Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations von Amin, Najaf, Belonogova, Nadezhda M, Jovanova, Olivera, Brouwer, Rutger W.W, van Rooij, Jeroen G.J, van den Hout, Mirjam C.G.N, Svishcheva, Gulnara R, Kraaij, Robert, Zorkoltseva, Irina V, Kirichenko, Anatoly V, Hofman, Albert, Uitterlinden, André G, van IJcken, Wilfred F.J, Tiemeier, Henning, Axenovich, Tatiana I, van Duijn, Cornelia M

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Underlying genetic variation in familial frontotemporal dementia: sequencing of 198 patients von Mol, Merel O., van Rooij, Jeroen G.J., Wong, Tsz H., Melhem, Shamiram, Verkerk, Annemieke J.M.H., Kievit, Anneke J.A., van Minkelen, Rick, Rademakers, Rosa, Pottier, Cyril, Kaat, Laura Donker, Seelaar, Harro, van Swieten, John C., Dopper, Elise G.P.

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A systematic analysis highlights multiple long non-coding RNAs associated with cardiometabolic disorders von Ghanbari, Mohsen, Peters, Marjolein J, de Vries, Paul S, Boer, Cindy G, van Rooij, Jeroen G J, Lee, Yu-Chi, Kumar, Vinod, Uitterlinden, André G, Ikram, M Arfan, Wijmenga, Cisca, Ordovas, Jose M, Smith, Caren E, van Meurs, Joyce B J, Erkeland, Stefan J, Franco, Oscar H, Dehghan, Abbas

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P1‐123: Differential Expression in Hippocampus of Alzheimer's Disease Patients von Rooij, Jeroen G.J., Meeter, Lieke H.H., Melhem, Shami, Nijholt, Diana, Rozemuller, Annemieke, Uitterlinden, Andre G., Meurs, Joyce, Van Swieten, John C.

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DIFFERENTIAL EXPRESSION IN HIPPOCAMPUS OF ALZHEIMER'S DISEASE PATIENTS von van Rooij, Jeroen G.J, Meeter, Lieke H.H, Melhem, Shami, Nijholt, Diana, Rozemuller, Annemieke, Uitterlinden, Andre G, van Meurs, Joyce, Van Swieten, John C

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Whole Exome Sequencing in Two Southeast Asian Families With Atypical Femur Fractures von Zhou, Wei, Nguyen, Hanh H., Laarschot, Denise M., Howe, Tet Sen, Koh, Joyce S.B., Milat, Frances, van Rooij, Jeroen G.J., Verlouw, Joost A.M., van der Eerden, Bram C.J., Stevenson, Mark, Thakker, Rajesh V., Zillikens, M. Carola, Ebeling, Peter R.

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P2‐024: Whole‐exome sequencing in dutch families with Alzheimer's disease von Wong, Tsz Hang, Lee, Sven J., Meeter, Lieke H.H., Rooij, Jeroen G.J., Ikram, M. Arfan, Minkelen, Rick, Uitterlinden, Andre G., Amin, Najaf, Duijn, Cornelia M., Swieten, John C.

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Whole-exome sequencing in dutch families with Alzheimer’s disease von Wong, Tsz Hang, van der Lee, Sven J, Meeter, Lieke H.H, van Rooij, Jeroen G.J, Ikram, M. Arfan, van Minkelen, Rick, Uitterlinden, Andre G, Amin, Najaf, van Duijn, Cornelia M, van Swieten, John C

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Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen G. J., Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J., Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, DeStefano, Anita L., Farrer, Lindsay A., Fox, Nick C., Galimberti, Daniela, Gille, Johan J. P., Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Marc, Lemstra, Afina W., Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel M. A. M., Marshall, Rachel, Martin, Eden R., Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel O., Morgan, Kevin, Myers, Richard M., Nacmias, Benedetta, Naj, Adam C., Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T., Riedel-Heller, Steffi G., Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S., Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D., Scheltens, Philip, Schott, Jonathan M., Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A., Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André G., van der Lee, Sven J., Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimon, Jordi, van Swieten, John C., Greicius, Michael D., Yokoyama, Jennifer S., Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M., van Duijn, Cornelia M., Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

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Risk Assessment for Hip and Knee Osteoarthritis Using Polygenic Risk Scores von Sedaghati‐Khayat, Bahar, Boer, Cindy G., Runhaar, Jos, Bierma‐Zeinstra, Sita M. A., Broer, Linda, Ikram, M. Arfan, Zeggini, Eleftheria, Uitterlinden, André G., Rooij, Jeroen G. J., Meurs, Joyce B. J.

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Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients von Zhou, Wei, Rooij, Jeroen GJ, Laarschot, Denise M, Zervou, Zografia, Bruggenwirth, Hennie, Appelman‐Dijkstra, Natasha M, Ebeling, Peter R, Demirdas, Serwet, Verkerk, Annemieke JMH, Zillikens, M Carola

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Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy von Holstege, Henne, van der Lee, Sven J, Hulsman, Marc, Wong, Tsz Hang, van Rooij, Jeroen Gj, Weiss, Marjan, Louwersheimer, Eva, Wolters, Frank J, Amin, Najaf, Uitterlinden, André G, Hofman, Albert, Ikram, M Arfan, van Swieten, John C, Meijers-Heijboer, Hanne, van der Flier, Wiesje M, Reinders, Marcel Jt, van Duijn, Cornelia M, Scheltens, Philip

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Molecular Pathways Involved in Frontotemporal Lobar Degeneration with TDP-43 Proteinopathy: What Can We Learn from Proteomics? von Mol, Merel O., Miedema, Suzanne S. M., van Swieten, John C., van Rooij, Jeroen G. J., Dopper, Elise G. P.

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Hippocampal transcriptome profiling combined with protein-protein interaction analysis elucidates Alzheimer's disease pathways and genes von van Rooij, Jeroen G.J., Meeter, Lieke H.H., Melhem, Shami, Nijholt, Diana A.T., Wong, Tsz Hang, Rozemuller, Annemieke, Uitterlinden, Andre G., van Meurs, Joyce G., van Swieten, John C.

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The Genetics of Atypical Femur Fractures—a Systematic Review von Zhou, Wei, van Rooij, Jeroen G. J., Ebeling, Peter R., Verkerk, Annemieke J. M. H., Zillikens, M. Carola

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Lifestyle Intervention Randomized Controlled Trial for Age-Related Macular Degeneration (AMD-Life): Study Design von de Koning-Backus, Alexandra P M, Kiefte-de Jong, Jessica C, van Rooij, Jeroen G J, Amd-Life Team, Uitterlinden, André G, Voortman, Trudy G, Meester-Smoor, Magda A, Klaver, Caroline C W

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Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch’s Membrane von Corominas, Jordi, Colijn, Johanna M., Geerlings, Maartje J., Pauper, Marc, Bakker, Bjorn, Amin, Najaf, Lores Motta, Laura, Kersten, Eveline, Garanto, Alejandro, Verlouw, Joost A.M., van Rooij, Jeroen G.J., Kraaij, Robert, de Jong, Paulus T.V.M., Hofman, Albert, Vingerling, Johannes R., Schick, Tina, Fauser, Sascha, de Jong, Eiko K., van Duijn, Cornelia M., Hoyng, Carel B., Klaver, Caroline C.W., den Hollander, Anneke I.

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Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors von Pankratz, Nathan, Wei, Peng, Brody, Jennifer A, Chen, Ming-Huei, de Vries, Paul S, Huffman, Jennifer E, Stimson, Mary Rachel, Auer, Paul L, Boerwinkle, Eric, Cushman, Mary, de Maat, Moniek P M, Folsom, Aaron R, Franco, Oscar H, Gibbs, Richard A, Haagenson, Kelly K, Hofman, Albert, Johnsen, Jill M, Kovar, Christie L, Kraaij, Robert, McKnight, Barbara, Metcalf, Ginger A, Muzny, Donna, Psaty, Bruce M, Tang, Weihong, Uitterlinden, André G, van Rooij, Jeroen G J, Dehghan, Abbas, O'Donnell, Christopher J, Reiner, Alex P, Morrison, Alanna C, Smith, Nicholas L

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EIF2AK3 variants in Dutch patients with Alzheimer's disease von Wong, Tsz Hang, van der Lee, Sven J., van Rooij, Jeroen G.J., Meeter, Lieke H.H., Frick, Petra, Melhem, Shamiram, Seelaar, Harro, Ikram, M. Arfan, Rozemuller, Annemieke J., Holstege, Henne, Hulsman, Marc, Uitterlinden, Andre, Neumann, Manuela, Hoozemans, Jeroen J.M., van Duijn, Cornelia M., Rademakers, Rosa, van Swieten, John C.

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Proteomics of the dentate gyrus reveals semantic‐dementia‐specific biology von Mol, Merel O., Melhem, Shamiram, Miedema, Suzanne S.M., Seelaar, Harro, Smit, August B., van Swieten, John C, van Rooij, Jeroen G.J.

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