Associated Papers
Analysis of genes implicated in non-obstructive azoospermia.
Wang J et al.
Steroids, 2025
Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia.
Malcher A et al.
Andrology, 2022
Analysis of variants in GATA4 and FOG2/ZFPM2 demonstrates benign contribution to 46,XY disorders of sex development.
van den Bergen JA et al.
Molecular Genetics & Genomic Medicine, 2020
Loss of Gata4 in Sertoli cells impairs the spermatogonial stem cell niche and causes germ cell exhaustion by attenuating chemokine signaling.
Chen SR et al.
Oncotarget, 2015
Human sex-determination and disorders of sex-development (DSD).
Bashamboo A et al.
Seminars in Cell & Developmental Biology, 2015
Genetic mutations and somatic anomalies in association with 46,XY gonadal dysgenesis.
Bastian C et al.
Fertility and Sterility, 2015
Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determination.
Bashamboo A et al.
Human Molecular Genetics, 2014
Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4.
Zhang W et al.
Plos One, 2014
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