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Manon S. Oud

Radboud University Nijmegen

19

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115

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Lack of evidence for a role of PIWIL1 variants in human male infertility.

2021 Cell
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A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships.

2021 Human Reproduction Update
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Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.

2021 Human Reproduction
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Variant PNLDC1, Defective piRNA Processing, and Azoospermia

2021 The New England Journal of Medicine
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TRIM71 deficiency causes germ cell loss during mouse embryogenesis and promotes human male infertility

2021 bioRxiv
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TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility

2021 Frontiers in Cell and Developmental Biology
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A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships

2021 medRxiv
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A de novo paradigm for male infertility

2021
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Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure

2021 Human Genetics
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Disease gene discovery in male infertility: past, present and future.

2020 Human Genetics
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Citations (19)