An M1AP homozygous splice‐site mutation associated with severe oligozoospermia in a consanguineous family

A systematic review and standardized clinical validity assessment of male infertility genes

(2019) Manon S Oud et al.   HUMAN REPRODUCTION

Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations

(2019) Weili Wang et al.   JOURNAL OF MEDICAL GENETICS

A homozygous FANCM frameshift pathogenic variant causes male infertility

(2018) Hao Yin et al.   GENETICS IN MEDICINE

Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans

(2017) Yue-Qiu Tan et al.   GENETICS IN MEDICINE

CDC14A phosphatase is essential for hearing and male fertility in mouse and human

(2017) Ayesha Imtiaz et al.   HUMAN MOLECULAR GENETICS

Spata19is critical for sperm mitochondrial function and male fertility

(2015) Yongjie Mi et al.   MOLECULAR REPRODUCTION AND DEVELOPMENT

A unique view on male infertility around the globe

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

Control of mammalian germ cell entry into meiosis

(2013) Chun-Wei Feng et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Meiosis I Arrest Abnormalities Lead to Severe Oligozoospermia in Meiosis 1 Arresting Protein (M1ap)-Deficient Mice1

(2012) Nelson Alexander Arango et al.   BIOLOGY OF REPRODUCTION

World Health Organization reference values for human semen characteristics*‡

(2009) Trevor G. Cooper et al.   HUMAN REPRODUCTION UPDATE

The biology of infertility: research advances and clinical challenges

(2008) Martin M Matzuk et al.   NATURE MEDICINE