Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Multi-dimensional clinical phenotyping of a national cohort of adult cystic fibrosis patients.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society - 1 Jan 2021

Conrad Douglas J, Billings Joanne, Teneback Charlotte, Koff Jonathan, Rosenbluth Daniel, Bailey Barbara A, Jain Raksha

Abstract excerpt

BACKGROUND: Cystic Fibrosis (CF) is a multi-systemic disorder resulting from genetic variation in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene which can result in bronchiectasis, chronic sinusitis, pancreatic malabsorption, cholestatic liver disease and distal intestinal obstructive syndrome. This study generates multi-dimensional clinical phenotypes that capture the complexity and spectrum...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cohort Studies
Share to Cystic Fibrosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to United States

Source

Identifiers

PMID: 32948498
DOI: 10.1016/j.jcf.2020.08.010

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multi-dimensional clinical phenotyping of a national cohort of adult cystic fibrosis patients.PMID 32948498Read ↗

Multidimensional clinical phenotyping of an adult cystic fibrosis patient population.Semantic proximity Read ↗

Symptom phenotyping in people with cystic fibrosis during acute pulmonary exacerbations using machine-learning K-means clustering analysis.Semantic proximity Read ↗

The Changing Epidemiology of Cystic Fibrosis: The Implications for Adult Care.Semantic proximity Read ↗

The demographics of adverse outcomes in cystic fibrosis.Semantic proximity Read ↗

CFTR genotype-phenotype associations and clinical outcomes in pediatric cystic fibrosis.Semantic proximity Read ↗

Epidemiological characteristics, disease spectrum and clinical pattern of the Egyptian children with cystic fibrosis; A single center registry.Semantic proximity Read ↗

Predictive factors of survival in people with cystic fibrosis from a Spanish rare disease registry.Semantic proximity Read ↗

Disease severity of people with cystic fibrosis carrying residual function mutations: Data from the ECFS Patient Registry.Semantic proximity Read ↗

Non-pulmonary chronic diseases in adults with cystic fibrosis: analysis of data from the Cystic Fibrosis Registry.Semantic proximity Read ↗

Refining the continuum of CFTR-associated disorders in the era of newborn screening.Semantic proximity Read ↗

Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole-Genome Analysis of 7,840 PatientsSemantic proximity Read ↗

Microbiomes without boundaries: cystic fibrosis ‘pulmotype’ classifications are dependent on algorithm choice and database size, and indicate continuous variationSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.