Christina K Rapp

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 8

Top Topics

Interstitial Lung Disease

Combination Therapy

Cell Cycle Arrest

Top Venues

International journal of molecular sciences

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaohua Yang, Maria Forstner, Christina K Rapp, Ina Rothenaigner, Yang Li, Kamyar Hadian, Matthias Griese
ABCA3 Deficiency-Variant-Specific Response to Hydroxychloroquine. International journal of molecular sciences 24 (9) (2023)
Xiaohua Yang, Christina K Rapp, Yang Li, Maria Forstner, Matthias Griese
Quantifying Functional Impairment of ABCA3 Variants Associated with Interstitial Lung Disease. International journal of molecular sciences 24 (8) (2023)
Xiaohua Yang, Christina K Rapp, Yang Li, Maria Forstner, Matthias Griese
Quantifying Functional Impairment of ABCA3 Variants Associated with Interstitial Lung Disease. International journal of molecular sciences 24 (8) (2023)
Xiaohua Yang, Christina K Rapp, Yang Li, Maria Forstner, Matthias Griese
Quantifying Functional Impairment of ABCA3 Variants Associated with Interstitial Lung Disease. International journal of molecular sciences 24 (8) (2023)
Xiaohua Yang, Christina K Rapp, Yang Li, Maria Forstner, Matthias Griese
Quantifying Functional Impairment of ABCA3 Variants Associated with Interstitial Lung Disease. International journal of molecular sciences 24 (8) (2023)
Xiaohua Yang, Maria Forstner, Christina K Rapp, Ina Rothenaigner, Yang Li, Kamyar Hadian, Matthias Griese
ABCA3 Deficiency-Variant-Specific Response to Hydroxychloroquine. International journal of molecular sciences 24 (9) (2023)
Christina K Rapp, Ine Van Dijck, Lucia Laugwitz, Mieke Boon, George Briassoulis, Stavroula Ilia, Birgit Kammer, Simone Reu, Stefanie Hornung, Rebecca Buchert, Linda Sofan, Tawfiq Froukh, Peter Witters, Daisy Rymen, Tobias B Haack, Marijke Proesmans, Matthias Griese
Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy. Clinical genetics 100 (4) (2021)
Luise A Schuch, Maria Forstner, Christina K Rapp, Yang Li, Desiree E C Smith, Marisa I Mendes, Florent Delhommel, Michael Sattler, Nagehan Emiralioğlu, Ekim Zihni Taşkiran, Diclehan Orhan, Emine Nural Kiper, Meino Rohlfs, Tim Jeske, Maximilian Hastreiter, Michael Gerstlauer, Alba Torrent Vernetta, Antonio Moreno-Galdó, Birgit Kammer, Frank Brasch, Simone Reu-Hofer, Matthias Griese
FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs! Clinical genetics 99 (6) (2021)