Maternal inflammation has a profound effect on cortical interneuron development in a stage and subtype-specific manner von Vasistha, Navneet A., Pardo-Navarro, Maria, Gasthaus, Janina, Weijers, Dilys, Müller, Michaela K., García-González, Diego, Malwade, Susmita, Korshunova, Irina, Pfisterer, Ulrich, von Engelhardt, Jakob, Hougaard, Karin S., Khodosevich, Konstantin

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Clinical and laboratory diversity of diffuse large B-cell lymphomas in children with Nijmegen breakage syndrome von Pastorczak, Agata, Szmyd, Bartosz, Braun, Marcin, Madzio, Joanna, Wypyszczak, Kamila, Sztromwasser, Pawel, Fendler, Wojciech, Wojtaszewska, Marzena, Chrzanowski, Jedrzej, Grajkowska, Wieslawa, Gregorek, Hanna, Wakulinska, Anna, Kazanowska, Bernarda, Krenova, Zdenka, Weijers, Dilys D, Kuiper, Roland P, Mlynarski, Wojciech

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Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations von Weijers, Dilys D., Hirsch, Steffen, Bakhuizen, Jette J., Engelen, Nienke, Kester, Lennart A., Kranendonk, Mariëtte E. G., Hiemcke‐Jiwa, Laura S., Vos‐Kerkhof, Evelien, Loeffen, Jan L. C., Autry, Robert J., Pajtler, Kristian W., Jäger, Natalie, Jongmans, Marjolijn C. J., Kuiper, Roland P.

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T‐cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD): Exploring treatment opportunities von Kroeze, Emma, Weijers, Dilys D., Kleisman, Michelle M., Ilan, Uri, Bladergroen, Reno S., Hagelaar, Rico, Meijerink, Jules P. P., Jongmans, Marjolijn C. J., Loeffen, Jan L. C., Kuiper, Roland P.

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High Prevalence of Constitutional Mismatch Repair Deficiency in a Pediatric T‐cell Lymphoblastic Lymphoma Cohort von Kroeze, Emma, Weijers, Dilys D., Hagleitner, Melanie M., Groot‐Kruseman, Hester A., Jongmans, Marjolijn C. J., Kuiper, Roland P., Pieters, Rob, Meijerink, Jules P. P., Loeffen, Jan L. C.

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Challenges of Neoantigen Targeting in Lynch Syndrome and Constitutional Mismatch Repair Deficiency Syndrome von Abidi, Asima, Gorris, Mark A. J., Brennan, Evan, Jongmans, Marjolijn C. J., Weijers, Dilys D., Kuiper, Roland P., de Voer, Richarda M., Hoogerbrugge, Nicoline, Schreibelt, Gerty, de Vries, I. Jolanda M.

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Sexually dimorphic perineuronal nets in the rodent and primate reproductive circuit von Ciccarelli, Alessandro, Weijers, Dilys, Kwan, William, Warner, Claire, Bourne, James, Gross, Cornelius T.

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Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations von Weijers, Dilys D, Hirsch, Steffen, Bakhuizen, Jette J, van Engelen, Nienke, Kester, Lennart A, Kranendonk, Mariëtte E.G, Hiemcke-Jiwa, Laura S, de Vos-Kerkhof, Evelien, Loeffen, Jan L.C, Autry, Robert J, Pajtler, Kristian W, Jäger, Natalie, Jongmans, Marjolijn C.J, Kuiper, Roland P

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De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay von Vissers, Lisenka E.L.M., Kalvakuri, Sreehari, de Boer, Elke, Geuer, Sinje, Oud, Machteld, van Outersterp, Inge, Kwint, Michael, Witmond, Melde, Kersten, Simone, Polla, Daniel L., Weijers, Dilys, Begtrup, Amber, McWalter, Kirsty, Ruiz, Anna, Gabau, Elisabeth, Morton, Jenny E.V., Griffith, Christopher, Weiss, Karin, Gamble, Candace, Bartley, James, Vernon, Hilary J., Brunet, Kendra, Ruivenkamp, Claudia, Kant, Sarina G., Kruszka, Paul, Larson, Austin, Afenjar, Alexandra, Billette de Villemeur, Thierry, Nugent, Kimberly, Raymond, F. Lucy, Venselaar, Hanka, Demurger, Florence, Soler-Alfonso, Claudia, Li, Dong, Bhoj, Elizabeth, Hayes, Ian, Hamilton, Nina Powell, Ahmad, Ayesha, Fisher, Rachel, van den Born, Myrthe, Willems, Marjolaine, Sorlin, Arthur, Delanne, Julian, Moutton, Sebastien, Christophe, Philippe, Mau-Them, Frederic Tran, Vitobello, Antonio, Goel, Himanshu, Massingham, Lauren, Phornphutkul, Chanika, Schwab, Jennifer, Keren, Boris, Charles, Perrine, Vreeburg, Maaike, De Simone, Lenika, Hoganson, George, Iascone, Maria, Milani, Donatella, Evenepoel, Lucie, Revencu, Nicole, Ward, D. Isum, Burns, Kaitlyn, Krantz, Ian, Raible, Sarah E., Murrell, Jill R., Wood, Kathleen, Cho, Megan T., van Bokhoven, Hans, Muenke, Maximilian, Kleefstra, Tjitske, Bodmer, Rolf, de Brouwer, Arjan P.M.

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Report of the sixth meeting of the European Consortium ‘Care for CMMRD’ (C4CMMRD), Paris, France, November 16th 2022 von Guerrini-Rousseau, Léa, Gallon, Richard, Pineda, Marta, Brugières, Laurence, Baert-Desurmont, Stéphanie, Corsini, Carole, Dangouloff-Ros, Volodia, Gorris, Mark A. J., Haberler, Christine, Hoarau, Pauline, Jongmans, Marjolijn C., Kloor, Matthias, Loeffen, Jan, Rigaud, Charlotte, Robbe, Julie, Vibert, Roseline, Weijers, Dilys, Wimmer, Katharina, Colas, Chrystelle

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Challenges of neoantigen targeting in lynch syndrome and constitutional mismatch repair deficiency syndrome von Abidi, Asima, Gorris, Mark A.J, Brennan, Evan, Jongmans, Marjolijn C.J, Weijers, Dilys D, Kuiper, Roland P, de Voer, Richarda M, Hoogerbrugge, Nicoline, Schreibelt, Gerty, de Vries, I. Jolanda M

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High Prevalence of Constitutional Mismatch Repair Deficiency in a Pediatric T-cell Lymphoblastic Lymphoma Cohort von Kroeze, Emma, Weijers, Dilys D, Hagleitner, Melanie M, De Groot-Kruseman, Hester A, Jongmans, Marjolijn C.J, Kuiper, Roland P, Pieters, Rob, Meijerink, Jules P.P, Loeffen, Jan L.C

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T-cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD): Exploring treatment opportunities von Kroeze, Emma, Weijers, Dilys D, Kleisman, Michelle M, Ilan, Uri, Bladergroen, Reno S, Hagelaar, Rico, Meijerink, Jules P.P, Jongmans, Marjolijn C.J, Loeffen, Jan L.C, Kuiper, Roland P

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