Amelia Shoemark

Broad Immunomodulatory Effects of the Dipeptidyl Peptidase-1 Inhibitor Brensocatib in Bronchiectasis: Data from the Phase 2, Double-Blind, Placebo-controlled WILLOW Trial

Upper-Airway Microbiome, Mucociliary Function, and Clinical Outcomes in Bronchiectasis: Data from the EMBARC-BRIDGE Study

Analyses of 1236 genotyped primary ciliary dyskinesia individuals identify regional clusters of distinct DNA variants and significant genotype–phenotype correlations

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules

The Association between Bronchiectasis and Chronic Obstructive Pulmonary Disease: Data from the European Bronchiectasis Registry (EMBARC)

Bronchiectasis and asthma: Data from the European Bronchiectasis Registry (EMBARC)

Airway IL-1β is related to disease severity and mucociliary function in bronchiectasis

Endotypes of Exacerbation in Bronchiectasis: An Observational Cohort Study

Objective sputum colour assessment and clinical outcomes in bronchiectasis: data from the European Bronchiectasis Registry (EMBARC)

Primary Ciliary Dyskinesia in Adult Bronchiectasis

Clinical outcomes of bronchiectasis in India: data from the EMBARC/Respiratory Research Network of India registry

A Hybrid Architecture (CO-CONNECT) to Facilitate Rapid Discovery and Access to Data Across the United Kingdom in Response to the COVID-19 Pandemic: Development Study

International consensus guideline for reporting transmission electron microscopy results in the diagnosis of primary ciliary dyskinesia (BEAT PCD TEM Criteria)

Physiological and Pathophysiological Aspects of Primary Cilia—A Literature Review with View on Functional and Structural Relationships in Cartilage

Time trends in diagnostic testing for PCD in Europe - Research letter.

International consensus guideline for reporting transmission electron microscopy results in the diagnosis of Primary Ciliary Dyskinesia

Primary Cilia Mediate Diverse Kinase Inhibitor Resistance Mechanisms in Cancer

Risk factors for situs defects and congenital heart disease in primary ciliary dyskinesia

An extracellular matrix fragment drives epithelial remodeling and airway hyperresponsiveness

Why, when and how to investigate primary ciliary dyskinesia in adult patients with bronchiectasis

The European Multicentre Bronchiectasis Audit and Research Collaboration (EMBARC) ERS Clinical Research Collaboration

X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia

Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus

Mutations in ZMYND10, a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms in Humans and Flies, Cause Primary Ciliary Dyskinesia

Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa

Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry

Mutations in<i>CCDC</i><i>39</i>and<i>CCDC</i><i>40</i>are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms

Recessive HYDIN mutations cause primary ciliary dyskinesia without situs abnomalities