Katherine Fleck
2025–2025 OpenAlex profile ↗
Reproducibility track record
1
assessed papers
98/100
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
Funders
—
Frequent co-authors
Institutions
University of Connecticut 1UConn Health 1
Geography (author institutions)
US 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 (6)
Request a reproduction →1 assessed by us (1 reproduced) · 5 not yet assessed — every PubMed paper on record, linked below.
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Developmental expression of the skeletal muscle determination gene, <i>MyoD</i> , is regulated by novel enhancer elements that interact with the core enhancer and distal regulatory region ↗bioRxiv (Cold Spring Harbor Laboratory) · 2026not yet assessed
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Disentangling spatial organization and splicing of rare intron classes in the human genome ↗bioRxiv (Cold Spring Harbor Laboratory) · 2025 · PMID 40832269not yet assessed
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Identity rather than 3D position informs splicing of rare introns in the human genomeiScience · 2025 · PMID 41561379L1 98/100
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Functional associations of evolutionarily recent human genes exhibit sensitivity to the 3D genome landscape and disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2024 · PMID 38559085not yet assessed
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The 3D genome landscape: Diverse chromosomal interactions and their functional implications ↗Frontiers in Cell and Developmental Biology · 2022 · PMID 36036013not yet assessed
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De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population ↗Proceedings of the National Academy of Sciences · 2020 · PMID 31964835not 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 “Fleck K” paper on PubMed ↗