Structure and reactivity of hexacoordinate hemoglobins von Kakar, Smita, Hoffman, Federico G., Storz, Jay F., Fabian, Marian, Hargrove, Mark S.

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Phylogenomic analyses data of the avian phylogenomics project von Jarvis, Erich D, Mirarab, Siavash, Aberer, Andre J, Li, Bo, Houde, Peter, Li, Cai, Ho, Simon Y W, Faircloth, Brant C, Nabholz, Benoit, Howard, Jason T, Suh, Alexander, Weber, Claudia C, da Fonseca, Rute R, Alfaro-Núñez, Alonzo, Narula, Nitish, Liu, Liang, Burt, Dave, Ellegren, Hans, Edwards, Scott V, Stamatakis, Alexandros, Mindell, David P, Cracraft, Joel, Braun, Edward L, Warnow, Tandy, Jun, Wang, Gilbert, M Thomas Pius, Zhang, Guojie

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Sustainable care for children with cancer: a Lancet Oncology Commission von Atun, Rifat, Bhakta, Nickhill, Denburg, Avram, Frazier, A Lindsay, Friedrich, Paola, Gupta, Sumit, Lam, Catherine G, Ward, Zachary J, Yeh, Jennifer M, Allemani, Claudia, Coleman, Michel P, Di Carlo, Veronica, Loucaides, Eva, Fitchett, Elizabeth, Girardi, Fabio, Horton, Susan E, Bray, Freddie, Steliarova-Foucher, Eva, Sullivan, Richard, Aitken, Joanne F, Banavali, Shripad, Binagwaho, Agnes, Alcasabas, Patricia, Antillon, Federico, Arora, Ramandeep S, Barr, Ronald D, Bouffet, Eric, Challinor, Julia, Fuentes-Alabi, Soad, Gross, Thomas, Hagander, Lars, Hoffman, Ruth I, Herrera, Cristian, Kutluk, Tezer, Marcus, Karen J, Moreira, Claude, Pritchard-Jones, Kathy, Ramirez, Oscar, Renner, Lorna, Robison, Leslie L, Shalkow, Jaime, Sung, Lillian, Yeoh, Allen, Rodriguez-Galindo, Carlos

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De novo variants in neurodevelopmental disorders with epilepsy von Heyne, Henrike O., Singh, Tarjinder, Stamberger, Hannah, Abou Jamra, Rami, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Guerrini, Renzo, Helbig, Katherine L., Koeleman, Bobby P. C., Kosmicki, Jack A., Linnankivi, Tarja, May, Patrick, Muhle, Hiltrud, Møller, Rikke S., Neubauer, Bernd A., Palotie, Aarno, Pendziwiat, Manuela, Striano, Pasquale, Tang, Sha, Wu, Sitao, Poduri, Annapurna, Weber, Yvonne G., Weckhuysen, Sarah, Sisodiya, Sanjay M., Daly, Mark J., Helbig, Ingo, Lal, Dennis, Lemke, Johannes R.

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Chronic stress disrupts fear extinction and enhances amygdala and hippocampal Fos expression in an animal model of post-traumatic stress disorder von Hoffman, Ann N., Lorson, Nickolaus G., Sanabria, Federico, Foster Olive, M., Conrad, Cheryl D.

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The phenotypic spectrum of SCN8A encephalopathy von Larsen, Jan, Carvill, Gemma L, Gardella, Elena, Kluger, Gerhard, Schmiedel, Gudrun, Barisic, Nina, Depienne, Christel, Brilstra, Eva, Mang, Yuan, Nielsen, Jens Erik Klint, Kirkpatrick, Martin, Goudie, David, Goldman, Rebecca, Jähn, Johanna A, Jepsen, Birgit, Gill, Deepak, Döcker, Miriam, Biskup, Saskia, McMahon, Jacinta M, Koeleman, Bobby, Harris, Mandy, Braun, Kees, de Kovel, Carolien G F, Marini, Carla, Specchio, Nicola, Djémié, Tania, Weckhuysen, Sarah, Tommerup, Niels, Troncoso, Monica, Troncoso, Ledia, Bevot, Andrea, Wolff, Markus, Hjalgrim, Helle, Guerrini, Renzo, Scheffer, Ingrid E, Mefford, Heather C, Møller, Rikke S

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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy von Syrbe, Steffen, Hedrich, Ulrike B S, Riesch, Erik, Djémié, Tania, Müller, Stephan, Møller, Rikke S, Maher, Bridget, Hernandez-Hernandez, Laura, Synofzik, Matthis, Caglayan, Hande S, Arslan, Mutluay, Serratosa, José M, Nothnagel, Michael, May, Patrick, Krause, Roland, Löffler, Heidrun, Detert, Katja, Dorn, Thomas, Vogt, Heinrich, Krämer, Günter, Schöls, Ludger, Mullis, Primus E, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Sterbova, Katalin, Craiu, Dana C, Hoffman-Zacharska, Dorota, Korff, Christian M, Weber, Yvonne G, Steinlin, Maja, Gallati, Sabina, Bertsche, Astrid, Bernhard, Matthias K, Merkenschlager, Andreas, Kiess, Wieland, Gonzalez, Michael, Züchner, Stephan, Palotie, Aarno, Suls, Arvid, De Jonghe, Peter, Helbig, Ingo, Biskup, Saskia, Wolff, Markus, Maljevic, Snezana, Schüle, Rebecca, Sisodiya, Sanjay M, Weckhuysen, Sarah, Lerche, Holger, Lemke, Johannes R

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De novo mutations in HCN1 cause early infantile epileptic encephalopathy von Nava, Caroline, Dalle, Carine, Rastetter, Agnès, Striano, Pasquale, de Kovel, Carolien G F, Nabbout, Rima, Cancès, Claude, Ville, Dorothée, Brilstra, Eva H, Gobbi, Giuseppe, Raffo, Emmanuel, Bouteiller, Delphine, Marie, Yannick, Trouillard, Oriane, Robbiano, Angela, Keren, Boris, Agher, Dahbia, Roze, Emmanuel, Lesage, Suzanne, Nicolas, Aude, Brice, Alexis, Baulac, Michel, Vogt, Cornelia, El Hajj, Nady, Schneider, Eberhard, Suls, Arvid, Weckhuysen, Sarah, Gormley, Padhraig, Lehesjoki, Anna-Elina, De Jonghe, Peter, Helbig, Ingo, Baulac, Stéphanie, Zara, Federico, Koeleman, Bobby P C, Haaf, Thomas, LeGuern, Eric, Depienne, Christel

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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy von Helbig, Ingo, Lopez-Hernandez, Tania, Shor, Oded, Galer, Peter, Ganesan, Shiva, Pendziwiat, Manuela, Rademacher, Annika, Ellis, Colin A., Hümpfer, Nadja, Schwarz, Niklas, Seiffert, Simone, Peeden, Joseph, Shen, Joseph, Štěrbová, Katalin, Hammer, Trine Bjørg, Møller, Rikke S., Shinde, Deepali N., Tang, Sha, Smith, Lacey, Poduri, Annapurna, Krause, Roland, Benninger, Felix, Helbig, Katherine L., Haucke, Volker, Weber, Yvonne G., Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Depienne, Christel, Guerrini, Renzo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby P.C., Komarek, Vladimir, Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Muhle, Hiltrud, Pal, Deb K., Palotie, Aarno, Rosenow, Felix, Schubert-Bast, Susanne, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Zara, Federico, Avillach, Paul, Bartels, Anna, Biswas, Sawona, Bourgeois, Florence, Devkota, Batsal, Glauser, Tracy, Hallinan, Barbara, Heath, Allison, Hirschhorn, Joel, Kilbourn, Judson, Kong, Sek Won, Krantz, Ian, Lee, In-Hee, Mandl, Kenneth D., Marsh, Eric, Sund, Kristen, Taylor, Deanne, White, Peter

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Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer von DONGHUI LI, DUELL, Eric J, ARSLAN, Alan A, BUENO-DE-MESQUITA, H. Bas, FUCHS, Charles S, GALLINGER, Steven, GROSS, Myron, HARTGE, Patricia, HOOVER, Robert N, HOLLY, Elizabeth A, JACOBS, Eric J, KLEIN, Alison P, KAI YU, LACROIX, Andrea, MANDELSON, Margaret T, PETERSEN, Gloria, WEI ZHENG, AGALLIU, Ilir, ALBANES, Demetrius, BOUTRON-RUAULT, Marie-Christine, BRACCI, Paige M, BURING, Julie E, CANZIAN, Federico, RISCH, Harvey A, CHANG, Kenneth, CHANOCK, Stephen J, COTTERCHIO, Michelle, GAZIANO, J. Michael, GIOVANNUCCI, Edward L, GOGGINS, Michael, HALLMANS, Göran, HANKINSON, Susan E, HOFFMAN BOLTON, Judith A, HUNTER, David J, OLSON, Sara H, HUTCHINSON, Amy, JACOBS, Kevinb, JENAB, Mazda, KHAW, Kay-Tee, KRAFT, Peter, KROGH, Vittorio, KURTZ, Robert C, MCWILLIAMS, Robert R, MENDELSOHN, Julie B, PATEL, Alpa V, KOOPERBERG, Charles, RABE, Kari G, RIBOLI, Elio, SHU, Xiao-Ou, TJØNNELAND, Anne, TOBIAS, Geoffrey S, TRICHOPOULOS, Dimitrios, VIRTAMO, Jarmo, VISVANATHAN, Kala, WATTERS, Joanne, HERBERT YU, WOLPIN, Brian M, LI JIAO, XIAOQUN DONG, WHEELER, Bill

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The Cysteine-Rich Region of Respiratory Syncytial Virus Attachment Protein Inhibits Innate Immunity Elicited by the Virus and Endotoxin von Polack, Fernando P., Irusta, Pablo M., Hoffman, Scott J., Schiatti, M. Paula, Melendi, Guillermina A., Delgado, M. Florencia, Laham, Federico R., Thumar, Bhagvanji, Hendry, R. Michael, Melero, Jose A., Karron, Ruth A., Collins, Peter L., Kleeberger, Steven R., Lamb, Robert A.

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Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders von Lal, Dennis, May, Patrick, Perez-Palma, Eduardo, Samocha, Kaitlin E., Kosmicki, Jack A., Robinson, Elise B., Moller, Rikke S., Krause, Roland, Nuernberg, Peter, Weckhuysen, Sarah, De Jonghe, Peter, Guerrini, Renzo, Niestroj, Lisa M., Du, Juliana, Marini, Carla, Ware, James S., Kurki, Mitja, Gormley, Padhraig, Tang, Sha, Wu, Sitao, Biskup, Saskia, Poduri, Annapurna, Neubauer, Bernd A., Koeleman, Bobby P. C., Helbig, Katherine L., Weber, Yvonne G., Helbig, Ingo, Majithia, Amit R., Palotie, Aarno, Daly, Mark J.

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Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly von Hardies, Katia, May, Patrick, Djémié, Tania, Tarta-Arsene, Oana, Deconinck, Tine, Craiu, Dana, Helbig, Ingo, Suls, Arvid, Balling, Rudy, Weckhuysen, Sarah, De Jonghe, Peter, Hirst, Jennifer

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Sustainable care for children with cancer: a Lancet Oncology Commission von Atun, Rifat, Bhakta, Nickhill, Denburg, Avram, Frazier, A Lindsay, Friedrich, Paola, Gupta, Sumit, Lam, Catherine G, Ward, Zachary J, Yeh, Jennifer M, Allemani, Claudia, Coleman, Michel P, Di Carlo, Veronica, Loucaides, Eva, Fitchett, Elizabeth, Girardi, Fabio, Horton, Susan E, Bray, Freddie, Steliarova-Foucher, Eva, Sullivan, Richard, Aitken, Joanne F, Banavali, Shripad, Binagwaho, Agnes, Alcasabas, Patricia, Antillon, Federico, Arora, Ramandeep S, Barr, Ronald D, Bouffet, Eric, Challinor, Julia, Fuentes-Alabi, Soad, Gross, Thomas, Hagander, Lars, Hoffman, Ruth I, Herrera, Cristian, Kutluk, Tezer, Marcus, Karen J, Moreira, Claude, Pritchard-Jones, Kathy, Ramirez, Oscar, Renner, Lorna, Robison, Leslie L, Shalkow, Jaime, Sung, Lillian, Yeoh, Allen, Rodriguez-Galindo, Carlos

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Chronic stress disrupts fear extinction and enhances amygdala and hippocampal Fos expression in an animal model of post-traumatic stress disorder: Stress and the regulation of memo... von HOFFMAN, Ann N, LORSON, Nickolaus G, SANABRIA, Federico, OLIVE, M. Foster, CONRAD, Cheryl D

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A bioartificial liver to treat severe acute liver failure von Rozga, J, Podesta, L, LePage, E, Morsiani, E, Moscioni, A D, Hoffman, A, Sher, L, Villamil, F, Woolf, G, McGrath, M

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Localization of a Susceptibility Gene for Familial Nonmedullary Thyroid Carcinoma to Chromosome 2q21 von McKay, James D., Lesueur, Fabienne, Jonard, Laurence, Pastore, Alessandro, Williamson, Jan, Hoffman, Linda, Burgess, John, Duffield, Anne, Papotti, Mauro, Stark, Markus, Sobol, Hagay, Maes, Béatrice, Murat, Arnaud, Kääriäinen, Helena, Bertholon-Grégoire, Mireille, Zini, Michele, Rossing, Mary Anne, Toubert, Marie-Elisabeth, Bonichon, Françoise, Cavarec, Marie, Bernard, Anne-Marie, Boneu, Andrée, Leprat, Frédéric, Haas, Oskar, Lasset, Christine, Schlumberger, Martin, Canzian, Federico, Goldgar, David E., Romeo, Giovanni

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Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4 von Leenders, Max, Bhattacharjee, Samsiddhi, Vineis, Paolo, Stevens, Victoria, Bueno-de-Mesquita, H. Bas, Shu, Xiao-Ou, Amundadottir, Laufey, Gross, Myron, Tobias, Geoffrey S., Wactawski-Wende, Jean, Arslan, Alan A., Duell, Eric J., Fuchs, Charles S., Gallinger, Steven, Hartge, Patricia, Hoover, Robert N., Holly, Elizabeth A., Jacobs, Eric J., Klein, Alison P., Kooperberg, Charles, LaCroix, Andrea, Li, Donghui, Mandelson, Margaret T., Olson, Sara H., Petersen, Gloria, Risch, Harvey A., Yu, Kai, Wolpin, Brian M., Zheng, Wei, Agalliu, Ilir, Albanes, Demetrius, Boutron-Ruault, Marie-Christine, Bracci, Paige M., Buring, Julie E., Canzian, Federico, Chang, Kenneth, Chanock, Stephen J., Cotterchio, Michelle, Gaziano, J. Michael, Giovanucci, Edward L., Goggins, Michael, Hallmans, Göran, Hankinson, Susan E., Hoffman-Bolton, Judith A., Hunter, David J., Hutchinson, Amy, Jacobs, Kevin B., Jenab, Mazda, Khaw, Kay-Tee, Kraft, Peter, Krogh, Vittorio, Kurtz, Robert C., McWilliams, Robert R., Mendelsohn, Julie B., Patel, Alpa V., Rabe, Kari G., Riboli, Elio, Tjønneland, Anne, Trichopoulos, Dimitrios, Virtamo, Jarmo, Visvanathan, Kala, Elena, Joanne W., Yu, Herbert, Zeleniuch-Jacquotte, Anne, Stolzenberg-Solomon, Rachael Z.

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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome von Suls, Arvid, Jaehn, Johanna A, Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C, Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M, Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S, Giraldez, Beatriz G, Serratosa, José, Lemke, Johannes R, Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S, Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D, Lehesjoki, Anna-Elina, de Witte, Peter A.M, Palotie, Aarno, Lerche, Holger, Esguerra, Camila V, De Jonghe, Peter, Helbig, Ingo, the EuroEPINOMICS RES Consortium

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Pathway analysis of genome-wide association study data highlights pancreatic development genes as susceptibility factors for pancreatic cancer von Li, Donghui, Duell, Eric J, Yu, Kai, Risch, Harvey A, Olson, Sara H, Kooperberg, Charles, Wolpin, Brian M, Jiao, Li, Dong, Xiaoqun, Wheeler, Bill, Arslan, Alan A, Bueno-de-Mesquita, H. Bas, Fuchs, Charles S, Gallinger, Steven, Gross, Myron, Hartge, Patricia, Hoover, Robert N, Holly, Elizabeth A, Jacobs, Eric J, Klein, Alison P, LaCroix, Andrea, Mandelson, Margaret T, Petersen, Gloria, Zheng, Wei, Agalliu, Ilir, Albanes, Demetrius, Boutron-Ruault, Marie-Christine, Bracci, Paige M, Buring, Julie E, Canzian, Federico, Chang, Kenneth, Chanock, Stephen J, Cotterchio, Michelle, Gaziano, J.Michael, Giovannucci, Edward L, Goggins, Michael, Hallmans, Göran, Hankinson, Susan E, Bolton, Judith Hoffman, Hunter, David J, Hutchinson, Amy, Jacobs, Kevin B, Jenab, Mazda, Khaw, Kay-Tee, Kraft, Peter, Krogh, Vittorio, Kurtz, Robert C, McWilliams, Robert R, Mendelsohn, Julie B, Patel, Alpa V, Rabe, Kari G, Riboli, Elio, Shu, Xiao-Ou, Tjønneland, Anne, Tobias, Geoffrey S, Trichopoulos, Dimitrios, Virtamo, Jarmo, Visvanathan, Kala, Watters, Joanne, Yu, Herbert, Zeleniuch-Jacquotte, Anne, Amundadottir, Laufey, Stolzenberg-Solomon, Rachael Z

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