All Stories

  1. CBLL1 is hypomethylated and correlates with cortical thickness in transgender men before gender affirming hormone treatment
  2. The Biological Basis of Gender Incongruence
  3. Editorial: Research in Transgender Healthcare: What Have We Learned and Where Are We Going?
  4. Research in Transgender Healthcare: What Have We Learned and Where are We Going?
  5. The Effects of Testosterone on the Brain of Transgender Men
  6. An Analysis of the Implication of Estrogens and Steroid Receptor Coactivators in the Genetic Basis of Gender Incongruence
  7. Epigenetics Is Implicated in the Basis of Gender Incongruence: An Epigenome-Wide Association Analysis
  8. Implications of the Estrogen Receptor Coactivators SRC1 and SRC2 in the Biological Basis of Gender Incongruence
  9. The (epi)genetic basis of gender incongruence
  10. Effects of adult male rat feminization treatments on brain morphology and metabolomic profile
  11. Analysis of Four Polymorphisms Located at the Promoter of the Estrogen Receptor Alpha ESR1 Gene in a Population With Gender Incongruence
  12. Molecular basis of Gender Dysphoria: androgen and estrogen receptor interaction
  13. Analyses of karyotype by G-banding and high-resolution microarrays in a gender dysphoria population
  14. Genotypes and Haplotypes of the Estrogen Receptor α Gene ( ESR1 ) Are Associated With Female-to-Male Gender Dysphoria
  15. The CYP17 MspA1 Polymorphism and the Gender Dysphoria
  16. Association Study of ERβ, AR, and CYP19A1 Genes and MtF Transsexualism
  17. The (CA)n Polymorphism of ERβ Gene is Associated with FtM Transsexualism
  18. Turner Syndrome and Sex Chromosomal Mosaicism
  19. Tall Stature and Gonadal Dysgenesis in a Non-Mosaic Girl 45,X
  20. Sexual dimorphism in hybrids rats
  21. The expression of brain sexual dimorphism in artificial selection of rat strains
  22. The role of the androgen receptor in CNS masculinization
  23. A Molecular Method for Classifying the Genotypes Obtained in a Breeding Colony from Testicular Feminized (Tfm) Rats
  24. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter→q11::q11→pter)
  25. Fluorescence in situ Hybridization of psu dic(X)(Xpter-Xq21::Xq21-Xpter) in Two Patients with Turner’s Syndrome
  26. Turner syndrome: a study of chromosomal mosaicism
  27. Optical density profile analysis of trypsin‐Giemsa bands in human X‐chromosomes