Evidence map›Paper›PMID 42138791›Full record

ArticleBehavior genetics2026

The Preprint Problem: Fringe, Genetically Informed Studies of Group Differences in Behavior Housed on Open Science Platforms.

Evan J Giangrande

Abstract read
PubMed Publisher
In one paragraph

Article in Behavior genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Evan J GiangrandeStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard Hospital, Cambridge, MA, USA. egiangrande@broadinstitute.org.ORCID http://orcid.org/0000-0002-8023-0062

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preprint servers and open science platforms have revolutionized the scientific process. A fundamental feature of these platforms is a lack of peer review-virtually anyone with an internet connection can upload their research in a few clicks. Although this setup has facilitated rapid dissemination of results and open access to research, it has also enabled fringe researchers to post and share pseudoscientific, genetically informed studies of differences in behavior that often advance racial hereditarian and eugenic claims. Because preprint archives are now routinely used by mainstream academics, preprints grant a degree of legitimacy to fringe research that otherwise may have been relegated to a blog post or fringe publication. Previous studies have documented individual examples of pseudoscientific, genetic studies of group differences being posted on preprint archives, but the scope of this problem remains unclear, making it difficult to formulate responses and potential solutions. The present study quantified and characterized pseudoscientific studies of group differences in behavior-including studies that used genetic methods-housed on popular preprint servers and open science collaboration platforms. Dozens of such preprints were identified. Preprinted studies on group differences often analyzed controversial phenotypes, most frequently intelligence and related traits, and furthered classical, widely rejected hereditarian and eugenic theories. Genetically informed analyses rested on fundamentally flawed assumptions about heritability and polygenic scores. The Preprint Problem is indicative of a broader effort to weaponize mainstream academic research and its mechanisms, including Open Science, and a recent resurgence of scientific racism and eugenics. Potential responses to these challenges are introduced.

Indexed as

EugenicsOpen scienceRacial hereditarianismScientific racismWeaponization

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.