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Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Tang, Clara Sze-Man; Gui, Hongsheng; Kapoor, Ashish; Kim, Jeong-Hyun; Luzón-Toro, Berta; Pelet, Anna; Burzynski, Grzegorz; Lantieri, Francesca; So, Man-Ting; Berrios, Courtney; Shin, Hyoung Doo; Fernández, Raquel M; Le, Thuy-Linh; Verheij, Joke B G M; Matera, Ivana; Cherny, Stacey S; Nandakumar, Priyanka; Cheong, Hyun Sub; Antiñolo, Guillermo; Amiel, Jeanne; Seo, Jeong-Meen; Kim, Dae-Yeon; Oh, Jung-Tak; Lyonnet, Stanislas; Borrego, Salud; Ceccherini, Isabella; Hofstra, Robert M W; Chakravarti, Aravinda; Kim, Hyun-Young; Sham, Pak Chung; Tam, Paul K H; Garcia-Barceló, Maria-Mercè.
Afiliación
  • Tang CS; Department of Surgery.
  • Gui H; Centre for Genomic Sciences.
  • Kapoor A; Dr Li Dak-Sum Research Centre, The University of Hong Kong - Karolinska Institutet Collaboration in Regenerative Medicine, Hong Kong SAR, China.
  • Kim JH; Department of Surgery.
  • Luzón-Toro B; Centre for Genomic Sciences.
  • Pelet A; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Burzynski G; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Lantieri F; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • So MT; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Berrios C; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Shin HD; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
  • Fernández RM; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Le TL; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.
  • Verheij JB; Department of Surgery.
  • Matera I; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Cherny SS; Research Institute for Basic Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Nandakumar P; Department of Life Science, Sogang University, Seoul 121-742, Republic of Korea.
  • Cheong HS; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • Antiñolo G; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Amiel J; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Seo JM; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
  • Kim DY; Department of Clinical Genetic, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Oh JT; UOC Genetica Medica, Istituto Giannina Gaslini, 16148 Genova, Italy.
  • Lyonnet S; Centre for Genomic Sciences.
  • Borrego S; Department of Psychiatry.
  • Ceccherini I; State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.
  • Hofstra RM; Center for Complex Disease Genomics, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
  • Chakravarti A; Department of Genetic Epidemiology, SNP Genetics, Inc., Seoul 121-742, Republic of Korea.
  • Kim HY; Department of Genetics, Reproduction and Fetal Medicine, Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville, Seville, Spain.
  • Sham PC; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain.
  • Tam PK; Laboratory of Embryology and Genetics of Congenital Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Institut Imagine, Paris, France.
  • Garcia-Barceló MM; Paris Descartes-Sorbonne Paris Cité University, Institut Imagine, Paris, France.
Hum Mol Genet ; 25(23): 5265-5275, 2016 12 01.
Article en En | MEDLINE | ID: mdl-27702942
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulina-1 / Semaforina-3A / Proteínas Proto-Oncogénicas c-ret / Enfermedad de Hirschsprung Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Neurregulina-1 / Semaforina-3A / Proteínas Proto-Oncogénicas c-ret / Enfermedad de Hirschsprung Tipo de estudio: Risk_factors_studies / Systematic_reviews Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article