination

(2013) Benoit Souquet et al.   PLoS Genetics

Mendelian genetics of male infertility

(2011) Kathleen Hwang et al.   Annals of the New York Academy of Sciences

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH