Publications of Darina Czamara

Czamara, D.; Eraslan, G.; Lahti, J.; Figueiredo, A. S.; Girchenko, P.; Lahti-Pulkkinen, M.; Hamalainen, E.; Kajantie, E.; Laivuori, H.; Villa, P. et al.; Reynolds, R.; Mueller, N.; Theis, F. J.; Raikkonen, K.; Binder, E.: GENOTYPE, PRENATAL ENVIRONMENT OR BOTH-WHAT SHAPES THE NEWBORN'S EPIGENOME? In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. 1037 - 1037. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, SCOTLAND, October 11, 2018 - October 15, 2018. (2019)

Czamara, D.; Eraslan, G.; Suarez, A.; Girchenko, P.; Lahti, J.; Lahti, M.; Hamalainen, E.; Kajantie, E.; Laivuori, H.; Reynolds, R. M. et al.; Kondofersky, I.; Mueller, N. S.; Theis, F. J.; Raikkonen, K.; Binder, E. B.: WHAT SHAPES THE CHILD'S EPIGENOME: GENOTYPE, PRENATAL ENVIRONMENT OR BOTH? In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. S985 - S985. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Dammering, F.; Martins, J.; Hoffmann, F.; Provencal, N.; de Punder, K.; Overfeld, J.; Czamara, D.; Rex-Haffner, M.; McEwen, L.; Kobor, M. et al.; Winter, S.; Buss, C.; Entringer, S.; Binder, E.; Heim, C.: Psychiatric symptom severity mediates the effect of adversity on epigenetic aging in children aged 3-5 years. In PSYCHONEUROENDOCRINOLOGY, 107, p. 30 - 30. 49th Annual Conference of the International-Society-of-Psychoneuroendocrinology - 50 Years of Psychoneuroendocrinology - Returning to Where It All Began, Milan, ITALY, August 29, 2019 - August 31, 2019. (2019)

Halldorsdottir, T.; Piechaczek, C.; Soares de Matos, A. P.; Czamara, D.; Pehl, V.; Wagenbuechler, P.; Feldmann, L.; Quickenstedt-Reinhardt, P.; Allgaier, A.-K.; Freisleder, F. J. et al.; Greimel, E.; Kvist, T.; Lahti, J.; Raikkonen, K.; Rex-Haffner, M.; Arnarson, E. O.; Craighead, E.; Schulte-Koerne, G.; Binder, E.: Polygenic risk: predicting depression outcomes in clinical and epidemiological cohorts of youth. In BEHAVIOR GENETICS, 49 (6), p. 556 - 556. 49th Annual Meeting of the Behavior-Genetics-Association (BGA), Karolinska Inst, Stockholm, SWEDEN, June 26, 2019 - June 29, 2019. (2019)

Kero, H.; Raikkonen, K.; Lahti, M.; Cattaneo, A.; Czamara, D.; Binder, E.; Lahti, J.: FOXO1 MODIFIES ASSOCIATIONS BETWEEN MATERNAL DEPRESSION AND ANXIETY DURING PREGNANCY AND OFFSPRING PSYCHIATRIC PROBLEMS IN EARLY CHILDHOOD. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, pp. S118 - S119. 27th World Congress of Psychiatric Genetics (WCPG), Los Angeles, CA, October 26, 2019 - October 31, 2019. (2019)

Papac-Milicevic, N.; Alic, L.; Czamara, D.; Gurbisz, M.; Ozsvar-Kozma, M.; Hoermann, G.; Rudnick, R. B.; Hartmann, A.; Hasslinger-Hutter, S.; Zipfels, P. et al.; Skerka, C.; Binder, E. B.; Binder, C. J.: VARIANTS WITHIN CFH, CFHR1 AND CFHR3 GENES INFLUENCE CFH BINDING TO MDA MODIFIED SURFACES. In MOLECULAR IMMUNOLOGY, 114, p. 421 - 421. 17th European Meeting on Complement in Human Disease (EMCHD), Madrid, SPAIN, September 14, 2019 - September 17, 2019. (2019)

Raikkonen, K.; Suarez, A.; Lahti, J.; Czamara, D.; Lahti, M.; Knight, A.; Girchenko, P.; Hamalainen, E.; Kajantie, E.; Laivuori, H. et al.; Villa, P.; Reynolds, R.; Smith, A.; Binder, E.: THE EPIGENETIC CLOCK AT BIRTH: ASSOCIATIONS WITH MATERNAL ANTENATAL DEPRESSION AND CHILD PSYCHIATRIC PROBLEMS. In EUROPEAN NEUROPSYCHOPHARMACOLOGY, 29, p. S748 - S748. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, October 13, 2017 - October 17, 2017. (2019)

Thomas, M.; Coope, A.; Falkenberg, C.; Dunlop, B.; Czamara, D.; Provencal, N.; Craighead, W. E.; Mayberg, H.; Nemeroff, C.; Binder, E. et al.; Nieratschker, V.: Investigation of MORC1 DNA methylation as biomarker of early life stress and depressive symptoms. In JOURNAL OF NEURAL TRANSMISSION, 126 (11), pp. 1543 - 1544. International Congress of the World-Association-for-Stress-Related-and-Anxiety-Disorders (WASAD), Wurzburg, GERMANY, October 03, 2019 - October 05, 2019. (2019)

Dieckmann, L.; Czamara, D.: Epigenetics of prenatal stress in humans: the current research landscape. CLINICAL EPIGENETICS 16 (1), 20 (2024)

Solomon, O.; Huen, K.; Yousefi, P.; Kupers, L. K.; Gonzalez, J. R.; Suderman, M.; Reese, S. E.; Page, C. M.; Gruzieva, O.; Rzehak, P. et al.; Gao, L.; Bakulski, K. M.; Novoloaca, A.; Allard, C.; Pappa, I.; Llambrich, M.; Vives, M.; Jima, D. D.; Kvist, T.; Baccarelli, A.; White, C.; Rezwan I, F.; Sharp, G. C.; Tindula, G.; Bergstrom, A.; Grote, V.; Dou, J. F.; Isaevska, E.; Magnus, M. C.; Corpeleijn, E.; Perron, P.; Jaddoe, V. W. V.; Nohr, E. A.; Maitre, L.; Foraster, M.; Hoyo, C.; Haberg, S. E.; Lahti, J.; DeMeo, D. L.; Zhang, H.; Karmaus, W.; Kull, I.; Koletzko, B.; Feinberg I, J.; Gagliardi, L.; Bouchard, L.; Ramlau-Hansen, C. H.; Tiemeier, H.; Santorelli, G.; Maguire, R. L.; Czamara, D.; Litonjua, A. A.; Langhendries, J.-P.; Plusquin, M.; Lepeule, J.; Binder, E. B.; Verduci, E.; Dwyer, T.; Carracedo, A.; Ferre, N.; Eskenazi, B.; Kogevinas, M.; Nawrot, T. S.; Munthe-Kaas, M. C.; Herceg, Z.; Relton, C.; Melen, E.; Gruszfeld, D.; Breton, C.; Fallin, M. D.; Ghantous, A.; Nystad, W.; Heude, B.; Snieder, H.; Hivert, M.-F.; Felix, J. F.; Sorensen, T. I. A.; Bustamante, M.; Murphy, S. K.; Raikkonen, K.; Oken, E.; Holloway, J. W.; Arshad, S. H.; London, S. J.; Holland, N.: Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation. MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH 789, 108415 (2022)

Huls, A.; Czamara, D.: Methodological challenges in constructing DNA methylation risk scores. EPIGENETICS 15 (1-2), pp. 1 - 11 (2020)

Kazmi, N.; Sharp, G. C.; Reese, S. E.; Vehmeijer, F. O.; Lahti, J.; Page, C. M.; Zhang, W.; Rifas-Shiman, S. L.; Rezwan, F. I.; Simpkin, A. J. et al.; Burrows, K.; Richardson, T. G.; Ferreira, D. L. S.; Fraser, A.; Harmon, Q. E.; Zhao, S.; Jaddoe, V. W. V.; Czamara, D.; Binder, E. B.; Magnus, M. C.; Haberg, S. E.; Nystad, W.; Nohr, E. A.; Starling, A. P.; Kechris, K. J.; Yang, I. V.; DeMeo, D. L.; Litonjua, A. A.; Baccarelli, A.; Oken, E.; Holloway, J. W.; Karmaus, W.; Arshad, S. H.; Dabelea, D.; Sorensen, T. I. A.; Laivuori, H.; Raikkonen, K.; Felix, J. F.; London, S. J.; Hivert, M.-F.; Gaunt, T. R.; Lawlor, D. A.; Relton, C. L.: Hypertensive Disorders of Pregnancy and DNA Methylation in Newborns Findings From the Pregnancy and Childhood Epigenetics Consortium. HYPERTENSION 74 (2), pp. 375 - 383 (2019)

Pham, H.; Thompson-Felix, T.; Czamara, D.; Rasmussen, J. M.; Lombroso, A.; Entringer, S.; Binder, E. B.; Wadhwa, P. D.; Buss, C.; ODonnell, K. J.: The effects of pregnancy, its progression, and its cessation on human (maternal) biological aging. CELL METABOLISM 36 (5), pp. 877 - 878 (2024)