CELSR2 is a candidate susceptibility gene in idiopathic scoliosis von Einarsdottir, Elisabet, Grauers, Anna, Wang, Jingwen, Jiao, Hong, Escher, Stefan A, Danielsson, Aina, Simony, Ane, Andersen, Mikkel, Christensen, Steen Bach, Åkesson, Kristina, Kou, Ikuyo, Khanshour, Anas M, Ohlin, Acke, Wise, Carol, Ikegawa, Shiro, Kere, Juha, Gerdhem, Paul

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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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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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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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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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Genetic Characterization of Cleveland Bay Horse Breed von Khanshour, Anas M., Hempsey, Eleanore K., Juras, Rytis, Cothran, E. Gus

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Characterization of the Polish Primitive Horse (Konik) maternal lines using mitochondrial D-loop sequence variation von Cieslak, Jakub, Wodas, Lukasz, Borowska, Alicja, Cothran, Ernest G, Khanshour, Anas M, Mackowski, Mariusz

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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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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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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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Genetic association and characterization of FSTL5 in isolated clubfoot von Khanshour, Anas M, Kidane, Yared H, Kozlitina, Julia, Cornelia, Reuel, Rafipay, Alexandra, De Mello, Vanessa, Weston, Mitchell, Paria, Nandina, Khalid, Aysha, Hecht, Jacqueline T, Dobbs, Matthew B, Richards, B Stephens, Vargesson, Neil, Hamra, F Kent, Wilson, Megan, Wise, Carol, Gurnett, Christina A, Rios, Jonathan J

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Y-Chromosomal Insights into Breeding History and Sire Line Genealogies of Arabian Horses von Remer, Viktoria, Bozlak, Elif, Felkel, Sabine, Radovic, Lara, Rigler, Doris, Grilz-Seger, Gertrud, Stefaniuk-Szmukier, Monika, Bugno-Poniewierska, Monika, Brooks, Samantha, Miller, Donald C, Antczak, Douglas F, Sadeghi, Raheleh, Cothran, Gus, Juras, Rytis, Khanshour, Anas M, Rieder, Stefan, Penedo, Maria C, Waiditschka, Gudrun, Kalinkova, Liliya, Kalashnikov, Valery V, Zaitsev, Alexander M, Almarzook, Saria, Reißmann, Monika, Brockmann, Gudrun A, Brem, Gottfried, Wallner, Barbara

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The cartilage matrisome in adolescent idiopathic scoliosis von Wise, Carol A., Sepich, Diane, Ushiki, Aki, Khanshour, Anas M., Kidane, Yared H., Makki, Nadja, Gurnett, Christina A., Gray, Ryan S., Rios, Jonathan J., Ahituv, Nadav, Solnica-Krezel, Lila

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Maternal phylogenetic relationships and genetic variation among Arabian horse populations using whole mitochondrial DNA D-loop sequencing von Khanshour, Anas M, Cothran, Ernest Gus

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Impaired glycine neurotransmission causes adolescent idiopathic scoliosis von Wang, Xiaolu, Yue, Ming, Cheung, Jason Rui 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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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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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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The cartilage matrisome in adolescent idiopathic scoliosis von Wise, Carol A, Sepich, Diane, Ushiki, Aki, Khanshour, Anas M, Kidane, Yared H, Makki, Nadja, Gurnett, Christina A, Gray, Ryan S, Rios, Jonathan J, Ahituv, Nadav, Solnica-Krezel, Lila

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The cartilage matrisome in adolescent idiopathic scoliosis von Carol A. Wise, Diane Sepich, Aki Ushiki, Anas M. Khanshour, Yared H. Kidane, Nadja Makki, Christina A. Gurnett, Ryan S. Gray, Jonathan J. Rios, Nadav Ahituv, Lila Solnica-Krezel

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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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