A C–H Functionalization Protocol for the Direct Synthesis of Benzobisthiazole Derivatives von Bon, Jennifer L, Feng, Daijun, Marder, Seth R, Blakey, Simon B

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Environmental Sensitivity of Ru(II) Complexes: The Role of the Accessory Ligands von Dixon, Eileen N, Snow, Michael Z, Bon, Jennifer L, Whitehurst, Alison M, DeGraff, Benjamin A, Trindle, Carl, Demas, James N

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ChemInform Abstract: A C-H Functionalization Protocol for the Direct Synthesis of Benzobisthiazole Derivatives von Bon, Jennifer L., Feng, Daijun, Marder, Seth R., Blakey, Simon B.

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ChemInform Abstract: Synthesis of Ruthenium(II) 2,6-Bis(imino)pyridyl Complexes for C-H Amination of Sulfamate Esters von Bon, Jennifer L., Blakey, Simon B.

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Human-to-monkey transfer learning identifies the frontal white matter as a key determinant for predicting monkey brain age von He, Sheng, Guan, Yi, Cheng, Chia Hsin, Moore, Tara L, Luebke, Jennifer I, Killiany, Ronald J, Rosene, Douglas L, Koo, Bang-Bon, Ou, Yangming

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, Michele, Vulto-van Silfhout, Anneke T., Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J., Stromme, Petter, Rosenfeld, Jill A., Shao, Yunru, Craigen, William J., Schaaf, Christian P., Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D., Nugent, Kimberly M., Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal, Patrier, Sophie, Lynch, Sally A., Kjaergaard, Susanne, Tørring, Pernille M., Brasch-Andersen, Charlotte, Ronan, Anne, van Haeringen, Arie, Anderson, Peter J., Powis, Zöe, Brunner, Han G., Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke H.M., van Bon, Bregje W.M., Lelieveld, Stefan, Gilissen, Christian, Nillesen, Willy M., Vissers, Lisenka E.L.M., Gecz, Jozef, Koolen, David A., Testa, Giuseppe, de Vries, Bert B.A.

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Outcomes of a Multicenter Training Program in Robotic Pancreatoduodenectomy (LAELAPS-3) von Zwart, Maurice J.W., Nota, Carolijn L.M., de Rooij, Thijs, van Hilst, Jony, te Riele, Wouter W., van Santvoort, Hjalmar C., Hagendoorn, Jeroen, Borei Rinkes, Inne H.M., van Dam, Jacob L., Latenstein, Anouk E.J., Takagi, Kosei, Tran, Khé T.C., Schreinemakers, Jennifer, van der Schelling, George P., Wijsman, Jan H., Festen, Sebastiaan, Daams, Freek, Luyer, Misha D., de Hingh, Ignace H.J.T., Mieog, Jan S.D., Bonsing, Bert A., Lips, Daan J., Hilal, Mohammed Abu, Busch, Olivier R., Saint-Marc, Olivier, Zehl, Herbert J., Zureikat, Amer H., Hogg, Melissa E., Molenaar, I. Quintus, Besselink, Marc G., Koerkamp, Bas Groot

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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling von Snijders Blok, Lot, Madsen, Erik, Juusola, Jane, Gilissen, Christian, Baralle, Diana, Reijnders, Margot R.F., Venselaar, Hanka, Helsmoortel, Céline, Cho, Megan T., Hoischen, Alexander, Vissers, Lisenka E.L.M., Koemans, Tom S., Wissink-Lindhout, Willemijn, Eichler, Evan E., Romano, Corrado, Van Esch, Hilde, Stumpel, Connie, Vreeburg, Maaike, Smeets, Eric, Oberndorff, Karin, van Bon, Bregje W.M., Shaw, Marie, Gecz, Jozef, Haan, Eric, Bienek, Melanie, Jensen, Corinna, Loeys, Bart L., Van Dijck, Anke, Innes, A. Micheil, Racher, Hilary, Vermeer, Sascha, Di Donato, Nataliya, Rump, Andreas, Tatton-Brown, Katrina, Parker, Michael J., Henderson, Alex, Lynch, Sally A., Fryer, Alan, Ross, Alison, Vasudevan, Pradeep, Kini, Usha, Newbury-Ecob, Ruth, Chandler, Kate, Male, Alison, Dijkstra, Sybe, Schieving, Jolanda, Giltay, Jacques, van Gassen, Koen L.I., Schuurs-Hoeijmakers, Janneke, Tan, Perciliz L., Pediaditakis, Igor, Haas, Stefan A., Retterer, Kyle, Reed, Patrick, Monaghan, Kristin G., Haverfield, Eden, Natowicz, Marvin, Myers, Angela, Kruer, Michael C., Stein, Quinn, Strauss, Kevin A., Brigatti, Karlla W., Keating, Katherine, Burton, Barbara K., Kim, Katherine H., Charrow, Joel, Norman, Jennifer, Foster-Barber, Audrey, Kline, Antonie D., Kimball, Amy, Zackai, Elaine, Harr, Margaret, Fox, Joyce, McLaughlin, Julie, Lindstrom, Kristin, Haude, Katrina M., van Roozendaal, Kees, Brunner, Han, Chung, Wendy K., Kooy, R. Frank, Pfundt, Rolph, Kalscheuer, Vera, Mehta, Sarju G., Katsanis, Nicholas, Kleefstra, Tjitske

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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females von Radio, Francesca Clementina, Ciolfi, Andrea, Levy, Michael A., Hernández-García, Andrés, Pedace, Lucia, Pantaleoni, Francesca, Liu, Zhandong, de Boer, Elke, Jackson, Adam, Bruselles, Alessandro, McConkey, Haley, Stellacci, Emilia, Lo Cicero, Stefania, Motta, Marialetizia, Carrozzo, Rosalba, McWalter, Kirsty, Desai, Megha, Monaghan, Kristin G., Telegrafi, Aida, Philippe, Christophe, Vitobello, Antonio, Au, Margaret, Grand, Katheryn, Baez, Joanne, Lindstrom, Kristin, Kulch, Peggy, Sebastian, Jessica, Madan-Khetarpal, Suneeta, Roadhouse, Chelsea, MacKenzie, Jennifer J., Monteleone, Berrin, Saunders, Carol J., Jean Cuevas, July K., Zhou, Dihong, Sawyer, Sarah L., Monteiro, Fabíola Paoli, Secches, Tania Vertemati, Kok, Fernando, Schultz-Rogers, Laura E., Morava, Eva, Klee, Eric W., Kemppainen, Jennifer, Iascone, Maria, Selicorni, Angelo, Tenconi, Romano, Pais, Lynn, Gallacher, Lyndon, Turnpenny, Peter D., Stals, Karen, Ellard, Sian, Cabet, Sara, Lesca, Gaetan, Pascal, Joset, Steindl, Katharina, Weiss, Karin, Carter, Melissa T., Kalsner, Louisa, de Vries, Bert B.A., van Bon, Bregje W., Wevers, Marijke R., Pfundt, Rolph, Stegmann, Alexander P.A., Kerr, Bronwyn, Chandler, Kate E., Sheehan, Willow, Elias, Abdallah F., Shinde, Deepali N., Towne, Meghan C., Robin, Nathaniel H., Goodloe, Dana, Vanderver, Adeline, Sherbini, Omar, Bluske, Krista, Faletra, Flavio, Musante, Luciana, Kurtz-Nelson, Evangeline C., Earl, Rachel K., Anderlid, Britt-Marie, Morin, Gilles, van Slegtenhorst, Marjon, Diderich, Karin E.M., Brooks, Alice S., Gribnau, Joost, Boers, Ruben G., Finestra, Teresa Robert, Carter, Lauren B., Rauch, Anita, Gasparini, Paolo, Boycott, Kym M., Barakat, Tahsin Stefan, Graham, John M., Faivre, Laurence, Banka, Siddharth, Wang, Tianyun, Eichler, Evan E., Dallapiccola, Bruno, Vissers, Lisenka E.L.M., Sadikovic, Bekim, Holder, Jimmy Lloyd, Tartaglia, Marco

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Single-cell RNA sequencing of neurofibromas reveals a tumor microenvironment favorable for neural regeneration and immune suppression in a neurofibromatosis type 1 porcine model von McLean, Dalton T, Meudt, Jennifer J, Lopez Rivera, Loren D, Schomberg, Dominic T, Pavelec, Derek M, Duellman, Tyler T, Buehler, Darya G, Schwartz, Patrick B, Graham, Melissa, Lee, Laura M, Graff, Keri D, Reichert, Jamie L, Bon-Durant, Sandra S, Konsitzke, Charles M, Ronnekleiv-Kelly, Sean M, Shanmuganayagam, Dhanansayan, Rubinstein, C Dustin

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Küry, Sébastien, van Woerden, Geeske M., Besnard, Thomas, Proietti Onori, Martina, Latypova, Xénia, Towne, Meghan C., Cho, Megan T., Ploeg, Melissa A., Sanders, Stephan, Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A., Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A., Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L., Deardorff, Matthew, Hoganson, George E., Bosanko, Katherine B., Johnson, Diana S., Dabir, Tabib, Holla, Øystein Lunde, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A., Grange, Dorothy K., van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Petrovski, Slavé, Retterer, Kyle, Eichler, Evan E., Rosenfeld, Jill A., Agrawal, Pankaj B., Bézieau, Stéphane, Odent, Sylvie, Mercier, Sandra

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Machine Learning Characterization of COPD Subtypes: Insights From the COPDGene Study von Castaldi, Peter J, Boueiz, Adel, Yun, Jeong, Estepar, Raul San Jose, Ross, James C, Washko, George, Cho, Michael H, Hersh, Craig P, Kinney, Gregory L, Young, Kendra A, Regan, Elizabeth A, Lynch, David A, Criner, Gerald J, Dy, Jennifer G, Rennard, Stephen I, Casaburi, Richard, Make, Barry J, Crapo, James, Silverman, Edwin K, Hokanson, John E

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Reduced Bone Density and Vertebral Fractures in Smokers. Men and COPD Patients at Increased Risk von Jaramillo, Joshua D, Wilson, Carla, Stinson, Douglas S, Stinson, Douglas J, Lynch, David A, Bowler, Russell P, Lutz, Sharon, Bon, Jessica M, Arnold, Ben, McDonald, Merry-Lynn N, Washko, George R, Wan, Emily S, DeMeo, Dawn L, Foreman, Marilyn G, Soler, Xavier, Lindsay, Sarah E, Lane, Nancy E, Genant, Harry K, Silverman, Edwin K, Hokanson, John E, Make, Barry J, Crapo, James D, Regan, Elizabeth A

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Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome von Rots, Dmitrijs, Bouman, Arianne, Yamada, Ayumi, Levy, Michael, Dingemans, Alexander J M, de Vries, Bert B A, Ruiterkamp-Versteeg, Martina, de Leeuw, Nicole, Ockeloen, Charlotte W, Pfundt, Rolph, de Boer, Elke, Kummeling, Joost, van Bon, Bregje, van Bokhoven, Hans, Kasri, Nael Nadif, Venselaar, Hanka, Alders, Marielle, Kerkhof, Jennifer, McConkey, Haley, Kuechler, Alma, Elffers, Bart, van Beeck Calkoen, Rixje, Hofman, Susanna, Valenzuela, Maria Irene, Srivastava, Siddharth, Frazier, Zoe, Maystadt, Isabelle, Piscopo, Carmelo, Merla, Giuseppe, Balasubramanian, Meena, Santen, Gijs W E, Metcalfe, Kay, Park, Soo-Mi, Pasquier, Laurent, Banka, Siddharth, Donnai, Dian, Weisberg, Daniel, Strobl-Wildemann, Gertrud, Wagemans, Annemieke, Vreeburg, Maaike, Baralle, Diana, Foulds, Nicola, Scurr, Ingrid, Brunetti-Pierri, Nicola, van Hagen, Johanna M, Bijlsma, Emilia K, Hakonen, Anna H, Courage, Carolina, Genevieve, David, Pinson, Lucile, Forzano, Francesca, Deshpande, Charu, Kluskens, Maria L, Welling, Lindsey, Plomp, Astrid S, Vanhoutte, Els K, Kalsner, Louisa, Hol, Janna A, Putoux, Audrey, Lazier, Johanna, Vasudevan, Pradeep, Ames, Elizabeth, O'Shea, Jessica, Lederer, Damien, Fleischer, Julie, Pauly, Melissa, Vasileiou, Georgia, Reis, André, Kiraly-Borri, Catherine, Bouman, Arjan, Barnett, Chris, Nezarati, Marjan, Borch, Lauren, Beunders, Gea, Özcan, Kübra, Miot, Stéphanie, Volker-Touw, Catharina M L, van Gassen, Koen L I, Cappuccio, Gerarda, Janssens, Katrien, Mor, Nofar, Shomer, Inna, Dominissini, Dan, Tedder, Matthew L, Sadikovic, Bekim, Brunner, Han G, Vissers, Lisenka E L M, Shinkai, Yoichi, Kleefstra, Tjitske

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Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome von Rots, Dmitrijs, Bouman, Arianne, Yamada, Ayumi, Levy, Michael, Dingemans, Alexander J.M., de Vries, Bert B.A., Ruiterkamp-Versteeg, Martina, de Leeuw, Nicole, Ockeloen, Charlotte W., Pfundt, Rolph, de Boer, Elke, Kummeling, Joost, van Bon, Bregje, van Bokhoven, Hans, Kasri, Nael Nadif, Venselaar, Hanka, Alders, Marielle, Kerkhof, Jennifer, McConkey, Haley, Kuechler, Alma, Elffers, Bart, van Beeck Calkoen, Rixje, Hofman, Susanna, Smith, Audrey, Valenzuela, Maria Irene, Srivastava, Siddharth, Frazier, Zoe, Maystadt, Isabelle, Piscopo, Carmelo, Merla, Giuseppe, Balasubramanian, Meena, Santen, Gijs W.E., Metcalfe, Kay, Park, Soo-Mi, Pasquier, Laurent, Banka, Siddharth, Donnai, Dian, Weisberg, Daniel, Strobl-Wildemann, Gertrud, Wagemans, Annemieke, Vreeburg, Maaike, Baralle, Diana, Foulds, Nicola, Scurr, Ingrid, Brunetti-Pierri, Nicola, van Hagen, Johanna M., Bijlsma, Emilia K., Hakonen, Anna H., Courage, Carolina, Genevieve, David, Pinson, Lucile, Forzano, Francesca, Deshpande, Charu, Kluskens, Maria L., Welling, Lindsey, Plomp, Astrid S., Vanhoutte, Els K., Kalsner, Louisa, Hol, Janna A., Putoux, Audrey, Lazier, Johanna, Vasudevan, Pradeep, Ames, Elizabeth, O'Shea, Jessica, Lederer, Damien, Fleischer, Julie, O'Connor, Mary, Pauly, Melissa, Vasileiou, Georgia, Reis, André, Kiraly-Borri, Catherine, Bouman, Arjan, Barnett, Chris, Nezarati, Marjan, Borch, Lauren, Beunders, Gea, Özcan, Kübra, Miot, Stéphanie, Volker-Touw, Catharina M.L., van Gassen, Koen L.I., Cappuccio, Gerarda, Janssens, Katrien, Mor, Nofar, Shomer, Inna, Dominissini, Dan, Tedder, Matthew L., Muir, Alison M., Sadikovic, Bekim, Brunner, Han G., Vissers, Lisenka E.L.M., Shinkai, Yoichi, Kleefstra, Tjitske

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Behavior Profiles at 2 Years for Children Born Extremely Preterm with Bronchopulmonary Dysplasia von Bell, Edward F., Grey, Scott F., Vohr, Betty R., Harmon, Heidi M., Logan, J. Wells, Colaizy, Tarah T., Peralta-Carcelen, Myriam A., McGowan, Elisabeth C., Stoll, Barbara J., Caplan, Michael S., Keszler, Martin, Hensman, Angelita M., Vieira, Elisa, Newman, Nancy S., Siner, Bonnie S., Pallotto, Eugenia K., Gauldin, Cheri, Holmes, Anne, Johnson, Kathy, Knutson, Allison, Schibler, Kurt, Gratton, Teresa L., Wuertz, Sandra, Adams-Chapman, Ira, Hale, Ellen C., Bottcher, Diane I., Goldberg, Ronald N., Goldstein, Ricki F., Malcolm, William F., Ashley, Patricia L., Finkle, Joanne, Bernhardt, Janice, Wilson Archer, Stephanie, Papile, Lu Ann, Hines, Abbey C., Gunn, Susan, Smiley, Lucy, Wright, Sharon L., Nelin, Leif D., Luzader, Patricia, Parikh, Nehal A., Newman, Jamie E., Leblond, David, Adams, Marian M., Huffman, Lynne C., Palmquist, Andrew W., Sankar, Meera N., Frantz, Ivan D., Fiascone, John M., Nylen, Ellen, Brussa, Ana K., Whitley, Sally, Garg, Meena, Vaucher, Yvonne E., Demetrio, Clarence, Rich, Wade, Hogden, Laurie A., Broadbent, Megan, Schmelzel, Mendi L., Walker, Jacky R., Watterberg, Kristi L., Ohls, Robin K., Backstrom Lacy, Conra, Fuller, Janell, Hanson, Mary Ruffner, Kuan, Elizabeth, Mancini, Toni, Bernbaum, Judy C., D'Angio, Carl T., Guillet, Ronnie, Lakshminrusimha, Satyan, Sacilowski, Michael G., Hunn, Julianne, Fallone, Cait, Vasil, Diana M., Chen, Lijun, De Leon, Maria M., Madden, Linda A., Sepulveda, Pollieanna, Faix, Roger G., Yoder, Bradley A., Baserga, Mariana, Bird, Karie, Burnett, Jill, Davis, Brandy, Elmont, Jennifer O., Jensen, Jennifer J., Loertscher, Manndi C., Maxson, Earl, Rau, Carrie A., Chawla, Sanjay, Bajaj, Monika, Johnson, Mary E., Wiggins, Stephanie A., Christensen, Mary K., Carlson, Martha, White, Diane F., Jacobs, Harris, Cervone, Patricia, Greisman, Sheila

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A Case Series of Familial ARID1B Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria von van der Sluijs, Pleuntje J, Alders, Mariëlle, Dingemans, Alexander J M, Parbhoo, Kareesma, van Bon, Bregje W, Dempsey, Jennifer C, Doherty, Dan, den Dunnen, Johan T, Gerkes, Erica H, Milller, Ilana M, Moortgat, Stephanie, Regier, Debra S, Ruivenkamp, Claudia A L, Schmalz, Betsy, Smol, Thomas, Stuurman, Kyra E, Vincent-Delorme, Catherine, de Vries, Bert B A, Sadikovic, Bekim, Hickey, Scott E, Rosenfeld, Jill A, Maystadt, Isabelle, Santen, Gijs W E

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A novel hTERT promoter–driven E1A therapeutic for ovarian cancer von Xie, Xiaoming, Hsu, Jennifer L, Choi, Min-Gew, Xia, Weiya, Yamaguchi, Hirohito, Chen, Chun-Te, Trinh, Bon Q, Lu, Zhen, Ueno, Naoto T, Wolf, Judith K, Bast, Jr, Robert C, Hung, Mien-Chie

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Socioeconomic disparities in changes to preterm birth and stillbirth rates during the first year of the COVID-19 pandemic: a study of 21 European countries von Zeitlin, Jennifer, Philibert, Marianne, Barros, Henrique, Broeders, Lisa, Cap, Jan, Draušnik, Željka, Engjom, Hilde, Farr, Alex, Fresson, Jeanne, Gatt, Miriam, Gissler, Mika, Heller, Günther, Isakova, Jelena, Källén, Karin, Kyprianou, Theopisti, Loghi, Marzia, Monteath, Kirsten, Mortensen, Laust, Rihs, Tonia, Sakkeus, Luule, Sikora, Izabela, Szamotulska, Katarzyna, Velebil, Petr, Verdenik, Ivan, Weber, Guy, Zile, Irisa, Zurriaga, Oscar, Smith, Lucy

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An annotated cDNA library of juvenile Euprymna scolopes with and without colonization by the symbiont Vibrio fischeri von Chun, Carlene K, Scheetz, Todd E, Bonaldo, Maria de Fatima, Brown, Bartley, Clemens, Anik, Crookes-Goodson, Wendy J, Crouch, Keith, DeMartini, Tad, Eyestone, Mari, Goodson, Michael S, Janssens, Bernadette, Kimbell, Jennifer L, Koropatnick, Tanya A, Kucaba, Tamara, Smith, Christina, Stewart, Jennifer J, Tong, Deyan, Troll, Joshua V, Webster, Sarahrose, Winhall-Rice, Jane, Yap, Cory, Casavant, Thomas L, McFall-Ngai, Margaret J, Soares, M Bento

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