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Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease.
Schiff, E R; Frampton, M; Ben-Yosef, N; Avila, B E; Semplici, F; Pontikos, N; Bloom, S L; McCartney, S A; Vega, R; Lovat, L B; Wood, E; Hart, A; Israeli, E; Crespi, D; Furman, M A; Mann, S; Murray, C D; Segal, A W; Levine, A P.
Afiliação
  • Schiff ER; Centre for Molecular Medicine, Division of Medicine, University College London, London, UK.
  • Frampton M; Centre for Molecular Medicine, Division of Medicine, University College London, London, UK.
  • Ben-Yosef N; Centre for Molecular Medicine, Division of Medicine, University College London, London, UK.
  • Avila BE; Inflammatory Bowel Disease Unit, Institute of Gastroenterology and Liver Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Semplici F; Medical and Population Genetics, Broad Institute, Cambridge, MA, USA.
  • Pontikos N; Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
  • Bloom SL; Centre for Molecular Medicine, Division of Medicine, University College London, London, UK.
  • McCartney SA; UCL Genetics Institute, Division of Biosciences, University College London, London, UK.
  • Vega R; Department of Gastroenterology, University College London Hospital, London, UK.
  • Lovat LB; Department of Gastroenterology, University College London Hospital, London, UK.
  • Wood E; Department of Gastroenterology, University College London Hospital, London, UK.
  • Hart A; Research Department of Tissue and Energy, Division of Surgery and Interventional Science, University College London, London, UK.
  • Israeli E; Gastroenterology Department, Homerton University Hospital, London, UK.
  • Crespi D; Gastroenterology Department, St Mark's Hospital, London, UK.
  • Furman MA; Inflammatory Bowel Disease Unit, Institute of Gastroenterology and Liver Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Mann S; Centre for Paediatric Gastroenterology, Royal Free Hospital, London, UK.
  • Murray CD; Centre for Paediatric Gastroenterology, Royal Free Hospital, London, UK.
  • Segal AW; Gastroenterology Department, Barnet General Hospital, London, UK.
  • Levine AP; Centre for Gastroenterology, Royal Free Hospital, London, UK.
Hum Genet ; 137(9): 723-734, 2018 Sep.
Article em En | MEDLINE | ID: mdl-30167848
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Doenças Inflamatórias Intestinais / Judeus / Fases de Leitura Aberta / Predisposição Genética para Doença / Proteína Adaptadora de Sinalização NOD2 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Hum Genet Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Doenças Inflamatórias Intestinais / Judeus / Fases de Leitura Aberta / Predisposição Genética para Doença / Proteína Adaptadora de Sinalização NOD2 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Hum Genet Ano de publicação: 2018 Tipo de documento: Article