Bone marrow adipocytes promote the regeneration of stem cells and haematopoiesis by secreting SCF von Zhou, Bo O., Yu, Hua, Yue, Rui, Zhao, Zhiyu, Rios, Jonathan J., Naveiras, Olaia, Morrison, Sean J.

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PIK3CA-related overgrowth spectrum (PROS): Diagnostic and testing eligibility criteria, differential diagnosis, and evaluation von Keppler-Noreuil, Kim M., Rios, Jonathan J., Parker, Victoria E.R., Semple, Robert K., Lindhurst, Marjorie J., Sapp, Julie C., Alomari, Ahmad, Ezaki, Marybeth, Dobyns, William, Biesecker, Leslie G.

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Geographical and sex‐specific effects of malathion insecticide selection in African fig fly Zaprionus indianus Gupta, 1970 (Diptera: Drosophilidae) von Oliveira Rios, Jonathan, Costa, Sávio Cunha, Conceição Galego, Luís Gustavo

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A Retrospective, Cross-Sectional Analysis of Motor Development, Cognition, and Mood in 87 Patients With Childhood-Onset Hereditary Spastic Paraplegias von Marvel, Brooke M., Smith, Linsley, Rios, Jonathan J., Christie, Michelle R.

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Viable mutations of mouse midnolin suppress B cell malignancies von Zhong, Xue, Peddada, Nagesh, Moresco, James J, Wang, Jianhui, Jiang, Yiao, Rios, Jonathan J, Moresco, Eva Marie Y, Choi, Jin Huk, Beutler, Bruce

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Deletion of Pax1 scoliosis-associated regulatory elements leads to a female-biased tail abnormality von Ushiki, Aki, Sheng, Rory R., Zhang, Yichi, Zhao, Jingjing, Nobuhara, Mai, Murray, Elizabeth, Ruan, Xin, Rios, Jonathan J., Wise, Carol A., Ahituv, Nadav

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Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly von Rios, Jonathan J, Paria, Nandina, Burns, Dennis K, Israel, Bonnie A, Cornelia, Reuel, Wise, Carol A, Ezaki, Marybeth

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DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis von Starokadomskyy, Petro, Gemelli, Terry, Rios, Jonathan J, Xing, Chao, Wang, Richard C, Li, Haiying, Pokatayev, Vladislav, Dozmorov, Igor, Khan, Shaheen, Miyata, Naoteru, Fraile, Guadalupe, Raj, Prithvi, Xu, Zhe, Xu, Zigang, Ma, Lin, Lin, Zhimiao, Wang, Huijun, Yang, Yong, Ben-Amitai, Dan, Orenstein, Naama, Mussaffi, Huda, Baselga, Eulalia, Tadini, Gianluca, Grunebaum, Eyal, Sarajlija, Adrijan, Krzewski, Konrad, Wakeland, Edward K, Yan, Nan, de la Morena, Maria Teresa, Zinn, Andrew R, Burstein, Ezra

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Molecular Dissection of Somatic Skeletal Disease in Neurofibromatosis Type 1 von Paria, Nandina, Khalid, Aysha, Shen, Bo, Lemoine, Ben, Chan, Jinyan, Kidane, Yared H, Oxendine, Ila, Cornelia, Reuel, Wise, Carol A, Rios, Jonathan J

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MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus von de Blank, Peter M K, Gross, Andrea M, Akshintala, Srivandana, Blakeley, Jaishri O, Bollag, Gideon, Cannon, Ashley, Dombi, Eva, Fangusaro, Jason, Gelb, Bruce D, Hargrave, Darren, Kim, AeRang, Klesse, Laura J, Loh, Mignon, Martin, Staci, Moertel, Christopher, Packer, Roger, Payne, Jonathan M, Rauen, Katherine A, Rios, Jonathan J, Robison, Nathan, Schorry, Elizabeth K, Shannon, Kevin, Stevenson, David A, Stieglitz, Elliot, Ullrich, Nicole J, Walsh, Karin S, Weiss, Brian D, Wolters, Pamela L, Yohay, Kaleb, Yohe, Marielle E, Widemann, Brigitte C, Fisher, Michael J

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Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci von Khanshour, Anas M, Kou, Ikuyo, Fan, Yanhui, Einarsdottir, Elisabet, Makki, Nadja, Kidane, Yared H, Kere, Juha, Grauers, Anna, Johnson, Todd A, Paria, Nandina, Patel, Chandreshkumar, Singhania, Richa, Kamiya, Nobuhiro, Takeda, Kazuki, Otomo, Nao, Watanabe, Kota, Luk, Keith D K, Cheung, Kenneth M C, Herring, John A, Rios, Jonathan J, Ahituv, Nadav, Gerdhem, Paul, Gurnett, Christina A, Song, You-Qiang, Ikegawa, Shiro, Wise, Carol A

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DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency von Logan, Clare V., Murray, Jennie E., Parry, David A., Robertson, Andrea, Bellelli, Roberto, Tarnauskaitė, Žygimantė, Challis, Rachel, Cleal, Louise, Borel, Valerie, Fluteau, Adeline, Santoyo-Lopez, Javier, Aitman, Timothy J., Biankin, Andrew V., Cooke, Susanna L., Humphrey, Wendy Inglis, Martin, Sancha, Mennie, Lynne, Meynert, Alison, Miedzybrodzka, Zosia, Murphy, Fiona, Nourse, Craig, Santoyo-Lopez, Javier, Semple, Colin A., Williams, Nicola, Aitman, Tim, Barroso, Inês, Basel, Donald, Bicknell, Louise S., Goel, Himanshu, Hu, Hao, Huff, Chad, Hutchison, Michele, Joyce, Caroline, Knox, Rachel, Lacroix, Amy E., Langlois, Sylvie, McCandless, Shawn, McCarrier, Julie, Metcalfe, Kay A., Morrissey, Rose, Murphy, Nuala, Netchine, Irène, O’Connell, Susan M., Olney, Ann Haskins, Paria, Nandina, Rosenfeld, Jill A., Sherlock, Mark, Syverson, Erin, White, Perrin C., Wise, Carol, Yu, Yao, Zacharin, Margaret, Banerjee, Indraneel, Reijns, Martin, Bober, Michael B., Semple, Robert K., Boulton, Simon J., Rios, Jonathan J., Jackson, Andrew P.

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Inheritance of Hb S and G6PD deficiency in a familiar group von Domingos, Claudia Bonini, Rios, Jonathan de Oliveira, Orlandini, Leticia Cardoso, Pereira, Lucas Ramos

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Deletion of GPIHBP1 causing severe chylomicronemia von Rios, Jonathan J., Shastry, Savitha, Jasso, Juan, Hauser, Natalie, Garg, Abhimanyu, Bensadoun, André, Cohen, Jonathan C., Hobbs, Helen H.

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Impaired glycine neurotransmission causes adolescent idiopathic scoliosis von Wang, Xiaolu, Yue, Ming, Cheung, Jason Pui Yin, Cheung, Prudence Wing Hang, Fan, Yanhui, Wu, Meicheng, Wang, Xiaojun, Zhao, Sen, Khanshour, Anas M, Rios, Jonathan J, Chen, Zheyi, Wang, Xiwei, Tu, Wenwei, Chan, Danny, Yuan, Qiuju, Qin, Dajiang, Qiu, Guixing, Wu, Zhihong, Zhang, Terry Jianguo, Ikegawa, Shiro, Wu, Nan, Wise, Carol A, Hu, Yong, Luk, Keith Dip Kei, Song, You-Qiang, Gao, Bo

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Genomic characterization of the adolescent idiopathic scoliosis-associated transcriptome and regulome von Makki, Nadja, Zhao, Jingjing, Liu, Zhaoyang, Eckalbar, Walter L, Ushiki, Aki, Khanshour, Anas M, Wu, Joe, Rios, Jonathan, Gray, Ryan S, Wise, Carol A, Ahituv, Nadav

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Os Desafios da Medicina Física e de Reabilitação em Portugal Durante a Pandemia por COVID-19 von Martins, Cristiana Lopes, Rios, Jonathan

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Doxil Synergizes with Cancer Immunotherapies to Enhance Antitumor Responses in Syngeneic Mouse Models von Rios-Doria, Jonathan, Durham, Nicholas, Wetzel, Leslie, Rothstein, Raymond, Chesebrough, Jon, Holoweckyj, Nicholas, Zhao, Wei, Leow, Ching Ching, Hollingsworth, Robert

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TBX6 missense variants expand the mutational spectrum in a non‐Mendelian inheritance disease von Chen, Weisheng, Lin, Jiachen, Wang, Lianlei, Li, Xiaoxin, Zhao, Sen, Liu, Jiaqi, Akdemir, Zeynep C., Zhao, Yanxue, Du, Renqian, Ye, Yongyu, Song, Xiaofei, Zhang, Yuanqiang, Yan, Zihui, Yang, Xinzhuang, Lin, Mao, Shen, Jianxiong, Wang, Shengru, Gao, Na, Yang, Ying, Liu, Ying, Li, Wenli, Liu, Jia, Zhang, Na, Yang, Xu, Xu, Yuan, Zhang, Jianguo, Delgado, Mauricio R., Posey, Jennifer E., Qiu, Guixing, Rios, Jonathan J., Liu, Pengfei, Wise, Carol A., Zhang, Feng, Wu, Zhihong, Lupski, James R., Wu, Nan

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RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation von Rios, Jonathan J., Li, Yang, Paria, Nandina, Bohlender, Ryan J., Huff, Chad, Rosenfeld, Jill A., Liu, Pengfei, Bi, Weimin, Haga, Kentaro, Fukuda, Mitsunori, Vashisth, Shayal, Kaur, Kiran, Chahrour, Maria H., Bober, Michael B., Duker, Angela L., Ladha, Farah A., Hanchard, Neil A., Atala, Kristhen, Khanshour, Anas M., Smith, Linsley, Wise, Carol A., Delgado, Mauricio R.

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