Developmental fluoxetine exposure in zebrafish reduces offspring basal cortisol concentration via life stage-dependent maternal transmission von Martinez, Rubén, Vera-Chang, Marilyn N, Haddad, Majd, Zon, Jessica, Navarro-Martin, Laia, Trudeau, Vance L, Mennigen, Jan A

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A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies von Joynt, Alyssa C. M., Deshwar, Ashish R., Zon, Jessica, Dupuis, Lucie, Wherrett, Diane K., Mendoza‐Londono, Roberto

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Waste pickers organizations and municipal selective waste collection: Sustainability indicators von Nogueira Zon, Jéssica Luiza, Jacobsen Leopoldino, Chaila, Yamane, Luciana Harue, Ribeiro Siman, Renato

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PROCEDIMENTO LEGAL PARA AVALIAR OS PROCESSOS DE PEDIDO DE OUTORGA PARA DILUIÇÃO DE EFLUENTES NO ESTADO DO ESPÍRITO SANTO von Siman, Renato Ribeiro, Baldam, Roquemar de Lima, Girondoli, Ludimila Marvila, Costa, Lourenço, Zon, Jessica Luiza Nogueira, Pereira, Flávio Raposo

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Developmental fluoxetine exposure in zebrafish reduces offspring basal cortisol concentration via life stage-dependent maternal transmission von Martinez, Ruben, Vera-Chang, Marilyn N, Haddad, Majd, Zon, Jessica, Navarro Martin, Laia, Trudeau, Vance L, Mennigen, Jan Alexander

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Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies von Nil, Zelha, Deshwar, Ashish R, Barish, Scott, Zhang, Xi, Choufani, Sanaa, Le Quesne Stabej, Polona, Hayes, Ian, Yap, Patrick, Haldeman-Englert, Chad, Wilson, Carolyn, Prescott, Trine, Tveten, Kristian, Vøllo, Arve, Haynes, Devon, Wheeler, Patricia G, Zon, Jessica, Cytrynbaum, Cheryl, Jobling, Rebekah, Blyth, Moira, Banka, Siddharth, Afenjar, Alexandra, Mignot, Cyril, Robin-Renaldo, Florence, Keren, Boris, Kanca, Oguz, Mao, Xiao, Wegner, Daniel J, Sisco, Kathleen, Shinawi, Marwan, Wangler, Michael F, Weksberg, Rosanna, Yamamoto, Shinya, Costain, Gregory, Bellen, Hugo J

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Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies von Nil, Zelha, Deshwar, Ashish R., Huang, Yan, Barish, Scott, Zhang, Xi, Choufani, Sanaa, Le Quesne Stabej, Polona, Hayes, Ian, Yap, Patrick, Haldeman-Englert, Chad, Wilson, Carolyn, Prescott, Trine, Tveten, Kristian, Vøllo, Arve, Haynes, Devon, Wheeler, Patricia G., Zon, Jessica, Cytrynbaum, Cheryl, Jobling, Rebekah, Blyth, Moira, Banka, Siddharth, Afenjar, Alexandra, Mignot, Cyril, Robin-Renaldo, Florence, Keren, Boris, Kanca, Oguz, Mao, Xiao, Wegner, Daniel J., Sisco, Kathleen, Shinawi, Marwan, Wangler, Michael F., Weksberg, Rosanna, Yamamoto, Shinya, Costain, Gregory, Bellen, Hugo J.

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Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications von Deshwar, Ashish R, Cytrynbaum, Cheryl, Murthy, Harsha, Zon, Jessica, Chitayat, David, Volpatti, Jonathan, Newbury-Ecob, Ruth, Ellard, Sian, Allen, Hana Lango, Yu, Emily P, Noche, Ramil, Walker, Suzi, Scherer, Stephen W, Mahida, Sonal, Elitt, Christopher M, Nicolas, Gaël, Goldenberg, Alice, Saugier-Veber, Pascale, Lecoquierre, Francois, Dabaj, Ivana, Meddaugh, Hannah, Marble, Michael, Keppler-Noreuil, Kim M, Drayson, Lucy, Barañano, Kristin W, Chassevent, Anna, Agre, Katie, Létard, Pascaline, Bilan, Frederic, Le Guyader, Gwenaël, Laquerrière, Annie, Ramsey, Keri, Henderson, Lindsay, Brady, Lauren, Tarnopolsky, Mark, Bainbridge, Matthew, Friedman, Jennifer, Capri, Yline, Athayde, Larissa, Kok, Fernando, Gurgel-Giannetti, Juliana, Ramos, Luiza L P, Blaser, Susan, Dowling, James J, Weksberg, Rosanna

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A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients von Wittmann Dayagi, Talya, Nirel, Ronit, Avrahami, Galia, Amar, Shira, Elitzur, Sarah, Fisher, Salvador, Gilead, Gil, Gilad, Oded, Goldberg, Tracie, Izraeli, Shai, Kadmon, Gili, Kaplan, Eytan, Krauss, Aviva, Michaeli, Orli, Stein, Jerry, Steinberg-Shemer, Orna, Tamary, Hannah, Tausky, Osnat, Toledano, Helen, Weissbach, Avichai, Yacobovich, Joanne, Yanir, Asaf D., Zon, Jessica, Nahum, Elhanan, Barzilai-Birenboim, Shlomit

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PROCEDIMENTO LEGAL PARA AVALIAR OS PROCESSOS DE PEDIDO DE OUTORGA PARA DILUIÇÃO DE EFLUENTES NO ESTADO DO ESPÍRITO SANTO von Siman, Renato Ribeiro, Baldam, Roquemar de Lima, Girondoli, Ludimila Marvila, Costa, Lourenço, Zon, Jessica Luiza Nogueira, Pereira, Flávio Raposo

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Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications von Deshwar, Ashish R, Cytrynbaum, Cheryl, Murthy, Harsha, Zon, Jessica, Chitayat, David, Volpatti, Jonathan, Newbury-Ecob, Ruth, Ellard, Sian, Lango Allen, Hana, Yu, Emily P, Noche, Ramil, Walker, Suzi, Scherer, Stephen W, Mahida, Sonal, Elitt, Christopher M, Nicolas, Gaël, Goldenberg, Alice, Saugier-Veber, Pascale, Lecoquierre, Francois, Dabaj, Ivana, Meddaugh, Hannah, Marble, Michael, Keppler-Noreuil, Kim M, Drayson, Lucy, Barañano, Kristin W, Chassevent, Anna, Agre, Katie, Létard, Pascaline, Bilan, Frederic, Le Guyader, Gwenaël, Laquerrière, Annie, Ramsey, Keri, Henderson, Lindsay, Brady, Lauren, Tarnopolsky, Mark, Bainbridge, Matthew, Friedman, Jennifer, Capri, Yline, Athayde, Larissa, Kok, Fernando, Gurgel-Giannetti, Juliana, Ramos, Luiza LP, Blaser, Susan, Dowling, James J, Weksberg, Rosanna

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Tumor-Infiltrating Lymphocyte Therapy or Ipilimumab in Advanced Melanoma von Rohaan, Maartje W., Borch, Troels H., van den Berg, Joost H., Met, Özcan, Kessels, Rob, Geukes Foppen, Marnix H., Stoltenborg Granhøj, Joachim, Nuijen, Bastiaan, Nijenhuis, Cynthia, Jedema, Inge, van Zon, Maaike, Scheij, Saskia, Beijnen, Jos H., Hansen, Marten, Voermans, Carlijn, Noringriis, Inge M., Monberg, Tine J., Holmstroem, Rikke B., Wever, Lidwina D.V., van Dijk, Marloes, Grijpink-Ongering, Lindsay G., Valkenet, Ludy H.M., Torres Acosta, Alejandro, Karger, Matthias, Borgers, Jessica S.W., ten Ham, Renske M.T., Retèl, Valesca P., van Harten, Wim H., Lalezari, Ferry, van Tinteren, Harm, van der Veldt, Astrid A.M., Hospers, Geke A.P., Stevense-den Boer, Marion A.M., Suijkerbuijk, Karijn P.M., Aarts, Maureen J.B., Piersma, Djura, van den Eertwegh, Alfons J.M., de Groot, Jan-Willem B., Vreugdenhil, Gerard, Kapiteijn, Ellen, Boers-Sonderen, Marye J., Fiets, W. Edward, van den Berkmortel, Franchette W.P.J., Ellebaek, Eva, Hölmich, Lisbet R., van Akkooi, Alexander C.J., van Houdt, Winan J., Wouters, Michel W.J.M., van Thienen, Johannes V., Blank, Christian U., Meerveld-Eggink, Aafke, Klobuch, Sebastian, Wilgenhof, Sofie, Schumacher, Ton N., Donia, Marco, Svane, Inge Marie, Haanen, John B.A.G.

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CXCR1 remodels the vascular niche to promote hematopoietic stem and progenitor cell engraftment von Blaser, Bradley W, Moore, Jessica L, Hagedorn, Elliott J, Li, Brian, Riquelme, Raquel, Lichtig, Asher, Yang, Song, Zhou, Yi, Tamplin, Owen J, Binder, Vera, Zon, Leonard I

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Community Forest Management: Weak States or Strong Communities? von Arts, Bas, Behagel, Jelle, De Koning, Jessica, Zon, Marieke Van der

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Thrombosis-Related Loss of Arterial Lines in the First Wave of COVID-19 and Non–COVID-19 Intensive Care Unit Patients von Zon, Rebecca L., Merz, Lauren E., Fields, Kara G., Grandoni, Jessica, Stuart, Jessica C., Occhiogrosso, Rachel H., Li, Linda, Baron, Rebecca M., Fredenburgh, Laura E., Woolley, Ann E., Connors, Jean M., Frendl, Gyorgy

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Clonal fate mapping quantifies the number of haematopoietic stem cells that arise during development von Henninger, Jonathan, Santoso, Buyung, Hans, Stefan, Durand, Ellen, Moore, Jessica, Mosimann, Christian, Brand, Michael, Traver, David, Zon, Leonard

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Hematopoietic defects in rps29 mutant zebrafish depend upon p53 activation von Taylor, Alison M, Humphries, Jessica M, White, Richard M, Murphey, Ryan D, Burns, Caroline E, Zon, Leonard I

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Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families von Mirabello, Lisa, Macari, Elizabeth R., Jessop, Lea, Ellis, Steven R., Myers, Timothy, Giri, Neelam, Taylor, Alison M., McGrath, Katherine E., Humphries, Jessica M., Ballew, Bari J., Yeager, Meredith, Boland, Joseph F., He, Ji, Hicks, Belynda D., Burdett, Laurie, Alter, Blanche P., Zon, Leonard, Savage, Sharon A.

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Loss of nr4a1 abrogates Fitness of asxl1-mutant Hematopoietic Clones von Avagyan, Serine, Henninger, Jonathan E, Mannherz, William P., Mistry, Meeta, Yang, Song, Weber, Margaret C., Moore, Jessica, Zon, Leonard I.

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Thrombosis-Related Loss of Arterial Lines in the First Wave of COVID-19 and Non–COVID-19 Intensive Care Unit Patients von Zon, Rebecca L., Merz, Lauren E., Fields, Kara G., Grandoni, Jessica, Stuart, Jessica C., Occhiogrosso, Rachel H., Li, Linda, Baron, Rebecca M., Fredenburgh, Laura E., Woolley, Ann E., Connors, Jean M., Frendl, Gyorgy

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