Brain Abnormalities in Patients with Germline Variants in H3F3 : Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors by Alves, C A P F, Sherbini, O, D'Arco, F, Steel, D, Kurian, M A, Radio, F C, Ferrero, G B, Carli, D, Tartaglia, M, Balci, T B, Powell-Hamilton, N N, Schrier Vergano, S A, Reutter, H, Hoefele, J, Günthner, R, Roeder, E R, Littlejohn, R O, Lessel, D, Lüttgen, S, Kentros, C, Anyane-Yeboa, K, Catarino, C B, Mercimek-Andrews, S, Denecke, J, Lyons, M J, Klopstock, T, Bhoj, E J, Bryant, L, Vanderver, A

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Genome-wide association analysis suggests novel loci for Hashimoto’s thyroiditis by Brčić, L., Barić, A., Gračan, S., Brekalo, M., Kaličanin, D., Gunjača, I., Torlak Lovrić, V., Tokić, S., Radman, M., Škrabić, V., Miljković, A., Kolčić, I., Štefanić, M., Glavaš-Obrovac, L., Lessel, D., Polašek, O., Zemunik, T., Barbalić, M., Punda, A., Boraska Perica, V.

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Paralog Studies Augment Gene Discovery: DDX and DHX Genes by Paine, Ingrid, Posey, Jennifer E., Grochowski, Christopher M., Jhangiani, Shalini N., Rosenheck, Sarah, Kleyner, Robert, Marmorale, Taylor, Yoon, Margaret, Wang, Kai, Robison, Reid, Cappuccio, Gerarda, Pinelli, Michele, Magli, Adriano, Coban Akdemir, Zeynep, Hui, Joannie, Yeung, Wai Lan, Wong, Bibiana K.Y., Ortega, Lucia, Bekheirnia, Mir Reza, Bierhals, Tatjana, Hempel, Maja, Johannsen, Jessika, Santer, René, Aktas, Dilek, Alikasifoglu, Mehmet, Bozdogan, Sevcan, Aydin, Hatip, Karaca, Ender, Bayram, Yavuz, Ityel, Hadas, Dorschner, Michael, White, Janson J., Wilichowski, Ekkehard, Wortmann, Saskia B., Casella, Erasmo B., Kitajima, Joao Paulo, Kok, Fernando, Monteiro, Fabiola, Muzny, Donna M., Bamshad, Michael, Gibbs, Richard A., Sutton, V. Reid, Van Esch, Hilde, Brunetti-Pierri, Nicola, Hildebrandt, Friedhelm, Brautbar, Ariel, Van den Veyver, Ignatia B., Glass, Ian, Lessel, Davor, Lyon, Gholson J., Lupski, James R.

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Werner syndrome. A prototypical form of segmental progeria. by Lessel, D, Oshima, J, Kubisch, C

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KIT mutations in primary mediastinal B-cell lymphoma by Nagel, P D, Stenzinger, A, Feld, F M, Herrmann, M D, Brüderlein, S, Barth, T F E, Marienfeld, R, Endris, V, Weichert, W, Debatin, K-M, Westhoff, M-A, Lessel, D, Möller, P, Lennerz, J K

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders by Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

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A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features by Saha, B., Lessel, D., Hisama, F.M., Leistritz, D.F., Friedrich, K., Martin, G.M., Kubisch, C., Oshima, J.

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Association Study between Polymorphisms in DNA Methylation-Related Genes and Testicular Germ Cell Tumor Risk by Grasso, Chiara, Popovic, Maja, Isaevska, Elena, Lazzarato, Fulvio, Fiano, Valentina, Zugna, Daniela, Pluta, John, Weathers, Benita, D'Andrea, Kurt, Almstrup, Kristian, Anson-Cartwright, Lynn, Bishop, D Timothy, Chanock, Stephen J, Chen, Chu, Cortessis, Victoria K, Dalgaard, Marlene D, Daneshmand, Siamak, Ferlin, Alberto, Foresta, Carlo, Frone, Megan N, Gamulin, Marija, Gietema, Jourik A, Greene, Mark H, Grotmol, Tom, Hamilton, Robert J, Haugen, Trine B, Hauser, Russ, Karlsson, Robert, Kiemeney, Lambertus A, Lessel, Davor, Lista, Patrizia, Lothe, Ragnhild A, Loveday, Chey, Meijer, Coby, Nead, Kevin T, Nsengimana, Jérémie, Skotheim, Rolf I, Turnbull, Clare, Vaughn, David J, Wiklund, Fredrik, Zheng, Tongzhang, Zitella, Andrea, Schwartz, Stephen M, McGlynn, Katherine A, Kanetsky, Peter A, Nathanson, Katherine L, Richiardi, Lorenzo

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Intake Patterns of Specific Alcoholic Beverages by Prostate Cancer Status by Lin, Hui-Yi, Tseng, Tung-Sung, Wang, Xinnan, Fang, Zhide, Zea, Arnold H, Wang, Liang, Pow-Sang, Julio, Tangen, Catherine M, Goodman, Phyllis J, Wolk, Alicja, Håkansson, Niclas, Kogevinas, Manolis, Llorca, Javier, Brenner, Hermann, Schöttker, Ben, Castelao, Jose Esteban, Gago-Dominguez, Manuela, Gamulin, Marija, Lessel, Davor, Claessens, Frank, Joniau, Steven, The Practical Consortium, Park, Jong Y

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Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma by Went, Molly, Sud, Amit, Försti, Asta, Halvarsson, Britt-Marie, Weinhold, Niels, Kimber, Scott, van Duin, Mark, Thorleifsson, Gudmar, Holroyd, Amy, Johnson, David C., Li, Ni, Orlando, Giulia, Law, Philip J., Ali, Mina, Chen, Bowang, Mitchell, Jonathan S., Gudbjartsson, Daniel F., Kuiper, Rowan, Stephens, Owen W., Bertsch, Uta, Broderick, Peter, Campo, Chiara, Bandapalli, Obul R, Einsele, Hermann, Gregory, Walter A., Gullberg, Urban, Hillengass, Jens, Hoffmann, Per, Jackson, Graham H., Jöckel, Karl-Heinz, Johnsson, Ellinor, Kristinsson, Sigurður Y., Mellqvist, Ulf-Henrik, Nahi, Hareth, Easton, Douglas, Pharoah, Paul, Dunning, Alison, Peto, Julian, Canzian, Federico, Swerdlow, Anthony, Eeles, Rosalind A., Kote-Jarai, Zsofia, Muir, Kenneth, Pashayan, Nora, Nickel, Jolanta, Nöthen, Markus M., Rafnar, Thorunn, Ross, Fiona M., da Silva Filho, Miguel Inacio, Thomsen, Hauke, Turesson, Ingemar, Vangsted, Annette, Andersen, Niels Frost, Waage, Anders, Walker, Brian A., Wihlborg, Anna-Karin, Broyl, Annemiek, Davies, Faith E., Thorsteinsdottir, Unnur, Langer, Christian, Hansson, Markus, Goldschmidt, Hartmut, Kaiser, Martin, Sonneveld, Pieter, Stefansson, Kari, Morgan, Gareth J., Hemminki, Kari, Nilsson, Björn, Houlston, Richard S.

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Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry by Matejcic, Marco, Saunders, Edward J., Dadaev, Tokhir, Brook, Mark N., Wang, Kan, Sheng, Xin, Olama, Ali Amin Al, Schumacher, Fredrick R., Ingles, Sue A., Govindasami, Koveela, Benlloch, Sara, Berndt, Sonja I., Albanes, Demetrius, Koutros, Stella, Muir, Kenneth, Stevens, Victoria L., Gapstur, Susan M., Tangen, Catherine M., Batra, Jyotsna, Clements, Judith, Gronberg, Henrik, Pashayan, Nora, Schleutker, Johanna, Wolk, Alicja, West, Catharine, Mucci, Lorelei, Kraft, Peter, Cancel-Tassin, Géraldine, Sorensen, Karina D., Maehle, Lovise, Grindedal, Eli M., Strom, Sara S., Neal, David E., Hamdy, Freddie C., Donovan, Jenny L., Travis, Ruth C., Hamilton, Robert J., Rosenstein, Barry, Lu, Yong-Jie, Giles, Graham G., Kibel, Adam S., Vega, Ana, Bensen, Jeanette T., Kogevinas, Manolis, Penney, Kathryn L., Park, Jong Y., Stanford, Janet L., Cybulski, Cezary, Nordestgaard, Børge G., Brenner, Hermann, Maier, Christiane, Kim, Jeri, Teixeira, Manuel R., Neuhausen, Susan L., De Ruyck, Kim, Razack, Azad, Newcomb, Lisa F., Lessel, Davor, Kaneva, Radka, Usmani, Nawaid, Claessens, Frank, Townsend, Paul A., Gago-Dominguez, Manuela, Roobol, Monique J., Menegaux, Florence, Khaw, Kay-Tee, Cannon-Albright, Lisa A., Pandha, Hardev, Thibodeau, Stephen N., Schaid, Daniel J., Wiklund, Fredrik, Chanock, Stephen J., Easton, Douglas F., Eeles, Rosalind A., Kote-Jarai, Zsofia, Conti, David V., Haiman, Christopher A.

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Werner-Syndrom by Lessel, D., Oshima, J., Kubisch, C.

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Werner-Syndrom. Eine prototypische Form der segmentalen Progerie by Lessel, D., Oshima, J., Kubisch, C.

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Identification of 22 novel loci associated with susceptibility to testicular germ cell tumors by Pluta, J, Pyle, L, Bishop, T, Benitez, J, Cortessis, V, Ferlin, A, Gietema, J, Greene, M, Grotmol, T, Gupta, R, Hamilton, R, Hildebrandt, M, Kiemeney, L, Lessel, D, Rafnar, T, Richiardi, L, Skotheim, R, Turnbull, C, Wiklund, F, Zheng, TZ, Rajpert-De Meyts, E, Schwartz, S, McGlynn, K, Kanetsky, P, Nathanson, K

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Onset of a fulminant malignant hyperthermia crisis. Case report of a 74-year-old patient with previously subclinical central core disease by Wejbora, M, Bornemann-Cimenti, H, Lessel, D, Mandl, C, Voit-Augustin, H, Schwarz, G

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Identification of 14 novel genetic loci for testicular germ cell tumor susceptibility by Pyle, LC, Pluta, J, Nead, KT, Mitra, N, Benitez, J, Bishop, DT, Cortessis, V, Ferlin, A, Gietema, J, Greene, M, Grotmol, T, Gupta, R, Hamilton, R, Hildebrandt, MA, Haugen, TB, Kiemeney, L, Kubisch, C, Lessel, D, Martin, P, Rafnar, T, Richiardi, L, Skotheim, R, Turnbull, C, Wiklund, F, Zheng, TZ, Rajpert-De Meyts, E, Schwartz, SM, McGlynn, KA, Kanetsky, PA, Nathanson, KL

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Werner-Syndrom: Eine prototypische Form der segmentalen Progerie by Lessel, D., Oshima, J., Kubisch, C.

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Werner syndrome. A prototypical form of segmental progeria. by Lessel, D, Oshima, J, Kubisch, C

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Erstmanifestation einer fulminanten Malignen-Hyperthermie-Krise: Fall eines 74-jährigen Patienten mit bislang subklinischer „central core disease by Wejbora, M., Bornemann-Cimenti, H., Lessel, D., Mandl, C., Voit-Augustin, H., Schwarz, G.

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A global surveillance system for crop diseases by Carvajal-Yepes, M, Cardwell, K, Nelson, A, Garrett, K A, Giovani, B, Saunders, D G O, Kamoun, S, Legg, J P, Verdier, V, Lessel, J, Neher, R A, Day, R, Pardey, P, Gullino, M L, Records, A R, Bextine, B, Leach, J E, Staiger, S, Tohme, J

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