Anzahl der Publikationen: 21
2024
Lanz, Anna-Lisa; Erdem, Serife; Ozcan, Alper; Ceylaner, Gulay; Cansever, Murat; Ceylaner, Serdar; Conca, Raffaele; Magg, Thomas; Acuto, Oreste; Latour, Sylvain; Klein, Christoph; Patiroglu, Turkan; Unal, Ekrem; Eken, Ahmet und Hauck, Fabian
(2024):
A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature.
In: Journal of Clinical Immunology, Bd. 44, 1
[PDF, 1MB]
2022
Ghalandary, Maryam; Li, Yue; Frohlich, Thomas; Magg, Thomas; Liu, Yanshan; Rohlfs, Meino; Hollizeck, Sebastian; Conca, Raffaele; Schwerd, Tobias; Uhlig, Holm H.; Bufler, Philip; Koletzko, Sibylle; Muise, Aleixo M.; Snapper, Scott B.; Hauck, Fabian; Klein, Christoph und Kotlarz, Daniel
(2022):
Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses.
In: Scientific Reports, Bd. 12, Nr. 1, 3906
Kolorz, Julian; Demir, Salih; Gottschlich, Adrian; Beirith, Iris; Ilmer, Matthias; Luethy, Daniel; Walz, Christoph; Dorostkar, Mario M.; Magg, Thomas; Hauck, Fabian; Schweinitz, Dietrich von; Kobold, Sebastian; Kappler, Roland und Berger, Michael
(2022):
The Neurokinin-1 Receptor Is a Target in Pediatric Rhabdoid Tumors.
In: Current Oncology, Bd. 29, Nr. 1: S. 94-110
Levy, Romain; Gothe, Florian; Momenilandi, Mana; Magg, Thomas; Materna, Marie; Peters, Philipp; Rädler, Johannes; Philippot, Quentin; Rack-Hoch, Anita Lena; Langlais, David; Bourgey, Mathieu; Lanz, Anna-Lisa; Ogishi, Masato; Rosain, Jeremie; Martin, Emmanuel; Latour, Sylvain; Vladikine, Natasha; Distefano, Marco; Khan, Taushif; Rapaport, Franck; Schulz, Marian S.; Holzer, Ursula; Fasth, Anders; Sogkas, Georgios; Speckmann, Carsten; Troilo, Arianna; Bigley, Venetia; Roppelt, Anna; Dinur-Schejter, Yael; Toker, Ori; Martinsen, Karen Helene Bronken; Sherkat, Roya; Somekh, Ido; Somech, Raz; Shouval, Dror S.; Kühl, Joern-Sven; Ip, Winnie; McDermott, Elizabeth M.; Cliffe, Lucy; Ozen, Ahmet; Baris, Safa; Rangarajan, Hemalatha G.; Jouanguy, Emmanuelle; Puel, Anne; Bustamante, Jacinta; Alyanakian, Marie-Alexandra; Fusaro, Mathieu; Wang, Yi; Kong, Xiao-Fei; Cobat, Aurelie; Boutboul, David; Castelle, Martin; Aguilar, Claire; Hermine, Olivier; Cheminant, Morgane; Suarez, Felipe; Yildiran, Alisan; Bousfiha, Aziz; Al-Mousa, Hamoud; Alsohime, Fahad; Cagdas, Deniz; Abraham, Roshini S.; Knutsen, Alan P.; Fevang, Borre; Bhattad, Sagar; Kiykim, Ayca; Erman, Baran; Arikoglu, Tugba; Unal, Ekrem; Kumar, Ashish; Geier, Christoph B.; Baumann, Ulrich; Neven, Benedicte; Rohlfs, Meino; Walz, Christoph; Abel, Laurent; Malissen, Bernard; Marr, Nico; Klein, Christoph; Casanova, Jean-Laurent; Hauck, Fabian und Beziat, Vivien
(2022):
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.
In: Journal of Experimental Medicine, Bd. 220, Nr. 2, e20220275
2021
Magg, Thomas; Okano, Tsubasa; Koenig, Lars M.; Boehmer, Daniel F. R.; Schwartz, Samantha L.; Inoue, Kento; Heimall, Jennifer; Licciardi, Francesco; Ley-Zaporozhan, Julia; Ferdman, Ronald M.; Caballero-Oteyza, Andres; Park, Esther N.; Calderon, Brenda M.; Dey, Debayan; Kanegane, Hirokazu; Cho, Kazutoshi; Montin, Davide; Reiter, Karl; Griese, Matthias; Albert, Michael H.; Rohlfs, Meino; Gray, Paul; Walz, Christoph; Conn, Graeme L.; Sullivan, Kathleen E.; Klein, Christoph; Morio, Tomohiro und Hauck, Fabian
(2021):
Heterozygous OAS1 gain-of-function variants cause an autoinflammatory immunodeficiency.
In: Science Immunology, Bd. 6, Nr. 60, eabf9564
Raedler, Johannes; Magg, Thomas; Rohlfs, Meino; Klein, Christoph; Vallée, Tanja; Hauck, Fabian und Albert, Michael H.
(2021):
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency.
In: Journal of clinical immunology, Bd. 41, Nr. 7: S. 1536-1548
[PDF, 2MB]
2020
Bitar, Michael; Boettcher, Marcus; Boldt, Andreas; Hauck, Fabian; Koehl, Ulrike; Liebert, Uwe G.; Magg, Thomas; Schulz, Marian S. und Sack, Ulrich
(2020):
Flow cytometric measurement of STAT5 phosphorylation in cytomegalovirus-stimulated T cells.
In: Cytometry Part A, Bd. 99, Nr. 8: S. 774-783
Boehmer, Daniel F. R.; Koehler, Lisa M.; Magg, Thomas; Metzger, Philipp; Rohlfs, Meino; Ahlfeld, Julia; Rack-Hoch, Anita; Reiter, Karl; Albert, Michael H.; Endres, Stefan; Rothenfusser, Simon; Klein, Christoph; König, Lars M. und Hauck, Fabian
(2020):
A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis-Like Hyperinflammation.
In: Journal of Allergy and Clinical Immunology-in Practice, Bd. 8, Nr. 9: S. 3102-3111
Heller, Stephanie; Koelsch, Uwe; Magg, Thomas; Krueger, Renate; Scheuern, Andrea; Schneider, Holm; Eichinger, Anna; Wahn, Volker; Unterwalder, Nadine; Lorenz, Myriam; Schwarz, Klaus; Meisel, Christian; Schulz, Ansgar; Hauck, Fabian und Bernuth, Horst von
(2020):
T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency.
In: Journal of Clinical Immunology, Bd. 40, Nr. 3: S. 421-434
2019
Li, Yue; Fuehrer, Marita; Bahrami, Ehsan; Socha, Piotr; Klaudel-Dreszler, Maja; Bouzidi, Amira; Liu, Yanshan; Lehle, Anna S.; Magg, Thomas; Hollizeck, Sebastian; Rohlfs, Meino; Conca, Raffaele; Field, Michael; Warner, Neil; Mordechai, Slae; Shteyer, Eyal; Turner, Dan; Boukari, Rachida; Belbouab, Reda; Walz, Christoph; Gaidt, Moritz M.; Hornung, Veit; Baumann, Bernd; Pannicke, Ulrich; Al Idrissi, Eman; Alghamdi, Hamza Ali; Sepulveda, Fernando E.; Gil, Marine; Basile, Genevieve de Saint; Honig, Manfred; Koletzko, Sibylle; Muise, Aleixo M.; Snapper, Scott B.; Schwarz, Klaus; Klein, Christoph und Kotlarz, Daniel
(2019):
Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 116, Nr. 3: S. 970-975
Somekh, Ido; Thian, Marini; Medgyesi, David; Gulez, Nesrin; Magg, Thomas; Gallon Duque, Alejandro; Stauber, Tali; Lev, Atar; Genel, Ferah; Unal, Ekrem; Simon, Amos J.; Lee, Yu Nee; Kalinichenko, Artem; Dmytrus, Jasmin; Kraakman, Michael J.; Schiby, Ginette; Rohlfs, Meino; Jacobson, Jeffrey M.; Ozer, Erdener; Akcal, Omer; Conca, Raffaele; Patiroglu, Turkan; Karakukcu, Musa; Ozcan, Alper; Shahin, Tala; Appella, Eliana; Tatematsu, Megumi; Martinez-Jaramillo, Catalina; Chinn, Ivan K.; Orange, Jordan S.; Milena Trujillo-Vargas, Claudia; Luis Franco, Jose; Hauck, Fabian; Somech, Raz; Klein, Christoph und Boztug, Kaan
(2019):
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis.
In: Blood, Bd. 134, Nr. 18: S. 1510-1516
Magg, Thomas; Shcherbina, Anna; Arslan, Duran; Desai, Mukesh M.; Wall, Sarah; Mitsialis, Vanessa; Conca, Raffaele; Unal, Ekrem; Karacabey, Neslihan; Mukhina, Anna; Rodina, Yulia; Taur, Prasad D.; Illig, David; Marquardt, Benjamin; Hollizeck, Sebastian; Jeske, Tim; Gothe, Florian; Schober, Tilmann; Rohlfs, Meino; Koletzko, Sibylle; Lurz, Eberhard; Muise, Aleixo M.; Snapper, Scott B.; Hauck, Fabian; Klein, Christoph und Kotlarz, Daniel
(2019):
CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease.
In: Inflammatory Bowel Diseases, Bd. 25, Nr. 11: S. 1788-1795
2018
Magg, Thomas; Schober, Tilmann; Walz, Christoph; Ley-Zaporozhan, Julia; Facchetti, Fabio; Klein, Christoph und Hauck, Fabian
(2018):
Epstein–Barr Virus+ Smooth Muscle Tumors as Manifestation of Primary Immunodeficiency Disorders.
In: Frontiers in Immunology, Bd. 9, 368
[PDF, 567kB]
Frowein, Julia von; Hauck, Stefanie M.; Kappler, Roland; Pagel, Philipp; Fleischmann, Katrin K.; Magg, Thomas; Cairo, Stefano; Roscher, Adelbert; Schweinitz, Dietrich von und Schmid, Irene
(2018):
MiR‐492 regulates metastatic properties of hepatoblastoma via CD44.
In: Liver International, Bd. 38, Nr. 7: S. 1280-1291
Kotlarz, Daniel; Marquardt, Benjamin; Baroy, Tuva; Lee, Way S.; Konnikova, Liza; Hollizeck, Sebastian; Magg, Thomas; Lehle, Anna S.; Walz, Christoph; Borggraefe, Ingo; Hauck, Fabian; Bufler, Philip; Conca, Raffaele; Wall, Sarah M.; Schumacher, Eva M.; Misceo, Doriana; Frengen, Eirik; Bentsen, Beint S.; Uhlig, Holm H.; Hopfner, Karl-Peter; Muise, Aleixo M.; Snapper, Scott B.; Stromme, Petter und Klein, Christoph
(2018):
Human TGF-beta 1 deficiency causes severe inflammatory bowel disease and encephalopathy.
In: Nature Genetics, Bd. 50, Nr. 3: S. 344-348
Magg, Thomas; Wiebking, Volker; Conca, Raffaele; Krebs, Stefan; Arens, Stefan; Schmid, Irene; Klein, Christoph; Albert, Michael H. und Hauck, Fabian
(2018):
IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T-Reg cell engraftment.
In: Clinical Immunology, Bd. 191: S. 52-58
2017
Hauck, Fabian; Magg, Thomas; Krolo, Ana; Bilic, Ivan; Hirschmugl, Tatjana; Laass, Martin; Rösen-Wolff, Angela; Luksch, Hella; Boztug, Kaan und Rösler, Joachim
(2017):
Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma.
In: Klinische Pädiatrie, Bd. 229, Nr. 3: S. 113-117
2016
Hagl, Beate; Heinz, Valerie; Schlesinger, Anne; Spielberger, Benedikt D.; Sawalle-Belohradsky, Julie; Senn-Rauh, Monika; Magg, Thomas; Boos, Annette C.; Hönig, Manfred; Schwarz, Klaus; Dückers, Gregor; Bernuth, Horst von; Pache, Christoph; Karitnig-Weiss, Cäcilia; Belohradsky, Bernd H.; Frank, Josef; Niehues, Tim; Wahn, Volker; Albert, Michael H.; Wollenberg, Andreas; Jansson, Annette F. und Renner, Ellen D.
(2016):
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children.
In: Pediatric Allergy and Immunology, Bd. 27, Nr. 2: S. 177-184
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