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Top Articles

#TitleJournalYearCitations
1Testosterone Replacement Effectively Inhibits the Development of Experimental Autoimmune Orchitis in Rats: Evidence for a Direct Role of Testosterone on Regulatory T Cell ExpansionJournal of Immunology2011163
2Sperm navigation along helical paths in 3D chemoattractant landscapesNature Communications2015157
3Testicular function and fertility preservation in male cancer patientsBest Practice and Research in Clinical Endocrinology and Metabolism2011147
4The epididymis, cytoplasmic droplets and male fertilityAsian Journal of Andrology2011135
5Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsyJournal of Developmental and Physical Disabilities2011132
6Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only SyndromePLoS ONE2011129
7Fertility preservation in boys: recent developments and new insights †Human Reproduction Open2020122
8Combined Effects of the VariantsFSHB−211G>T andFSHR2039A>G on Male Reproductive ParametersJournal of Clinical Endocrinology and Metabolism2012116
9Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with ObesityCell Metabolism2016110
10Doping with anabolic androgenic steroids (AAS): Adverse effects on non-reproductive organs and functionsReviews in Endocrine and Metabolic Disorders201599
11Sperm competition and the evolution of spermatogenesisMolecular Human Reproduction201482
12Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile malesEuropean Journal of Human Genetics201380
13Specific immune cell and cytokine characteristics of human testicular germ cell neoplasiaHuman Reproduction201676
14ENDOCRINE HISTORY: The history of discovery, synthesis and development of testosterone for clinical useEuropean Journal of Endocrinology201971
15Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male InfertilityAmerican Journal of Human Genetics202068
16Quantitative bioimaging of platinum in polymer embedded mouse organs using laser ablation ICP-MSMetallomics201367
17Aquaporin Isoforms Involved in Physiological Volume Regulation of Murine Spermatozoa1Biology of Reproduction200965
18Semen quality and fertility in adult long-term survivors of childhood acute lymphoblastic leukemiaFertility and Sterility201160
19Epigenetic germline mosaicism in infertile menHuman Molecular Genetics201558
20Causes of hypogonadotropic hypogonadism predict response to gonadotropin substitution in adultsAndrology201657
21Aquaporin AQP11 in the testis: molecular identity and association with the processing of residual cytoplasm of elongated spermatidsReproduction201055
22Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization - a preliminary reportAndrology201454
23Klinefelter SyndromeDeutsches Ärzteblatt International201353
24Aquaporins in the human testis and spermatozoa – identification, involvement in sperm volume regulation and clinical relevanceJournal of Developmental and Physical Disabilities201050
25Presence of histone H3 acetylated at lysine 9 in male germ cells and its distribution pattern in the genome of human spermatozoaReproduction, Fertility and Development201144
26Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca 2+ signalingEMBO Journal202042
27Coiled sperm from infertile patients: characteristics, associated factors and biological implicationHuman Reproduction200940
28Non-Viral Generation of Marmoset Monkey iPS Cells by a Six-Factor-in-One-Vector ApproachPLoS ONE201539
29A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyJournal of Assisted Reproduction and Genetics201738
30A common haplotype of protamine 1 and 2 genes is associated with higher sperm countsJournal of Developmental and Physical Disabilities201037
31CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis moduleNature Communications202036
32Spermatogenic and sperm quality differences in an experimental model of metabolic syndrome and hypogonadal hypogonadismReproduction201135
33Can germ cell neoplasia in situ be diagnosed by measuring serum levels of microRNA371a-3p?Journal of Cancer Research and Clinical Oncology201735
34Disturbed spermatogenesis associated with thickened lamina propria of seminiferous tubules is not caused by dedifferentiation of myofibroblastsHuman Reproduction201132
35Fact or fictionSpermatogenesis201230
36High-resolution analysis of germ cells from men with sex chromosomal aneuploidies reveals normal transcriptome but impaired imprintingClinical Epigenetics201930
37Germ cell dynamics in the testis of the postnatal common marmoset monkey (Callithrix jacchus)Reproduction201028
38DMRT1 mutations are rarely associated with male infertilityFertility and Sterility201428
39Hormonal male contraception in men with normal and subnormal semen parametersJournal of Developmental and Physical Disabilities201127
40The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKAJournal of Biological Chemistry202027
41A germ cell‐specific ageing pattern in otherwise healthy menAging Cell202027
42Ageing in men with normal spermatogenesis alters spermatogonial dynamics and nuclear morphology in Sertoli cellsAndrology201926
43The humanRHOXgene cluster: target genes and functional analysis of gene variants in infertile menHuman Molecular Genetics201625
44FSHB −211 G>T Polymorphism as Predictor for TESE Success in Patients With Unexplained AzoospermiaJournal of Clinical Endocrinology and Metabolism201925
45Healthy ageing and spermatogenesisReproduction202123
46MANAGEMENT OF ENDOCRINE DISEASE: Female sexual dysfunction for the endocrinologistEuropean Journal of Endocrinology202023
47Germ cell loss is associated with fading Lin28a expression in a mouse model for Klinefelter's syndromeReproduction201421
48Aberrant ocular architecture and function in patients with Klinefelter syndromeScientific Reports201721
49FSHB ‐211G>T stratification for follicle‐stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadismAndrology201520
50The FSHB −211G>T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndromeEuropean Journal of Human Genetics201518