Madeline Carrellas
Brigham and Women's Hospital
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Publication
Featured researches published by Madeline Carrellas.
Alimentary Pharmacology & Therapeutics | 2017
Rachel W. Winter; Emily Collins; Bonnie Cao; Madeline Carrellas; Crowell Am; Joshua R. Korzenik
Vitamin D has been linked to disease activity among patients with inflammatory bowel diseases (IBD). Prior investigation has also suggested that vitamin D levels may affect duration of therapy with anti‐tumour necrosis factor‐α (anti‐TNF‐α) medications among patients with IBD.
Inflammatory Bowel Diseases | 2018
Jodie Ouahed; William Gordon; James Canavan; Huanyu Zhou; Sarah Du; David von Schack; Kathleen Phillips; Lu Wang; W. Augustine Dunn; Michael Field; Shelby Friel; Alexandra Griffith; Spencer Evans; Sophia Tollefson; Madeline Carrellas; Bonnie Cao; Ami Merker; Athos Bousvaros; Dror S. Shouval; Kenneth E. Hung; Christopher Lepsy; Lovisa Afzelius; Joshua R. Korzenik; Scott B. Snapper; Bwh Crohn’s
Background Transcriptional profiling has been performed on biopsies from ulcerative colitis patients. Limitations in prior studies include the variability introduced by inflammation, anatomic site of biopsy, extent of disease, and medications. We sought to more globally understand the variability of gene expression from patients with ulcerative colitis to advance our understanding of its pathogenesis and to guide clinical study design. Methods We performed transcriptional profiling on 13 subjects, including pediatric and adult patients from 2 hospital sites. For each patient, we collected 6 biopsies from macroscopically inflamed tissue and 4 biopsies from macroscopically healthy-appearing tissue. Isolated RNA was used for microarray gene expression analysis utilizing Affymetrix Human Primeview microarrays. Ingenuity pathway analysis was used to assess over-representation of gene ontology and biological pathways. RNAseq was also performed, and differential analysis was assessed to compare affected vs unaffected samples. Finally, we modeled the minimum number of biopsies required to reliably detect gene expression across different subject numbers. Results Transcriptional profiles co-clustered independently of the hospital collection site, patient age, sex, and colonic location, which parallels prior gene expression findings. A small set of genes not previously described was identified. Our modeling analysis reveals the number of biopsies and patients per cohort to yield reliable results in clinical studies. Conclusions Key findings include concordance, including some expansion, of previously published gene expression studies and similarity among different age groups. We also established a reliable statistical model for biopsy collection for future clinical studies.
Digestive Diseases and Sciences | 2016
Edward L. Barnes; Alison Goldin; Rachel W. Winter; Emily Collins; Bonnie Cao; Madeline Carrellas; Crowell Am; Korzenik
Gastroenterology | 2015
Matthew Lucci; Emily Collins; Bonnie Cao; Madeline Carrellas; Anne Marie Crowell; Justine States; Michael Currier; Beth-Ann Norton; Joshua R. Korzenik
Gastroenterology | 2018
Jessica R. Allegretti; Zain Kassam; Madeline Carrellas; Mark Smith; Ylaine Geradin; Sonia Timberlake; Daniel S. Pratt; Joshua R. Korzenik
Gastroenterology | 2017
Rachel W. Winter; Madeline Carrellas; Ami Merker; Joshua R. Korzenik
Gastroenterology | 2016
Rachel W. Winter; Madeline Carrellas; Emily Collins; Ami Merker; Joshua R. Korzenik
Gastroenterology | 2016
Jessica R. Allegretti; Madeline Carrellas; Matthew J. Hamilton; Sonia Friedman; Joshua R. Korzenik
Gastroenterology | 2016
Ronak V. Patel; Edward L. Barnes; Emily Collins; Bonnie Cao; Madeline Carrellas; Anne Marie Crowell; Justine States; Shelley Hurwitz; Joshua R. Korzenik
Gastroenterology | 2015
Punyanganie S. de Silva; Aoibhlinn M. O'Toole; Madeline Carrellas; Emily Collins; Joshua R. Korzenik; Deanna Nguyen; Ashwin N. Ananthakrishnan; Sonia Friedman