Stephanie Hirtz

1.4k total citations
23 papers, 985 citations indexed

About

Stephanie Hirtz is a scholar working on Pulmonary and Respiratory Medicine, Physiology and Emergency Medical Services. According to data from OpenAlex, Stephanie Hirtz has authored 23 papers receiving a total of 985 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Pulmonary and Respiratory Medicine, 6 papers in Physiology and 5 papers in Emergency Medical Services. Recurrent topics in Stephanie Hirtz's work include Cystic Fibrosis Research Advances (15 papers), Neonatal Respiratory Health Research (15 papers) and Asthma and respiratory diseases (6 papers). Stephanie Hirtz is often cited by papers focused on Cystic Fibrosis Research Advances (15 papers), Neonatal Respiratory Health Research (15 papers) and Asthma and respiratory diseases (6 papers). Stephanie Hirtz collaborates with scholars based in Germany, United States and Australia. Stephanie Hirtz's co-authors include Marcus Mall, Jolanthe Schatterny, Julia Duerr, Karl Kunzelmann, Carsten Schultz, Tanja Gonska, Richard C. Boucher, Simon Y. Graeber, H. H. Seydewitz and Zhe Zhou-Suckow and has published in prestigious journals such as Gastroenterology, PLoS ONE and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Stephanie Hirtz

22 papers receiving 972 citations

Peers

Countries citing papers authored by Stephanie Hirtz

Since Specialization

Citations

This map shows the geographic impact of Stephanie Hirtz's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stephanie Hirtz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephanie Hirtz more than expected).

Fields of papers citing papers by Stephanie Hirtz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephanie Hirtz. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stephanie Hirtz. The network helps show where Stephanie Hirtz may publish in the future.

Co-authorship network of co-authors of Stephanie Hirtz

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Hirtz. A scholar is included among the top collaborators of Stephanie Hirtz based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephanie Hirtz. Stephanie Hirtz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Intestinal current measurement detects age-dependent differences in CFTR function in rectal epithelium 2025 ·Frontiers in Pharmacology ·Simon Y. Graeber, Olaf Sommerburg, (unknown), (unknown), Stephanie Hirtz, (unknown), (unknown), Julia Duerr, Marcus Mall	0
2	Effects of lumacaftor—ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function in F508del homozygous patients with cystic fibrosis aged 2–11 years 2023 ·Frontiers in Pharmacology ·(unknown), Simon Y. Graeber, Susanne Hämmerling, (unknown), (unknown), Mirjam Stahl, Stephanie Hirtz, (unknown), Marcus Mall, Olaf Sommerburg	1
3	Lack of IL-1 Receptor Signaling Reduces Spontaneous Airway Eosinophilia in Juvenile Mice with Muco-Obstructive Lung Disease 2019 ·American Journal of Respiratory Cell and Molecular Biology ·Ryan Brown, Michelle T. Paulsen, (unknown), Jolanthe Schatterny, Angela Frank, Stephanie Hirtz, (unknown), Declan Doherty, Matthias Hagner, Clifford C. Taggart, Sinéad Weldon, Marcus Mall	5
4	Effects of Lumacaftor–Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic Fibrosis 2018 ·American Journal of Respiratory and Critical Care Medicine ·Simon Y. Graeber, Christian Dopfer, Lutz Naehrlich, (unknown), (unknown), Stephanie Hirtz, Sabine Wege, Heimo Mairbäurl, Marie Dorda, Rebecca Hyde, (unknown), (unknown), Sebastian Fischer, Marcus Mall, Burkhard Tümmler	83
5	Effects of Lumacaftor-Ivacaftor Therapy on CFTR Function in Phe508del Homozygous Patients with Cystic Fibrosis 2018 ·(unknown), Christian Dopfer, Lutz Naehrlich, (unknown), (unknown), Stephanie Hirtz, Sabine Wege, (unknown), Marie Dorda, Rebecca Hyde, (unknown), (unknown), Sebastian Fischer, Marcus Mall, (unknown)	8
6	Impaired mucus clearance exacerbates allergen-induced type 2 airway inflammation in juvenile mice 2016 ·Journal of Allergy and Clinical Immunology ·Benedikt Fritzsching, Matthias Hagner, Lu Dai, (unknown), Raman Agrawal, (unknown), (unknown), Jolanthe Schatterny, Stephanie Hirtz, Ryan Brown, Michelle Goritzka, Julia Duerr, Zhe Zhou-Suckow, Marcus Mall	18
7	Hypoxic Epithelial Necrosis Triggers Neutrophilic Inflammation via IL-1 Receptor Signaling in Cystic Fibrosis Lung Disease 2015 ·American Journal of Respiratory and Critical Care Medicine ·Benedikt Fritzsching, Zhe Zhou-Suckow, Joanna Trojanek, Susanne Schubert, Jolanthe Schatterny, Stephanie Hirtz, Raman Agrawal, Thomas Muley, Nicolas Kahn, Carsten Sticht, Nikolas Gunkel, Tobias Welte, Scott H. Randell, Florian Länger, Philipp A. Schnabel, Felix Herth, Marcus Mall	81
8	Airway Mucus Obstruction Triggers Macrophage Activation and Matrix Metalloproteinase 12–Dependent Emphysema 2014 ·American Journal of Respiratory Cell and Molecular Biology ·Joanna Trojanek, Amanda Cobos‐Correa, (unknown), Michael Kormann, Susanne Schubert, Zhe Zhou-Suckow, Raman Agrawal, Julia Duerr, (unknown), Jolanthe Schatterny, Stephanie Hirtz, Olaf Sommerburg, Dominik Hartl, Carsten Schultz, Marcus Mall	80
9	Lack of Neutrophil Elastase Reduces Inflammation, Mucus Hypersecretion, and Emphysema, but Not Mucus Obstruction, in Mice with Cystic Fibrosis–like Lung Disease 2014 ·American Journal of Respiratory and Critical Care Medicine ·Stefanie Gehrig, Julia Duerr, Michael Weitnauer, (unknown), Simon Y. Graeber, Jolanthe Schatterny, Stephanie Hirtz, Abderrazzaq Belaaouaj, Alexander H. Dalpke, Carsten Schultz, Marcus Mall	121
10	Hypertonic Saline Is Effective in the Prevention and Treatment of Mucus Obstruction, but Not Airway Inflammation, in Mice with Chronic Obstructive Lung Disease 2013 ·American Journal of Respiratory Cell and Molecular Biology ·Simon Y. Graeber, Zhe Zhou-Suckow, Jolanthe Schatterny, Stephanie Hirtz, Richard C. Boucher, Marcus Mall	39
11	CFTR Regulates Early Pathogenesis of Chronic Obstructive Lung Disease in βENaC-Overexpressing Mice 2012 ·PLoS ONE ·Bjarki Jóhannesson, Stephanie Hirtz, Jolanthe Schatterny, Carsten Schultz, Marcus Mall	46
12	In vivomonitoring of cystic fibrosis-like lung disease in mice by volumetric computed tomography 2011 ·European Respiratory Journal ·Mark O. Wielpütz, Monika Eichinger, Zhe Zhou, Karin Leotta, Stephanie Hirtz, Sönke Bartling, Willi Semmler, (unknown), Michael Puderbach, Marcus Mall	41
13	The K+ Channel Opener 1-EBIO Potentiates Residual Function of Mutant CFTR in Rectal Biopsies from Cystic Fibrosis Patients 2011 ·PLoS ONE ·(unknown), Stephanie Hirtz, Julia Duerr, Daniel Wenning, Irmgard Eichler, H. H. Seydewitz, Margarida D. Amaral, Marcus Mall	34
14	Allergic airway inflammation induces a pro-secretory epithelial ion transport phenotype in mice 2010 ·European Respiratory Journal ·Pinelopi Anagnostopoulou, Lu Dai, Jolanthe Schatterny, Stephanie Hirtz, Julia Duerr, Marcus Mall	50
15	Airways surface liquid depletion causes MMP-12 dependent emphysema in βENaC-overexpressing mice 2009 ·Journal of Cystic Fibrosis ·Susanne Schubert‐Bast, Joanna Trojanek, (unknown), (unknown), Zhe Zhou, Diana Treis, Long‐Jun Dai, Jolanthe Schatterny, Stephanie Hirtz, (unknown), Marcus Mall	4
16	Preventive but Not Late Amiloride Therapy Reduces Morbidity and Mortality of Lung Disease in βENaC-overexpressing Mice 2008 ·American Journal of Respiratory and Critical Care Medicine ·Zhe Zhou, Diana Treis, Susanne Schubert‐Bast, (unknown), Jolanthe Schatterny, Stephanie Hirtz, Julia Duerr, Richard C. Boucher, Marcus Mall	90
17	CFTR Cl− channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis 2004 ·Gastroenterology ·Stephanie Hirtz, Tanja Gonska, H. H. Seydewitz, Jörg Thomas, (unknown), Joachim Kuehr, M. Brandis, Irmgard Eichler, (unknown), (unknown), Celeste Barreto, Anabela S. Ramalho, Margarida D. Amaral, Karl Kunzelmann, Marcus Mall	105
18	Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis 2004 ·Journal of Cystic Fibrosis ·Marcus Mall, Stephanie Hirtz, Tanja Gonska, Karl Kunzelmann	36
19	The ΔF508 mutation results in loss of CFTR function and mature protein in native human colon 2003 ·Gastroenterology ·Marcus Mall, Silvia M. Kreda, April Mengos, Timothy J. Jensen, Stephanie Hirtz, H. H. Seydewitz, James R. Yankaskas, Karl Kunzelmann, John R. Riordan, Richard C. Boucher	84
20	Activation of ion secretion via proteinase-activated receptor-2 in human colon 2002 ·American Journal of Physiology-Gastrointestinal and Liver Physiology ·Marcus Mall, Tanja Gonska, Jörg Thomas, Stephanie Hirtz, Rainer Schreiber, Karl Kunzelmann	56

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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