Peroxisomes can oxidize medium‐ and long‐chain fatty acids through a pathway involving ABCD3 and HSD17B4 von Violante, Sara, Achetib, Nihad, Roermund, Carlo W. T., Hagen, Jacob, Dodatko, Tetyana, Vaz, Frédéric M., Waterham, Hans R., Chen, Hongjie, Baes, Myriam, Yu, Chunli, Argmann, Carmen A., Houten, Sander M.

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Proliferative potential and resistance to immune checkpoint blockade in lung cancer patients von Pabla, Sarabjot, Conroy, Jeffrey M, Nesline, Mary K, Glenn, Sean T, Papanicolau-Sengos, Antonios, Burgher, Blake, Hagen, Jacob, Giamo, Vincent, Andreas, Jonathan, Lenzo, Felicia L, Yirong, Wang, Dy, Grace K, Yau, Edwin, Early, Amy, Chen, Hongbin, Bshara, Wiam, Madden, Katherine G, Shirai, Keisuke, Dragnev, Konstantin, Tafe, Laura J, Marin, Daniele, Zhu, Jason, Clarke, Jeff, Labriola, Matthew, McCall, Shannon, Zhang, Tian, Zibelman, Matthew, Ghatalia, Pooja, Araujo-Fernandez, Isabel, Singavi, Arun, George, Ben, MacKinnon, Andrew Craig, Thompson, Jonathan, Singh, Rajbir, Jacob, Robin, Dressler, Lynn, Steciuk, Mark, Binns, Oliver, Kasuganti, Deepa, Shah, Neel, Ernstoff, Marc, Odunsi, Kunle, Kurzrock, Razelle, Gardner, Mark, Galluzzi, Lorenzo, Morrison, Carl

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HEPES activates a MiT/TFE-dependent lysosomal-autophagic gene network in cultured cells: A call for caution von Tol, Marc J., van der Lienden, Martijn J.C., Gabriel, Tanit L., Hagen, Jacob J., Scheij, Saskia, Veenendaal, Tineke, Klumperman, Judith, Donker-Koopman, Wilma E., Verhoeven, Arthur J., Overkleeft, Hermen, Aerts, Johannes M., Argmann, Carmen A., van Eijk, Marco

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A next generation sequencing based approach to identify extracellular vesicle mediated mRNA transfers between cells von Yang, Jialiang, Hagen, Jacob, Guntur, Kalyani V, Allette, Kimaada, Schuyler, Sarah, Ranjan, Jyoti, Petralia, Francesca, Gesta, Stephane, Sebra, Robert, Mahajan, Milind, Zhang, Bin, Zhu, Jun, Houten, Sander, Kasarskis, Andrew, Vishnudas, Vivek K, Akmaev, Viatcheslav R, Sarangarajan, Rangaprasad, Narain, Niven R, Schadt, Eric E, Argmann, Carmen A, Tu, Zhidong

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Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas von Zhong, Guojie, Ahimaz, Priyanka, Edwards, Nicole A., Hagen, Jacob J., Faure, Christophe, Lu, Qiao, Kingma, Paul, Middlesworth, William, Khlevner, Julie, El Fiky, Mahmoud, Schindel, David, Fialkowski, Elizabeth, Kashyap, Adhish, Forlenza, Sophia, Kenny, Alan P., Zorn, Aaron M., Shen, Yufeng, Chung, Wendy K.

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Novel, Compound Heterozygous, Single-Nucleotide Variants in MARS2 Associated with Developmental Delay, Poor Growth, and Sensorineural Hearing Loss von Webb, Bryn D., Wheeler, Patricia G., Hagen, Jacob J., Cohen, Ninette, Linderman, Michael D., Diaz, George A., Naidich, Thomas P., Rodenburg, Richard J., Houten, Sander M., Schadt, Eric E.

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Development and analytical validation of a next-generation sequencing based microsatellite instability (MSI) assay von Pabla, Sarabjot, Andreas, Jonathan, Lenzo, Felicia L, Burgher, Blake, Hagen, Jacob, Giamo, Vincent, Nesline, Mary K, Wang, Yirong, Gardner, Mark, Conroy, Jeffrey M, Papanicolau-Sengos, Antonios, Morrison, Carl, Glenn, Sean T

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Evaluation of the Surrogator® system to increase pheasant and quail abundance von Thacker, Eric T., Hamm, Robert L., Hagen, Jacob, Davis, Craig A., Guthery, Fred

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A temporal classifier predicts histopathology state and parses acute-chronic phasing in inflammatory bowel disease patients von Peters, Lauren A., Friedman, Joshua R., Stojmirovic, Aleksandar, Hagen, Jacob, Houten, Sander, Dodatko, Tetyana, Amaro, Mariana P., Restrepo, Paula, Chai, Zhi, Rodrigo Mora, J., Raymond, Holly A., Curran, Mark, Dobrin, Radu, Das, Anuk, Xiong, Huabao, Schadt, Eric E., Argmann, Carmen, Losic, Bojan

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Evaluation of leg banding and attachment of radio-transmitters on ring-necked pheasant chicks von Carroll, J. Matthew, Hamm, R. Lee, Hagen, Jacob M, Davis, Craig A, Guthery, Fred S

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Correction to: Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH von Zhu, Na, Swietlik, Emilia M, Welch, Carrie L, Pauciulo, Michael W, Hagen, Jacob J, Zhou, Xueya, Guo, Yicheng, Karten, Johannes, Pandya, Divya, Tilly, Tobias, Lutz, Katie A, Martin, Jennifer M, Treacy, Carmen M, Rosenzweig, Erika B, Krishnan, Usha, Coleman, Anna W, Gonzaga-Jauregui, Claudia, Lawrie, Allan, Trembath, Richard C, Wilkins, Martin R, Morrell, Nicholas W, Shen, Yufeng, Gräf, Stefan, Nichols, William C, Chung, Wendy K

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Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas von Zhong, Guojie, Ahimaz, Priyanka, Edwards, Nicole A., Hagen, Jacob J., Faure, Christophe, Lu, Qiao, Kingma, Paul, Middlesworth, William, Khlevner, Julie, El Fiky, Mahmoud, Schindel, David, Fialkowski, Elizabeth, Kashyap, Adhish, Forlenza, Sophia, Kenny, Alan P., Zorn, Aaron M., Shen, Yufeng, Chung, Wendy K.

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Altered Fat Tissue Distribution in Young Adult Men Who Had Low Birth Weight von Rasmussen, Eva Lind, Malis, Charlotte, Jensen, Christine Bjørn, Jensen, Jens-Erik Beck, Storgaard, Heidi, Poulsen, Pernille, Pilgaard, Kasper, Schou, Jacob Hagen, Madsbad, Sten, Astrup, Arne, Vaag, Allan

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Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease von Xiao, Feng, Zhang, Xiaoran, Morton, Sarah U., Kim, Seong Won, Fan, Youfei, Gorham, Joshua M., Zhang, Huan, Berkson, Paul J., Mazumdar, Neil, Cao, Yangpo, Chen, Jian, Hagen, Jacob, Liu, Xujie, Zhou, Pingzhu, Richter, Felix, Shen, Yufeng, Ward, Tarsha, Gelb, Bruce D., Seidman, Jonathan G., Seidman, Christine E., Pu, William T.

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A disorder-related variant (E420K) of a PP2A-regulatory subunit (PPP2R5D) causes constitutively active AKT-mTOR signaling and uncoordinated cell growth von Papke, Cinta M., Smolen, Kali A., Swingle, Mark R., Cressey, Lauren, Heng, Richard A., Toporsian, Mourad, Deng, Liyong, Hagen, Jacob, Shen, Yufeng, Chung, Wendy K., Kettenbach, Arminja N., Honkanen, Richard E.

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Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH von Zhu, Na, Swietlik, Emilia M, Welch, Carrie L, Pauciulo, Michael W, Hagen, Jacob J, Zhou, Xueya, Guo, Yicheng, Karten, Johannes, Pandya, Divya, Tilly, Tobias, Lutz, Katie A, Martin, Jennifer M, Treacy, Carmen M, Rosenzweig, Erika B, Krishnan, Usha, Coleman, Anna W, Gonzaga-Jauregui, Claudia, Lawrie, Allan, Trembath, Richard C, Wilkins, Martin R, Morrell, Nicholas W, Shen, Yufeng, Gräf, Stefan, Nichols, William C, Chung, Wendy K

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Bi‐allelic PAGR1 variants are associated with microcephaly and a severe neurodevelopmental disorder: Genetic evidence from two families von Daum, Hagit, Ganapathi, Mythily, Hirsch, Yoel, Griffin, Emily L., LeDuc, Charles A., Hagen, Jacob, Yagel, Simcha, Meiner, Vardiella, Chung, Wendy K., Mor‐Shaked, Hagar

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Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellu... von Ma, Mengqi, Ganapathi, Mythily, Zheng, Yiming, Tan, Kai-Li, Kanca, Oguz, Bove, Kevin E., Quintanilla, Norma, Sag, Sebnem O., Temel, Sehime G., LeDuc, Charles A., McPartland, Amanda J., Pereira, Elaine M., Shen, Yufeng, Hagen, Jacob, Thomas, Christie P., Nguyen Galván, Nhu Thao, Pan, Xueyang, Lu, Shenzhao, Rosenfeld, Jill A., Calame, Daniel G., Wangler, Michael F., Lupski, James R., Pehlivan, Davut, Hertel, Paula M., Chung, Wendy K., Bellen, Hugo J.

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Tissue specific expression of myosin IC isoforms von Sielski, Neil L, Ihnatovych, Ivanna, Hagen, Jacob J, Hofmann, Wilma A

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Germline deletion of Krüppel-like factor 14 does not increase risk of diet induced metabolic syndrome in male C57BL/6 mice von Argmann, Carmen A., Violante, Sara, Dodatko, Tetyana, Amaro, Mariana P., Hagen, Jacob, Gillespie, Virginia L., Buettner, Christoph, Schadt, Eric E., Houten, Sander M.

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