Common DNA methylation alterations in multiple brain regions in autism von Ladd-Acosta, C, Hansen, K D, Briem, E, Fallin, M D, Kaufmann, W E, Feinberg, A P

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Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP) von Reitz, C, Tosto, G, Vardarajan, B, Rogaeva, E, Ghani, M, Rogers, R S, Conrad, C, Haines, J L, Pericak-Vance, M A, Fallin, M D, Foroud, T, Farrer, L A, Schellenberg, G D, George-Hyslop, P S, Mayeux, R

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Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults von Matteini, A.M., Li, J., Lange, E.M., Tanaka, T., Lange, L.A., Tracy, R.P., Wang, Y., Biggs, M.L., Arking, D.E., Fallin, M.D., Chakravarti, A., Psaty, B.M., Bandinelli, S., Ferrucci, L., Reiner, A.P., Walston, J.D.

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Simple biologically informed inflammatory index of two serum cytokines predicts 10 year all-cause mortality in older adults von Varadhan, Ravi, Yao, Wenliang, Matteini, Amy, Beamer, Brock A, Xue, Qian-Li, Yang, Huanle, Manwani, Bhavish, Reiner, Alexander, Jenny, Nancy, Parekh, Neel, Fallin, M Daniele, Newman, Anne, Bandeen-Roche, Karen, Tracy, Russell, Ferrucci, Luigi, Walston, Jeremy

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Determining source strength of semivolatile organic compounds using measured concentrations in indoor dust von Shin, H.-M., McKone, T. E., Nishioka, M. G., Fallin, M. D., Croen, L. A., Hertz-Picciotto, I., Newschaffer, C. J., Bennett, D. H.

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Markers of B-vitamin deficiency and frailty in older women von Matteini, A. M., Walston, J. D., Fallin, M. D., Bandeen-Roche, K., Kao, W. H. L., Semba, R. D., Allen, R. H., Guralnik, J., Fried, L. P., Stabler, S. P.

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The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study von Benke, K.S., Carlson, M.C., Doan, B.Q., Walston, J.D., Xue, Q.L., Reiner, A.P., Fried, L.P., Arking, D.E., Chakravarti, A., Fallin, M.D.

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β2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort von CHESLACK-POSTAVA, K, FALLIN, M. D, AVRAMOPOULOS, D, CONNORS, S. L, ZIMMERMAN, A. W, EBERHART, C. G, NEWSCHAFFER, C. J

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Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty von Matteini, Amy M., Walston, J. D., Bandeen-Roche, K., Arking, D. E., Allen, R. H., Fried, L. P., Chakravarti, A., Stabler, S. P., Fallin, M. D.

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High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts von Park, J W, Cai, J, McIntosh, I, Jabs, E W, Fallin, M D, Ingersoll, R, Hetmanski, J B, Vekemans, M, Attie-Bitach, T, Lovett, M, Scott, A F, Beaty, T H

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Haplotype Diversity in 11 Candidate Genes Across Four Populations von Beaty, T. H, Fallin, M. D, Hetmanski, J. B, McIntosh, I, Chong, S. S, Ingersoll, R, Sheng, X, Chakraborty, R, Scott, A. F

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Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations von BEATY, T. H, HETMANSKI, J. B, JABS, E. W, CHONG, S. S, CHEAH, F. S. H, WU-CHOU, Y. H, CHEN, P. K, CHIU, Y. F, YEOW, V, NG, I. S. L, CHENG, J, HUANG, S, FALLIN, M. D, YE, X, WANG, H, INGERSOLL, R, SCOTT, A. F, PARK, J. W, SULL, J. W, MCINTOSH, I, LIANG, K. Y, VANDERKOLK, C. A, REDETT, R. J, BOYADJIEV, S. A

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Exploring biologically relevant pathways in frailty von Ho, Yen-Yi, Matteini, Amy M, Beamer, Brock, Fried, Linda, Xue, Qian-li, Arking, Dan E, Chakravarti, Aravinda, Fallin, M Daniele, Walston, Jeremy

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Heritability Estimates of Endophenotypes of Long and Health Life: The Long Life Family Study von Matteini, Amy M., Fallin, M. Daniele, Kammerer, Candace M., Schupf, Nicole, Yashin, Anatoli I., Christensen, Kaare, Arbeev, Konstantin G., Barr, Graham, Mayeux, Richard, Newman, Anne B., Walston, Jeremy D.

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Scaling of the surface vasculature on the human placenta von Leonard, A S, Lee, J, Schubert, D, Croen, L A, Fallin, M D, Newschaffer, C J, Walker, C K, Salafia, C M, Morgan, S P, Vvedensky, D D

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Heritability of platelet function in families with premature coronary artery disease von BRAY, P. F., MATHIAS, R. A., FARADAY, N., YANEK, L. R., FALLIN, M. D., HERRERA‐GALEANO, J. E., WILSON, A. F., BECKER, L. C., BECKER, D. M.

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Dense SNP association study for bipolar I disorder on chromosome 18p11 suggests two loci with excess paternal transmission von MULLE, J. G, FALLIN, M. D, LASSETER, V. K, MCGRATH, J. A, WOLYNIEC, P. S, PULVER, A. E

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Variants in the gene encoding C3 are associated with asthma and related phenotypes among African Caribbean families von Barnes, K C, Grant, A V, Baltadzhieva, D, Zhang, S, Berg, T, Shao, L, Zambelli-Weiner, A, Anderson, W, Nelsen, A, Pillai, S, Yarnall, D P, Dienger, K, Ingersoll, R G, Scott, A F, Fallin, M D, Mathias, R A, Beaty, T H, Garcia, J G N, Wills-Karp, M

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Strategy to Control Type I Error Increases Power to Identify Genetic Variation Using the Full Biological Trajectory von Benke, K. S., Wu, Y., Fallin, D. M., Maher, B., Palmer, L. J.

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The Changing Epidemiology of Autism Spectrum Disorders von Lyall, Kristen, Croen, Lisa, Daniels, Julie, Fallin, M. Daniele, Ladd-Acosta, Christine, Lee, Brian K, Park, Bo Y, Snyder, Nathaniel W, Schendel, Diana, Volk, Heather, Windham, Gayle C, Newschaffer, Craig

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