| Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice BI Laufer, K Mantha, ML Kleiber, EJ Diehl, SMF Addison, SM Singh Disease models & mechanisms 6 (4), 977-992, 2013 | 143 | 2013 |
| Associative DNA methylation changes in children with prenatal alcohol exposure BI Laufer, J Kapalanga, CA Castellani, EJ Diehl, L Yan, SM Singh Epigenomics 7 (8), 1259-1274, 2015 | 117 | 2015 |
| DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks CA Castellani, BI Laufer, MG Melka, EJ Diehl, RL O’Reilly, SM Singh BMC medical genomics 8, 1-12, 2015 | 78 | 2015 |
| DNA methylation signature for EZH2 functionally classifies sequence variants in three PRC2 complex genes S Choufani, WT Gibson, AL Turinsky, BHY Chung, T Wang, K Garg, ... The American Journal of Human Genetics 106 (5), 596-610, 2020 | 74 | 2020 |
| Long-term genomic and epigenomic dysregulation as a consequence of prenatal alcohol exposure: a model for fetal alcohol spectrum disorders ML Kleiber, EJ Diehl, BI Laufer, K Mantha, A Chokroborty-Hoque, ... Frontiers in genetics 5, 161, 2014 | 70 | 2014 |
| Alteration of gene expression, DNA methylation, and histone methylation in free radical scavenging networks in adult mouse hippocampus following fetal alcohol exposure EJ Chater-Diehl, BI Laufer, CA Castellani, BL Alberry, SM Singh PloS one 11 (5), e0154836, 2016 | 66 | 2016 |
| Long-term alterations to the brain transcriptome in a maternal voluntary consumption model of fetal alcohol spectrum disorders ML Kleiber, BI Laufer, E Wright, EJ Diehl, SM Singh Brain research 1458, 18-33, 2012 | 65 | 2012 |
| Changes to histone modifications following prenatal alcohol exposure: An emerging picture EJ Chater-Diehl, BI Laufer, SM Singh Alcohol 60, 41-52, 2017 | 57 | 2017 |
| Long-term alterations to DNA methylation as a biomarker of prenatal alcohol exposure: From mouse models to human children with fetal alcohol spectrum disorders BI Laufer, EJ Chater-Diehl, J Kapalanga, SM Singh Alcohol 60, 67-75, 2017 | 55 | 2017 |
| Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature D Rots, E Chater-Diehl, AJM Dingemans, SJ Goodman, MT Siu, ... The American Journal of Human Genetics 108 (6), 1053-1068, 2021 | 53 | 2021 |
| Anatomy of DNA methylation signatures: Emerging insights and applications E Chater-Diehl, SJ Goodman, C Cytrynbaum, AL Turinsky, S Choufani, ... The American Journal of Human Genetics, 2021 | 42 | 2021 |
| New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome E Chater-Diehl, R Ejaz, C Cytrynbaum, MT Siu, A Turinsky, S Choufani, ... BMC medical genomics 12, 1-14, 2019 | 32 | 2019 |
| Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variation SJ Goodman, CL Burton, DT Butcher, MT Siu, M Lemire, E Chater-Diehl, ... Journal of neurodevelopmental disorders 12, 1-15, 2020 | 31 | 2020 |
| Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder J Courraud, E Chater-Diehl, B Durand, M Vincent, ... Genetics in Medicine 23 (11), 2150-2159, 2021 | 26 | 2021 |
| DNA methylation in psychosis: insights into etiology and treatment CA Castellani, MG Melka, EJ Diehl, BI Laufer, RL O’Reilly, SM Singh Epigenomics 7 (1), 67-74, 2015 | 24 | 2015 |
| DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes Z Awamleh, E Chater-Diehl, S Choufani, E Wei, RR Kianmahd, A Yu, ... European Journal of Human Genetics 30 (6), 695-702, 2022 | 21 | 2022 |
| EHMT1 pathogenic variants and 9q34. 3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome SJ Goodman, C Cytrynbaum, BHY Chung, E Chater-Diehl, C Aziz, ... Journal of Translational Genetics and Genomics, 2020 | 19 | 2020 |
| Human COL5A1 polymorphisms and quadriceps muscle–tendon mechanical stiffness in vivo EA Kirk, CW Moore, EJ Chater‐Diehl, SM Singh, CL Rice Experimental physiology 101 (12), 1581-1592, 2016 | 16 | 2016 |
| X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition JR Volpatti, MM Ghahramani-Seno, M Mansat, N Sabha, E Sarikaya, ... Acta neuropathologica 144 (3), 537-563, 2022 | 14 | 2022 |
| Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012 H Anderson‐Schmidt, O Beltcheva, MD Brandon, EM Byrne, EJ Diehl, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013 | 13 | 2013 |
