8 Einträge gefunden

1. New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics

   1. Begemann, Anaïs
   2. Sticht, Heinrich
   3. Begtrup, Amber
   4. Vitobello, Antonio
   5. Faivre, Laurence
   6. Banka, Siddharth
   7. Alhaddad, Bader

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Shared genetic etiology of obesity-related traits and Barrett's esophagus/adenocarcinoma:Insights from genome-wide association studies

   1. Böhmer, Anne Christin
   2. Hecker, Julian
   3. Schröder, Julia
   4. Gharahkhani, Puya
   5. May, Andrea
   6. Gerges, Christian
   7. Anders, Mario

   2020 - Forschungsinformationssystem des UKE
3. Nine newly identified individuals refine the phenotype associated with MYT1L mutations

   1. Windheuser, Isabelle C
   2. Becker, Jessica
   3. Cremer, Kirsten
   4. Hundertmark, Hela
   5. Yates, Laura M
   6. Mangold, Elisabeth
   7. Peters, Sophia

   2020 - Forschungsinformationssystem des UKE
4. Identification of loci of functional relevance to Barrett's esophagus and esophageal adenocarcinoma: Cross-referencing of expression quantitative trait loci data from disease-relevant tissues with genetic association data

   1. Schröder, Julia
   2. Schüller, Vitalia
   3. May, Andrea
   4. Gerges, Christian
   5. Anders, Mario
   6. Becker, Jessica
   7. Hess, Timo

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
5. The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma risk

   1. Becker, Jessica
   2. May, Andrea
   3. Gerges, Christian
   4. Anders, Mario
   5. Schmidt, Claudia
   6. Veits, Lothar
   7. Noder, Tania

   2016 - Forschungsinformationssystem des UKE - frei zugänglich
6. Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis

   1. Gharahkhani, Puya
   2. Fitzgerald, Rebecca C
   3. Vaughan, Thomas L
   4. Palles, Claire
   5. Gockel, Ines
   6. Tomlinson, Ian
   7. Buas, Matthew F

   2016 - Forschungsinformationssystem des UKE
7. Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

   1. Becker, Jessica
   2. May, Andrea
   3. Gerges, Christian
   4. Anders, Mario
   5. Veits, Lothar
   6. Weise, Katharina
   7. Czamara, Darina

   2015 - Forschungsinformationssystem des UKE
8. De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment

   1. Hempel, Maja
   2. Cremer, Kirsten
   3. Ockeloen, Charlotte W
   4. Lichtenbelt, Klaske D
   5. Herkert, Johanna C
   6. Denecke, Jonas
   7. Haack, Tobias B

   2015 - Forschungsinformationssystem des UKE