| Metabolic programming of MEST DNA methylation by intrauterine exposure to gestational diabetes mellitus N El Hajj, G Pliushch, E Schneider, M Dittrich, T Müller, M Korenkov, ... Diabetes 62 (4), 1320-1328, 2013 | 311 | 2013 |
| De novo mutations in HCN1 cause early infantile epileptic encephalopathy C Nava, C Dalle, A Rastetter, P Striano, CGF de Kovel, R Nabbout, ... Nature genetics 46 (6), 640-645, 2014 | 246 | 2014 |
| Epigenetics and life-long consequences of an adverse nutritional and diabetic intrauterine environment N El Hajj, E Schneider, H Lehnen, T Haaf Reproduction 148 (6), R111-R120, 2014 | 229 | 2014 |
| Methylation status of imprinted genes and repetitive elements in sperm DNA from infertile males N El Hajj, U Zechner, E Schneider, A Tresch, J Gromoll, T Hahn, ... Sexual Development 5 (2), 60-69, 2011 | 172 | 2011 |
| Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns E Schneider, G Pliushch, N El Hajj, D Galetzka, A Puhl, M Schorsch, ... Nucleic acids research 38 (12), 3880-3890, 2010 | 142 | 2010 |
| A novel DFNB1 deletion allele supports the existence of a distant cis‐regulatory region that controls GJB2 and GJB6 expression E Wilch, H Azaiez, RA Fisher, J Elfenbein, A Murgia, R Birkenhäger, ... Clinical genetics 78 (3), 267-274, 2010 | 98 | 2010 |
| Quantitative methylation analysis of developmentally important genes in human pregnancy losses after ART and spontaneous conception U Zechner, G Pliushch, E Schneider, N El Hajj, A Tresch, Y Shufaro, ... Molecular human reproduction 16 (9), 704-713, 2010 | 92 | 2010 |
| Extreme methylation values of imprinted genes in human abortions and stillbirths G Pliushch, E Schneider, D Weise, N El Hajj, A Tresch, L Seidmann, ... The American journal of pathology 176 (3), 1084-1090, 2010 | 90 | 2010 |
| Epigenetic dysregulation in the developing Down syndrome cortex N El Hajj, M Dittrich, J Böck, TFJ Kraus, I Nanda, T Müller, L Seidmann, ... Epigenetics 11 (8), 563-578, 2016 | 78 | 2016 |
| Epigenetic dysregulation in the prefrontal cortex of suicide completers E Schneider, N El Hajj, F Müller, B Navarro, T Haaf Cytogenetic and genome research 146 (1), 19-27, 2015 | 61 | 2015 |
| Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing … E Schneider, T Märker, A Daser, G Frey-Mahn, V Beyer, R Farcas, ... Human molecular genetics 18 (4), 655-666, 2009 | 60 | 2009 |
| Differences in DNA Methylation Patterns and Expression of the CCRK Gene in Human and Nonhuman Primate Cortices R Farcas, E Schneider, K Frauenknecht, I Kondova, R Bontrop, J Bohl, ... Molecular biology and evolution 26 (6), 1379-1389, 2009 | 56 | 2009 |
| In vitro maturation of oocytes is not associated with altered deoxyribonucleic acid methylation patterns in children from in vitro fertilization or intracytoplasmic sperm injection G Pliushch, E Schneider, T Schneider, N El Hajj, S Rösner, T Strowitzki, ... Fertility and Sterility 103 (3), 720-727. e1, 2015 | 50 | 2015 |
| Widespread differences in cortex DNA methylation of the “language gene” CNTNAP2 between humans and chimpanzees E Schneider, N El Hajj, S Richter, J Roche-Santiago, I Nanda, ... Epigenetics 9 (4), 533-545, 2014 | 41 | 2014 |
| Epigenetic heterogeneity of developmentally important genes in human sperm: implications for assisted reproduction outcome J Kuhtz, E Schneider, N El Hajj, L Zimmermann, O Fust, B Linek, R Seufert, ... Epigenetics 9 (12), 1648-1658, 2014 | 33 | 2014 |
| CpG sites with continuously increasing or decreasing methylation from early to late human fetal brain development E Schneider, M Dittrich, J Böck, I Nanda, T Müller, L Seidmann, T Tralau, ... Gene 592 (1), 110-118, 2016 | 28 | 2016 |
| Assisted reproductive technologies and the placenta: clinical, morphological, and molecular outcomes L Riesche, MS Bartolomei Seminars in Reproductive Medicine 36 (03/04), 240-248, 2018 | 24 | 2018 |
| Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices E Schneider, S Mayer, N El Hajj, LR Jensen, AW Kuss, H Zischler, ... Cytogenetic and genome research 136 (4), 278-287, 2012 | 24 | 2012 |
| Fulminant hepatic failure requiring liver transplantation in 22q13. 3 deletion syndrome O Bartsch, E Schneider, N Damatova, R Weis, M Tufano, R Iorio, A Ahmed, ... American Journal of Medical Genetics Part A 152 (8), 2099-2102, 2010 | 16 | 2010 |
| A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices E Schneider, LR Jensen, R Farcas, I Kondova, RE Bontrop, B Navarro, ... Cytogenetic and genome research 136 (2), 97-106, 2012 | 14 | 2012 |
