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Showing results 1 to 9 of 9

	Title	Author(s)	Issue Date
	A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis Journal:Scientific Reports	Kou, I Watanabe, K Takahashi, Y Momozawa, Y Khanshour, A Grauers, A Zhou, H Liu, G Fan, Y Takeda, K Ogura, Y Zhou, T Iwasaki, Y Kubo, M Wu, Z Matsumoto, M JSCRG, J TSRHCCG, T Einarsdottir, E Kere, J Huang, D Qiu, G Qiu, Y Wise, CA Song, Y WU, N SU, P Gerdhem, P Ikegawa, S	2018
	A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis Journal:Journal of Human Genetics	Takeda, K Kou, I Otomo, N Grauers, A Fan, YH Ogura, Y Takahashi, Y Momozawa, Y Einarsdottir, E Kere, J Japan Scoliosis Clinical Research Group (JSCRG)Matsumoto, M Qiu, Y Song, YQ Gerdhem, P Watanabe, K Ikegawa, S	2019
	Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia Journal:American Journal of Human Genetics	Feuk, L Kalervo, A LipsanenNyman, M Skaug, J Nakabayashi, K Finucane, B Hartung, D Innes, M Kerem, B Nowaczyk, MJ Rivlin, J Roberts, W Senman, L Summers, A Szatmari, P Wong, V Vincent, JB Zeesman, S Osborne, LR Cardy, JO Kere, J Scherer, SW HannulaJouppi, K	2006
	An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis Journal:Scientific Reports	Ogura, Y Takeda, K Kou, I Khanshour, A Grauers, A Zhou, H LIU, G Fan, Y ZHOU, T WU, Z Takahashi, Y Matsumoto, M Einarsdottir, E Kere, J Huang, D QIU, G XU, L QIU, Y WISE, SA Song, Y WU, N SU, P Gerdhem, P Watanabe, K Ikegawa, S	2018
	Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF Journal:Developmental Biology	Pispa, J Jung, HS Jernvall, J Kettunen, P Mustonen, T Tabata, MJ Kere, J Thesleff, I	1999
	Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci Journal:Human Molecular Genetics	Khanshour, AM Kou, I Fan, Y Einarsdottir, E Makki, N Kidane, YH Kere, J Grauers, A Johnson, TA Paria, N Patel, C Singhania, R Kamiya, N Takeda, K Otomo, N Watanabe, K Luk, KDK Cheung, KMC Herring, JA Rios, JJ Ahituv, N Gerdhem, P Gurnett, CA Song, Y Ikegawa, S Wise, CA	2018
	Human chromosome 7: DNA sequence and biology Journal:Science	Scherer, SW Cheung, J MacDonald, JR Osborne, LR Nakabayashi, K Herbrick, JA Carson, AR ParkerKatiraee, L Skaug, J Khaja, R Zhang, J Hudek, AK Li, M Haddad, M Duggan, GE Fernandez, BA Kanematsu, E Gentles, S Christopoulos, CC Choufani, S Kwasnicka, D Zheng, XH Lai, Z Nusskern, D Zhang, Q Gu, Z Lu, F Zeesman, S Nowaczyk, MJ Teshima, I Chitayat, D Shuman, C Weksberg, R Zackai, EH Grebe, TA Cox, SR Kirkpatrick, SJ Rahman, N Friedman, JM Heng, HHQ Pelicci, PG LoCoco, F Belloni, E Shaffer, LG Pober, B Morton, CC Gusella, JF Bruns, GAP Korf, BR Quade, BJ Ligon, AH Ferguson, H Higgins, AW Leach, NT Herrick, SR Lemyre, E Farra, CG Kim, HG Summers, AM Gripp, KW Roberts, W Szatmari, P Winsor, EJT Grzeschik, KH Teebi, A Minassian, BA Kere, J Armengol, L Pujana, MA Estivill, X Wilson, MD Koop, BF Tosi, S Moore, GE Boright, AP Zlotorynski, E Kerem, B Kroisel, PM Petek, E Oscier, DG Mould, SJ Döhner, H Döhner, K Rommens, JM Vincent, JB Venter, JC Li, PW Mural, RJ Adams, MD Tsui, LC	2003
	Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly Journal:Human Molecular Genetics	Scherer, SW Poorkaj, P Massa, H Soder, S Allen, T Nunes, M Geshuri, D Wong, E Belloni, E Little, S Zhou, L Becker, D Kere, J Ignatius, J Niikawa, N Fukushima, Y Hasegawa, T Weissenbach, J Boncinelli, E Trask, B Tsui, L-C Evans, JP	1994
	Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31 Journal:Genome Research	Höglund, P Haila, S Scherer, SW Tsui, LC Green, ED Weissenbach, J Holmberg, C De La Chapelle, A Kere, J	1996

Showing results 1 to 9 of 9