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Frank Tüttelmann

University of Münster

130

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2328

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A de novo paradigm for male infertility

2021 bioRxiv
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Pituitary response to GnRH stimulation tests in different FSHB-211 G/T genotypes.

2021 Human Reproduction
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Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.

2021 Human Reproduction
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Lack of evidence for a role of PIWIL1 variants in human male infertility.

2021 Cell
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O-118 New insight into the genetic contribution of common variants to the development of extreme phenotypes of unexplained male infertility: a multicenter genome-wide association study

2021 Human Reproduction
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Identifying a genomic region at Chromosome 11p.14.1 that is associated to FSH serum level in men with unexplained male infertility

2021 European Urology
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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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TRIM71 deficiency causes germ cell loss during mouse embryogenesis and promotes human male infertility

2021 bioRxiv
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Can Unlikely Neanderthal Chloride Channel CLC-2 Gene Variants Provide Insights in Modern Human Infertility?

2021 Cellular Physiology and Biochemistry
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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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