Pigmentation, pleiotropy, and genetic pathways in humans and mice.

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

5 citing papers in PubMed, 23 citations in OpenAlex.

1. Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.PloS one · 2013
   Article
2. A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3.Human genetics · 2005
   Article
3. Characterization of genes modulated during pheomelanogenesis using differential display.Proceedings of the National Academy of Sciences of the United States of America · 1998
   Article
4. Waardenburg syndrome.Journal of medical genetics · 1997
   Review
5. The ocular albinism type 1 gene product is a membrane glycoprotein localized to melanosomes.Proceedings of the National Academy of Sciences of the United States of America · 1996
   Article

Corrections and comments

• Comment on
  A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2.1995

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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