|
| 36997603 | DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia. | Commun Biol | 2023 |
| 38073178 | Genome sequencing of Pakistani families with male infertility identifies deleterious genotypes in SPAG6, CCDC9, TKTL1, TUBA3C, and M1AP. | | 2023 |
| 36631630 | Microdeletions and microduplications linked to severe congenital disorders in infertile men. | | 2023 |
| 37316461 | Urinary microRNA profiling in pregnant women identifies placental microRNAs that are candidate biomarkers for monitoring placental health. | | 2023 |
| 36572685 | Diverse monogenic subforms of human spermatogenic failure. | | 2022 |
| 35966513 | Novel Early Pregnancy Multimarker Screening Test for Preeclampsia Risk Prediction. | Frontiers in Cardiovascular Medicine | 2022 |
| 35450731 | Corrigendum to "Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health" [Placenta 116 (2021) 2-11]. | Placenta | 2022 |
| 35821576 | Maternal Pyelonephritis as a Potential Cause of Perinatal Periventricular Venous Infarction in Term-Born Children. | Journal of Child Neurology | 2022 |
| 36078883 | Screening of Gestational Diabetes and Its Risk Factors: Pregnancy Outcome of Women with Gestational Diabetes Risk Factors According to Glycose Tolerance Test Results. | Journal of Clinical Medicine | 2022 |
| 35551712 | Value of soluble fms-like tyrosine kinase-1/placental growth factor test in third trimester of pregnancy for predicting preeclampsia in asymptomatic women. | Journal of Perinatal Medicine | 2022 |
| 35535697 | Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient management. | Human Reproduction | 2022 |
| 35850260 | DDB1- and CUL4-associated factor 12-like protein 1 (Dcaf12l1) is not essential for male fertility in mice. | Developmental Biology | 2022 |
| 34755838 | Translational aspects of novel findings in genetics of male infertility-status quo 2021. | British Medical Bulletin | 2021 |
| 31955275 | Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives. | Human Genetics | 2021 |
| 33781384 | A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humans. | Elife | 2021 |
| 33663810 | Current knowledge on genetic variants shaping placental transcriptome and their link to gestational and postnatal health. | Placenta | 2021 |
| 33296094 | NR5A1 c.991-1GÂ >Â C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance. | Clin Endocrinol (Oxf) | 2021 |
| 34398675 | Recurrent Pregnancy Loss and Concealed Long-QT Syndrome. | J Am Heart Assoc | 2021 |
| 34368147 | Coordinated Expressional Landscape of the Human Placental miRNome and Transcriptome. | Frontiers in Cell and Developmental Biology | 2021 |
| 32755415 | C-allele of rs4769613 Near Represents a High-Confidence Placental Risk Factor for Preeclampsia. | Hypertension | 2020 |
| 32395752 | Single-Tube Multimarker Assay for Estimating the Risk to Develop Preeclampsia. | journal of applied laboratory medicine, The | 2020 |
| 32462745 | The decline of FANCM immunohistochemical expression in prostate cancer stroma correlates with the grade group. | Pathology International | 2020 |
| 31242935 | Parent-of-origin-specific allelic expression in the human placenta is limited to established imprinted loci and it is stably maintained across pregnancy. | Clinical Epigenetics | 2019 |
| 30865269 | Systematic review of the monogenetic causes of male infertility: the first step towards diagnostic gene panels in the andrology clinic. | Human Reproduction | 2019 |
| 31108506 | Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome. | Hum Mol Genet | 2019 |
| 31244887 | The Effect of Genetic Variation on the Placental Transcriptome in Humans. | Frontiers in Genetics | 2019 |
| 29617818 | FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age women. | Human Reproduction | 2018 |
| 30075111 | Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive Azoospermia. | American Journal of Human Genetics | 2018 |
| 30429575 | Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 30224653 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. | Nat Genet | 2018 |
| 27864361 | Causes of male infertility: a 9-year prospective monocentre study on 1737 patients with reduced total sperm counts. | Human Reproduction | 2017 |
| 28345611 | Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families. | Scientific Reports | 2017 |
| 28334513 | The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young men. | Andrology | 2017 |
| 28446590 | Effects of RNA integrity on transcript quantification by total RNA sequencing of clinically collected human placental samples. | FASEB Journal | 2017 |
| 28739976 | Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. | Hypertension | 2017 |
| 29264510 | Genetics of Sex Hormone-Binding Globulin and Testosterone Levels in Fertile and Infertile Men of Reproductive Age. | Journal of the Endocrine Society | 2017 |
| 27603899 | Stanniocalcin-1 Hormone in Nonpreeclamptic and Preeclamptic Pregnancy: Clinical, Life-Style, and Genetic Modulators. | Journal of Clinical Endocrinology and Metabolism | 2016 |
| 27174393 | Response to "Annexin A5 haplotype M2 is not a risk factor for recurrent miscarriages in Northern Europe, is there sufficient evidence?". | Reproductive BioMedicine Online | 2016 |
| 27929073 | RNA sequencing of chorionic villi from recurrent pregnancy loss patients reveals impaired function of basic nuclear and cellular machinery. | Scientific Reports | 2016 |
| 26268791 | Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomes. | Scientific Reports | 2015 |
| 25543204 | CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs. | Human Genetics | 2015 |
| 25666259 | Extensive load of somatic CNVs in the human placenta. | Scientific Reports | 2015 |
| 25820123 | 'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'. | Andrology | 2015 |
| 25853576 | Haplotype phasing and inheritance of copy number variants in nuclear families. | PLoS ONE | 2015 |
| 26135579 | Annexin A5 Promoter Haplotype M2 Is Not a Risk Factor for Recurrent Pregnancy Loss in Northern Europe. | PLoS ONE | 2015 |
| 24954895 | Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. | Am J Hum Genet | 2014 |
| 24718625 | Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T. | PLoS ONE | 2014 |
| 24827138 | Structural genomic variation as risk factor for idiopathic recurrent miscarriage. | Human Mutation | 2014 |
| 23499152 | A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage. | Fertility and Sterility | 2013 |
| 24035309 | Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination. | Placenta | 2013 |