|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, 2013
|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
|Transcriptional plasticity promotes primary and acquired resistance to BET inhibition|
P Rathert, M Roth, T Neumann, F Muerdter, JS Roe, M Muhar, S Deswal, ...
Nature 525 (7570), 543-547, 2015
|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), 1-12, 2015
|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
|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
|Single nucleotide polymorphisms and the future of genetic epidemiology|
NJ Schork, D Fallin, JS Lanchbury
Clinical genetics 58 (4), 250-264, 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
|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
|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
|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
|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
|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
|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
|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
|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, 81-102, 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
|KLOTHO allele status and the risk of early-onset occult coronary artery disease|
DE Arking, DM Becker, LR Yanek, D Fallin, DP Judge, TF Moy, LC Becker, ...
The American Journal of Human Genetics 72 (5), 1154-1161, 2003
|The prevalence of voice disorders among day care center teachers compared with nurses: a questionnaire and clinical study|
E Sala, A Laine, S Simberg, J Pentti, J Suonpää
Journal of Voice 15 (3), 413-423, 2001
|Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign|
JD Groman, TW Hefferon, T Casals, L Bassas, X Estivill, M Des Georges, ...
The American Journal of Human Genetics 74 (1), 176-179, 2004