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M. Rohlfs · SciRah

Researcher profile · Semantic Scholar

M. Rohlfs

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M. Rohlfs — researcher profile on SciRah

h-index: 25
Works: 78
Citations: 1,673

Most-cited papers

Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases
Yue Li, Marita Führer, E. Bahrami, P. Socha +32 more
2018Proceedings of the National Academy of Sciences of the United States of America158 citations Open access
Semantic Scholar
Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency.
Anna S. Lehle, H. Farin, Benjamin Marquardt, Birgitta E. Michels +28 more
2019Gastroenterology114 citations Open access
Semantic Scholar
A human immunodeficiency syndrome caused by mutations in CARMIL2
T. Schober, T. Magg, M. Laschinger, M. Rohlfs +16 more
2017Nature Communications107 citations Open access
Semantic Scholar
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes
Maximilian Witzel, Daniel Petersheim, Yanxin Fan, E. Bahrami +20 more
2017Nature Genetics97 citations Open access
Semantic Scholar
Epithelial sodium channel (ENaC) is multi-ubiquitinated at the cell surface.
D. Wiemuth, Ying Ke, M. Rohlfs, F. McDonald
2007Biochemical Journal78 citations Open access
Semantic Scholar
Heterozygous OAS1 Gain-of-Function Variants Cause an Autoinflammatory Immunodeficiency
T. Magg, Tsubasa Okano, Lars M. Koenig, D. Boehmer +24 more
2021Science immunology62 citations Open access
Semantic Scholar
CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis.
I. Somekh, M. Thian, David Medgyesi, N. Gulez +32 more
2019Blood62 citations Open access
Semantic Scholar
CLEC12A and CD33 co-expression as preferential target on pediatric AML for combinatorial immunotherapy.
Semjon Willier, P. Rothämel, M. Hastreiter, Jonas Wilhelm +10 more
2020Blood57 citations
Semantic Scholar
Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition
Piotr Grabowski, Sebastian Hesse, Sebastian Hollizeck, M. Rohlfs +10 more
2019Molecular & Cellular Proteomics57 citations Open access
Semantic Scholar
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
A. Schmidt, M. Danyel, K. Grundmann, T. Brunet +168 more
2024Nature Genetics50 citations Open access
Semantic Scholar
Scoping review of biological treatment of deficiency of interleukin-36 receptor antagonist (DITRA) in children and adolescents
T. Hospach, Fabian Glowatzki, Friederike Blankenburg, Dennis Conzelmann +7 more
2019Pediatric Rheumatology Online Journal45 citations Open access
Semantic Scholar
Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma
I. Somekh, Benjamin Marquardt, Yanshan Liu, M. Rohlfs +15 more
2018Journal of Clinical Immunology45 citations
Semantic Scholar
OAS1/RNase L executes RIG-I ligand–dependent tumor cell apoptosis
D. Boehmer, Simone Formisano, C. C. de Oliveira Mann, Stephan A. Mueller +13 more
2021Science immunology43 citations
Semantic Scholar
The Actinome of Dictyostelium discoideum in Comparison to Actins and Actin-Related Proteins from Other Organisms
Jayabalan Joseph, P. Fey, Nagendran Ramalingam, Xiao Liu +5 more
2008PLoS ONE43 citations Open access
Semantic Scholar
Leukemia-induced dysfunctional TIM-3+CD4+ bone marrow T cells increase risk of relapse in pediatric B-precursor ALL patients
Franziska Blaeschke, Semjon Willier, D. Stenger, Mareike Lepenies +10 more
2020Leukemia40 citations
Semantic Scholar
Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells
A. Eken, M. Cansever, I. Somekh, Yoko Mizoguchi +12 more
2019Journal of Clinical Immunology40 citations
Semantic Scholar
A novel VPS13B mutation in Cohen syndrome: a case report and review of literature
S. Momtazmanesh, Elham Rayzan, S. Shahkarami, M. Rohlfs +2 more
2020BMC Medical Genetics37 citations Open access
Semantic Scholar
Abatacept for treatment-refractory pediatric CTLA4-haploinsufficiency.
Anna-Lisa Lanz, M. Riester, Philip Peters, T. Schwerd +9 more
2021Clinical Immunology32 citations
Semantic Scholar
Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
Marcin Łyszkiewicz, Natalia Ziȩtara, Laura Frey, U. Pannicke +22 more
2020Nature Communications31 citations Open access
Semantic Scholar
Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
R. Lévy, F. Gothe, M. Momenilandi, T. Magg +78 more
2022Journal of Experimental Medicine30 citations Open access
Semantic Scholar
FARS1‐related disorders caused by bi‐allelic mutations in cytosolic phenylalanyl‐tRNA synthetase genes: Look beyond the lungs!
Luise A. Schuch, M. Forstner, Christina K. Rapp, Yang Li +18 more
2021Clinical Genetics30 citations Open access
Semantic Scholar
CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease.
T. Magg, A. Shcherbina, D. Arslan, M. Desai +22 more
2019Inflammatory Bowel Diseases28 citations Open access
Semantic Scholar
A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis–Like Hyperinflammation
D. Boehmer, L. Koehler, T. Magg, Philipp Metzger +10 more
2020Journal of Allergy and Clinical Immunology: In Practice27 citations Open access
Semantic Scholar
First detected geographical cluster of BoDV-1 encephalitis from same small village in two children: therapeutic considerations and epidemiological implications
Leonie Grosse, V. Lieftüchter, Y. Vollmuth, F. Hoffmann +18 more
2023Infection26 citations Open access
Semantic Scholar
Deficiency in X-linked inhibitor of apoptosis protein promotes susceptibility to microbial triggers of intestinal inflammation
A. Strigli, S. Gopalakrishnan, Yvonne Zeissig, M. Basic +29 more
2021Science immunology26 citations
Semantic Scholar
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes
Monika I. Linder, Yoko Mizoguchi, Sebastian Hesse, Gergely Csaba +29 more
2022Blood24 citations Open access
Semantic Scholar
Tumor suppressor Hippo/MST1 kinase mediates chemotaxis by regulating spreading and adhesion
Yulia Artemenko, Petros Batsios, Jane S. Borleis, Z. Gagnon +6 more
2012Proceedings of the National Academy of Sciences of the United States of America24 citations Open access
Semantic Scholar
The Ste20-like kinase SvkA of Dictyostelium discoideum is essential for late stages of cytokinesis
M. Rohlfs, R. Arasada, Petros Batsios, J. Janzen +1 more
2007Journal of Cell Science24 citations
Semantic Scholar
SmartPhase: Accurate and fast phasing of heterozygous variant pairs for genetic diagnosis of rare diseases
Paul Hager, H. Mewes, M. Rohlfs, C. Klein +1 more
2020PLoS Comput. Biol.21 citations Open access
Semantic Scholar
Dye-ligand chromatographic purification of intact multisubunit membrane protein complexes: application to the chloroplast H+-FoF1-ATP synthase.
H. Seelert, A. Poetsch, M. Rohlfs, Norbert A. Dencher
2000Biochemical Journal18 citations Open access
Semantic Scholar
A Rare Case of Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS) Presenting With Hemophagocytosis Complicated With Hodgkin Lymphoma.
M. Cansever, Natalia Ziȩtara, Samuel C. C. Chiang, A. Ozcan +10 more
2020Journal of pediatric hematology/oncology16 citations
Semantic Scholar
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation
K. Tanita, Akihiro Hoshino, K. Imadome, T. Kamiya +15 more
2019Frontiers in Pediatrics16 citations Open access
Semantic Scholar
NOX1 Regulates Collective and Planktonic Cell Migration: Insights From Patients With Pediatric-Onset IBD and NOX1 Deficiency.
R. Khoshnevisan, Michael Anderson, Stephen J. Babcock, Sierra Anderson +17 more
2020Inflammatory Bowel Diseases15 citations Open access
Semantic Scholar
Refractory and Fatal Presentation of Severe Autoimmune Hemolytic Anemia in a Child With the DNASE1L3 Mutation Complicated With an Additional DOCK8 Variant.
Ayşenur Paç Kısaarslan, M. Witzel, E. Unal, M. Rohlfs +5 more
2020Journal of pediatric hematology/oncology14 citations
Semantic Scholar
Human MD2 deficiency-an inborn error of immunity with pleiotropic features.
Yue Li, Zi-Qi Yu, M. Schenk, Irena Lagovsky +10 more
2022Journal of Allergy and Clinical Immunology12 citations Open access
Semantic Scholar
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
T. Brunet, B. Zott, V. Lieftüchter, D. Lenz +45 more
2023Genetics in Medicine11 citations Open access
Semantic Scholar
Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR)
F. Rahmani, Elham Rayzan, M. Rahmani, S. Shahkarami +19 more
2020Immunological Investigations11 citations
Semantic Scholar
Common Variable Immune Deficiency, Autoimmune Hemolytic Anemia and Pancytopenia associated with a Defect in IKAROS
Ebru Yılmaz, H. Kuehn, Eda Odakir, Julie E. Niemela +12 more
2020Journal of pediatric hematology/oncology10 citations Open access
Semantic Scholar
C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.
Friedrich G. Kapp, S. Kretschmer, Cora C. A. Beckmann, Lena Wäsch +28 more
2023Clinical Immunology9 citations
Semantic Scholar
The centrosomal component CEP161 of Dictyostelium discoideum interacts with the Hippo signaling pathway
S. Sukumaran, Rosemarie Blau-Wasser, M. Rohlfs, Christoph Gallinger +2 more
2015Cell Cycle9 citations Open access
Semantic Scholar
Characterization of the Ste20-like kinase Krs1 of Dictyostelium discoideum.
R. Arasada, H. Son, Nagendran Ramalingam, L. Eichinger +2 more
2006European Journal of Cell Biology9 citations
Semantic Scholar
Properties of the Kinesin-1 motor DdKif3 from Dictyostelium discoideum.
Christian Röhlk, M. Rohlfs, Sven Leier, M. Schliwa +3 more
2008European Journal of Cell Biology8 citations
Semantic Scholar
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency
Johannes Raedler, T. Magg, M. Rohlfs, C. Klein +3 more
2021Journal of Clinical Immunology7 citations Open access
Semantic Scholar
Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings.
V. Chongsrisawat, Narissara Suratannon, P. Chatchatee, Rungnapa Ittiwut +7 more
2022Inflammatory Bowel Diseases6 citations Open access
Semantic Scholar
Novel G6PC3 Mutations in patients with Congenital Neutropenia: Case reports and Review of the Literature.
S. F. Maroufi, Zoha Shaka, Helia Mojtabavi, Mona Sadeghalvad +7 more
2021Endocrine, Metabolic & Immune Disorders - Drug Targets6 citations
Semantic Scholar
Alternative Splicing Rescues Loss of Common Gamma Chain Function and Results in IL-21R-like Deficiency
D. Illig, M. Navratil, J. Kelečić, R. Conca +9 more
2019Journal of Clinical Immunology6 citations
Semantic Scholar
Valosin-containing protein-regulated endoplasmic reticulum stress causes NOD2-dependent inflammatory responses
M. Ghalandary, Yue Li, T. Fröhlich, T. Magg +13 more
2022Scientific Reports5 citations Open access
Semantic Scholar
DNAH11 and a Novel Genetic Variant Associated with Situs Inversus: A Case Report and Review of the Literature
F. Sodeifian, Noosha Samieefar, S. Shahkarami, Elham Rayzan +5 more
2023Case Reports in Medicine4 citations Open access
Semantic Scholar
A 3-year- old boy with an Xp21 deletion syndrome: A case report.
Shaghayegh Sadeghmousavi, S. Shahkarami, Elham Rayzan, S. Ahmed +4 more
2022Endocrine, Metabolic & Immune Disorders - Drug Targets4 citations
Semantic Scholar
Clinical and genomic features of Iranian patients with very early onset IBD
Mahya Haghipanah, Pejman Rohani, M. Rohlfs, S. Shahrokh +10 more
2026Pediatric Research3 citations
Semantic Scholar

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