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Birte Zurek

TRIM27 Negatively Regulates NOD2 by Ubiquitination and Proteasomal Degradation
2012 · Birte Zurek, Ida Schoultz, et al. · PLoS ONE · 122
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
2021 · Birte Zurek, Kornelia Ellwanger, et al. · European Journal of Human Genetics · 101
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NOD-Like Receptor Activation by Outer Membrane Vesicles from Vibrio cholerae Non-O1 Non-O139 Strains Is Modulated by the Quorum-Sensing Regulator HapR
2011 · H. Bielig, P. K. Rompikuntal, et al. · Infection and Immunity · 94
Mutational analysis of human NOD1 and NOD2 NACHT domains reveals different modes of activation
2011 · Birte Zurek, Martina Proell, et al. · Innate Immunity · 77
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
2021 · Leslie Matalonga, Carles Hernández-Ferrer, et al. · European Journal of Human Genetics · 71
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Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
2025 · Steven Laurie, Wouter Steyaert, et al. · Nature Medicine · 70
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The Cofilin Phosphatase Slingshot Homolog 1 (SSH1) Links NOD1 Signaling to Actin Remodeling
2014 · Harald Bielig, Katja Lautz, et al. · PLoS Pathogens · 53
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A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome
2020 · Antonio Atalaia, Rachel Thompson, et al. · Orphanet Journal of Rare Diseases · 40
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Solving the unsolved rare diseases in Europe
2021 · Holm Graessner, Birte Zurek, et al. · European Journal of Human Genetics · 35
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A role for quorum sensing in regulating innate immune responses mediated byVibrio choleraeouter membrane vesicles (OMVs)
2011 · Harald Bielig, Mitesh Dongre, et al. · Gut Microbes · 33
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A function for AAMP in Nod2-mediated NF-κB activation
2009 · H. Bielig, B. Zurek, et al. · Molecular Immunology · 32
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
2023 · Burcu Yaldiz, Erdi Kucuk, et al. · Human Genomics · 30
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Engagement of Nucleotide-binding Oligomerization Domain-containing Protein 1 (NOD1) by Receptor-interacting Protein 2 (RIP2) Is Insufficient for Signal Transduction
2014 · Sophie Mayle, Joseph P. Boyle, et al. · Journal of Biological Chemistry · 30
Solving unsolved rare neurological diseases—a Solve-RD viewpoint
2021 · Rebecca Schüle, Dagmar Timmann, et al. · European Journal of Human Genetics · 19
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14
2023 · Adam Jackson, Sheng-Jia Lin, et al. · Human Genetics and Genomics Advances · 14
Cell-Based Reporter Assay to Analyze Activation of Nod1 and Nod2
2011 · Birte Zurek, Harald Bielig, et al. · Methods in molecular biology · 14
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis
2021 · Elke de Boer, Charlotte W. Ockeloen, et al. · European Journal of Human Genetics · 12
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An interconnected data infrastructure to support large-scale rare disease research
2024 · Lennart F Johansson, Steve Laurie, et al. · GigaScience · 11
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A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing
2023 · Anne-Sophie Denommé-Pichon, Leslie Matalonga, et al. · Genetics in Medicine · 10
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease
2025 · Vicente A. Yépez, German Demidov, et al. · Nature Genetics · 8
Model matchmaking via the Solve-RD Rare Disease Models & Mechanisms Network (RDMM-Europe)
2024 · Kornelia Ellwanger, Julie A. Brill, et al. · Lab Animal · 5
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Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant
2021 · Elke de Boer, Burcu Yaldiz, et al. · European Journal of Medical Genetics · 5
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Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
2025 · Steven Laurie, Wouter Steyaert, et al. · Nature Medicine · 2
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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis
2021 · Elke de Boer, Charlotte W. Ockeloen, et al. · European Journal of Human Genetics · 2
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Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
2021 · Birte Zurek, Kornelia Ellwanger, et al. · European Journal of Human Genetics · 1
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Works count: 59
Citation count: 1,093
H-index: 16
I10-index: 23
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