Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density von Chesi, Alessandra, Wagley, Yadav, Johnson, Matthew E., Manduchi, Elisabetta, Su, Chun, Lu, Sumei, Leonard, Michelle E., Hodge, Kenyaita M., Pippin, James A., Hankenson, Kurt D., Wells, Andrew D., Grant, Struan F. A.

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Mapping effector genes at lupus GWAS loci using promoter Capture-C in follicular helper T cells von Su, Chun, Johnson, Matthew E., Torres, Annabel, Thomas, Rajan M., Manduchi, Elisabetta, Sharma, Prabhat, Mehra, Parul, Le Coz, Carole, Leonard, Michelle E., Lu, Sumei, Hodge, Kenyaita M., Chesi, Alessandra, Pippin, James, Romberg, Neil, Grant, Struan F. A., Wells, Andrew D.

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Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes von Mishra, Rajashree, Chesi, Alessandra, Cousminer, Diana L, Hawa, Mohammad I, Bradfield, Jonathan P, Hodge, Kenyaita M, Guy, Vanessa C, Hakonarson, Hakon, Mauricio, Didac, Schloot, Nanette C, Yderstræde, Knud B, Voight, Benjamin F, Schwartz, Stanley, Boehm, Bernhard O, Leslie, Richard David, Grant, Struan F A

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Epigenetic associations with neonatal age in infants born very preterm, particularly among genes involved in neurodevelopment von Hodge, Kenyaita M., Burt, Amber A., Camerota, Marie, Carter, Brian S., Check, Jennifer, Conneely, Karen N., Helderman, Jennifer, Hofheimer, Julie A., Hüls, Anke, McGowan, Elisabeth C., Neal, Charles R., Pastyrnak, Steven L., Smith, Lynne M., DellaGrotta, Sheri A., Dansereau, Lynne M., O’Shea, T. Michael, Marsit, Carmen J., Lester, Barry M., Everson, Todd M.

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Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human Liver von Çalışkan, Minal, Manduchi, Elisabetta, Rao, H. Shanker, Segert, Julian A., Beltrame, Marcia Holsbach, Trizzino, Marco, Park, YoSon, Baker, Samuel W., Chesi, Alessandra, Johnson, Matthew E., Hodge, Kenyaita M., Leonard, Michelle E., Loza, Baoli, Xin, Dong, Berrido, Andrea M., Hand, Nicholas J., Bauer, Robert C., Wells, Andrew D., Olthoff, Kim M., Shaked, Abraham, Rader, Daniel J., Grant, Struan F.A., Brown, Christopher D.

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Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci von Hammond, Reza K., Pahl, Matthew C., Su, Chun, Cousminer, Diana L., Leonard, Michelle E., Lu, Sumei, Doege, Claudia A., Wagley, Yadav, Hodge, Kenyaita M., Lasconi, Chiara, Johnson, Matthew E., Pippin, James A., Hankenson, Kurt D., Leibel, Rudolph L., Chesi, Alessandra, Wells, Andrew D., Grant, Struan F. A.

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Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant complex traits von Pahl, Matthew C., Doege, Claudia A., Hodge, Kenyaita M., Littleton, Sheridan H., Leonard, Michelle E., Lu, Sumei, Rausch, Rick, Pippin, James A., De Rosa, Maria Caterina, Basak, Alisha, Bradfield, Jonathan P., Hammond, Reza K., Boehm, Keith, Berkowitz, Robert I., Lasconi, Chiara, Su, Chun, Chesi, Alessandra, Johnson, Matthew E., Wells, Andrew D., Voight, Benjamin F., Leibel, Rudolph L., Cousminer, Diana L., Grant, Struan F. A.

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CRISPR‐Cas9–Mediated Genome Editing Confirms EPDR1 as an Effector Gene at the BMD GWAS‐Implicated ‘STARD3NL’ Locus von Pippin, James A, Chesi, Alessandra, Wagley, Yadav, Su, Chun, Pahl, Matthew C, Hodge, Kenyaita M, Johnson, Matthew E, Wells, Andrew D, Hankenson, Kurt D, Grant, Struan F A

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First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes von Cousminer, Diana L, Ahlqvist, Emma, Mishra, Rajashree, Andersen, Mette K, Chesi, Alessandra, Hawa, Mohammad I, Davis, Asa, Hodge, Kenyaita M, Bradfield, Jonathan P, Zhou, Kaixin, Guy, Vanessa C, Åkerlund, Mikael, Wod, Mette, Fritsche, Lars G, Vestergaard, Henrik, Snyder, James, Højlund, Kurt, Linneberg, Allan, Käräjämäki, Annemari, Brandslund, Ivan, Kim, Cecilia E, Witte, Daniel, Sørgjerd, Elin Pettersen, Brillon, David J, Pedersen, Oluf, Beck-Nielsen, Henning, Grarup, Niels, Pratley, Richard E, Rickels, Michael R, Vella, Adrian, Ovalle, Fernando, Melander, Olle, Harris, Ronald I, Varvel, Stephen, Grill, Valdemar E R, Hakonarson, Hakon, Froguel, Philippe, Lonsdale, John T, Mauricio, Didac, Schloot, Nanette C, Khunti, Kamlesh, Greenbaum, Carla J, Åsvold, Bjørn Olav, Yderstræde, Knud B, Pearson, Ewan R, Schwartz, Stanley, Voight, Benjamin F, Hansen, Torben, Tuomi, Tiinamaija, Boehm, Bernhard O, Groop, Leif, Leslie, R David, Grant, Struan F A

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A Global Perspective of Latent Autoimmune Diabetes in Adults von Mishra, Rajashree, Hodge, Kenyaita M., Cousminer, Diana L., Leslie, Richard D., Grant, Struan F.A.

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Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC von Mishra, Rajashree, Akerlund, Mikael, Cousminer, Diana L., Ahlqvist, Emma, Bradfield, Jonathan P., Chesi, Alessandra, Hodge, Kenyaita M., Guy, Vanessa C., Brillon, David J., Pratley, Richard E., Rickels, Michael R., Vella, Adrian, Ovalle, Fernando, Harris, Ronald I., Melander, Olle, Varvel, Stephen, Hakonarson, Hakon, Froguel, Phillippe, Lonsdale, John T., Mauricio, Didac, Schloot, Nanette C., Khunti, Kamlesh, Greenbaum, Carla J., Yderstraede, Knud B., Tuomi, Tiinamaija, Voight, Benjamin F., Schwartz, Stanley, Boehm, Bernhard O., Groop, Leif, Leslie, Richard David, Grant, Struan F. A.

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IL-1 Transcriptional Responses to Lipopolysaccharides Are Regulated by a Complex of RNA Binding Proteins von Shi, Lihua, Song, Li, Maurer, Kelly, Dou, Ying, Patel, Vishesh R., Su, Chun, Leonard, Michelle E., Lu, Sumei, Hodge, Kenyaita M., Torres, Annabel, Chesi, Alessandra, Grant, Struan F. A., Wells, Andrew D., Zhang, Zhe, Petri, Michelle A., Sullivan, Kathleen E.

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Type 1 diabetes in Africa: an immunogenetic study in the Amhara of North-West Ethiopia von Balcha, Shitaye A., Demisse, Abayneh G., Mishra, Rajashree, Vartak, Tanwi, Cousminer, Diana L., Hodge, Kenyaita M., Voight, Benjamin F., Lorenz, Kim, Schwartz, Stanley, Jerram, Samuel T., Gamper, Arla, Holmes, Alice, Wilson, Hannah F., Williams, Alistair J. K., Grant, Struan F. A., Leslie, R. David, Phillips, David I. W., Trimble, Elisabeth R.

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Epigenetic associations in HPA axis genes related to bronchopulmonary dysplasia and antenatal steroids von Hodge, Kenyaita M., Zhabotynsky, Vasyl, Burt, Amber A., Carter, Brian S., Fry, Rebecca C., Helderman, Jennifer, Hofheimer, Julie A., McGowan, Elisabeth C., Neal, Charles R., Pastyrnak, Steven L., Smith, Lynne M., DellaGrotta, Sheri A., Dansereau, Lynne M., Lester, Barry M., Marsit, Carmen J., O’Shea, T. Michael, Everson, Todd M.

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245-OR: CIS-Regulatory Architecture of Human ESC-Derived Hypothalamic Neuron Differentiation Aids in Variant-to-Gene Mapping of Type 2 Diabetes Related Traits von PAHL, MATTHEW C., LITTLETON, SHERIDAN H., DOEGE, CLAUDIA, HODGE, KENYAITA M., LEONARD, MICHELLE, LU, SUMEI, HAMMOND, REZA, BOEHM, KEITH, LASCONI, CHIARA, SU, CHUN, CHESI, ALESSANDRA, PIPPIN, JAMES A., JOHNSON, MATTHEW, WELLS, ANDREW D., VOIGHT, BENJAMIN F., LEIBEL, RUDOLPH, GRANT, STRUAN F., COUSMINER, DIANA L.

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305-OR: Genomic Basis to Shared Influences on Pubertal Timing and Type 2 Diabetes von COUSMINER, DIANA L., MISHRA, RAJASHREE, ARGENZIANO, MARIANA A., MANDUCHI, ELISABETTA, HODGE, KENYAITA M., SU, CHUN, LEONARD, MICHELLE, LU, SUMEI, PIPPIN, JAMES A., JOHNSON, MATTHEW, WELLS, ANDREW D., CHESI, ALESSANDRA, VOIGHT, BENJAMIN F., GRANT, STRUAN F.

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Variant‐to‐gene mapping in human microglial cell models with CRISPR validation implicates RTFDC1 at the Alzheimer’s disease ‘CASS4’ locus von Burton, Elizabeth, Argenziano, Mariana, Cook, Kieona, Lu, Sumei, Manduchi, Elisabetta, Leonard, Michelle E, Hodge, Kenyaita M, Wang, Li‐San, Schellenberg, Gerard D., Johnson, Matthew E, Pippin, James A, Wells, Andrew D, Anderson, Stewart A, Brown, Christopher D., Grant, Struan F.A., Chesi, Alessandra

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114-OR: T1DM in the Chronically Undernourished: Rural Ethiopia von TRIMBLE, ELISABETH R., BALCHA, SHITAYE A., DEMISSE, ABAYNEH G., COUSMINER, DIANA L., MISHRA, RAJASHREE, VOIGHT, BENJAMIN F., LORENZ, KIMBERLY, VARTAK, TANWI, JERRAM, SAMUEL T., HODGE, KENYAITA M., SCHWARTZ, STANLEY, HOLMES, ALICE, GAMPER, ARLA, WILSON, HANNAH F., WILLIAMS, ALISTAIR J., LESLIE, RICHARD D., GRANT, STRUAN F., PHILLIPS, DAVID I.W.

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Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3′ UTR of FAIM2 von Littleton, Sheridan H., Trang, Khanh B., Volpe, Christina M., Cook, Kieona, DeBruyne, Nicole, Maguire, Jean Ann, Weidekamp, Mary Ann, Hodge, Kenyaita M., Boehm, Keith, Lu, Sumei, Chesi, Alessandra, Bradfield, Jonathan P., Pippin, James A., Anderson, Stewart A., Wells, Andrew D., Pahl, Matthew C., Grant, Struan F.A.

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Variant-to-Gene-Mapping Analyses Reveal a Role for the Hypothalamus in Genetic Susceptibility to Inflammatory Bowel Disease von Lasconi, Chiara, Pahl, Matthew C., Cousminer, Diana L., Doege, Claudia A., Chesi, Alessandra, Hodge, Kenyaita M., Leonard, Michelle E., Lu, Sumei, Johnson, Matthew E., Su, Chun, Hammond, Reza K., Pippin, James A., Terry, Natalie A., Ghanem, Louis R., Leibel, Rudolph L., Wells, Andrew D., Grant, Struan F.A.

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