Verena Kolbe
2015–2020 OpenAlex profile ↗
Reproducibility track record
5
assessed papers
83/100
mean reproducibility
3
reproduced (C1–C2)
1
flagged
0
total citations
flag rate:
20%
(1/5)
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
—
Funders
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Frequent co-authors
Georg Rosenberger 5Sina Renner 3Karen W. Gripp 2Malik Alawi 2Katja Kloth 2Deborah L. Stabley 2Laura Baker 2Maja Hempel 2Janine Altmüller 2Patroula Smpokou 1
Institutions
Universität Hamburg 5University Medical Center Hamburg-Eppendorf 5University of Cologne 2Alfred I. duPont Hospital for Children 2Community Health Systems - Dupont Hospital 2Kinderkrebs-Zentrum Hamburg 1
Geography (author institutions)
DE 5US 2CA 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 (5)
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Exome sequencing in 38 patients with intracranial aneurysms and subarachnoid hemorrhage.⚑
2020 78/100 ⚑
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The novel duplication HRAS c.186_206dup p.(Glu62_Arg68dup): clinical and functional aspects.
2020 L1 No computation
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Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
2019 L1 93/100
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16p13.11 microdeletion uncovers loss-of-function of a MYH11 missense variant in a patient with megacystis-microcolon-intestinal-hypoperistalsis syndrome.
2019 L1 78/100
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An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences.
2015 L1 No computation