Michael Kutsche
2026–2026 OpenAlex profile ↗
Reproducibility track record
1
assessed papers
89/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
0
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
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Funders
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Frequent co-authors
Altfeld Marcus 1Christian Schlein 1Brigitte Beifuss 1Jana Hennesen 1Felix R. Stahl 1Maria Pujantell 1Christian Kubisch 1Felix Flomm 1Veit Hornung 1Marie Eggers 1
Institutions
Leibniz Institute of Virology (LIV) 1HNO Bad Bramstedt 1Centre for Structural Systems Biology 1Institute of Virology of the Slovak Academy of Sciences 1Institute of Immunology 1Universität Hamburg 1
Geography (author institutions)
DE 1SK 1HR 1ES 1CZ 1NL 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
Complete publication record (20)
Request a reproduction →1 assessed by us (1 reproduced) · 19 not yet assessed — every PubMed paper on record, linked below.
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Structural modeling and functional characterization of a novel gain-of-function TLR8 variant causing severe inflammatory syndromeJCI Insight · 2026 · PMID 41729082L1 89/100
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Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male ↗American Journal of Medical Genetics Part A · 2026 · PMID 41851022not yet assessed
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Structural modeling and functional characterization of a novel gain-of-function TLR8 variant causing severe inflammatory syndrome ↗DESY Publication Database (PUBDB) (Deutsches Elektronen-Synchrotron) · 2026not yet assessed
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A novel <scp><i>TTC26</i></scp> variant in a patient with hexadactyly, pituitary stalk interruption, hepatopathy, nephropathy, and bilateral lip‐palate cleft: A case report and expansion of the phenotype ↗American Journal of Medical Genetics Part A · 2023 · PMID 38135897not yet assessed
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Thoracic Aortic Disease in Patients with Heterozygous Variants in FBN2 ↗The Thoracic and Cardiovascular Surgeon · 2022not yet assessed
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Inherited Aortic Disease: Expanding the Diagnostic Yield Using Next-Generation Sequencing ↗The Thoracic and Cardiovascular Surgeon · 2021not yet assessed
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Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study ↗British Journal of Cancer · 2020 · PMID 32451468not yet assessed
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Pilot Study: Maternal Betamethasone Administration Has Long Term Effects on Umbilical Cord Glucose Levels in Human FetusesUWA Profiles and Research Repository (University of Western Australia) · 2011not yet assessed
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MLPA screening in the<i>BRCA1</i>gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases ↗Human Mutation · 2008 · PMID 18431737not yet assessed
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Reduced GABAergic transmission and number of hippocampal perisomatic inhibitory synapses in juvenile mice deficient in the neural cell adhesion molecule L1 ↗Molecular and Cellular Neuroscience · 2004 · PMID 15121190not yet assessed
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Neural cell adhesion molecule L1 is required for fasciculation and routing of thalamocortical fibres and corticothalamic fibres ↗Neuroscience Research · 2004 · PMID 15041201not yet assessed
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Tenascin-N: characterization of a novel member of the tenascin family that mediates neurite repulsion from hippocampal explants ↗Molecular and Cellular Neuroscience · 2003 · PMID 12812753not yet assessed
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Structure of the murine tenascin-R gene and functional characterisation of the promoter ↗Biochemical and Biophysical Research Communications · 2003 · PMID 12927810not yet assessed
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The Neural Recognition Molecule L1 Is a Sialic Acid-binding Lectin for CD24, Which Induces Promotion and Inhibition of Neurite Outgrowth ↗Journal of Biological Chemistry · 2001 · PMID 11283023not yet assessed
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Severe hydrocephalus in L1-deficient mice ↗Brain Research · 2001 · PMID 11164829not yet assessed
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Selective Malformation of the Splenic White Pulp Border in L1-Deficient Mice ↗The Journal of Immunology · 2000 · PMID 10946272not yet assessed
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Promoters controlling expression of the alternative nitrogenase and the molybdenum uptake system in Rhodobacter capsulatus are activated by NtrC, independent of sigma54, and repressed by molybdenum ↗Journal of Bacteriology · 1996 · PMID 8606177not yet assessed
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Regulation of Molybdenum and Alternative Nitrogenases in the Photosynthetic Purple Bacterium Rhodobacter Capsulatus ↗Current plant science and biotechnology in agriculture · 1995not yet assessed
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Characterization of <i>anf</i> genes specific for the alternative nitrogenase and identification of <i>nif</i> genes required for both nitrogenases in <i>Rhodobacter capsulatus</i> ↗Molecular Microbiology · 1993 · PMID 8332060not yet assessed
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Functional analysis of the cysteine motifs in the ferredoxin-like protein FdxN ofRhizobium meliloti involved in symbiotic nitrogen fixation ↗Molecular and General Genetics MGG · 1992 · PMID 1603075not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
No ORCID on record to anchor it (≈⅓ of researchers have none), so this rests on name disambiguation alone. See every “Kutsche M” paper on PubMed ↗