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
- The TGFβ system and TIMP1 and 3 genotypes in Turner syndrome—Relation with aortic congenital malformationsLukas Ochsner Reynaud Ridder, Kirstine Stochholm, Kristian Havmand Mortensen, N.H. Andersen, Claus Højbjerg Gravholt · 2023 · Clinical Endocrinology
- Survey of gene, lncRNA and transposon transcription patterns in four mouse organs highlights shared and organ-specific sex-biased regulationQinwei 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
- Functional and regulatory aspects of oxidative stress response in X monosomyVinayak S. Biradar, Shriram N. Rajpathak, Suraj R. Joshi, Deepti Dileep Deobagkar · 2021 · In Vitro Cellular & Developmental Biology - Animal
- DNA Hypermethylation and a Specific Methylation Spectrum on the X Chromosome in Turner Syndrome as Determined by Nanopore SequencingXin Fan, Beibei Zhang, Lijun Fan, Jiajia Chen, Chang Su, Bingyan Cao, Liya Wei, Miao Qin, Chunxiu Gong · 2022 · Journal of Personalized Medicine
- Reliable detection of sex chromosome abnormalities by quantitative fluorescence polymerase chain reactionCamilla 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)
- Epigenetics: Future prospective in human disorders and therapeuticsShriram N. Rajpathak, Vinayak S. Biradar, Deepti Dileep Deobagkar · 2021 · Elsevier eBooks
- Rethinking rare disease: longevity-enhancing drug targets through X-linked aneuploidyJake P. Taylor‐King · 2021 · Trends in Genetics
- PGCLCs of human 45,XO reveal pathogenetic pathways of neurocognitive and psychosocial disordersDantong Shang, Tian Lan, Yue Wang, Xuanyu Li, Quanyi Liu, Huimin Dong, Bo Xu, Hanhua Cheng, Rongjia Zhou · 2022 · Cell & Bioscience
- Adult Care of Turner SyndromeClaus Højbjerg Gravholt, Mette Hansen Viuff, Kirstine Stochholm, N.H. Andersen · 2018 · Elsevier eBooks
- Rare Turner syndrome and lupus coexistence with insights from DNA methylation patternsGülşah Kavrul Kayaalp, Desiré Casares‐Marfil, Sezgin Şahin, Özgür Kasapçopur, Betül Sözeri, Nuray Aktay Ayaz, Amr H. Sawalha · 2024 · Clinical Immunology
- International Symposium on Ruminant Physiology: Developmental epigenetics—Understanding genetic and sexually dimorphic responses to parental diet and outcomes following assisted reproductionKevin D. Sinclair · 2024 · Journal of Dairy Science
- Associations of Karyotype and Age at Diagnosis with Physical Features and Comorbidities in Turner Syndrome: A Single-Site ExperienceBeáta Vida, Olga Török, Enikő Felszeghy, Mónika Orosz, Zoárd Tibor Krasznai, Zoltán Tándor, Attila Jakab, Tamás Deli · 2025 · The Application of Clinical Genetics
- Characterizing the Human Fetal Perimeiotic 45,X Ovary at Single-Cell ResolutionSinead 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
- Epigenetic age acceleration in Turner and Klinefelter syndrome: Correlations with clinical aging markersEmma Bruun Johannsen, Jesper Just, Simon Chang, Anne H Skakkebaek, Claus Højbjerg Gravholt · 2025 · Clinical Epigenetics
- Integrative Analyses of Genes Associated With Otologic Disorders in Turner SyndromeRuoyan Xue, Qi Tang, Yongli Zhang, Mengyao Xie, Chen Li, Shu Wang, Hua Yang · 2022 · Frontiers in Genetics
- When Does the Epigenome Become “Sexy”?Anna K. Naumova · 2018 · BioEssays
- The pattern of X-inactivation in Human X-linked Disorders and their Model Organisms: A literature reviewYixin Zhou · 2020 · E3S Web of Conferences
- The Heart and Vasculature in Turner Syndrome: Development, Surveillance, and ManagementLuciana Young, Michael Silberbach · 2020 · Springer eBooks
- Molecular Mechanisms of Distinct DiseasesAdnan Batman, İrem Yalım Camcı, Elif Kadioglu, Kezban Uçar Çifci, Berçem Yeman-Kıyak, Servet Tunoğlu, Ezgi Nurdan Yenilmez Tunoğlu, Yusuf Tutar · 2021 · IntechOpen eBooks
- Inverse regulatory mechanisms in aneuploidyShuai Zhang, Lin Sun · 2022 · Scientia Sinica Vitae
- Human X-chromosome inactivation: Complexity and clinical implicationsMaría José Navarro-Cobos, Karanveer Bhangu, Carolyn J. Brown · 2023 · Elsevier eBooks
- Genetics of Sex Differences in ImmunityShani Talia Gal-Oz, Tal Shay · 2023 · Current topics in microbiology and immunology
- Lebensqualität von kleinwüchsigen Kindern und Jugendlichen und WachstumshormontherapieJulia 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
- Stem cell epigenetics in development and diseaseWei Qiang Seow, Lillian Yuxian Lim, Dewei Kong, Adrian Kee Keong Teo · 2023 · Elsevier eBooks
- System biology approach to delineate expressional difference in the blood mononuclear cells between healthy and Turner syndrome individualsAnam Farooqui, Naaila Tamkeen, Safia Tazyeen, Sher Ali, Romana Ishrat · 2024 · Egyptian Journal of Medical Human Genetics
- A Turner-szindróma áttekintése az újabb genetikai ismeretek és a multidiszciplináris beteggondozás tekintetébenNikolett Jusztina Beniczky, Nikolette Szücs, Balázs Gellén, Rita Ágnes Bertalan · 2024 · Orvosi Hetilap
- Genetic analysis of Turner syndrome in Tunisian patientsOlfa 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
- Cell Cycle Kinetics and Sister Chromatid Exchange in Mosaic Turner SyndromeMiriam 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
- Survey of gene, lncRNA and transposon transcription patterns in four mouse organs highlights shared and organ-specific sex-biased regulationQinwei 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)
- Turner SyndromePreeti Singh, Sangeeta Yadav · 2024 · Springer eBooks
- Adult care of Turner syndrome womenClaus Højbjerg Gravholt · 2024 · Elsevier eBooks
- Abnormal methylation of ST8SIA4 in low-motility sperm: A genome-wide identification approachChia‐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
- Clinical analysis of karyotypes and phenotypes in 87 cases of Turner syndrome during transitional periodJuan Luo, Luhong Yang, Hongxi Guo, Hui Jun Yao, Xiaohong Chen, Lifang Feng · 2025 · BMC Pediatrics
- Turner disease: A contemporary clinical approachMilina Tančić‐Gajić, Bojana Tesla, Marija Miletić, Milos M. Stojanovic, Svetlana Vujović · 2025 · Medicinska istrazivanja
- Clinical and Genotypic Insights into Turner SyndromeMounam Chattopadhyay, Anindya Mukherjee, Pranab Kumar Sahana · 2025 · Journal of the ASEAN Federation of Endocrine Societies
- Genes with abnormal DNA methylation in chorionic villi of spontaneous abortions with monosomy XEkaterina 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
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
- Additional file 1 of X chromosome dosage and the genetic impact across human tissuesMette 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
- Additional file 1 of A cross-cohort analysis of autosomal DNA methylation sex differences in the term placentaAmy M. Inkster, Victor Yuan, Chaini Konwar, Allison Matthews, Carolyn J. Brown, Wendy P. Robinson · 2021 · Figshare
- Additional file 2 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosisIngo 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
- Additional file 1 of System biology approach to delineate expressional difference in the blood mononuclear cells between healthy and Turner syndrome individualsAnam Farooqui, Naaila Tamkeen, Safia Tazyeen, Ali, Sher, Romana Ishrat · 2024 · Figshare
- Additional file 1 of Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolismShanie 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
- Additional file 2 of X chromosome dosage and the genetic impact across human tissuesMette 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
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Zhu, Detu · 2024 · Figshare
- Additional file 3 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosisIngo 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
- Additional file 4 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosisIngo 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
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2023 · Figshare
- 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 RNAsLuo, Yumei, Yapei Chen, Lingxia Ge, Zhou, Guanqing, Yaoyong Chen, Detu Zhu · 2024 · Figshare
- Additional file 5 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosisIngo 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
- Additional file 1 of Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosisIngo 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
- Plasticity of X-chromosome inactivation in female reproductionAlejandro Cáceres, Albert Alegret-García, Alicia Barberan, Mariona Bustamante, Varun B. Dwaraka, Ryan C. Smith, Luis Alberto Pérez Jurado, Juan R. González · 2026 · Research Square
- Evolution of the human & mouse X-chromosome inactivation regulatory networkOlga Rosspopoff · 2018 · theses.fr (ABES)
- Human Sex Chromosome Biology in the Genomic EraMaike Bensberg, Alia W. Johnson, Hannah C. Kubinski, Mahitha Chaturvedula, Adrianna K. San Roman · 2026 · Annual Review of Genomics and Human Genetics
- Influence of X-Chromosome Inactivation in Pathogenesis of Turner SyndromeAna Maria Grigore, Lavinia Caba, Vlad Teodor Iacob, Lucian-Mihai Antoci, Monica-Cristina Pânzaru, Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza · 2026 · Epigenomes
- New genomic understanding and challenges in clinical care of Turner syndromeClaus 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
- Genome Aging in Women: Hematopoietic Loss of X Chromosome as An ExemplarXihan Guo, Xueqin Dai · 2026 · Aging Cell