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Karoline Fiedler

University of Toronto

17

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117

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Novel CARMIL2 loss-of-function variants are associated with pediatric inflammatory bowel disease.

2021 Scientific Reports
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Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease.

2021 Scientific Reports
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Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated with Monogenic Variants, Identified by Whole-exome Sequencing in 1000 Children at a Single Center

2020 Gastroenterology
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Natural History of Very Early Onset Inflammatory Bowel Disease in North America: A Retrospective Cohort Study.

2020 Inflammatory Bowel Diseases
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204 – Surgery in Very Early Onset Inflammatory Bowel Disease (Veoibd): Results from a Large, Multi-Center North American Cohort

2019 Gastroenterology
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Application of Whole Exome Sequencing in Congenital Secretory Diarrhea Diagnosis

2019 Journal of Pediatric Gastroenterology and Nutrition
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Su1795 – Utilization of Anti-TNF Therapy (BIOLOGICS) in Children with Very Early Onset Inflammatory Bowel Disease (Veoibd) in a Large North American Cohort

2019 Gastroenterology
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A13 WHOLE EXOME SEQUENCING OF OVER 1000 PEDIATRIC IBD PATIENTS FROM A SINGLE CENTRE IDENTIFIES MONOGENIC FORMS OF IBD.

2018
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587 - Whole Exome Sequencing of over 1000 Pediatric IBD Patients from a Single Centre on an Expanded Gene Panel Identifies Monogenic Forms of IBD

2018 Gastroenterology
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Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn′s Disease

2017 bioRxiv
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Citations (5)