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This page is alzhub.org's plain-English summary of a published study, not the paper itself. It is generated from the record we hold for this study, sourced and linked below — check the original for the full text and methods.

✓ Peer-reviewed alzhub usefulness score 44 out of 100. Genetics

Topic: Brain proteins, microglia and lab models

Imprinted genes are epigenetically modified genes whose expression is determined according to their parent of origin. They are involved in embryonic development, and imprinting dysregulation is linked to cancer, obesity, diabetes, and behavioral disorders such as autism and bipolar disease. Herein, we train a statistical model based on DNA sequence characteristics that not only identifies potentially imprinted genes, but also predicts the parental allele from which they are expressed. Of 23,788 annotated autosomal mouse genes, our model identifies 600 (2.5%) to be potentially imprinted, 64% of which are predicted to exhibit maternal expression. These predictions allowed for the identification of putative candidate genes for complex conditions where parent-of-origin effects are involved, including Alzheimer disease, autism, bipolar disorder, diabetes, male sexual orientation, obesity, and schizophrenia. We observe that the number, type, and relative orientation of repeated elements flanking a gene are particularly important in predicting whether a gene is imprinted.

Cite this study APA, Vancouver, BibTeX · download .bib or .ris

APA 7th

Luedi, P. P., Hartemink, A. J., & Jirtle, R. L. (2005). Genome-wide prediction of imprinted murine genes. Genome research. https://doi.org/10.1101/gr.3303505

Vancouver

Luedi PP, Hartemink AJ, Jirtle RL. Genome-wide prediction of imprinted murine genes. Genome research. 2005. doi:10.1101/gr.3303505. PMID: 15930497.

BibTeX

@article{luedi2005-15930497,
  author  = {Luedi, P. P. and Hartemink, A. J. and Jirtle, R. L.},
  title   = {{Genome-wide prediction of imprinted murine genes}},
  journal = {Genome research},
  year    = {2005},
  doi     = {10.1101/gr.3303505},
  pmid    = {15930497},
  url     = {https://doi.org/10.1101/gr.3303505}
}

Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.

Key findings

Why it matters

This work used a statistical model in mice to predict potentially imprinted genes, including some put forward as candidate genes for conditions where parent-of-origin effects are involved, such as Alzheimer disease. It is a prediction study in mice and does not show that these genes cause or can be used to treat Alzheimer disease.

Study details

How this study scored 44/100
How this study's score is builtJournal tier 7 of 10; Journal's citation record 3 of 4; Study design 0 of 12; Strength of evidence 1 of 5; Peer-review validation 10 of 10; How recent 1 of 5; Sample size 0 of 4; Effect reported 2 of 3; Studied in people 0 of 3; Randomized / blinded 0 of 2; Times cited 5 of 7; Citations per year 3 of 5; Impact for its field and year left out, no data; Cited by studies here 0 of 6; Still being cited 1 of 4; Senior author's track record 3 of 4; Institution's track record 2 of 3; Multicenter collaboration 1 of 3; Indexed in PubMed 2 of 2; Free to read 0 of 2. 41 of the 94 points it could be judged on, which is 44 of 100. Total 44 of 100.41 of the 94 points we could judge = 44 of 100

Published in a peer-reviewed journal. Scored zero for study design, sample size and randomized / blinded because the record does not state it. We have no data on impact for its field and year, so that was left out: it earned 41 of the 94 points we could judge it on, which is 44 out of 100.

ComponentPointsWhy
Journal tier 7 / 10 Tier 3 — peer-reviewed journal (Genome research)
Journal's citation record 3 / 4 Genome Research: journal h-index 399 (OpenAlex, 2026-10-29)
Study design 0 / 12 No study design recorded — scores zero, not guessed (not stated in the record — scored 0)
Strength of evidence 1 / 5 Rated “low” in our summary
Peer-review validation 10 / 10 Peer-reviewed. Published as an article in a named peer-reviewed journal.
How recent 1 / 5 2005 — older than 20 years, still counted
Sample size 0 / 4 Participant count not stated — scores zero (not stated in the record — scored 0)
Effect reported 2 / 3 Effect reported as a number, without an interval or test
Studied in people 0 / 3 Laboratory or animal study (title names “murine”) — scores zero
Randomized / blinded 0 / 2 No randomization or blinding stated — scores zero (not stated in the record — scored 0)
Times cited 5 / 7 Cited 259 times (OpenAlex, 2026-10-10)
Citations per year 3 / 5 11.3 citations a year over 23 year(s) since 2005
Impact for its field and year — / 6 No field-weighted citation impact (OpenAlex has none yet) — left out of this score
Cited by studies here 0 / 6 No other study in this library cites it
Still being cited 1 / 4 Cited 6 times in 2024–2026 (2026 still in progress; OpenAlex)
Senior author's track record 3 / 4 Last-listed author Randy L. Jirtle: h-index 76 (OpenAlex, whole career)
Institution's track record 2 / 3 Duke University: institution h-index 1,541 (OpenAlex)
Multicenter collaboration 1 / 3 OpenAlex lists 2 institution(s) in 1 country
Indexed in PubMed 2 / 2 Indexed in PubMed (PMID 15930497)
Free to read 0 / 2 Behind a paywall — scores zero
Points 41 / 94 Scored on 19 of 20 parts. We have no data for the rest, so they are left out: 41 of the 94 points we could judge it on is 44 out of 100.
Total 44 / 100 —

What each of these 20 components measures, and what this score is not →

Read the original

Full text: free to read — PubMed Central lists this copy as free to read: the link above (checked 10 Oct 2026).

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