A Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans1
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Title
A Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans1
Authors
Keywords
-
Journal
BIOLOGY OF REPRODUCTION
Volume 93, Issue 3, Pages -
Publisher
Oxford University Press (OUP)
Online
2015-07-23
DOI
10.1095/biolreprod.115.131185
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Note: Only part of the references are listed.- Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility
- (2014) D Lo Giacco et al. JOURNAL OF MEDICAL GENETICS
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- X Chromosome-Linked CNVs in Male Infertility: Discovery of Overall Duplication Load and Recurrent, Patient-Specific Gains with Potential Clinical Relevance
- (2014) Chiara Chianese et al. PLoS One
- Independent specialization of the human and mouse X chromosomes for the male germ line
- (2013) Jacob L Mueller et al. NATURE GENETICS
- Genome-Wide Landscapes of Human Local Adaptation in Asia
- (2013) Wei Qian et al. PLoS One
- Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1
- (2013) Alexandra M. Lopes et al. PLoS Genetics
- AZFc Deletions and Spermatogenic Failure: A Population-Based Survey of 20,000 Y Chromosomes
- (2012) Steven G. Rozen et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development
- (2012) S. Ledig et al. EUROPEAN JOURNAL OF ENDOCRINOLOGY
- Transcriptional regulation of human-specific SVAF1 retrotransposons by cis-regulatory MAST2 sequences
- (2012) Anastasia A. Zabolotneva et al. GENE
- Efficient typing of copy number variations in a segmental duplication-mediated rearrangement hotspot using multiplex competitive amplification
- (2012) Renqian Du et al. JOURNAL OF HUMAN GENETICS
- Additional genomic duplications in AZFc underlie the b2/b3 deletion-associated risk of spermatogenic impairment in Han Chinese population
- (2011) Chuncheng Lu et al. HUMAN MOLECULAR GENETICS
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- 5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome
- (2009) A. Damert et al. GENOME RESEARCH
- The avian Z-linked gene DMRT1 is required for male sex determination in the chicken
- (2009) Craig A. Smith et al. NATURE
- Large, rare chromosomal deletions associated with severe early-onset obesity
- (2009) Elena G. Bochukova et al. NATURE
- Mutation of the Mouse Syce1 Gene Disrupts Synapsis and Suggests a Link between Synaptonemal Complex Structural Components and DNA Repair
- (2009) Ewelina Bolcun-Filas et al. PLoS Genetics
- Comparative Analysis of Testis Protein Evolution in Rodents
- (2008) L. M. Turner et al. GENETICS
- Partial AZFc deletions and duplications: clinical correlates in the Italian population
- (2008) Claudia Giachini et al. HUMAN GENETICS
- A robust statistical method for case-control association testing with copy number variation
- (2008) Chris Barnes et al. NATURE GENETICS
- Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
- (2008) Joshua M Korn et al. NATURE GENETICS
- The biology of infertility: research advances and clinical challenges
- (2008) Martin M Matzuk et al. NATURE MEDICINE
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