| The changing epidemiology of autism spectrum disorders K Lyall, L Croen, J Daniels, MD Fallin, C Ladd-Acosta, BK Lee, BY Park, ... Annual review of public health 38 (1), 81-102, 2017 | 1258 | 2017 |
| DNA methylation age of blood predicts all-cause mortality in later life RE Marioni, S Shah, AF McRae, BH Chen, E Colicino, SE Harris, J Gibson, ... Genome biology 16, 1-12, 2015 | 1207 | 2015 |
| Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis Y Liu, MJ Aryee, L Padyukov, MD Fallin, E Hesselberg, A Runarsson, ... Nature biotechnology 31 (2), 142-147, 2013 | 1110 | 2013 |
| DNA methylation in newborns and maternal smoking in pregnancy: genome-wide consortium meta-analysis BR Joubert, JF Felix, P Yousefi, KM Bakulski, AC Just, C Breton, ... The American Journal of Human Genetics 98 (4), 680-696, 2016 | 941 | 2016 |
| Intra-individual change over time in DNA methylation with familial clustering HT Bjornsson, MI Sigurdsson, MD Fallin, RA Irizarry, T Aspelund, H Cui, ... Jama 299 (24), 2877-2883, 2008 | 844 | 2008 |
| Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies AE Jaffe, P Murakami, H Lee, JT Leek, MD Fallin, AP Feinberg, RA Irizarry International journal of epidemiology 41 (1), 200-209, 2012 | 756 | 2012 |
| A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ... Nature genetics 42 (6), 525-529, 2010 | 690 | 2010 |
| Single nucleotide polymorphisms and the future of genetic epidemiology NJ Schork, D Fallin, JS Lanchbury Clinical genetics 58 (4), 250-264, 2000 | 603 | 2000 |
| An integrated epigenetic and genetic approach to common human disease HT Bjornsson, MD Fallin, AP Feinberg TRENDS in Genetics 20 (8), 350-358, 2004 | 549 | 2004 |
| Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes G Jun, AC Naj, GW Beecham, LS Wang, J Buros, PJ Gallins, JD Buxbaum, ... Archives of neurology 67 (12), 1473-1484, 2010 | 516 | 2010 |
| Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data D Fallin, NJ Schork The American Journal of Human Genetics 67 (4), 947-959, 2000 | 511 | 2000 |
| Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease D Fallin, A Cohen, L Essioux, I Chumakov, M Blumenfeld, D Cohen, ... Genome research 11 (1), 143-151, 2001 | 508 | 2001 |
| Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ... Nature genetics 49 (7), 978-985, 2017 | 500 | 2017 |
| Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4, and the risk of late-onset Alzheimer disease in African Americans C Reitz, G Jun, A Naj, R Rajbhandary, BN Vardarajan, LS Wang, ... Jama 309 (14), 1483-1492, 2013 | 476 | 2013 |
| Bipolar I disorder and schizophrenia: a 440–single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios MD Fallin, VK Lasseter, D Avramopoulos, KK Nicodemus, PS Wolyniec, ... The American Journal of Human Genetics 77 (6), 918-936, 2005 | 466 | 2005 |
| Results of a high-resolution genome screen of 437 Alzheimer's disease families D Blacker, L Bertram, AJ Saunders, TJ Moscarillo, MS Albert, H Wiener, ... Human molecular genetics 12 (1), 23-32, 2003 | 445 | 2003 |
| Personalized epigenomic signatures that are stable over time and covary with body mass index AP Feinberg, RA Irizarry, D Fradin, MJ Aryee, P Murakami, T Aspelund, ... Science translational medicine 2 (49), 49ra67-49ra67, 2010 | 401 | 2010 |
| Common DNA methylation alterations in multiple brain regions in autism C Ladd-Acosta, KD Hansen, E Briem, MD Fallin, WE Kaufmann, ... Molecular psychiatry 19 (8), 862-871, 2014 | 387 | 2014 |
| Meta-analysis of 32 genome-wide linkage studies of schizophrenia MYM Ng, DF Levinson, SV Faraone, BK Suárez, LE DeLisi, T Arinami, ... Molecular psychiatry 14 (8), 774-785, 2009 | 377 | 2009 |
| Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia Molecular autism 8, 1-17, 2017 | 360 | 2017 |
Christine Ladd-AcostaAssociate Professor, Johns Hopkins Bloomberg School of Public HealthVerified email at jhsph.edu
