Nicola Iuso
2024–2024 OpenAlex profile ↗
Reproducibility track record
1
assessed papers
58/100
mean reproducibility
0
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
Jonas Bahn 1Jenny Krause 1Alena Laschtowitz 1André Franke 1Lilly K. Kunzmann 1Lise Katrine Engesæter 1Hilla Gilladi 1Laura Liebig 1Anne-Marie Schäfer 1Ansgar W. Lohse 1
Institutions
Universität Hamburg 1University Medical Center Hamburg-Eppendorf 1ERN RARE-LIVER 1Charité - Universitätsmedizin Berlin 1Max Delbrück Center 1Oslo University Hospital 1
Geography (author institutions)
DE 1NO 1SE 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 (9)
Request a reproduction →1 assessed by us (0 reproduced) · 8 not yet assessed — every PubMed paper on record, linked below.
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Intergenic risk variant rs56258221 skews the fate of naive CD4+ T cells via miR4464-BACH2 interplay in primary sclerosing cholangitisCell Reports Medicine · 2024 · PMID 38901430L1 58/100
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Mapping the human genetic architecture of COVID-19 ↗Nature · 2021 · PMID 34237774not yet assessed
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Association of Toll-like receptor 7 variants with life-threatening COVID-19 disease in males: findings from a nested case-control study ↗eLife · 2021 · PMID 33650967not yet assessed
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Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males ↗EBioMedicine · 2021 · PMID 33647767not yet assessed
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Severe COVID-19 in Hospitalized Carriers of Single CFTR Pathogenic Variants ↗Journal of Personalized Medicine · 2021 · PMID 34203982not yet assessed
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Identification of a New Mutation in RSK2, the Gene for Coffin–Lowry Syndrome (CLS), in Two Related Patients with Mild and Atypical Phenotypes ↗Brain Sciences · 2021 · PMID 34439726not yet assessed
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Post-Mendelian genetic model in COVID-19 ↗medRxiv · 2021not yet assessed
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not yet assessed
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Private somatic mutations identified with liquid biopsy lead tumor progression in solid cancers ↗Journal of Cancer Metastasis and Treatment · 2020not 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 “Iuso N” paper on PubMed ↗