High-resolution Russian–German beamline at BESSY von Molodtsov, S. L., Fedoseenko, S. I., Vyalikh, D. V., Iossifov, I. E., Follath, R., Gorovikov, S. A., Brzhezinskaya, M. M., Dedkov, Y. S., Püttner, R., Schmidt, J.-S., Adamchuk, V. K., Gudat, W., Kaindl, G.

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Commissioning results and performance of the high-resolution Russian–German Beamline at BESSY II von Fedoseenko, S.I, Vyalikh, D.V, Iossifov, I.E, Follath, R, Gorovikov, S.A, Püttner, R, Schmidt, J.-S, Molodtsov, S.L, Adamchuk, V.K, Gudat, W, Kaindl, G

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The Russian-German Soft X-Ray Beamline at BESSY II von Vyalikh, D V, Fedoseenko, S I, Iossifov, I E, Follath, R, Gorovikov, S A, Molodtsov, S L, Schmidt, J-S, Puttner, R, Adamchuk, V K, Gudat, W, Kaindl, G

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Development and present status of the Russian–German soft X-ray beamline at BESSY II von Fedoseenko, S.I., Iossifov, I.E., Gorovikov, S.A., Schmidt, J.-S., Follath, R., Molodtsov, S.L., Adamchuk, V.K., Kaindl, G.

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High-resolution Russian-German beamline at BESSY : Material Sciences at BESSY von MOLODTSOV, S. L, FEDOSEENKO, S. I, ADAMCHUK, V. K, GUDAT, W, KAINDL, G, VYALIKH, D. V, IOSSIFOV, I. E, FOLLATH, R, GOROVIKOV, S. A, BRZHEZINSKAYA, M. M, DEDKOV, Y. S, PÜTTNER, R, SCHMIDT, J.-S

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Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk von Castel, Stephane E., Cervera, Alejandra, Mohammadi, Pejman, Aguet, François, Reverter, Ferran, Wolman, Aaron, Guigo, Roderic, Iossifov, Ivan, Vasileva, Ana, Lappalainen, Tuuli

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Damaging de novo mutations diminish motor skills in children on the autism spectrum von Buja, Andreas, Volfovsky, Natalia, Krieger, Abba M., Lord, Catherine, Lash, Alex E., Wigler, Michael, Iossifov, Ivan

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Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA von Turner, Tychele N., Hormozdiari, Fereydoun, Duyzend, Michael H., McClymont, Sarah A., Hook, Paul W., Iossifov, Ivan, Raja, Archana, Baker, Carl, Hoekzema, Kendra, Stessman, Holly A., Zody, Michael C., Nelson, Bradley J., Huddleston, John, Sandstrom, Richard, Smith, Joshua D., Hanna, David, Swanson, James M., Faustman, Elaine M., Bamshad, Michael J., Stamatoyannopoulos, John, Nickerson, Deborah A., McCallion, Andrew S., Darnell, Robert, Eichler, Evan E.

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Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis,... von Cheng, R, Juo, S H, Loth, J E, Nee, J, Iossifov, I, Blumenthal, R, Sharpe, L, Kanyas, K, Lerer, B, Lilliston, B, Smith, M, Trautman, K, Gilliam, T C, Endicott, J, Baron, M

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De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies von Homsy, Jason, Zaidi, Samir, Shen, Yufeng, Ware, James S., Samocha, Kaitlin E., Karczewski, Konrad J., DePalma, Steven R., McKean, David, Wakimoto, Hiroko, Gorham, Josh, Jin, Sheng Chih, Deanfield, John, Giardini, Alessandro, Porter, George A., Kim, Richard, Bilguvar, Kaya, López-Giráldez, Francesc, Tikhonova, Irina, Mane, Shrikant, Romano-Adesman, Angela, Qi, Hongjian, Vardarajan, Badri, Ma, Lijiang, Daly, Mark, Roberts, Amy E., Russell, Mark W., Mital, Seema, Newburger, Jane W., Gaynor, J. William, Breitbart, Roger E., Iossifov, Ivan, Ronemus, Michael, Sanders, Stephan J., Kaltman, Jonathan R., Seidman, Jonathan G., Brueckner, Martina, Gelb, Bruce D., Goldmuntz, Elizabeth, Lifton, Richard P., Seidman, Christine E., Chung, Wendy K.

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Mapping and characterization of structural variation in 17,795 human genomes von Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.

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The contribution of de novo coding mutations to autism spectrum disorder von Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali T., Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jeffrey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael

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Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction von Shi, Xi, Lu, Congyi, Corman, Alba, Nikish, Alexandra, Zhou, Yang, Platt, Randy J., Iossifov, Ivan, Zhang, Feng, Pan, Jen Q., Sanjana, Neville E.

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Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants von Einson, Jonah, Glinos, Dafni, Boerwinkle, Eric, Castaldi, Peter, Darbar, Dawood, de Andrade, Mariza, Ellinor, Patrick, Fornage, Myriam, Gabriel, Stacey, Germer, Soren, Gibbs, Richard, Hersh, Craig P, Johnsen, Jill, Kaplan, Robert, Konkle, Barbara A, Kooperberg, Charles, Nassir, Rami, Loos, Ruth J F, Meyers, Deborah A, Mitchell, Braxton D, Psaty, Bruce, Vasan, Ramachandran S, Rich, Stephen S, Rienstra, Michael, Rotter, Jerome I, Saferali, Aabida, Shoemaker, Moore Benjamin, Silverman, Edwin, Smith, Albert Vernon, Mohammadi, Pejman, Castel, Stephane E, Iossifov, Ivan, Lappalainen, Tuuli

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Mast-cell leukemia exome sequencing reveals a mutation in the IgE mast-cell receptor β chain and KIT V654A von Spector, M S, Iossifov, I, Kritharis, A, He, C, Kolitz, J E, Lowe, S W, Allen, S L

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De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms von Jansen, Sandra, van der Werf, Ilse M, Innes, A Micheil, Afenjar, Alexandra, Agrawal, Pankaj B, Anderson, Ilse J, Atwal, Paldeep S, van Binsbergen, Ellen, van den Boogaard, Marie-José, Castiglia, Lucia, Coban-Akdemir, Zeynep H, van Dijck, Anke, Doummar, Diane, van Eerde, Albertien M, van Essen, Anthonie J, van Gassen, Koen L, Guillen Sacoto, Maria J, van Haelst, Mieke M, Iossifov, Ivan, Jackson, Jessica L, Judd, Elizabeth, Kaiwar, Charu, Keren, Boris, Klee, Eric W, Klein Wassink-Ruiter, Jolien S, Meuwissen, Marije E, Monaghan, Kristin G, de Munnik, Sonja A, Nava, Caroline, Ockeloen, Charlotte W, Pettinato, Rosa, Racher, Hilary, Rinne, Tuula, Romano, Corrado, Sanders, Victoria R, Schnur, Rhonda E, Smeets, Eric J, Stegmann, Alexander P A, Stray-Pedersen, Asbjørg, Sweetser, David A, Terhal, Paulien A, Tveten, Kristian, VanNoy, Grace E, de Vries, Petra F, Waxler, Jessica L, Willing, Marcia, Pfundt, Rolph, Veltman, Joris A, Kooy, R Frank, Vissers, Lisenka E L M, de Vries, Bert B A

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Are Non-Euro Area EU Countries Importing Low Inflation from the Euro Area? von Iossifov, Plamen, Podpiera, Jiri

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Interest Rate Elasticity of Residential Housing Prices von Iossifov, Plamen, Cihák, Martin, Shanghavi, Amar

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Estimation of a Behavioral Equilibrium Exchange Rate Model for Ghana von Loukoianova, Elena, Iossifov, Plamen

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De novo mutations in congenital heart disease with neurodevelopmental and other birth defects von Homsy, J, Zaidi, S, Shen, Y, Ware, JS, Samocha, KE, Wakimoto, H, Gorham, J, Chih Jin, S, Deanfield, J, Giardini, A, Porter Jr., GA, Kim, R, Bilguvar, K, Lopez, F, Tikhonova, I, Mane, S, Romano Adesman, A, Qi, H, Vardarajan, B, Ma, L, Daly, M, Roberts, AE, Russell, MW, Mital, S, Newburger, JW, Gaynor, JW, Breitbart, RE, Iossifov, I, Ronemus, M, Sanders, SJ, Kaltman, JR, Seidman, JG, Brueckner, M, Gelb, BD, Goldmuntz, E, Lifton, RP, Seidman, CE, Chung, WK

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