Commitment and oncogene-induced plasticity of human stem cell-derived pancreatic acinar and ductal organoids von Huang, Ling, Desai, Ridhdhi, Conrad, Daniel N., Leite, Nayara C., Akshinthala, Dipikaa, Lim, Christine Maria, Gonzalez, Raul, Muthuswamy, Lakshmi B., Gartner, Zev, Muthuswamy, Senthil K.

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A large-scale proteomics resource of circulating extracellular vesicles for biomarker discovery in pancreatic cancer von Bockorny, Bruno, Muthuswamy, Lakshmi, Huang, Ling, Hadisurya, Marco, Maria Lim, Christine, Tsai, Leo L, Gill, Ritu R, Wei, Jesse L, Bullock, Andrea J, Grossman, Joseph E, Besaw, Robert J, Narasimhan, Supraja, Tao, Weiguo Andy, Perea, Sofia, Sawhney, Mandeep S, Freedman, Steven D, Hildago, Manuel, Iliuk, Anton, Muthuswamy, Senthil K

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Leveraging Protein Homeostasis as a Disease-modifying Strategy von Lim, Christine Maria

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Large scale proteomics of circulating extracellular vesicles to reveal novel biomarkers for pancreatic cancer von Bockorny, Bruno, Muthuswamy, Lakshmi, Huang, Ling, Hadisurya, Marco, Tsai, Leo, Gill, Ritu R., Wei, Jesse, Bullock, Andrea J., Grossman, Joseph Elan, Besaw, Robert J., Lim, Christine Maria, Narasimhan, Supraja, Perea, Sofia, Sawhney, Mandeep, Tao, W. Andy, Freedman, Steven, Hidalgo, Manuel, Iliuk, Anton, Muthuswamy, Senthil

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Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism von Chahrour, Maria H, Yu, Timothy W, Lim, Elaine T, Ataman, Bulent, Coulter, Michael E, Hill, R Sean, Stevens, Christine R, Schubert, Christian R, Greenberg, Michael E, Gabriel, Stacey B, Walsh, Christopher A

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Using Whole-Exome Sequencing to Identify Inherited Causes of Autism von Yu, Timothy W., Chahrour, Maria H., Coulter, Michael E., Jiralerspong, Sarn, Okamura-Ikeda, Kazuko, Ataman, Bulent, Schmitz-Abe, Klaus, Harmin, David A., Adli, Mazhar, Malik, Athar N., D’Gama, Alissa M., Lim, Elaine T., Sanders, Stephan J., Mochida, Ganesh H., Partlow, Jennifer N., Sunu, Christine M., Felie, Jillian M., Rodriguez, Jacqueline, Nasir, Ramzi H., Ware, Janice, Joseph, Robert M., Hill, R. Sean, Kwan, Benjamin Y., Al-Saffar, Muna, Mukaddes, Nahit M., Hashmi, Asif, Balkhy, Soher, Gascon, Generoso G., Hisama, Fuki M., LeClair, Elaine, Poduri, Annapurna, Oner, Ozgur, Al-Saad, Samira, Al-Awadi, Sadika A., Bastaki, Laila, Ben-Omran, Tawfeg, Teebi, Ahmad S., Al-Gazali, Lihadh, Eapen, Valsamma, Stevens, Christine R., Rappaport, Leonard, Gabriel, Stacey B., Markianos, Kyriacos, State, Matthew W., Greenberg, Michael E., Taniguchi, Hisaaki, Braverman, Nancy E., Morrow, Eric M., Walsh, Christopher A.

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Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder von Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S, Zhang, Xiaochang, D'Gama, Alissa M, Kim, Sonia N, Hill, Robert Sean, Goldberg, Arthur P, Poultney, Christopher, Minshew, Nancy J, Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J, Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M, Weiss, Lauren A, Fromer, Menachem, Chiocchetti, Andreas G, Freitag, Christine M, Church, George M, Scherer, Stephen W, Buxbaum, Joseph D, Walsh, Christopher A

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Ciliated muconodular papillary tumor: a solitary peripheral lung nodule in a teenage girl von Lau, Kah Weng, MBBS, DPhil (Oxon), Aubry, Marie-Christine, MD, Tan, Gek San, MSc, Lim, Chong Hee, MBBS, FRCSEd, Takano, Angela Maria, MD

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Measuring social determinants of health in the All of Us Research Program von Tesfaye, Samantha, Cronin, Robert M., Lopez-Class, Maria, Chen, Qingxia, Foster, Christopher S., Gu, Callie A., Guide, Andrew, Hiatt, Robert A., Johnson, Angelica S., Joseph, Christine L. M., Khatri, Parinda, Lim, Sokny, Litwin, Tamara R., Munoz, Fatima A., Ramirez, Andrea H., Sansbury, Heather, Schlundt, David G., Viera, Emma N., Dede-Yildirim, Elif, Clark, Cheryl R.

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Phase 3 Trial of Selpercatinib in Advanced RET-Mutant Medullary Thyroid Cancer von Hadoux, Julien, Elisei, Rossella, Brose, Marcia S., Hoff, Ana O., Robinson, Bruce G., Gao, Ming, Jarzab, Barbara, Isaev, Pavel, Kopeckova, Katerina, Wadsley, Jonathan, Führer, Dagmar, Keam, Bhumsuk, Bardet, Stéphane, Sherman, Eric J., Tahara, Makoto, Hu, Mimi I., Singh, Ravinder, Lin, Yan, Soldatenkova, Victoria, Wright, Jennifer, Lin, Boris, Maeda, Patricia, Capdevila, Jaume, Wirth, Lori J.

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Zeolite Beta Formation from Clear Sols: Silicate Speciation, Particle Formation and Crystallization Monitored by Complementary Analysis Methods von Castro, Maria, Haouas, Mohamed, Lim, Ivy, Bongard, Hans J., Schüth, Ferdi, Taulelle, Francis, Karlsson, Gunnel, Alfredsson, Viveka, Breyneart, Eric, Kirschhock, Christine E. A., Schmidt, Wolfgang

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Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale von Junker, Johanna, Lange, Lara M., Vollstedt, Eva‐Juliane, Roopnarain, Karisha, Doquenia, Maria Leila M., Annuar, Azlina Ahmad, Avenali, Micol, Bardien, Soraya, Bahr, Natascha, Ellis, Melina, Galandra, Caterina, Gasser, Thomas, Heutink, Peter, Illarionova, Anastasia, Kanana, Yuliia, Keller Sarmiento, Ignacio J., Kumar, Kishore R., Lim, Shen‐Yang, Madoev, Harutyun, Mata, Ignacio F., Mencacci, Niccolò E., Nalls, Mike A., Padmanabhan, Shalini, Shambetova, Cholpon, Solle, J. C., Tan, Ai‐Huey, Trinh, Joanne, Valente, Enza Maria, Singleton, Andrew, Blauwendraat, Cornelis, Lohmann, Katja, Fang, Zih‐Hua, Klein, Christine, Junker, Johanna, Lange, Lara M., Vollstedt, Eva‐Juliane, Roopnarain, Karisha, Doquenia, Maria Leila M., Annuar, Azlina Ahmad, Avenali, Micol, Bardien, Soraya, Bahr, Natascha, Ellis, Melina, Galandra, Caterina, Gasser, Thomas, Heutink, Peter, Illarionova, Anastasia, Kanana, Yuliia, Keller, Ignacio J., Kumar, Kishore R., Lim, Shen‐Yang, Madoev, Harutyun, Mata, Ignacio F., Mencacci, Niccolò E., Nalls's, Mike A., Padmanabhan, Shalini, Shambetova, Cholpon, Solle, J., Tan, Ai‐Huey, Trinh, Joanne, Valente, Enza Maria, Singleton, Andrew, Blauwendraat, Cornelis, Lohmann, Katja, Fang, Zih‐Hua, Klein, Christine

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GP2: The Global Parkinson's Genetics Program

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Oxygen in patients with fibrotic interstitial lung disease: an international Delphi survey von Lim, Rachel K, Humphreys, Christopher, Morisset, Julie, Holland, Anne E, Johannson, Kerri A

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A sustained type I IFN-neutrophil-IL-18 axis drives pathology during mucosal viral infection von Lebratti, Tania, Lim, Ying Shiang, Cofie, Adjoa, Andhey, Prabhakar, Jiang, Xiaoping, Scott, Jason, Fabbrizi, Maria Rita, Ozantürk, Ayşe Naz, Pham, Christine, Clemens, Regina, Artyomov, Maxim, Dinauer, Mary, Shin, Haina

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Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial von Brose, Marcia S, Dr, Nutting, Christopher M, Prof, Jarzab, Barbara, Prof, Elisei, Rossella, Prof, Siena, Salvatore, MD, Bastholt, Lars, MD, de la Fouchardiere, Christelle, MD, Pacini, Furio, Prof, Paschke, Ralf, Prof, Shong, Young Kee, Prof, Sherman, Steven I, Prof, Smit, Johannes W A, Prof, Chung, John, MD, Kappeler, Christian, PhD, Peña, Carol, PhD, Molnár, István, MD, Schlumberger, Martin J, Prof

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High prevalence of adrenal insufficiency at diagnosis and headache recovery in surgically resected Rathke’s cleft cysts—a large retrospective single center study von Langlois, Fabienne, Manea, Anamaria, Lim, Dawn Shao Ting, McCartney, Shirley, Yedinak, Christine G., Cetas, Justin S., Fleseriu, Maria

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Automated and Continuous Monitoring of Animal Welfare through Digital Alerting von Do, Johnny P, Defensor, Erwin B, Ichim, Christine V, Lim, Maria A, Mechanic, Jordan A, Rabe, Mark D, Schaevitz, Laura R

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A second update on mapping the human genetic architecture of COVID-19 von Jansen, Philip, Nakanishi, Tomoko, Priest, James, Turebayeva, Gulsimzhan, Bouab, Meriem, Bourque, Guillaume, Tse, Sze Man, Faucon, Annika B, Jensen, Björn-Erik Ole, Bals, Robert, Noor, Abdul, Liontos, Angelos, Azuure, Clinton, Blanco-Grau, Albert, Casalone, Elisabetta, Bellelli, Giuseppe, Kurihara, Hayato, Farré, Xavier, Hunkapiller, Julie, Kim, Jin Yong, Lee, Ji Yeon, Jung, Keum Ji, Bretherick, Andrew D, Ostermann, Marlies, Ryan, Lucy, Briton, Kate, Cutler, Sean, Springle, Philippa, Goodwin, Emma, Tibke, Clare, Farley, Sean, Bradley-Potts, Joanne, Whileman, Amanda, Kaye, Callum, Preston, Stephen, Cupitt, Jason, Jakkula, Srinivas, Lamb, Thomas, Hudson, Anne, Clark, Richard, Hudig, Lisa, Roberts, Abigail, Slevin, Kathryn, Thomas, Vicky, Chisholm, Catherine, Scanlon, Jeremy, Jones, Helen, Riches, Joanne, Anderson, Susan, Davies, Rhys, Tebbutt, Julie, Conyngham, Jo-Anna, Hobden, Gillian, Collier, Dawn, Durga, Latha, Wilson, Alison, Finnell, Jez, Serrano-Ruiz, Alfredo, Turner, Patricia, Turney, Sharon, Tutt, Gabriella, Varghese, Mathew, Stuart, Carmel, Wood, Stephen, Cother, Naiara, Brady, Ailbhe, Arden, Tracie, Capps, Nigel, Lennon, Liz, Joseph, Sibet, Jennings, Claire, Revill, Adam, Fletcher, Jo, Sutherland, Isobel, Kaye, Duncan, Whitbread, Jennifer, Hector, Gemma, Goddard, Peter, Lauder, Christen, Oosthuyzen, Wilna, Szoor-Mcelhinney, Helen, Upadhyay, Kamlesh J, Joshi, Chaitanya G, Kabata, Hiroki, Mikami, Yohei, Sonobe, Kazunari, Tateno, Hiroki, Yoshihara, Tomoyuki, Kuwahara, Naota, Sugiura, Hisatoshi, Ishihara, Sayoko, Ismail, Said I, Feng, Yen-Chen Anne, Castano, Luis, Ceballos, Francisco C, Aguado, Jose María, Carbonell, Cristina, Werge, Thomas, Wilson, Daniel J, Serra-Llovich, Alex

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Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine

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