![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2022
Solomon, Olivia; Huen, Karen; Yousefi, Paul; Kupers, Leanne K.; Gonzalez, Juan R.; Suderman, Matthew; Reese, Sarah E.; Page, Christian M.; Gruzieva, Olena; Rzehak, Peter; Gao, Lu; Bakulski, Kelly M.; Novoloaca, Alexei; Allard, Catherine; Pappa, Irene; Llambrich, Maria; Vives, Marta; Jima, Dereje D.; Kvist, Tuomas; Baccarelli, Andrea; White, Cory; Rezwan, Faisal I.; Sharp, Gemma C.; Tindula, Gwen; Bergstrom, Anna; Grote, Veit; Dou, John F.; Isaevska, Elena; Magnus, Maria C.; Corpeleijn, Eva; Perron, Patrice; Jaddoe, Vincent W. V.; Nohr, Ellen A.; Maitre, Lea; Foraster, Maria; Hoyo, Cathrine; Haberg, Siri E.; Lahti, Jari; DeMeo, Dawn L.; Zhang, Hongmei; Karmaus, Wilfried; Kull, Inger; Koletzko, Berthold; Feinberg, Jason I.; Gagliardi, Luigi; Bouchard, Luigi; Ramlau-Hansen, Cecilia Host; Tiemeier, Henning; Santorelli, Gillian; Maguire, Rachel L.; Czamara, Darina; Litonjua, Augusto A.; Langhendries, Jean-Paul; Plusquin, Michelle; Lepeule, Johanna; Binder, Elisabeth B.; Verduci, Elvira; Dwyer, Terence; Carracedo, Angel; Ferre, Natalia; Eskenazi, Brenda; Kogevinas, Manolis; Nawrot, Tim S.; Munthe-Kaas, Monica C.; Herceg, Zdenko; Relton, Caroline; Melen, Erik; Gruszfeld, Dariusz; Breton, Carrie; Fallin, M. D.; Ghantous, Akram; Nystad, Wenche; Heude, Barbara; Snieder, Harold; Hivert, Marie-France; Felix, Janine F.; Sorensen, Thorkild I. A.; Bustamante, Mariona; Murphy, Susan K.; Raikkonen, Katri; Oken, Emily; Holloway, John W.; Arshad, Syed Hasan; London, Stephanie J. und Holland, Nina
(2022):
Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation.
In: Mutation Research-Reviews in Mutation Research, Bd. 789, 108415
2018
Luijk, Rene; Wu, Haoyu; Ward-Caviness, Cavin K.; Hannon, Eilis; Carnero-Montoro, Elena; Min, Josine L.; Mandaviya, Pooja; Müller-Nurasyid, Martina; Mei, Hailiang; Maarel, Silvere M. van der; Relton, Caroline; Mill, Jonathan; Waldenberger, Melanie; Bell, Jordana T.; Jansen, Rick; Zhernakova, Alexandra; Franke, Lude; Hoen, Peter A. C. 't; Boomsma, Dorret I.; Duijn, Cornelia M. van; Greevenbroek, Marleen M. J. van 
ORCID: https://orcid.org/0000-0002-2989-1631; Veldink, Jan H.; Wijmenga, Cisca; Meurs, Joyce van; Daxinger, Lucia; Slagboom, P. Eline; Zwet, Erik W. van und Heijmans, Bastiaan T.
(2018):
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation.
In: Nature Communications, Bd. 9, 3738
[PDF, 988kB]
ORCID: https://orcid.org/0000-0002-2989-1631; Veldink, Jan H.; Wijmenga, Cisca; Meurs, Joyce van; Daxinger, Lucia; Slagboom, P. Eline; Zwet, Erik W. van und Heijmans, Bastiaan T.
(2018):
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation.
In: Nature Communications, Bd. 9, 3738
[PDF, 988kB]