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EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: state‐of‐the‐art 2013

Andrology (Oxford), 2014-01, Vol.2 (1), p.5-19

2014

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Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest

Human reproduction (Oxford), 2019-11, Vol.34 (11), p.2112-2119

2019

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Novel genetic aspects of Klinefelter's syndrome

Molecular human reproduction, 2010-06, Vol.16 (6), p.386-395

2010

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O-153 Unravelling the causes of male infertility: the role of genetics

Human reproduction (Oxford), 2022-06, Vol.37 (Supplement_1)

Tüttelmann, F

2022

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

Human reproduction (Oxford), 2021-12, Vol.37 (1), p.178-189

2021

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Pathogenic gene variants in CCDC39 , CCDC40 , RSPH1 , RSPH9 , HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility

Frontiers in genetics, 2023-02, Vol.14, p.1117821-1117821

2023

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

Cell, 2021-04, Vol.184 (8), p.1941-1942

2021

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Andrologische Diagnostik vor einer reproduktionsmedizinischen Behandlung

Gynäkologische Endokrinologie, 2019-10, Vol.17 (4), p.257-275

2019

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Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes

Andrology (Oxford), 2020-03, Vol.8 (2), p.434-441

2020

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Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

International journal of andrology, 2010-08, Vol.33 (4), p.642-649

2010

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Analysis of copy number variation in men with non‐obstructive azoospermia

Andrology (Oxford), 2022-11, Vol.10 (8), p.1593-1604

2022

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DNA methylation in spermatozoa as a prospective marker in andrology

Andrology (Oxford), 2013-09, Vol.1 (5), p.731-740

2013

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FSHB ‐211G>T stratification for follicle‐stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism

Andrology (Oxford), 2015-11, Vol.3 (6), p.1050-1053

2015

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Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy

International journal of andrology, 2011-08, Vol.34 (4pt1), p.291-298

2011

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Is the FSHR 2039A>G variant associated with susceptibility to testicular germ cell cancer?

Andrology (Oxford), 2018-01, Vol.6 (1), p.176-183

2018

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Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Human reproduction (Oxford), 2014-05, Vol.29 (5), p.1114-1115

2014

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Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Human reproduction (Oxford), 2013-11, Vol.28 (11), p.3155-3160

2013

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ESHRE Task Force on Ethics and Law 21: genetic screening of gamete donors: ethical issues

Human reproduction (Oxford), 2014-07, Vol.29 (7), p.1353-1359

2014

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O-137 Functional characterisation of three human male infertility associated X-linked genes using Drosophila melanogaster as model organism

Human reproduction (Oxford), 2024-07, Vol.39 (Supplement_1)

2024

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Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization – a preliminary report

Andrology (Oxford), 2014-03, Vol.2 (2), p.275-281

2014

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Aquaporins in the human testis and spermatozoa - identification, involvement in sperm volume regulation and clinical relevance

International journal of andrology, 2010-08, Vol.33 (4), p.629-641

2010

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Genetische Aspekte bei Spermatogenesestörungen

Medizinische Genetik, 2011-06, Vol.23 (2), p.259-266

Tüttelmann, F.

2011

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European Academy of Andrology (EAA) guidelines on investigation, treatment and monitoring of functional hypogonadism in males

Andrology (Oxford), 2020-09, Vol.8 (5), p.970-987

2020

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O-089 A Genome Wide Association Study in men with unexplained infertility identifies nine SNPs at the FSHB locus to be associated with Follicle Stimulating Hormone level

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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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

European urology, 2021-06, Vol.79, p.S391

2021

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EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: state‐of‐the‐art 2013

Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest

Novel genetic aspects of Klinefelter's syndrome

O-153 Unravelling the causes of male infertility: the role of genetics

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

Pathogenic gene variants in CCDC39 , CCDC40 , RSPH1 , RSPH9 , HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility

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

Andrologische Diagnostik vor einer reproduktionsmedizinischen Behandlung

Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

Analysis of copy number variation in men with non‐obstructive azoospermia

DNA methylation in spermatozoa as a prospective marker in andrology

FSHB ‐211G>T stratification for follicle‐stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy

Is the FSHR 2039A>G variant associated with susceptibility to testicular germ cell cancer?

Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

Y-chromosome microdeletions are not associated with SHOX haploinsufficiency

ESHRE Task Force on Ethics and Law 21: genetic screening of gamete donors: ethical issues

O-137 Functional characterisation of three human male infertility associated X-linked genes using Drosophila melanogaster as model organism

Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization – a preliminary report

Aquaporins in the human testis and spermatozoa - identification, involvement in sperm volume regulation and clinical relevance

Genetische Aspekte bei Spermatogenesestörungen

European Academy of Andrology (EAA) guidelines on investigation, treatment and monitoring of functional hypogonadism in males

O-089 A Genome Wide Association Study in men with unexplained infertility identifies nine SNPs at the FSHB locus to be associated with Follicle Stimulating Hormone level

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

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