Disease genetics: insights into missing heritability.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

12 citing papers in PubMed.

1. Transgenerational epigenetic self-memory ofEpigenetics · 2024
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2. Paternal developmental thyrotoxicosis disrupts neonatal leptin leading to increased adiposity and altered physiology of the melanocortin system.Frontiers in endocrinology · 2023
   Article
3. Concurrent outcomes from multiple approaches of epistasis analysis for human body mass index associated loci provide insights into obesity biology.Scientific reports · 2022
   Article
4. Thyroid hormone elicits intergenerational epigenetic effects on adult social behavior and fetal brain expression of autism susceptibility genes.Frontiers in neuroscience · 2022
   Article
5. Thyroid hormone influences brain gene expression programs and behaviors in later generations by altering germ line epigenetic information.Molecular psychiatry · 2020
   Article
6. Thyroid hormone action in the developing testis: intergenerational epigenetics.The Journal of endocrinology · 2020
   Review
7. Recent technical advances in proteomics.F1000Research · 2019
   Review
8. The search for gene-gene interactions in genome-wide association studies: challenges in abundance of methods, practical considerations, and biological interpretation.Annals of translational medicine · 2018
   Article
9. A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family.Heredity · 2018
   Article
10. Assessing the Heritability of Complex Traits in Humans: Methodological Challenges and Opportunities.Current genomics · 2017
    Review
11. Genome-wide identification of long noncoding RNAs in rat models of cardiovascular and renal disease.Hypertension (Dallas, Tex. : 1979) · 2015
    Article
12. SNP characteristics predict replication success in association studies.Human genetics · 2014
    Article

Corrections and comments

• Comment on
  Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome.2014

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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