Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults by 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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Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP) by 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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Simple biologically informed inflammatory index of two serum cytokines predicts 10 year all-cause mortality in older adults by 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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Markers of B-vitamin deficiency and frailty in older women by 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 by 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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Transcobalamin-II variants, decreased vitamin B12 availability and increased risk of frailty by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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Strategy to Control Type I Error Increases Power to Identify Genetic Variation Using the Full Biological Trajectory by Benke, K. S., Wu, Y., Fallin, D. M., Maher, B., Palmer, L. J.

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The Changing Epidemiology of Autism Spectrum Disorders by 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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Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis by Liu, Yun, Aryee, Martin J, Padyukov, Leonid, Fallin, M Daniele, Hesselberg, Espen, Runarsson, Arni, Reinius, Lovisa, Acevedo, Nathalie, Taub, Margaret, Ronninger, Marcus, Shchetynsky, Klementy, Scheynius, Annika, Kere, Juha, Alfredsson, Lars, Klareskog, Lars, Ekström, Tomas J, Feinberg, Andrew P

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DNA methylation age of blood predicts all-cause mortality in later life by Marioni, Riccardo E, Shah, Sonia, McRae, Allan F, Chen, Brian H, Colicino, Elena, Harris, Sarah E, Gibson, Jude, Henders, Anjali K, Redmond, Paul, Cox, Simon R, Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G, Montgomery, Grant W, Feinberg, Andrew P, Fallin, M Daniele, Multhaup, Michael L, Jaffe, Andrew E, Joehanes, Roby, Schwartz, Joel, Just, Allan C, Lunetta, Kathryn L, Murabito, Joanne M, Starr, John M, Horvath, Steve, Baccarelli, Andrea A, Levy, Daniel, Visscher, Peter M, Wray, Naomi R, Deary, Ian J

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth by Hannon, Eilis, Schendel, Diana, Ladd-Acosta, Christine, Grove, Jakob, Hansen, Christine Søholm, Andrews, Shan V, Hougaard, David Michael, Bresnahan, Michaeline, Mors, Ole, Hollegaard, Mads Vilhelm, Bækvad-Hansen, Marie, Hornig, Mady, Mortensen, Preben Bo, Børglum, Anders D, Werge, Thomas, Pedersen, Marianne Giørtz, Nordentoft, Merete, Buxbaum, Joseph, Daniele Fallin, M, Bybjerg-Grauholm, Jonas, Reichenberg, Abraham, Mill, Jonathan

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Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation by Solomon, Olivia, Huen, Karen, Yousefi, Paul, Küpers, Leanne K., González, Juan R., Suderman, Matthew, Reese, Sarah E., Page, Christian M., Gruzieva, Olena, Rzehak, Peter, Gao, Lu, Bakulski, Kelly M., Novoloaca, Alexei, Allard, Catherine, Pappa, Irene, Llambrich, Maria, Vives, Marta, Jima, Dereje D., Kvist, Tuomas, Baccarelli, Andrea, White, Cory, Rezwan, Faisal I., Sharp, Gemma C., Tindula, Gwen, Bergström, Anna, Grote, Veit, Dou, John F., Isaevska, Elena, Magnus, Maria C., Corpeleijn, Eva, Perron, Patrice, Jaddoe, Vincent W.V., Nohr, Ellen A., Maitre, Lea, Foraster, Maria, Hoyo, Cathrine, Håberg, Siri E., Lahti, Jari, DeMeo, Dawn L., Zhang, Hongmei, Karmaus, Wilfried, Kull, Inger, Koletzko, Berthold, Feinberg, Jason I., Gagliardi, Luigi, Bouchard, Luigi, Ramlau-Hansen, Cecilia Høst, Tiemeier, Henning, Santorelli, Gillian, Maguire, Rachel L., Czamara, Darina, Litonjua, Augusto A., Langhendries, Jean-Paul, Plusquin, Michelle, Lepeule, Johanna, Binder, Elisabeth B., Verduci, Elvira, Dwyer, Terence, Carracedo, Ángel, Ferre, Natalia, Eskenazi, Brenda, Kogevinas, Manolis, Nawrot, Tim S., Munthe-Kaas, Monica C., Herceg, Zdenko, Relton, Caroline, Melén, Erik, Gruszfeld, Dariusz, Breton, Carrie, Fallin, M.D., Ghantous, Akram, Nystad, Wenche, Heude, Barbara, Snieder, Harold, Hivert, Marie-France, Felix, Janine F., Sørensen, Thorkild I.A., Bustamante, Mariona, Murphy, Susan K., Raikkönen, Katri, Oken, Emily, Holloway, John W., Arshad, Syed Hasan, London, Stephanie J., Holland, Nina

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Presence of an epigenetic signature of prenatal cigarette smoke exposure in childhood by Ladd-Acosta, Christine, Shu, Chang, Lee, Brian K., Gidaya, Nicole, Singer, Alison, Schieve, Laura A., Schendel, Diana E., Jones, Nicole, Daniels, Julie L., Windham, Gayle C., Newschaffer, Craig J., Croen, Lisa A., Feinberg, Andrew P., Daniele Fallin, M.

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