MND1 enables homologous recombination in somatic cells primarily outside the context of replication von Koob, Lisa, Friskes, Anoek, Bergen, Louise, Feringa, Femke M., Broek, Bram, Koeleman, Emma S., Beek, Ellis, Schubert, Michael, Blomen, Vincent A., Brummelkamp, Thijn R., Krenning, Lenno, Medema, René H.

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Nordisk teater i Montevideo: Kontextrelaterad reception av Henrik Ibsen och August Strindberg von von Bergen, Louise

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Nordisk teater i Montevideo Kontextrelaterad reception av Henrik Ibsen och August Strindberg von von Bergen Louise 1940- , Stockholms universitet, Institutionen för litteraturvetenskap och idéhistoria, von Bergen Louise 1940-, Stockholm University, Department of Literature Science and History of Ideas

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Integrated multi-omics for rapid rare disease diagnosis on a national scale von Lunke, Sebastian, Bouffler, Sophie E., Patel, Chirag V., Sandaradura, Sarah A., Wilson, Meredith, Pinner, Jason, Hunter, Matthew F., Barnett, Christopher P., Wallis, Mathew, Kamien, Benjamin, Tan, Tiong Y., Freckmann, Mary-Louise, Chong, Belinda, Phelan, Dean, Francis, David, Kassahn, Karin S., Ha, Thuong, Gao, Song, Arts, Peer, Jackson, Matilda R., Scott, Hamish S., Eggers, Stefanie, Rowley, Simone, Boggs, Kirsten, Rakonjac, Ana, Brett, Gemma R., de Silva, Michelle G., Springer, Amanda, Ward, Michelle, Stallard, Kirsty, Simons, Cas, Conway, Thomas, Halman, Andreas, Van Bergen, Nicole J., Sikora, Tim, Semcesen, Liana N., Stroud, David A., Compton, Alison G., Thorburn, David R., Bell, Katrina M., Sadedin, Simon, North, Kathryn N., Christodoulou, John, Stark, Zornitza

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Placental Complement Activation in Fetal and Neonatal Alloimmune Thrombocytopenia: An Observational Study von de Vos, Thijs W., Winkelhorst, Dian, Baelde, Hans J., Dijkstra, Kyra L., van Bergen, Rianne D. M., van der Meeren, Lotte E., Nikkels, Peter G. J., Porcelijn, Leendert, van der Schoot, C. Ellen, Vidarsson, Gestur, Eikmans, Michael, Kapur, Rick, van der Keur, Carin, Trouw, Leendert A., Oepkes, Dick, Lopriore, Enrico, van der Hoorn, Marie-Louise P., Bos, Manon, de Haas, Masja

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Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction von Demange, Perline A., Malanchini, Margherita, Mallard, Travis T., Biroli, Pietro, Cox, Simon R., Grotzinger, Andrew D., Tucker-Drob, Elliot M., Abdellaoui, Abdel, Arseneault, Louise, van Bergen, Elsje, Boomsma, Dorret I., Caspi, Avshalom, Corcoran, David L., Domingue, Benjamin W., Harris, Kathleen Mullan, Ip, Hill F., Mitchell, Colter, Moffitt, Terrie E., Poulton, Richie, Prinz, Joseph A., Sugden, Karen, Wertz, Jasmin, Williams, Benjamin S., de Zeeuw, Eveline L., Belsky, Daniel W., Harden, K. Paige, Nivard, Michel G.

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The effectiveness of secondary-school based interventions on the future physical activity of adolescents in Aotearoa New Zealand: a modelling study von Bergen, Tom, Richards, Justin, Kira, Geoff, Kim, Alice Hyun Min, Signal, Louise, Mizdrak, Anja

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Determinants of Future Physical Activity Participation in New Zealand Adolescents across Sociodemographic Groups: A Descriptive Study von Bergen, Tom, Kim, Alice Hyun Min, Mizdrak, Anja, Signal, Louise, Kira, Geoff, Richards, Justin

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Parental Leave for Residents and Pediatric Training Programs von Takagishi, Jennifer, Garagozlo, Katiana

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Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe – A multi-professional survey study von Koido, Kati, Malmgren, Charlotta Ingvoldstad, Pojskic, Lejla, Almos, Peter Z., Bergen, Sarah E., Borg, Isabella, Božina, Nada, Coviello, Domenico A., Degenhardt, Franziska, Ganoci, Lana, Jensen, Uffe B., Durand-Lennad, Louise, Laurent-Levinson, Claudine, McQuillin, Andrew, Navickas, Alvydas, Pace, Nikolai P., Paneque, Milena, Rietschel, Marcella, Grigoroiu-Serbanescu, Maria, Soller, Maria Johansson, Suvisaari, Jaana, Utkus, Algirdas, Van Assche, Evelien, Vissouze, Lily, Zuckerman, Shachar, Chaumette, Boris, Tammimies, Kristiina

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Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder von Hughes, Timothy, Sønderby, Ida E., Polushina, Tatiana, Hansson, Lars, Holmgren, Asbjørn, Athanasiu, Lavinia, Melbø-Jørgensen, Christian, Hassani, Sahar, Hoeffding, Louise K., Herms, Stefan, Bergen, Sarah E., Karlsson, Robert, Song, Jie, Rietschel, Marcella, Nöthen, Markus M., Forstner, Andreas J., Hoffmann, Per, Hultman, Christina M., Landén, Mikael, Cichon, Sven, Werge, Thomas, Andreassen, Ole A., Le Hellard, Stephanie, Djurovic, Srdjan

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Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study von Mittendorf, Kathleen F, Hunter, Jessica Ezzell, Schneider, Jennifer L, Shuster, Elizabeth, Rope, Alan F, Zepp, Jamilyn, Gilmore, Marian J, Muessig, Kristin R, Davis, James V, Kauffman, Tia L, Bergen, Kellene M, Wiesner, Georgia L, Acheson, Louise S, Peterson, Susan K, Syngal, Sapna, Reiss, Jacob A, Goddard, Katrina A B

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Care of Adolescent Parents and Their Children von Powers, Makia E, Takagishi, Jennifer

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Identification of a Bipolar Disorder Vulnerable Gene CHDH at 3p21.1 von Chang, Hong, Li, Lingyi, Peng, Tao, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Xiao, Xiao, Li, Ming

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Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting von Clarke, Elizabeth V., Muessig, Kristin R., Zepp, Jamilyn, Hunter, Jessica E., Syngal, Sapna, Acheson, Louise S., Wiesner, Georgia L., Peterson, Susan K., Bergen, Kellene M., Shuster, Elizabeth, Davis, James V., Schneider, Jennifer L., Kauffman, Tia L., Gilmore, Marian J., Reiss, Jacob A., Rope, Alan F., Cook, Jennifer E., Goddard, Katrina A. B.

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Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction von Demange, Perline A, Malanchini, Margherita, Mallard, Travis T, Biroli, Pietro, Cox, Simon R, Grotzinger, Andrew D, Tucker-Drob, Elliot M, Abdellaoui, Abdel, Arseneault, Louise, van Bergen, Elsje, Boomsma, Dorret I, Caspi, Avshalom, Corcoran, David L, Domingue, Benjamin W, Harris, Kathleen Mullan, Ip, Hill F, Mitchell, Colter, Moffitt, Terrie E, Poulton, Richie, Prinz, Joseph A, Sugden, Karen, Wertz, Jasmin, Williams, Benjamin S, de Zeeuw, Eveline L, Belsky, Daniel W, Harden, K Paige, Nivard, Michel G

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Investigating the genetic architecture of non-cognitive skills using GWAS-by-subtraction von Demange, Perline A., Malanchini, Margherita, Mallard, Travis T., Biroli, Pietro, Cox, Simon R., Grotzinger, Andrew D., Tucker-Drob, Elliot M., Abdellaoui, Abdel, Arseneault, Louise, van Bergen, Elsje, Boomsma, Dorret I., Caspi, Avshalom, Corcoran, David L., Domingue, Benjamin W., Harris, Kathleen Mullan, Ip, Hill F., Mitchell, Colter, Moffitt, Terrie E., Poulton, Richie, Prinz, Joseph A., Sugden, Karen, Wertz, Jasmin, Williams, Benjamin S., de Zeeuw, Eveline L., Belsky, Daniel W., Harden, K. Paige, Nivard, Michel G.

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Placental Complement Activation in Fetal and Neonatal Alloimmune Thrombocytopenia: An Observational Study von Vos, Thijs W. de, Winkelhorst, Dian, Baelde, Hans J, Dijkstra, Kyra L, Bergen, Rianne D. M. van, Meeren, Lotte E. van der, Nikkels, Peter G. J, Porcelijn, Leendert, Schoot, C. Ellen van der, Vidarsson, Gestur, Eikmans, Michael, Kapur, Rick, Keur, Carin van der, Trouw, Leendert A, Oepkes, Dick, Lopriore, Enrico, Hoorn, Marie-Louise P. van der, Bos, Manon, Haas, Masja de

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Placental complement activation in fetal and neonatal alloimmune thrombocytopenia: An observational study von de Vos, Thijs W, Winkelhorst, Dian, Baelde, Hans J, Dijkstra, Kyra L, van Bergen, Rianne D.M, van der Meeren, Lotte E, Nikkels, Peter G.J, Porcelijn, Leendert, van der Schoot, C. Ellen, Vidarsson, Gestur, Eikmans, Michael, Kapur, Rick, van der Keur, Carin, Trouw, Leendert A, Oepkes, Dick, Lopriore, Enrico, van der Hoorn, Marie Louise P, Bos, Manon, de Haas, Masja

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Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives von Hunter, Jessica Ezzell, Arnold, Kathleen A., Cook, Jennifer E., Zepp, Jamilyn, Gilmore, Marian J., Rope, Alan F., Davis, James V., Bergen, Kellene M., Esterberg, Elizabeth, Muessig, Kristin R., Peterson, Susan K., Syngal, Sapna, Acheson, Louise, Wiesner, Georgia, Reiss, Jacob, Goddard, Katrina A. B.

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