Widespread DNA hypomethylation and differential gene expression in Turner syndrome

Trolle, Christian, Nielsen, Morten Muhlig, Skakkebæk, Anne, Lamy, Philippe, Vang, Søren, Hedegaard, Jakob, Nordentoft, Iver, Ørntoft, Torben Falck +2 more·2016·Scientific Reports

Cited by (158)

Items 101–158 of 158

  1. The TGFβ system and TIMP1 and 3 genotypes in Turner syndrome—Relation with aortic congenital malformations
    Lukas Ochsner Reynaud Ridder, Kirstine Stochholm, Kristian Havmand Mortensen, N.H. Andersen, Claus Højbjerg Gravholt · 2023 · Clinical Endocrinology
  2. Survey of gene, lncRNA and transposon transcription patterns in four mouse organs highlights shared and organ-specific sex-biased regulation
    Qinwei Kim-Wee Zhuang, Klara Bauermeister, José Héctor Gálvez, Najla AlOgayil, Enkhjin Batdorj, Fernando Pardo‐Manuel de Villena, Teruko Taketo, Guillaume Bourque, Anna K. Naumova · 2025 · Genome biology
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    Vinayak S. Biradar, Shriram N. Rajpathak, Suraj R. Joshi, Deepti Dileep Deobagkar · 2021 · In Vitro Cellular & Developmental Biology - Animal
  4. DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore Sequencing
    Xin Fan, Beibei Zhang, Lijun Fan, Jiajia Chen, Chang Su, Bingyan Cao, Liya Wei, Miao Qin, Chunxiu Gong · 2022 · Journal of Personalized Medicine
  5. Reliable detection of sex chromosome abnormalities by quantitative fluorescence polymerase chain reaction
    Camilla Mains Balle, Dorte Launholt Lildballe, Ivonne Alexandra Bedei, Ruth Luschka, Anne H Skakkebaek, Simon Chang, Zeynep Agirman, Jan Keller, Axel Weber, Ramón E. Schäfer et al. · 2025 · Clinical Chemistry and Laboratory Medicine (CCLM)
  6. Epigenetics: Future prospective in human disorders and therapeutics
    Shriram N. Rajpathak, Vinayak S. Biradar, Deepti Dileep Deobagkar · 2021 · Elsevier eBooks
  7. Rethinking rare disease: longevity-enhancing drug targets through X-linked aneuploidy
    Jake P. Taylor‐King · 2021 · Trends in Genetics
  8. PGCLCs of human 45,XO reveal pathogenetic pathways of neurocognitive and psychosocial disorders
    Dantong Shang, Tian Lan, Yue Wang, Xuanyu Li, Quanyi Liu, Huimin Dong, Bo Xu, Hanhua Cheng, Rongjia Zhou · 2022 · Cell & Bioscience
  9. Adult Care of Turner Syndrome
    Claus Højbjerg Gravholt, Mette Hansen Viuff, Kirstine Stochholm, N.H. Andersen · 2018 · Elsevier eBooks
  10. Rare Turner syndrome and lupus coexistence with insights from DNA methylation patterns
    Gülşah Kavrul Kayaalp, Desiré Casares‐Marfil, Sezgin Şahin, Özgür Kasapçopur, Betül Sözeri, Nuray Aktay Ayaz, Amr H. Sawalha · 2024 · Clinical Immunology
  11. International Symposium on Ruminant Physiology: Developmental epigenetics—Understanding genetic and sexually dimorphic responses to parental diet and outcomes following assisted reproduction
    Kevin D. Sinclair · 2024 · Journal of Dairy Science
  12. Associations of Karyotype and Age at Diagnosis with Physical Features and Comorbidities in Turner Syndrome: A Single-Site Experience
    Beáta Vida, Olga Török, Enikő Felszeghy, Mónika Orosz, Zoárd Tibor Krasznai, Zoltán Tándor, Attila Jakab, Tamás Deli · 2025 · The Application of Clinical Genetics
  13. Characterizing the Human Fetal Perimeiotic 45,X Ovary at Single-Cell Resolution
    Sinead Mary McGlacken-Byrne, Ignacio del Valle, Theodoros Xenakis, Jenifer P. Suntharalingham, Lydia Nel, Danielle Liptrot, Berta Crespo, Olumide Kayode Ogunbiyi, Paola Niola, Tony Brooks et al. · 2025 · Journal of the Endocrine Society
  14. Epigenetic age acceleration in Turner and Klinefelter syndrome: Correlations with clinical aging markers
    Emma Bruun Johannsen, Jesper Just, Simon Chang, Anne H Skakkebaek, Claus Højbjerg Gravholt · 2025 · Clinical Epigenetics
  15. Integrative Analyses of Genes Associated With Otologic Disorders in Turner Syndrome
    Ruoyan Xue, Qi Tang, Yongli Zhang, Mengyao Xie, Chen Li, Shu Wang, Hua Yang · 2022 · Frontiers in Genetics
  16. When Does the Epigenome Become “Sexy”?
    Anna K. Naumova · 2018 · BioEssays
  17. The pattern of X-inactivation in Human X-linked Disorders and their Model Organisms: A literature review
    Yixin Zhou · 2020 · E3S Web of Conferences
  18. The Heart and Vasculature in Turner Syndrome: Development, Surveillance, and Management
    Luciana Young, Michael Silberbach · 2020 · Springer eBooks
  19. Molecular Mechanisms of Distinct Diseases
    Adnan Batman, İrem Yalım Camcı, Elif Kadioglu, Kezban Uçar Çifci, Berçem Yeman-Kıyak, Servet Tunoğlu, Ezgi Nurdan Yenilmez Tunoğlu, Yusuf Tutar · 2021 · IntechOpen eBooks
  20. Inverse regulatory mechanisms in aneuploidy
    Shuai Zhang, Lin Sun · 2022 · Scientia Sinica Vitae
  21. Human X-chromosome inactivation: Complexity and clinical implications
    María José Navarro-Cobos, Karanveer Bhangu, Carolyn J. Brown · 2023 · Elsevier eBooks
  22. Genetics of Sex Differences in Immunity
    Shani Talia Gal-Oz, Tal Shay · 2023 · Current topics in microbiology and immunology
  23. Lebensqualität von kleinwüchsigen Kindern und Jugendlichen und Wachstumshormontherapie
    Julia Quitmann, Gerhard Binder, Stefanie Witt, Monika Bullinger, Janika Blömeke, Susanne Fricke‐Otto, Berthold P. Hauffa, Sabine Kahrs, Carl‐Joachim Partsch, Anja Christine Rohenkohl et al. · 2023 · Monatsschrift Kinderheilkunde
  24. Stem cell epigenetics in development and disease
    Wei Qiang Seow, Lillian Yuxian Lim, Dewei Kong, Adrian Kee Keong Teo · 2023 · Elsevier eBooks
  25. System biology approach to delineate expressional difference in the blood mononuclear cells between healthy and Turner syndrome individuals
    Anam Farooqui, Naaila Tamkeen, Safia Tazyeen, Sher Ali, Romana Ishrat · 2024 · Egyptian Journal of Medical Human Genetics
  26. A Turner-szindróma áttekintése az újabb genetikai ismeretek és a multidiszciplináris beteggondozás tekintetében
    Nikolett Jusztina Beniczky, Nikolette Szücs, Balázs Gellén, Rita Ágnes Bertalan · 2024 · Orvosi Hetilap
  27. Genetic analysis of Turner syndrome in Tunisian patients
    Olfa Siala, Fatma Laadhar, Mouna Feki Mnif, Wajdi Sefi, Faten Hadj Kacem, Mohamed A. Kessentini, Mohamed Abid, Faïza Fakhfakh · 2023 · Journal of The Arab Society for Medical Research
  28. Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner Syndrome
    Miriam Beatriz Goulart, Eduardo Vieira Neto, Daniela R. Ney Garcia, Marilia Martins Guimarães, Isaías Soares de Paiva, Karina de Ferran, Nathalia Correia Krause dos Santos, Luciana Santos Barbosa, Amanda Faria de Figueiredo, Maria Cecília Menks Ribeiro et al. · 2024 · Life
  29. Survey of gene, lncRNA and transposon transcription patterns in four mouse organs highlights shared and organ-specific sex-biased regulation
    Qinwei Kim-Wee Zhuang, Klara Bauermeister, José Héctor Gálvez, Najla AlOgayil, Enkhjin Batdorj, Fernando Pardo‐Manuel de Villena, Teruko Taketo, Guillaume Bourque, Anna K. Naumova · 2024 · bioRxiv (Cold Spring Harbor Laboratory)
  30. Turner Syndrome
    Preeti Singh, Sangeeta Yadav · 2024 · Springer eBooks
  31. Adult care of Turner syndrome women
    Claus Højbjerg Gravholt · 2024 · Elsevier eBooks
  32. Abnormal methylation of ST8SIA4 in low-motility sperm: A genome-wide identification approach
    Chia‐Ching Chang, Li‐Chun Liu, Yu-Ting Chou, Chia-Wei Chen, Chih-Chi Guo, Chying‐Chyuan Chan, Ta-Jen Lin, C H Chen, Ming-Tzeung Chung · 2025 · Taiwanese Journal of Obstetrics and Gynecology
  33. Clinical analysis of karyotypes and phenotypes in 87 cases of Turner syndrome during transitional period
    Juan Luo, Luhong Yang, Hongxi Guo, Hui Jun Yao, Xiaohong Chen, Lifang Feng · 2025 · BMC Pediatrics
  34. Turner disease: A contemporary clinical approach
    Milina Tančić‐Gajić, Bojana Tesla, Marija Miletić, Milos M. Stojanovic, Svetlana Vujović · 2025 · Medicinska istrazivanja
  35. Clinical and Genotypic Insights into Turner Syndrome
    Mounam Chattopadhyay, Anindya Mukherjee, Pranab Kumar Sahana · 2025 · Journal of the ASEAN Federation of Endocrine Societies
  36. Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy X
    Ekaterina N. Tolmacheva, Д. И. Жигалина, Oksana Yu. Vasilyeva, Victoria V. Demeneva, S. A. Filatova, Daniil G. Shevtsov, Е. А. Фонова, Elena A. Sazhenova, Nikitina Tv, И. Н. Лебедев et al. · 2025 · Journal of Assisted Reproduction and Genetics
  37. Additional file 8 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
  38. Additional file 1 of X chromosome dosage and the genetic impact across human tissues
    Mette Hansen Viuff, Anne H Skakkebaek, Emma Bruun Johannsen, Simon Chang, Steen B. Pedersen, Katrine Meyer Lauritsen, Pedersen, Mette Glavind Bülow, Christian Trolle, Jesper Just, Gravholt, Claus H. · 2023 · Figshare
  39. Additional file 1 of A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta
    Amy M. Inkster, Victor Yuan, Chaini Konwar, Allison Matthews, Carolyn J. Brown, Wendy P. Robinson · 2021 · Figshare
  40. Additional file 2 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis
    Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Woo, Marcel S., Lena Kristina Pfeffer, Jana K. Sonner, Uwe Borgmeyer et al. · 2024 · Figshare
  41. Additional file 1 of System biology approach to delineate expressional difference in the blood mononuclear cells between healthy and Turner syndrome individuals
    Anam Farooqui, Naaila Tamkeen, Safia Tazyeen, Ali, Sher, Romana Ishrat · 2024 · Figshare
  42. Additional file 1 of Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolism
    Shanie Landen, Macsue Jacques, Danielle Hiam, Javier Alvarez‐Romero, Harvey, Nicholas R., Haupt, Larisa M., Lyn Robyn Griffiths, Kevin J. Ashton, Séverine Lamon, Sarah Amandine Caroline Voisin et al. · 2021 · Figshare
  43. Additional file 2 of X chromosome dosage and the genetic impact across human tissues
    Mette Hansen Viuff, Anne H Skakkebaek, Emma Bruun Johannsen, Simon Chang, Steen B. Pedersen, Katrine Meyer Lauritsen, Pedersen, Mette Glavind Bülow, Christian Trolle, Jesper Just, Gravholt, Claus H. · 2023 · Figshare
  44. Additional file 6 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Zhu, Detu · 2024 · Figshare
  45. Additional file 3 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis
    Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Woo, Marcel S., Lena Kristina Pfeffer, Jana K. Sonner, Uwe Borgmeyer et al. · 2024 · Figshare
  46. Additional file 4 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis
    Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Woo, Marcel S., Lena Kristina Pfeffer, Jana K. Sonner, Uwe Borgmeyer et al. · 2024 · Figshare
  47. Additional file 7 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
  48. Additional file 5 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
  49. Additional file 1 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2023 · Figshare
  50. Additional file 4 of Competing endogenous RNA network analysis of Turner syndrome patient-specific iPSC-derived cardiomyocytes reveals dysregulation of autosomal heart development genes by altered dosages of X-inactivation escaping non-coding RNAs
    Luo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
  51. Additional file 5 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis
    Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Woo, Marcel S., Lena Kristina Pfeffer, Jana K. Sonner, Uwe Borgmeyer et al. · 2024 · Figshare
  52. Additional file 1 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis
    Ingo Winschel, Anne Willing, Jan Broder Engler, Mark Walkenhorst, Nina Meurs, Lars Binkle-Ladisch, Woo, Marcel S., Lena Kristina Pfeffer, Jana K. Sonner, Uwe Borgmeyer et al. · 2024 · Figshare
  53. Plasticity of X-chromosome inactivation in female reproduction
    Alejandro Cáceres, Albert Alegret-García, Alicia Barberan, Mariona Bustamante, Varun B. Dwaraka, Ryan C. Smith, Luis Alberto Pérez Jurado, Juan R. González · 2026 · Research Square
  54. Evolution of the human & mouse X-chromosome inactivation regulatory network
    Olga Rosspopoff · 2018 · theses.fr (ABES)
  55. Human Sex Chromosome Biology in the Genomic Era
    Maike Bensberg, Alia W. Johnson, Hannah C. Kubinski, Mahitha Chaturvedula, Adrianna K. San Roman · 2026 · Annual Review of Genomics and Human Genetics
  56. Influence of X-Chromosome Inactivation in Pathogenesis of Turner Syndrome
    Ana Maria Grigore, Lavinia Caba, Vlad Teodor Iacob, Lucian-Mihai Antoci, Monica-Cristina Pânzaru, Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza · 2026 · Epigenomes
  57. New genomic understanding and challenges in clinical care of Turner syndrome
    Claus Højbjerg Gravholt, Camilla Mains Balle, Emma Bruun Johannsen, Line Balsby Valsted, Etki Albayrak Rasborg Hartogsohn, Ivonne Alexandra Bedei, Jesper Just, Philippe Ferdinand Backeljauw, Kirstine Stochholm · 2026 · The Lancet Diabetes & Endocrinology
  58. Genome Aging in Women: Hematopoietic Loss of X Chromosome as An Exemplar
    Xihan Guo, Xueqin Dai · 2026 · Aging Cell