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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Genome‐Wide Association Meta‐Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci von McIntosh, Laura A., Marion, Miranda C., Sudman, Marc, Comeau, Mary E., Becker, Mara L., Bohnsack, John F., Fingerlin, Tasha E., Griffin, Thomas A., Haas, J. Peter, Lovell, Daniel J., Maier, Lisa A., Nigrovic, Peter A., Prahalad, Sampath, Punaro, Marilynn, Rosé, Carlos D., Wallace, Carol A., Wise, Carol A., Moncrieffe, Halima, Howard, Timothy D., Langefeld, Carl D., Thompson, Susan D.

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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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Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review von Smith, Elisabeth J, Allantaz, Florence, Bennett, Lynda, Zhang, Dongping, Gao, Xiaochong, Wood, Geryl, Kastner, Daniel L, Punaro, Marilynn, Aksentijevich, Ivona, Pascual, Virginia, Wise, Carol A

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Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes von SHARMA, Swarkar, XIAOCHONG GAO, GURNETT, Christina A, GRANT, Struan F. A, HAKONARSON, Hakon, DORMANS, John P, HERRING, John A, GORDON, Derek, WISE, Carol A, LONDONO, Douglas, DEVROY, Shonn E, MAULDIN, Kristen N, FRANKEL, Jessica T, BRANDON, January M, DONGPING ZHANG, LI, Quan-Zhen, DOBBS, Matthew B

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Pyrin Binds the PSTPIP1/CD2BP1 Protein, Defining Familial Mediterranean Fever and PAPA Syndrome as Disorders in the Same Pathway von Shoham, Nitza G., Centola, Michael, Mansfield, Elizabeth, Hull, Keith M., Wood, Geryl, Wise, Carol A., Kastner, Daniel L.

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Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis von Yu, Hao, Khanshour, Anas M, Ushiki, Aki, Otomo, Nao, Koike, Yoshinao, Einarsdottir, Elisabet, Fan, Yanhui, Antunes, Lilian, Kidane, Yared H, Cornelia, Reuel, Sheng, Rory R, Zhang, Yichi, Pei, Jimin, Grishin, Nick V, Evers, Bret M, Cheung, Jason Pui Yin, Herring, John A, Terao, Chikashi, Song, You-Qiang, Gurnett, Christina A, Gerdhem, Paul, Ikegawa, Shiro, Rios, Jonathan J, Ahituv, Nadav, Wise, Carol A

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Saturation mutagenesis defines novel mouse models of severe spine deformity von Rios, Jonathan J., Denton, Kristin, Yu, Hao, Manickam, Kandamurugu, Garner, Shannon, Russell, Jamie, Ludwig, Sara, Rosenfeld, Jill A., Liu, Pengfei, Munch, Jake, Sucato, Daniel J., Beutler, Bruce, Wise, Carol A.

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Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study von Otomo, Nao, Khanshour, Anas M, Koido, Masaru, Takeda, Kazuki, Momozawa, Yukihide, Kubo, Michiaki, Kamatani, Yoichiro, Herring, John A, Ogura, Yoji, Takahashi, Yohei, Minami, Shohei, Uno, Koki, Kawakami, Noriaki, Ito, Manabu, Sato, Tatsuya, Watanabe, Kei, Kaito, Takashi, Yanagida, Haruhisa, Taneichi, Hiroshi, Harimaya, Katsumi, Taniguchi, Yuki, Shigematsu, Hideki, Iida, Takahiro, Demura, Satoru, Sugawara, Ryo, Fujita, Nobuyuki, Yagi, Mitsuru, Okada, Eijiro, Hosogane, Naobumi, Kono, Katsuki, Nakamura, Masaya, Chiba, Kazuhiro, Kotani, Toshiaki, Sakuma, Tsuyoshi, Akazawa, Tsutomu, Suzuki, Teppei, Nishida, Kotaro, Kakutani, Kenichiro, Tsuji, Taichi, Sudo, Hideki, Iwata, Akira, Inami, Satoshi, Wise, Carol A, Kochi, Yuta, Matsumoto, Morio, Ikegawa, Shiro, Watanabe, Kota, Terao, Chikashi

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Interrogating Causal Effects of Body Composition and Puberty‐Related Risk Factors on Adolescent Idiopathic Scoliosis: A Two‐Sample Mendelian Randomization Study von Ghanbari, Faegheh, Otomo, Nao, Gamache, Isabel, Iwami, Takuro, Koike, Yoshinao, Khanshour, Anas M., Ikegawa, Shiro, Wise, Carol A., Terao, Chikashi, Manousaki, Despoina

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Deep Learning-Based Automated Measurement of Murine Bone Length in Radiographs von Rong, Ruichen, Denton, Kristin, Jin, Kevin W, Quan, Peiran, Wen, Zhuoyu, Kozlitina, Julia, Lyon, Stephen, Wang, Aileen, Wise, Carol A, Beutler, Bruce, Yang, Donghan M, Li, Qiwei, Rios, Jonathan J, Xiao, Guanghua

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Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16... von Giampietro, Philip F., Pourquie, Olivier, Raggio, Cathy, Ikegawa, Shiro, Turnpenny, Peter D., Gray, Ryan, Dunwoodie, Sally L., Gurnett, Christina A., Alman, Benjamin, Cheung, Kenneth, Kusumi, Kenro, Hadley‐Miller, Nancy, Wise, Carol A.

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Mutations Preventing Regulated Exon Skipping in MET Cause Osteofibrous Dysplasia von Gray, Mary J., Kannu, Peter, Sharma, Swarkar, Neyt, Christine, Zhang, Dongping, Paria, Nandina, Daniel, Philip B., Whetstone, Heather, Sprenger, Hans-Georg, Hammerschmidt, Philipp, Weng, Angela, Dupuis, Lucie, Jobling, Rebekah, Mendoza-Londono, Roberto, Dray, Michael, Su, Peiqiang, Wilson, Megan J., Kapur, Raj P., McCarthy, Edward F., Alman, Benjamin A., Howard, Andrew, Somers, Gino R., Marshall, Christian R., Manners, Simon, Flanagan, Adrienne M., Rathjen, Karl E., Karol, Lori A., Crawford, Haemish, Markie, David M., Rios, Jonathan J., Wise, Carol A., Robertson, Stephen P.

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ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease von Hayes, Madeline, Gao, Xiaochong, Yu, Lisa X, Paria, Nandina, Henkelman, R. Mark, Wise, Carol A., Ciruna, Brian

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Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasia von Patel, Chandreshkumar, Khanshour, Anas M., Wilkes, David, Rios, Jonathan J., Sheff, Kelly W., Nassi, Lorien, Wise, Carol A.

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TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data von Londono, Douglas, Buyske, Steven, Finch, Stephen J, Sharma, Swarkar, Wise, Carol A, Gordon, Derek

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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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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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Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways von Gladman, Dafna, Begovich, Ann B, Liao, Wilson, Nair, Rajan P, Bowcock, Anne M, Ruether, Andreas, Voorhees, John J, Schrodi, Steven J, Rahman, Proton, Goldgar, David, Fischer, Judith, Weichenthal, Michael, Guthery, Stephen L, Menter, Alan, Gudjonsson, Johann E, Ding, Jun, Tejasvi, Trilokraj, Kwok, Pui-Yan, Elder, James T, Duffin, Kristina Callis, Li, Yun, Prahalad, Sampath, Abecasis, Gonçalo R, Schreiber, Stefan, Feng, Bing-Jian, Wise, Carol A, Lathrop, G Mark, Krueger, Gerald G, Stuart, Philip E, Helms, Cynthia

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Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis von Martin, Carol-Anne, Murray, Jennie E, Carroll, Paula, Leitch, Andrea, Mackenzie, Karen J, Halachev, Mihail, Fetit, Ahmed E, Keith, Charlotte, Bicknell, Louise S, Fluteau, Adeline, Gautier, Philippe, Hall, Emma A, Joss, Shelagh, Soares, Gabriela, Silva, João, Bober, Michael B, Duker, Angela, Wise, Carol A, Quigley, Alan J, Phadke, Shubha R, Wood, Andrew J, Vagnarelli, Paola, Jackson, Andrew P

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