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

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis.

Pediatric research - 1 Feb 2021

Zysman-Colman Zofia N, Kilberg Marissa J, Harrison Victor S, Chesi Alessandra, Grant Struan F A, Mitchell Jonathan, Sheikh Saba, Hadjiliadis Denis, Rickels Michael R, Rubenstein Ronald C, Kelly Andrea

Abstract excerpt

BACKGROUND: Despite improved health, shorter stature is common in cystic fibrosis (CF). We aimed to describe height velocity (HV) and contribution of height-related genetic variants to height (HT) in CF. METHODS: HV cohort: standard deviation scores (-Z) for HT, mid-parental height-adjusted HT (MPAH), and HV were generated using our Pediatric Center's CF Foundation registry data. HV-Z was compared with population...

Read the complete abstract on PubMed

Topics

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

Share to Body Height
Share to Cystic Fibrosis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cystic Fibrosis Transmembrane Conductance Regulator

Share to Electronic Health Records

Share to Exocrine Pancreatic Insufficiency

Share to Pediatrics

Share to Puberty

Share to Registries

Source

Open in PubMed Open full text

Identifiers

PMID: 32386398
DOI: 10.1038/s41390-020-0940-4
PMCID: PMC7649126

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis.PMID 32386398Read ↗

Adult height variants affect birth length and growth rate in children.Semantic proximity Read ↗

Height matters-from monogenic disorders to normal variation.Semantic proximity Read ↗

Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966.Semantic proximity Read ↗

A polygenic score for height identifies an unmeasured genetic predisposition among pediatric patients with idiopathic short stature.Semantic proximity Read ↗

Using height association studies to gain insights into human idiopathic short and syndromic stature phenotypes.Semantic proximity Read ↗

Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height.Semantic proximity Read ↗

Trans-ancestral genome-wide association study of longitudinal pubertal height growth and shared heritability with adult health outcomes.Semantic proximity Read ↗

Reaching new heights: insights into the genetics of human stature.Semantic proximity Read ↗

Recent progress in the study of the genetics of height.Semantic proximity Read ↗

Progress in genome-wide association studies of human height.Semantic proximity Read ↗

Novel signals and polygenic score for height are associated with pubertal growth traits in Southwestern American Indians.Semantic proximity Read ↗

Genetic short stature.Semantic proximity Read ↗

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