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X-Chromosome Inactivation Patterns and Androgen Receptor Functionality Influence Phenotype and Social Characteristics as Well as Pharmacogenetics of Testosterone Therapy in Klinefelter Patients

The journal of clinical endocrinology and metabolism, 2004-12, Vol.89 (12), p.6208-6217

2004

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OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotations

BMC bioinformatics, 2023-07, Vol.24 (1), p.300-300

2023

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Pharmacogenetics of FSH Action in the Male

Frontiers in endocrinology (Lausanne), 2019-02, Vol.10, p.47-47

2019

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Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males

European journal of human genetics : EJHG, 2013-09, Vol.21 (9), p.1012-1015

2013

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Non-viral generation of marmoset monkey iPS cells by a six-factor-in-one-vector approach

PloS one, 2015-03, Vol.10 (3), p.e0118424-e0118424

2015

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Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives

Asian journal of andrology, 2014-09, Vol.16 (5), p.669-674

2014

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Separation of somatic and germ cells is required to establish primate spermatogonial cultures

Human reproduction (Oxford), 2014-09, Vol.29 (9), p.2018-2031

2014

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A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

The journal of clinical endocrinology and metabolism, 2022-07, Vol.107 (8), p.2350-2361

2022

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Derivation of male germ cells from bone marrow stem cells

Laboratory investigation, 2006-07, Vol.86 (7), p.654-663

2006

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Epigenetic germline mosaicism in infertile men

Human molecular genetics, 2015-03, Vol.24 (5), p.1295-1304

2015

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Epigenetic regulation of the RHOX homeobox gene cluster and its association with human male infertility

Human molecular genetics, 2014-01, Vol.23 (1), p.12-23

2014

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Testicular blood supply is altered in the 41,XXY Klinefelter syndrome mouse model

Scientific reports, 2020-09, Vol.10 (1), p.14369-14369, Article 14369

2020

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Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism

European journal of endocrinology, 2005-12, Vol.153 (6), p.845

2005

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Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients

The journal of clinical endocrinology and metabolism, 2007-09, Vol.92 (9), p.3458-3465

2007

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Genetic complexity of FSH receptor function

Trends in endocrinology and metabolism, 2005-10, Vol.16 (8), p.368-373

2005

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Maternal Smoking and Developmental Changes in Luteinizing Hormone (LH) and the LH Receptor in the Fetal Testis

The journal of clinical endocrinology and metabolism, 2009-12, Vol.94 (12), p.4688-4695

2009

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Ovarian Response to Follicle-Stimulating Hormone (FSH) Stimulation Depends on the FSH Receptor Genotype

The journal of clinical endocrinology and metabolism, 2000-09, Vol.85 (9), p.3365-3369

2000

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Molecular Aging Markers in Patients with Klinefelter Syndrome

Aging and disease, 2020-06, Vol.11 (3), p.470-476

2020

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De novo methylation in male germ cells of the common marmoset monkey occurs during postnatal development and is maintained in vitro

Epigenetics, 2017-07, Vol.12 (7), p.527-539

2017

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Direct but no transgenerational effects of decitabine and vorinostat on male fertility

PloS one, 2015-02, Vol.10 (2), p.e0117839-e0117839

2015

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The FSHB -211G>T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndrome

European journal of human genetics : EJHG, 2015-05, Vol.23 (5), p.700-703

2015

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Male 41, XXY Mice as a Model for Klinefelter Syndrome: Hyperactivation of Leydig Cells

Endocrinology (Philadelphia), 2010-06, Vol.151 (6), p.2898-2910

2010

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The origin of the RB1 imprint

PloS one, 2013-11, Vol.8 (11), p.e81502-e81502

2013

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Male Hypogonadism Caused by Homozygous Deletion of Exon 10 of the Luteinizing Hormone (LH) Receptor: Differential Action of Human Chorionic Gonadotropin and LH

The journal of clinical endocrinology and metabolism, 2000-06, Vol.85 (6), p.2281-2286

2000

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Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome

European journal of endocrinology, 2010-01, Vol.162 (1), p.169

2010

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X-Chromosome Inactivation Patterns and Androgen Receptor Functionality Influence Phenotype and Social Characteristics as Well as Pharmacogenetics of Testosterone Therapy in Klinefelter Patients

OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotations

Pharmacogenetics of FSH Action in the Male

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males

Non-viral generation of marmoset monkey iPS cells by a six-factor-in-one-vector approach

Bringing epigenetics into the diagnostics of the andrology laboratory: challenges and perspectives

Separation of somatic and germ cells is required to establish primate spermatogonial cultures

A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels

Derivation of male germ cells from bone marrow stem cells

Epigenetic germline mosaicism in infertile men

Epigenetic regulation of the RHOX homeobox gene cluster and its association with human male infertility

Testicular blood supply is altered in the 41,XXY Klinefelter syndrome mouse model

Role of sequence variations of the GnRH receptor and G protein-coupled receptor 54 gene in male idiopathic hypogonadotropic hypogonadism

Clinical, Endocrinological, and Epigenetic Features of the 46,XX Male Syndrome, Compared with 47,XXY Klinefelter Patients

Genetic complexity of FSH receptor function

Maternal Smoking and Developmental Changes in Luteinizing Hormone (LH) and the LH Receptor in the Fetal Testis

Ovarian Response to Follicle-Stimulating Hormone (FSH) Stimulation Depends on the FSH Receptor Genotype

Molecular Aging Markers in Patients with Klinefelter Syndrome

De novo methylation in male germ cells of the common marmoset monkey occurs during postnatal development and is maintained in vitro

Direct but no transgenerational effects of decitabine and vorinostat on male fertility

The FSHB -211G>T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndrome

Male 41, XXY Mice as a Model for Klinefelter Syndrome: Hyperactivation of Leydig Cells

The origin of the RB1 imprint

Male Hypogonadism Caused by Homozygous Deletion of Exon 10 of the Luteinizing Hormone (LH) Receptor: Differential Action of Human Chorionic Gonadotropin and LH

Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome

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