The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease by Van Den Bogaert, Ann, Schumacher, Johannes, Schulze, Thomas G., Otte, Andreas C., Ohlraun, Stephanie, Kovalenko, Svetlana, Becker, Tim, Freudenberg, Jan, Jönsson, Erik G., Mattila-Evenden, Marja, Sedvall, Göran C., Czerski, Piotr M., Kapelski, Pawel, Hauser, Joanna, Maier, Wolfgang, Rietschel, Marcella, Propping, Peter, Nöthen, Markus M., Cichon, Sven

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Risk of malignancy in 22q11.2 deletion syndrome by Stevens, Toer, Werff ten Bosch, Jutte, De Rademaeker, Marjan, Van Den Bogaert, Ann, Akker, Machiel

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Major affective disorders and schizophrenia: a common molecular signature? by Bogaert, Ann Van Den, Del-Favero, Jurgen, Broeckhoven, Christine Van

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Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles by Parijs, Ilse, Brison, Nathalie, Vancoillie, Leen, Baetens, Machteld, Blaumeiser, Bettina, Boulanger, Sébastien, Désir, Julie, Dimitrov, Boyan, Fieremans, Nathalie, Janssens, Katrien, Janssens, Sandra, Marichal, Axel, Menten, Björn, Meunier, Colombine, Van Berkel, Kim, Van Den Bogaert, Ann, Devriendt, Koenraad, Van Den Bogaert, Kris, Vermeesch, Joris Robert

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Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study by Muys, Joke, Jacquemyn, Yves, Blaumeiser, Bettina, Bourlard, Laura, Brison, Nathalie, Bulk, Saskia, Chiarappa, Patrizia, De Leener, Anne, De Rademaeker, Marjan, Désir, Julie, Destrée, Anne, Devriendt, Koenraad, Dheedene, Annelies, Duquenne, Armelle, Fieuw, Annelies, Fransen, Erik, Gatot, Jean‐Stéphane, Jamar, Mauricette, Janssens, Sandra, Kerstjens, Jorien, Keymolen, Kathelijn, Lederer, Damien, Menten, Björn, Pichon, Bruno, Rombout, Sonia, Sznajer, Yves, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vermeesch, Joris, Janssens, Katrien

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Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges by Vanakker, Olivier, Vilain, Catheline, Janssens, Katrien, Van der Aa, Nathalie, Smits, Guillaume, Bandelier, Claude, Blaumeiser, Bettina, Bulk, Saskia, Caberg, Jean-Hubert, De Leener, Anne, De Rademaeker, Marjan, de Ravel, Thomy, Desir, Julie, Destree, Anne, Dheedene, Annelies, Gaillez, Stéphane, Grisart, Bernard, Hellin, Ann-Cécile, Janssens, Sandra, Keymolen, Kathelijn, Menten, Björn, Pichon, Bruno, Ravoet, Marie, Revencu, Nicole, Rombout, Sonia, Staessens, Catherine, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vermeesch, Joris R, Kooy, Frank, Sznajer, Yves, Devriendt, Koen

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The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations by Muys, Joke, Blaumeiser, Bettina, Jacquemyn, Yves, Bandelier, Claude, Brison, Nathalie, Bulk, Saskia, Chiarappa, Patrizia, Courtens, Winnie, De Leener, Anne, De Rademaeker, Marjan, Désir, Julie, Destrée, Anne, Devriendt, Koenraad, Dheedene, Annelies, Fieuw, Annelies, Fransen, Erik, Gatot, Jean‐Stéphane, Holmgren, Philip, Jamar, Mauricette, Janssens, Sandra, Keymolen, Kathelijn, Lederer, Damien, Menten, Björn, Meuwissen, Marije, Parmentier, Benoit, Pichon, Bruno, Rombout, Sonia, Sznajer, Yves, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vanakker, Olivier, Vermeesch, Joris, Janssens, Katrien

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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder by Cichon, Sven, Winge, Ingeborg, Mattheisen, Manuel, Georgi, Alexander, Karpushova, Anna, Freudenberg, Jan, Freudenberg-Hua, Yun, Babadjanova, Gulia, Van Den Bogaert, Ann, Abramova, Lilia I., Kapiletti, Sofia, Knappskog, Per M., McKinney, Jeffrey, Maier, Wolfgang, Abou Jamra, Rami, Schulze, Thomas G., Schumacher, Johannes, Propping, Peter, Rietschel, Marcella, Haavik, Jan, Nöthen, Markus M.

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Response to Zhang et al (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major Depression. Neuron 45, 11-16 by Van Den Bogaert, Ann, De Zutter, Sonia, Heyrman, Lien, Mendlewicz, Julien, Adolfsson, Rolf, Van Broeckhoven, Christine, Del-Favero, Jurgen

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Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16 by Zhou, Zhifeng, Peters, Eric J, Hamilton, Steven P, McMahon, Francis, Thomas, Christee, McGrath, Patrick J, Rush, John, Trivedi, Madhukar H, Charney, Dennis S, Roy, Alec, Wisniewski, Stephen, Lipsky, Robert, Goldman, David

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Response to Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16 by Van Den Bogaert, Ann, De Zutter, Sonia, Heyrman, Lien, Mendlewicz, Julien, Adolfsson, Rolf, Van Broeckhoven, Christine, Del-Favero, Jurgen

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Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16 by Glatt, Charles E, Carlson, Elaine, Taylor, Travis R, Risch, Neil, Reus, Victor I, Schaefer, Catherine A

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Radiation Dose Homogeneity in an EORTC Multicenter Trial on Breast Irradiation by Ptaszynski, Walter Van den Bogaert, Jean-Claude Horiot, Philip Poortmans, Alain Fourquet, Henk Struikmans, Harry Bartelink, Marianne Pierart, Laurence Collette, Emmanuel van der Schueren, Ann-Marie

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Risk of malignancy in 22q11.2 deletion syndrome by Stevens, Toer, van der Werff Ten Bosch, Jutte, De Rademaeker, Marjan, Van Den Bogaert, Ann, van den Akker, Machiel

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The BElgian PREnatal MicroArray (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations by Muys, Joke, Blaumeiser, Bettina, Jacquemyn, Yves, Bandelier, Claude, Brison, Nathalie, BULK, Saskia, Chiarappa, Patrizia, COURTENS, Winnie, De Leener, Anne, De Rademaeker, Marjan, Desir, Julie, Destree, Anne, Devriendt, Koenraad, Dheedene, Annelies, Fieuw, Annelies, Fransen, Erik, GATOT, Jean-Stéphane, Holmgren, Philip, JAMAR, Mauricette, Janssens, Sandra, Keymolen, Kathelijn, Lederer, Damien, Menten, Bjorn, Meuwissen, Marije, Parmentier, Benoit, Pichon, Bruno, Rombout, Sonia, Sznajer, Yves, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vanakker, Olivier, Vermeesch, Joris, Janssens, Katrien

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How do people living with chronic conditions and their informal caregivers experience primary care? A phenomenological‐hermeneutical study by Boeykens, Dagje, Sirimsi, Muhammed Mustafa, Timmermans, Lotte, Hartmann, Maja Lopez, Anthierens, Sibyl, De Loof, Hans, De Vliegher, Kristel, Foulon, Veerle, Huybrechts, Ine, Lahousse, Lies, Pype, Peter, Schoenmakers, Birgitte, Van Bogaert, Peter, Van den Broeck, Kris, Van Hecke, Ann, Verhaeghe, Nick, Vermandere, Mieke, Verté, Emily, Van de Velde, Dominique, De Vriendt, Patricia

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Metastases of primary mixed no-special type and lobular breast cancer display an exclusive lobular histology by Zels, Gitte, Van Baelen, Karen, De Schepper, Maxim, Borremans, Kristien, Geukens, Tatjana, Isnaldi, Edoardo, Izci, Hava, Leduc, Sophia, Mahdami, Amena, Maetens, Marion, Nguyen, Ha Linh, Pabba, Anirudh, Richard, François, Van Cauwenberge, Josephine, Smeets, Ann, Nevelsteen, Ines, Neven, Patrick, Wildiers, Hans, Van Den Bogaert, Wouter, Floris, Giuseppe, Desmedt, Christine

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Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results by Van Hoovels, Lieve, Vander Cruyssen, Bert, Sieghart, Daniela, Bonroy, Carolien, Nagy, Eszter, Pullerits, Rille, Čučnik, Saša, Dahle, Charlotte, Heijnen, Ingmar, Bernasconi, Luca, Benkhadra, Farid, Bogaert, Laura, Van Den Bremt, Stefanie, Van Liedekerke, Ann, Vanheule, Geert, Robbrecht, Johan, Studholme, Lucy, Wirth, Claudine, Müller, Rüdiger, Kyburz, Diego, Sjöwall, Christopher, Kastbom, Alf, Ješe, Rok, Jovancevic, Boja, Kiss, Emese, Jacques, Peggy, Aletaha, Daniel, Steiner, Guenter, Verschueren, Patrick, Bossuyt, Xavier

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Intra-patient and inter-metastasis heterogeneity of HER2-low status in metastatic breast cancer by Geukens, Tatjana, De Schepper, Maxim, Richard, François, Maetens, Marion, Van Baelen, Karen, Mahdami, Amena, Nguyen, Ha-Linh, Isnaldi, Edoardo, Leduc, Sophia, Pabba, Anirudh, Zels, Gitte, Mertens, Freya, Vander Borght, Sara, Smeets, Ann, Nevelsteen, Ines, Punie, Kevin, Neven, Patrick, Wildiers, Hans, Van Den Bogaert, Wouter, Floris, Giuseppe, Desmedt, Christine

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A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity by De Bruyne, Marieke, Bogaert, Delfien J., Venken, Koen, Van den Bossche, Lien, Bonroy, Carolien, Roels, Lisa, Tavernier, Simon J., van de Vijver, Els, Driessen, Ann, van Gijn, Marielle, Gámez-Diaz, Laura, Elewaut, Dirk, Grimbacher, Bodo, Haerynck, Filomeen, Moes, Nicolette, Dullaers, Melissa

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