Publikationen von Rohlfs, Meino

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Anzahl der Publikationen: 35

Zeitschriftenartikel

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

Sadeghmousavi, Shaghayegh; Shahkarami, Sepideh; Rayzan, Elham; Ahmed, Souran; Gharalari, Farzaneh Hosseini; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima (2022): A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report. In: Endocrine Metabolic & Immune Disorders - Drug Targets, Bd. 22, Nr. 8: S. 881-887

Chongsrisawat, Voranush; Suratannon, Narissara; Chatchatee, Pantipa; Ittiwut, Rungnapa; Ittiwut, Chupong; Weerapakorn, Wanlapa; Theamboonlers, Apiradee; Rohlfs, Meino; Klein, Christoph; Kotlarz, Daniel und Suphapeetiporn, Kanya (2022): Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings. In: Inflammatory Bowel Diseases, Bd. 28, Nr. 9: S. 1458-1461

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

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

Boehmer, Daniel F. R.; Formisano, Simone; Mann, Carina C. de Oliveira; Mueller, Stephan A.; Kluge, Michael; Metzger, Philipp; Rohlfs, Meino; Hoerth, Christine; Kocheise, Lorenz; Lichtenthaler, Stefan F.; Hopfner, Karl-Peter; Endres, Stefan; Rothenfusser, Simon; Friedel, Caroline C.; Duewell, Peter; Schnurr, Max und Koenig, Lars M. (2021): OAS1/RNase L executes RIG-I ligand-dependent tumor cell apoptosis. In: Science Immunology, Bd. 6, Nr. 61, eabe2550

Duztas, Demet Teker; Al-Shadfan, Lina; Ozturk, Hakan; Yazan, Hakan; Cakir, Erkan; Unver, Nurcan; Ekinci, Ozgur; Dalgic, Buket; Rohlfs, Meino; Jeske, Tim; Klein, Christoph; Kotlarz, Daniel und Gurkan, Odul Egritas (2021): New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX);Granulomas in Lung and Duodenum. In: Pediatric and Developmental Pathology, Bd. 24, Nr. 3, 1093526621998868: S. 252-257

Kisaarslan, Aysenur Pac; Witzel, Maximilam; Unal, Ekrem; Rohlfs, Meino; Akyildiz, Basaknur; Dogan, Muhammet E.; Poyrazoglu, Hakan; Klein, Christoph und Patiroglu, Turkan (2021): Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant. In: Journal of Pediatric Hematology Oncology, Bd. 43, Nr. 3, E452-E456

Lanz, Anna-Lisa; Riester, Martin; Peters, Philipp; Schwerd, Tobias; Lurz, Eberhard; Hajji, Mohammad Samer; Rohlfs, Meino; Ley-Zaporozhan, Julia; Walz, Christoph; Kotlarz, Daniel; Klein, Christoph; Albert, Michael H. und Hauck, Fabian (2021): Abatacept for treatment-refractory pediatric CTLA4-haploinsufficiency. In: Clinical Immunology, Bd. 229, 108779

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

Maroufi, Seyed F.; Shaka, Zoha; Mojtabavi, Helia; Sadeghalvad, Mona; Rayzan, Elham; Sedighi, Iraj; Shahkarami, Sepideh; Najafi, Mehri; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima (2021): Novel G6PC3 Mutations in Patients with Congenital Neutropenia: Case Reports and Review of the Literature. In: Endocrine Metabolic & Immune Disorders-Drug Targets, Bd. 21, Nr. 9: S. 1660-1668

Schuch, Luise A.; Forstner, Maria; Rapp, Christina K.; Li, Yang; Smith, Desiree E. C.; Mendes, Marisa I.; Delhommel, Florent; Sattler, Michael; Emiralioglu, Nagehan; Taskiran, Ekim Z.; Orhan, Diclehan; Kiper, Nural; Rohlfs, Meino; Jeske, Tim; Hastreiter, Maximilian; Gerstlauer, Michael; Torrent-Vernetta, Alba; Moreno-Galdo, Antonio; Kammer, Birgit; Brasch, Frank; Reu-Hofer, Simone und Griese, Matthias (2021): FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs! In: Clinical Genetics, Bd. 99, Nr. 6: S. 789-801

Strigli, Anne; Gopalakrishnan, Shreya; Zeissig, Yvonne; Basic, Marijana; Wang, Jun; Schwerd, Tobias; Doms, Shauni; Peuker, Kenneth; Hartwig, Jelka; Harder, Jürgen; Hoenscheid, Pia; Arnold, Philipp; Kurth, Thomas; Rost, Fabian; Petersen, Britt-Sabina; Forster, Michael; Franke, Andre; Kelsen, Judith R.; Rohlfs, Meino; Klein, Christoph; Muise, Aleixo M.; Warner, Neil; Nambu, Ryusuke; Mayerle, Julia; Toeroek, Helga-Paula; Linkermann, Andreas; Muders, Michael H.; Baretton, Gustavo B.; Hampe, Jochen; Aust, Daniela E.; Baines, John F.; Bleich, Andre und Zeissig, Sebastian (2021): Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation. In: Science Immunology, Bd. 6, Nr. 65, eabf7473

Willier, Semjon; Rothamel, Paula; Hastreiter, Maximilian; Wilhelm, Jonas; Stenger, Dana; Blaeschke, Franziska; Rohlfs, Meino; Kaeuferle, Theresa; Schmid, Irene; Albert, Michael H.; Binder, Vera; Subklewe, Marion; Klein, Christoph und Feuchtinger, Tobias (2021): CLEC12A and CD33 coexpression as a preferential target for pediatric AML combinatorial immunotherapy. In: Blood, Bd. 137, Nr. 8: S. 1037-1049

Yilmaz, Ebru; Kuehn, Hye S.; Odakir, Eda; Niemela, Julie E.; Ozcan, Alper; Eken, Ahmet; Rohlfs, Meino; Cansever, Murat; Gok, Veysel; Aydin, Firdevs; Karakukcu, Musa; Hauck, Fabian; Klein, Christoph; Unal, Ekrem; Rosenzweig, Sergio D. und Patiroglu, Turkan (2021): Common Variable Immunodeficiency, Autoimmune Hemolytic Anemia, and Pancytopenia Associated With a Defect in IKAROS. In: Journal of Pediatric Hematology Oncology, Bd. 43, Nr. 3, E351-E357

Hager, Paul; Mewes, Hans-Werner; Rohlfs, Meino; Klein, Christoph und Jeske, Tim (2020): SmartPhase: Accurate and fast phasing of heterozygous variant pairs for genetic diagnosis of rare diseases.
In: PLOS Computational Biology 16(2), e1007613 [PDF, 869kB]

Momtazmanesh, Sara; Rayzan, Elham; Shahkarami, Sepideh; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima (2020): A novelVPS13Bmutation in Cohen syndrome: a case report and review of literature. In: BMC Medical Genetics, Bd. 21, Nr. 1, 140

Cansever, Murat; Zietara, Natalia; Chiang, Samuel C. C.; Ozcan, Alper; Yilmaz, Ebru; Karakukcu, Musa; Rohlfs, Meino; Somekh, Ido; Canoz, Ozlem; Abdulrezzak, Ummuhan; Bryceson, Yenan; Klein, Christoph; Unal, Ekrem und Patiroglu, Turkan (2020): A Rare Case of Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS) Presenting With Hemophagocytosis Complicated With Hodgkin Lymphoma. In: Journal of Pediatric Hematology Oncology, Bd. 42, Nr. 2: S. 156-159

Khoshnevisan, Razieh; Anderson, Michael; Babcock, Stephen; Anderson, Sierra; Illig, David; Marquardt, Benjamin; Sherkat, Roya; Schroeder, Katrin; Moll, Franziska; Hollizeck, Sebastian; Rohlfs, Meino; Walz, Christoph; Adibi, Peyman; Rezaei, Abbas; Andalib, Alireza; Koletzko, Sibylle; Muise, Aleixo M.; Snapper, Scott B.; Klein, Christoph; Thiagarajah, Jay R. und Kotlarz, Daniel (2020): NOX1 Regulates Collective and Planktonic Cell Migration: Insights From Patients With Pediatric-Onset IBD and NOX1 Deficiency. In: Inflammatory Bowel Diseases, Bd. 26, Nr. 8: S. 1166-1176

Rahmani, Farzaneh; Rayzan, Elham; Rahmani, Mohammad Reza; Shahkarami, Sepideh; Zoghi, Samaneh; Rezaei, Arezoo; Aryan, Zahra; Najaf, Mehri; Rohlfs, Meino; Jeske, Tim; Aflatoonian, Majid; Chavoshzadeh, Zahra; Farahnnand, Fatemeh; Motamed, Farzaneh; Rohani, Pejman; Alinnadadi, Hossein; Mandaviani, Alireza; Mansouri, Mahboubeh; Tavakol, Marzieh; Vanderberg, Mirjam; Kotlarz, Daniel; Klein, Christoph und Rezaei, Nima (2020): Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR). In: Immunological Investigations, Bd. 50, Nr. 4: S. 445-459

Lyszkiewicz, Marcin; Zietara, Natalia; Frey, Laura; Pannicke, Ulrich; Stern, Marcel; Liu, Yanshan; Fan, Yanxin; Puchalka, Jacek; Hollizeck, Sebastian; Somekh, Ido; Rohlfs, Meino; Yilmaz, Tugba; Unal, Ekrem; Karakukcu, Musa; Patiroglu, Türkan; Kellerer, Christina; Karasu, Ebru; Sykora, Karl-Walter; Lev, Atar; Simon, Amos; Somech, Raz; Roesler, Joachim; Hoenig, Manfred; Keppler, Oliver T.; Schwarz, Klaus und Klein, Christoph (2020): Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells. In: Nature Communications, Bd. 11, Nr. 1, 1031 [PDF, 3MB]

Blaeschke, Franziska; Willier, Semjon; Stenger, Dana; Lepenies, Mareike; Horstmann, Martin A.; Escherich, Gabriele; Zimmermann, Martin; Ringeling, Francisca Rojas; Canzar, Stefan; Kaeuferle, Theresa; Rohlfs, Meino; Binder, Vera; Klein, Christoph und Feuchtinger, Tobias (2020): Leukemia-induced dysfunctional TIM-3(+)CD4(+) bone marrow T cells increase risk of relapse in pediatric B-precursor ALL patients. In: Leukemia, Bd. 34, Nr. 10: S. 2607-2620

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

Tanita, Kay; Hoshino, Akihiro; Imadome, Ken-Ichi; Kamiya, Takahiro; Inoue, Kento; Okano, Tsubasa; Yeh, Tzu-wen; Yanagimachi, Masakatsu; Shiraishi, Akira; Ishimura, Masataka; Schober, Tilmann; Rohlfs, Meino; Takagi, Masatoshi; Imai, Kohsuke; Takada, Hidetoshi; Ohga, Shouichi; Klein, Christoph; Morio, Tomohiro und Kanegane, Hirokazu (4. Februar 2019): Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation. In: Frontiers in Pediatrics, Bd. 7, 15: S. 1-6 [PDF, 1MB]

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

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

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

Eken, Ahmet; Cansever, Murat; Somekh, Ido; Mizoguchi, Yoko; Zietara, Natalia; Okus, Fatma Zehra; Erdem, Serife; Canatan, Halit; Akyol, Sefika; Ozcan, Alper; Karakukcu, Musa; Hollizeck, Sebastian; Rohlfs, Meino; Unal, Ekrem; Klein, Christoph und Patiroglu, Turkan (2019): Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells. In: Journal of Clinical Immunology, Bd. 39, Nr. 4: S. 391-400

Grabowski, Piotr; Hesse, Sebastian; Hollizeck, Sebastian; Rohlfs, Meino; Behrends, Uta; Sherkat, Roya; Tamary, Hannah; Unal, Ekrem; Somech, Raz; Patiroglu, Turkan; Canzar, Stefan; Ten Bosch, Jutte van der Werff; Klein, Christoph und Rappsilber, Juri (2019): Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition. In: Molecular & Cellular Proteomics, Bd. 18, Nr. 4: S. 760-772

Illig, David; Navratil, Marta; Kelecic, Jadranka; Conca, Raffaele; Hojsak, Iva; Jadresin, Oleg; Coric, Marijana; Vukovic, Jurica; Rohlfs, Meino; Hollizeck, Sebastian; Bohne, Jens; Klein, Christoph und Kotlarz, Daniel (2019): Alternative Splicing Rescues Loss of Common Gamma Chain Function and Results in IL-21R-like Deficiency. In: Journal of Clinical Immunology, Bd. 39, Nr. 2: S. 207-215

Hospach, Toni; Glowatzki, Fabian; Blankenburg, Friederike; Conzelmann, Dennis; Stirnkorb, Christian; Müllerschön, Chris Sandra; Driesch, Peter von den; Köhler, Lisa Maria; Rohlfs, Meino; Klein, Christoph und Hauck, Fabian (2019): Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents. In: Pediatric Rheumatology, Bd. 17, 37

Somekh, Ido; Marquardt, Benjamin; Liu, Yanshan; Rohlfs, Meino; Hollizeck, Sebastian; Karakukcu, Musa; Unal, Ekrem; Yilmaz, Ebru; Patiroglu, Turkan; Cansever, Murat; Frizinsky, Shirly; Vishnvenska-Dai, Vicktoria; Rechavi, Erez; Stauber, Tali; Simon, Amos J.; Lev, Atar; Klein, Christoph; Kotlarz, Daniel und Somech, Raz (2018): Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma. In: Journal of Clinical Immunology, Bd. 38, Nr. 6: S. 699-710

Witzel, Maximilian; Petersheim, Daniel; Fan, Yanxin; Bahrami, Ehsan; Racek, Tomas; Rohlfs, Meino; Puchalka, Jacek; Mertes, Christian; Gagneur, Julien; Ziegenhain, Christoph; Enard, Wolfgang; Stray-Pedersen, AsbJörg; Arkwright, Peter D.; Abboud, Miguel R.; Pazhakh, Vahid; Lieschke, Graham J.; Krawitz, Peter M.; Dahlhoff, Maik; Schneider, Marlon R.; Wolf, Eckhard; Horny, Hans-Peter; Schmidt, Heinrich; Schäffer, Alejandro A. und Klein, Christoph (2017): Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes. In: Nature Genetics, Bd. 49, Nr. 5: S. 742-752

Joseph, Jayabalan M.; Fey, Petra; Ramalingam, Nagendran; Liu, Xiao I.; Rohlfs, Meino; Noegel, Angelika A.; Müller-Taubenberger, Annette; Glöckner, Gernot und Schleicher, Michael (9. Juli 2008): The actinome of Dictyostelium discoideum in comparison to actins and actin-related proteins from other organisms.
In: PLOS ONE 3(7), e2654 [PDF, 957kB]

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