Cardiac myocyte miR-29 promotes pathological remodeling of the heart by activating Wnt signaling von Sassi, Y, Avramopoulos, P, Ramanujam, D, Grueter, L, Werfel, S, Giosele, S, Brunner, A-D, Esfandyari, D, Papadopoulou, AS, De Strooper, B, Huebner, N, Kumarswamy, R, Thum, T, Yin, X, Mayr, M, Laggerbauer, B, Engelhardt, S

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Atmospheric Pollution and Hospitalization for Cardiovascular and Respiratory Diseases in the City of Manaus from 2008 to 2012 von Pamplona, Ysabely de A. P., Arbex, Marcos A., Martins, Lourdes C., Sacramento, Daniel S.

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First Principle Study of the Mechanical Properties and Phonon Dispersion of the Iron Pnictide Compound EuFe2As2 von Omboga, N. K., Nyawere, P. W. O., Otieno, C. O.

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High-throughput sequencing of the synaptome in major depressive disorder von Pirooznia, M, Wang, T, Avramopoulos, D, Potash, J B, Zandi, P P, Goes, F S

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O-band QKD link over a multiple ONT loaded carrier-grade GPON for FTTH applications von Makris, N., Ntanos, A., Papageorgopoulos, A., Stathopoulos, T., Konteli, P., Stathis, A., Giannoulis, G., Tsoni, I., Setaki, F., Zavitsanos, D., Lyberopoulos, G., Avramopoulos, H., Syvridis, D., Kanellos, G. T.

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Analog fiber-wireless downlink transmission of IFoF/mmWave over in-field deployed legacy PON infrastructure for 5G fronthauling von Kanta, K., Pagano, A., Ruggeri, E., Agus, M., Stratakos, I., Mercinelli, R., Vagionas, C., Toumasis, P., Kalfas, G., Giannoulis, G., Miliou, A., Lentaris, G., Apostolopoulos, D., Pleros, N., Soudris, D., Avramopoulos, H.

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End-to-End Real-Time Service Provisioning Over a SDN-Controllable Analog mmWave Fiber -Wireless 5G X-Haul Network von Vagionas, C., Maximidis, R., Stratakos, I., Margaris, A., Mesodiakaki, A., Gatzianas, M., Kanta, K., Toumasis, P., Giannoulis, G., Apostolopoulos, D., Papatheofanous, E. A., Lentaris, G., Reisis, D., Soudris, D., Tsagkaris, K., Argyris, N., Syrivelis, D., Bakopoulos, P., Oldenbeuving, R. M., Roeloffzen, C. G. H., van Dijk, P. W. L., Dimogiannis, I., Kontogiannis, A., Avramopoulos, H., Miliou, A., Pleros, N., Kalfas, G.

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program von Taliun, Daniel, Kessler, Michael D., Carlson, Jedidiah, Taliun, Sarah A. Gagliano, Kang, Hyun Min, Pitsillides, Achilleas N., Emde, Anne-Katrin, Clarke, Wayne E., Shetty, Amol C., Wong, Quenna, Bobo, Dean M., Aguet, François, Albert, Christine, Aslibekyan, Stella, Barnard, John, Barr, R. Graham, Barwick, Lucas, Becker, Lewis C., Bielak, Lawrence F., Blangero, John, Bowden, Donald W., Burchard, Esteban G., Chalazan, Brandon, Chasman, Daniel I., Chen, Yii-Der Ida, Choi, Seung Hoan, Chung, Mina K., Curran, Joanne E., Daya, Michelle, Ellinor, Patrick T., Fatkin, Diane, Fingerlin, Tasha, Forer, Lukas, Franceschini, Nora, Germer, Soren, Gladwin, Mark T., Hall, Michael E., He, Jiang, Johnsen, Jill M., Johnson, Andrew D., Kardia, Sharon L. R., Klemmer, Robert, Kooperberg, Charles, Köttgen, Anna, Lange, Leslie A., Lin, Xihong, Lin, Keng-Han, Liu, Chunyu, Loos, Ruth J. F., Gerszten, Robert, Lunetta, Kathryn L., Mak, Angel C. Y., Manichaikul, Ani, Manning, Alisa K., Mathias, Rasika A., McManus, David D., McGarvey, Stephen T., Meigs, James B., Minear, Mollie A., Mitchell, Braxton D., Mohanty, Sanghamitra, Montasser, May E., Montgomery, Courtney, Morrison, Alanna C., Murabito, Joanne M., Natale, Andrea, Nelson, Sarah C., Palmer, Nicholette D., Pankratz, Nathan, Peyser, Patricia A., Post, Wendy S., Psaty, Bruce M., Rao, D. C., Reiner, Alexander P., Roden, Dan, Rotter, Jerome I., Schoenherr, Sebastian, Seo, Jeong-Sun, Sheu, Wayne H., Smith, Nicholas L., Smith, Jennifer A., Stilp, Adrienne M., Telen, Marilyn, Thornton, Timothy A., Tracy, Russell P., Van Den Berg, David J., Vasan, Ramachandran S., Vrieze, Scott, Weng, Lu-Chen, Zhao, Xutong, Boerwinkle, Eric, Gibbs, Richard, Rich, Stephen S., Silverman, Edwin K., Qasba, Pankaj, Gan, Weiniu, Zöllner, Sebastian, Wilson, James G., Laurie, Cathy C., Jaquish, Cashell E.

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Toward efficient, reliable, and autonomous optical networks: the ORCHESTRA solution [Invited] von Christodoulopoulos, K., Bernini, G., Roccato, D., Percelsi, A., Morro, R., Avramopoulos, H., Castoldi, P., Layec, P., Bigo, S., Delezoide, C., Sambo, N., Kretsis, A., Sartzetakis, I., Sgambelluri, A., Argyris, N., Kanakis, G., Giardina, P.

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Bipolar I Disorder and Schizophrenia: A 440–Single-Nucleotide Polymorphism Screen of 64 Candidate Genes among Ashkenazi Jewish Case-Parent Trios von Fallin, M. Daniele, Lasseter, Virginia K., Avramopoulos, Dimitrios, Nicodemus, Kristin K., Wolyniec, Paula S., McGrath, John A., Steel, Gary, Nestadt, Gerald, Liang, Kung-Yee, Huganir, Richard L., Valle, David, Pulver, Ann E.

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Structural variants caused by Alu insertions are associated with risks for many human diseases von Payer, Lindsay M., Steranka, Jared P., Yang, Wan Rou, Kryatova, Maria, Medabalimi, Sibyl, Ardeljan, Daniel, Liu, Chunhong, Boeke, Jef D., Avramopoulos, Dimitri, Burns, Kathleen H.

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Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data von Wainschtein, Pierrick, Jain, Deepti, Zheng, Zhili, Cupples, L. Adrienne, Shadyab, Aladdin H., McKnight, Barbara, Shoemaker, Benjamin M., Mitchell, Braxton D., Psaty, Bruce M., Kooperberg, Charles, Liu, Ching-Ti, Albert, Christine M., Roden, Dan, Chasman, Daniel I., Darbar, Dawood, Lloyd-Jones, Donald M., Arnett, Donna K., Regan, Elizabeth A., Boerwinkle, Eric, Rotter, Jerome I., O’Connell, Jeffrey R., Yanek, Lisa R., de Andrade, Mariza, Allison, Matthew A., McDonald, Merry-Lynn N., Chung, Mina K., Fornage, Myriam, Chami, Nathalie, Smith, Nicholas L., Ellinor, Patrick T., Vasan, Ramachandran S., Mathias, Rasika A., Loos, Ruth J. F., Rich, Stephen S., Lubitz, Steven A., Heckbert, Susan R., Redline, Susan, Guo, Xiuqing, Chen, Y. -D Ida, Laurie, Cecelia A., Hernandez, Ryan D., McGarvey, Stephen T., Goddard, Michael E., Laurie, Cathy C., North, Kari E., Lange, Leslie A., Weir, Bruce S., Yengo, Loic, Yang, Jian, Visscher, Peter M.

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SynaptomeDB: an ontology-based knowledgebase for synaptic genes von PIROOZNIA, Mehdi, TAO WANG, AVRAMOPOULOS, Dimitrios, VALLE, David, THOMAS, Gareth, HUGANIR, Richard L, GOES, Fernando S, POTASH, James B, ZANDI, Peter P

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Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants von Zhang, Siwei, Zhang, Hanwen, Zhou, Yifan, Qiao, Min, Zhao, Siming, Kozlova, Alena, Shi, Jianxin, Sanders, Alan R., Wang, Gao, Luo, Kaixuan, Sengupta, Subhajit, West, Siobhan, Qian, Sheng, Streit, Michael, Avramopoulos, Dimitrios, Cowan, Chad A., Chen, Mengjie, Pang, Zhiping P., Gejman, Pablo V., He, Xin, Duan, Jubao

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Effect of Citalopram on Agitation in Alzheimer Disease: The CitAD Randomized Clinical Trial von Porsteinsson, Anton P, Drye, Lea T, Pollock, Bruce G, Devanand, D. P, Frangakis, Constantine, Ismail, Zahinoor, Marano, Christopher, Meinert, Curtis L, Mintzer, Jacobo E, Munro, Cynthia A, Pelton, Gregory, Rabins, Peter V, Rosenberg, Paul B, Schneider, Lon S, Shade, David M, Weintraub, Daniel, Yesavage, Jerome, Lyketsos, Constantine G

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Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes von Guipponi, Michel, Santoni, Federico A, Setola, Vincent, Gehrig, Corinne, Rotharmel, Maud, Cuenca, Macarena, Guillin, Olivier, Dikeos, Dimitris, Georgantopoulos, Georgios, Papadimitriou, George, Curtis, Logos, Méary, Alexandre, Schürhoff, Franck, Jamain, Stéphane, Avramopoulos, Dimitri, Leboyer, Marion, Rujescu, Dan, Pulver, Ann, Campion, Dominique, Siderovski, David P, Antonarakis, Stylianos E

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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene von Sobreira, Nara L M, Cirulli, Elizabeth T, Avramopoulos, Dimitrios, Wohler, Elizabeth, Oswald, Gretchen L, Stevens, Eric L, Ge, Dongliang, Shianna, Kevin V, Smith, Jason P, Maia, Jessica M, Gumbs, Curtis E, Pevsner, Jonathan, Thomas, George, Valle, David, Hoover-Fong, Julie E, Goldstein, David B

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Clonal haematopoiesis and risk of chronic liver disease von Wong, Waihay J., Emdin, Connor, Bick, Alexander G., Zekavat, Seyedeh M., Niroula, Abhishek, Pirruccello, James P., Dichtel, Laura, Griffin, Gabriel, Uddin, Md Mesbah, Gibson, Christopher J., Kovalcik, Veronica, Lin, Amy E., McConkey, Marie E., Vromman, Amelie, Sellar, Rob S., Kim, Peter G., Agrawal, Mridul, Weinstock, Joshua, Long, Michelle T., Yu, Bing, Banerjee, Rajarshi, Nicholls, Rowan C., Dennis, Andrea, Kelly, Matt, Loh, Po-Ru, McCarroll, Steve, Boerwinkle, Eric, Vasan, Ramachandran S., Jaiswal, Siddhartha, Johnson, Andrew D., Chung, Raymond T., Corey, Kathleen, Levy, Daniel, Ballantyne, Christie, Ebert, Benjamin L., Natarajan, Pradeep

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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response von Luo, Yang, Kanai, Masahiro, Choi, Wanson, Li, Xinyi, Sakaue, Saori, Yamamoto, Kenichi, Ogawa, Kotaro, Gutierrez-Arcelus, Maria, Gregersen, Peter K., Stuart, Philip E., Elder, James T., Forer, Lukas, Schönherr, Sebastian, Fuchsberger, Christian, Smith, Albert V., Fellay, Jacques, Carrington, Mary, Haas, David W., Guo, Xiuqing, Palmer, Nicholette D., Chen, Yii-Der Ida, Rotter, Jerome I., Taylor, Kent D., Rich, Stephen S., Correa, Adolfo, Wilson, James G., Kathiresan, Sekar, Cho, Michael H., Metspalu, Andres, Esko, Tonu, Okada, Yukinori, Han, Buhm, McLaren, Paul J., Raychaudhuri, Soumya

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Angled 3D Glass-to-Silicon Photonics Coupling Interface von Poulopoulos, G., Kalavrouziotis, D., Macdonald, J. R., Mitchell, P., Psaila, N., Avramopoulos, H.

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