Andrea Schams

German Center for Lung Research — Germany

Medicine · Health Sciences

15h-index1.6kcitations28works0.02yr avg
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Research Topics

Neonatal Respiratory Health Research(19), Congenital Diaphragmatic Hernia Studies(7), Medical Imaging and Pathology Studies(5), RNA Interference and Gene Delivery(4), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis(4)

Publications28 total

Pulmonary Alveolar Proteinosis: a 3-country cohort study Greece, Türkiye, Cyprus
2025
Kinderlungenregister (chILD-EU) – Zusammenarbeit führt zu Fortschritten bei den seltenen und interstitiellen Lungenerkrankungen
Klinische Pädiatrie·2023
Autoimmune Pulmonary Alveolar Proteinosis (aPAP) in Greece: 20 years in progress
2023· 1 cited
COVID-19 in patients with Pulmonary Alveolar Proteinosis A European multicenter study
2022· 1 cited
COVID-19 in patients with pulmonary alveolar proteinosis: a European multicentre study
ERJ Open Research·2022· 11 citedOpen Access
Pulmonary interstitial Glycogenosis – a systematic analysis of new cases
2018· 1 cited
Lung disease caused by non-null ABCA3 mutations: long-term follow-up
2018
Pulmonary interstitial glycogenosis – A systematic analysis of new cases
Respiratory Medicine·2018· 35 citedOpen Access
International management platform for children’s interstitial lung disease (chILD-EU)
Thorax·2017· 95 citedOpen Access
<i>In vivo</i>genome editing using nuclease-encoding mRNA corrects SP-B deficiency
2016· 1 cited
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3
Molecular Medicine·2016· 26 citedOpen Access
Cardiovascular risk in pulmonary alveolar proteinosis
Expert Review of Respiratory Medicine·2015· 3 cited
Persistent Tachypnea of Infancy. Usual and Aberrant
American Journal of Respiratory and Critical Care Medicine·2015· 68 citedOpen Access
Categorizing diffuse parenchymal lung disease in children
Orphanet Journal of Rare Diseases·2015· 52 citedOpen Access
Surfactant proteins in pediatric interstitial lung disease
Pediatric Research·2015· 33 citedOpen Access
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
BMC Pulmonary Medicine·2015· 73 citedOpen Access
In vivo genome editing using nuclease-encoding mRNA corrects SP-B deficiency
Nature Biotechnology·2015· 137 cited
Genotype alone does not predict the clinical course of<i>SFTPC</i>deficiency in paediatric patients
European Respiratory Journal·2015· 90 citedOpen Access
Long-term follow-up and treatment of congenital alveolar proteinosis
BMC Pediatrics·2011· 35 citedOpen Access
Expression of therapeutic proteins after delivery of chemically modified mRNA in mice
Nature Biotechnology·2011· 730 cited
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Frequent Co-authors

Matthias Griese(26), Matthias Kappler(9), Frank Brasch(8), Nicolaus Schwerk(6), Dominik Hartl(5), Simone Reu(5), Julia Ley‐Zaporozhan(5), Traudl Wesselak(5), Peter Lohse(5), Daniela Rauch(5), Spyros A. Papiris(5), Maria Kallieri(5), Lykourgos Kolilekas(5), Andriana Ι. Papaioannou(5), Effrosyni D. Manali(5), Meike Hengst(4), Martin Wetzke(4), Ralf Zarbock(4), Jan Ripper(4), Michael Kormann(3)