ReviewJournal of psychopathology and clinical science2026
Why psychopathology research should avoid studying one mental disorder at a time: An intergenerational and developmental evidence base for understanding "p".
Review in Journal of psychopathology and clinical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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
3 citing papers in PubMed.
- Remembering the bad times: Autobiographical memory fluency, specificity, and fading affect bias in adolescents at clinical risk of affective disorder.Journal of child psychology and psychiatry, and allied disciplines · 2026Article
- Longitudinal Transitions Between Internalizing and Externalizing Symptoms and Associations with Substance Use among US Young Adults, 2016-2023.Epidemiology (Cambridge, Mass.) · 2026Article
- Associations of general and specific psychopathology factors by age 35 with dementia after age 50: a Swedish population-based sibling comparison study.Molecular psychiatry · 2026Article
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9 authors.
Funding
Abstract
Most etiological research on mental disorders tries to find specific causes of specific disorders. However, the search for causal specificity has been elusive. In fact, new evidence reveals that the major etiological factors are transdiagnostic. One possible reason for why the search for specificity has been elusive is that most disorders are more similar than they are distinct, an idea that prompted research on "p"-the tendency of a person to develop a wide range of different mental disorders. Here we bring together data from unique sources to provide the intergenerational and developmental empirical evidence base for understanding "p." Men and women with a history of mental disorders tend to mate with partners who are also prone to have mental disorders, but not necessarily the same disorders. This creates a situation whereby their offspring, whether through genetic and/or environmental transmission, are at heightened risk of developing a variety of different mental disorders, but which specific disorder offspring ultimately develop is not easy to predict. Given that offspring inherit these multiple liabilities, it may not surprise that these liabilities manifest as different disorders at different points throughout their lives, but which disorder emerges at a particular time is difficult to foretell. The intergenerational and developmental evidence about the familiality and course of mental disorders helps to deconstruct "p" and invites psychopathology research and clinical science to reconsider their common approach to studying one mental disorder at a time. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
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Registered trials
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 Socratic graph.