Britt-Sabina Petersen (Britt-Sabina Löscher)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 10

Top Venues

Gut

Scientific reports

European journal of human genetics : EJHG

Science translational medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Andreea Zamfir-Taranu, Britt-Sabina Petersen, Diab M Husein, Abdullah Hoter, Koldo Garcia, Usune Etxeberria, Lucía Gayoso, Gabriele Mayr, Clara Nilholm, Rita J Gustafsson, Oliver Ozaydin, Tenghao Zheng, Cristina Esteban-Blanco, Isotta Bozzarelli, Ferdinando Bonfiglio, Sandra Rizk, Andre Franke, Luis Bujanda, Hassan Y Naim, Bodil Ohlsson, Mauro D'Amato
Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patients. Gut (2023)
Xiaojun Jiang, Annika Bergquist, Britt-Sabina Petersen, Geetha Venkatesh, Jeff E Mold, Kristian Holm, Jon Kristen Laerdahl, Sigrid S Skånland, Kimia T Maleki, Martin Cornillet Jeannin, Kjetil Taskén, Andre Franke, Tom H Karlsen, Niklas K Björkström, Espen Melum
A heterozygous germline CD100 mutation in a family with primary sclerosing cholangitis. Science translational medicine 13 (582) (2021)
Anna Foley, Emma Phoebe Halmos, Diab M Husein, Sasha Rachel Fehily, Britt-Sabina Petersen, Andre Franke, Hassan Y Naim, Peter R Gibson, Mauro D'Amato
Adult sucrase-isomaltase deficiency masquerading as IBS. Gut (2021)
Lea Južnić, Kenneth Peuker, Anne Strigli, Mario Brosch, Alexander Herrmann, Robert Häsler, Michael Koch, Liz Matthiesen, Yvonne Zeissig, Britt-Sabina Petersen, Alexander Nuber, Gunnar Schotta, Volker Neumeister, Triantafyllos Chavakis, Thomas Kurth, Mathias Lesche, Andreas Dahl, Anne von Mässenhausen, Andreas Linkermann, Stefan Schreiber, Konrad Aden, Philip C Rosenstiel, Andre Franke, Jochen Hampe, Sebastian Zeissig
SETDB1 is required for intestinal epithelial differentiation and the prevention of intestinal inflammation. Gut 70 (3) (2020)
Jörn F Ziegler, Chotima Böttcher, Marilena Letizia, Cansu Yerinde, Hao Wu, Inka Freise, Yasmina Rodriguez-Sillke, Ani K Stoyanova, Martin E Kreis, Patrick Asbach, Désirée Kunkel, Josef Priller, Ioannis Anagnostopoulos, Anja A Kühl, Konstanze Miehle, Michael Stumvoll, Florian Tran, Broder Fredrich, Michael Forster, Andre Franke, Christian Bojarski, Rainer Glauben, Britt-Sabina Petersen, Britta Siegmund, Carl Weidinger
Leptin induces TNFα-dependent inflammation in acquired generalized lipodystrophy and combined Crohn's disease. Nature communications 10 (1) (2019)
Simone Lipinski, Britt-Sabina Petersen, Matthias Barann, Agnes Piecyk, Florian Tran, Gabriele Mayr, Marlene Jentzsch, Konrad Aden, Stephanie T Stengel, Ulrich C Klostermeier, Vrunda Sheth, David Ellinghaus, Tobias Rausch, Jan O Korbel, Michael Nothnagel, Michael Krawczak, Christian Gilissen, Joris A Veltman, Michael J Forster, Peter Forster, Clarence C Lee, Annette Fritscher-Ravens, Stefan Schreiber, Andre Franke, Philip C Rosenstiel
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2. Cold Spring Harbor molecular case studies 5 (1) (2019)
Britt-Sabina Petersen, Bernd Bokemeyer, Christian Wenker, Stefan Hoby, Katrin Baumgartner, Hermann Will, Marc P Hoeppner, Stefan Schreiber, Ingo Mecklenburg, Andre Franke
First known case of paediatric inflammatory bowel disease in a western lowland gorilla may be linked to a familial mutation in the MEFV gene. Gut 69 (6) (2019)
Urszula Lechowicz, Tomasz Gambin, Agnieszka Pollak, Anna Podgorska, Piotr Stawinski, Andre Franke, Britt-Sabina Petersen, Malgorzata Firczuk, Monika Oldak, Henryk Skarzynski, Rafal Ploski
Iterative Sequencing and Variant Screening (ISVS) as a novel pathogenic mutations search strategy - application for TMPRSS3 mutations screen. Scientific reports 7 (1) (2017)
Yvonne Zeissig, Britt-Sabina Petersen, Andre Franke, Richard S Blumberg, Sebastian Zeissig
Rare phenotypes in the understanding of autoimmunity. Immunology and cell biology 94 (10) (2016)
Matthias Baumann, Elisabeth Steichen-Gersdorf, Birgit Krabichler, Britt-Sabina Petersen, Ulrike Weber, Wolfgang M Schmidt, Johannes Zschocke, Thomas Müller, Reginald E Bittner, Andreas R Janecke
Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype-phenotype correlation. European journal of human genetics : EJHG 25 (2) (2016)

Britt-Sabina Petersen.css-eqlu8i{font-size:small;padding-left:4px;} (Britt-Sabina Löscher)

Publication Activity (10 Years)

Top Topics

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Britt-Sabina Petersen (Britt-Sabina Löscher)