Abstract
The Broader Autism Phenotype (BAP), or “subclinical” autistic traits found in relatives of autistic individuals and the general population, has mainly been studied as a genetic endophenotype. Three decades of heritability research have developed reliable measurement tools and deepened understanding of autism’s genetic architecture, but they have left a fundamental question largely unasked: what is it like to have BAP? This paper argues that BAP is not just a “mild” form of autism, and that the structural dynamics causing disadvantages for diagnosed autistic individuals also affect those who carry these traits without a diagnosis. Recognizing this has direct implications for how researchers, clinicians, and policymakers approach this population. Using Bourdieu’s sociology of practice, particularly the concepts of habitus, field, cultural capital, and symbolic violence, along with the neurodiversity paradigm and social model of disability, we propose a social-relational framework for understanding high-BAP experiences. This model explains why individuals with high BAP often experience structural disadvantages as personal failure, why masking is a form of cultural labor rather than symptom masking, and why the lack of explanatory frameworks for BAP experience itself can be harmful. We also address the limitations of familial BAP research samples, explore what lived neurodivergence looks like within neurotypical environments, and outline implications for research methods, clinical practice, and theories of neurocognitive diversity. The paper concludes by applying the Bourdieusian perspective to psychology itself, questioning what it means that a research tradition has spent 30 years measuring traits whose human significance it has largely chosen not to examine.
Introduction
Psychology has recognized for 30 years that autistic traits exist in the general population, cluster in families, and can be measured in individuals who will never be diagnosed (Constantino & Todd, 2003; Hurley et al., 2007; Robinson et al., 2016). However, it has paid less attention to what those people’s lives are actually like. The Broader Autism Phenotype (BAP), a group of “subclinical” autism traits found in both relatives of autistic individuals and the general population, has been studied primarily to assess its heritability, identify neurobiological links, and include it in genome-wide studies. Yet researchers have not systematically asked what it is like to have BAP. This paper considers that asymmetry as its starting point. The BAP is not just an underexplored area in need of further research; it is a case study of what happens when a research tradition organizes inquiry around etiology while treating lived experience as a secondary concern.
We understand the origins of high-BAP traits much better than we understand what those traits mean for the individuals who possess them—how they navigate social worlds shaped by different cognitive styles, and what daily interactions cost them. High-BAP individuals navigate social fields organized around neurotypical norms of interaction, communication, and social performance, yet lack any framework to name that mismatch as structural. The effort required to meet baseline expectations for acceptable participation goes largely unrecognized—by interaction partners, employers, and, frequently, the individuals themselves. And when that labor goes unrecognized, when no explanatory framework exists to name the mismatch as structural, the social verdict tends to be absorbed as self-understanding. Understanding why requires a different theoretical vocabulary than psychology has typically brought to BAP. This paper proposes a Bourdieusian social-relational framework to account for what heritability research has left unexamined, and considers what that reframing reveals about the disciplinary commitments that have kept experiential questions secondary to etiological ones.
What BAP Research Has Taught Us (and What It Hasn’t)
The BAP emerged in the 1990s from observations that relatives of autistic children often displayed subclinical traits across social reciprocity, communication, and cognitive flexibility (Bolton et al., 1994; Piven et al., 1997). BAP became a tool for understanding heritability, serving as an endophenotype to identify genetic variants (Gottesman & Gould, 2003). This approach proved effective in advancing genetic research on autism (Geschwind, 2011; St Pourcain et al., 2018; Virkud et al., 2009). Family studies showed higher BAP traits in first-degree relatives, with twin research indicating moderate to high heritability across BAP domains (Losh et al., 2008; Piven et al., 1997; Sung et al., 2005). Standardized tools such as the Broader Autism Phenotype Questionnaire (BAPQ), Social Responsiveness Scale, and Autism Spectrum Quotient were used in this research (Baron-Cohen et al., 2001; Constantino et al., 2003; Hurley et al., 2007; Sucksmith et al., 2011). This work helped clarify autism’s genetic architecture, supporting the view that autism lies at the extreme end of a continuous spectrum of traits rather than constituting a discrete category (Constantino & Todd, 2003; Robinson et al., 2016). Researchers also used BAP to identify biological pathways involved in autism, including those related to synaptic function, neuronal development, and social communication (Geschwind, 2011; Sasson et al., 2013).
The Limits of an Etiological Framework
BAP research has concentrated on relatives of autistic individuals, treating high-BAP traits as markers of genetic liability. That focus has served the etiological questions it was designed to answer. What it has not done is account for the social and cognitive experiences associated with those traits, and this gap is not unique to BAP research. Across psychology, wherever subclinical trait elevations are studied (e.g., elevated ADHD symptoms that fall short of diagnosis, subclinical depression or anxiety), sophisticated measurement tools and growing neurobiological knowledge coexist with a limited understanding of how these individuals actually navigate their lives. This leaves clinicians with precise measurements and a limited understanding of what to do with them.
But this limitation is not only one of scope. The underlying premise of any purely biological account of autism or BAP is that there is a discrete, definable “autistic brain” or stable neurobiological autistic or BAP profile. This does not hold up under scrutiny. Neurobiological heterogeneity within autism consistently exceeds differences between diagnostic groups, and no reliable biomarkers cleanly demarcate autistic from non-autistic neurology (Lai et al., 2014; Lombardo et al., 2019). It is not simply a measurement problem awaiting a more sensitive instrument. Diagnostic categories are not neutral descriptions of pre-existing biological kinds; they are produced within institutional fields shaped by clinical consensus, research funding priorities, and the habitus of those with the power to define disorder (Jutel, 2009; Rosenberg, 2002). BAP is no exception. What exists are shared biologies and shared forms of life—real, consequential, and varying continuously across the population—but these do not resolve into a fixed biological type waiting to be discovered. The concept will remain incomplete, not because research is insufficiently advanced but because a fully determinate biological BAP was never there to be found. 1 Recognizing this does not invalidate heritability research; it clarifies what that research can and cannot tell us, and why experiential and sociological questions are not secondary add-ons but irreducible dimensions of what BAP actually is.
For BAP, this etiological focus leaves many questions unanswered. We can measure BAP traits but know little about how high-BAP individuals experience social interactions, relationships, work, or daily life (Demizu et al., 2022). BAP traits are enacted and perceived in social contexts, yet we do not understand how others interpret high-BAP individuals or how this affects their social experiences. Evidence suggests that poor mental health linked to autistic traits often results from social experiences mediated by self-efficacy, motivation, and loneliness, emphasizing the social context over the traits themselves (Ai et al., 2024; Camus et al., 2025). Unlike diagnosed autistic individuals, those with high-BAP traits usually lack community, identity, or narratives for their experiences, leaving meaningful differences unrecognized without diagnosis validation or support (Ardeleanu et al., 2025; Belcher et al., 2023; Botha & Frost, 2020; French & Cassidy, 2026; Leedham et al., 2020). The heritability focus also obscures whether and when support for high-BAP individuals would help, and which types of support are most effective.
Beyond the Familial Focus: A Sampling Problem
Before examining the sampling limitations of familial BAP research, it is important to clarify what I mean by “high BAP” throughout this paper. The term refers to individuals who score in elevated ranges on standardized measures of autistic traits, typically one or more standard deviations above population means on instruments like the BAPQ, but who do not meet diagnostic criteria for autism spectrum disorder. Population studies suggest approximately 15–20% of individuals fall into this range, though prevalence estimates vary depending on the measure and cutoff used (Sasson et al., 2013; Wainer et al., 2011).
Critically, “high BAP” is not synonymous with “almost autistic” or “mild autism.” It describes a particular profile of traits that may or may not be associated with functional difficulties, distress, or desire for support. The designation is dimensional and descriptive rather than categorical and pathological (Sasson & Bottema-Beutel, 2022). It indicates where someone falls on a continuum of trait expression, not whether they have a disorder. Even where high-BAP and diagnosed autistic individuals show similar behaviors, such as camouflaging, the mechanisms and motivations involved may differ in ways that matter for understanding and support (Milner et al., 2023).
While studying BAP primarily in families made sense for genetic research, it has created a significant sampling bias. We have been examining a specific subgroup of high-BAP individuals and implicitly treating them as representative of everyone with these traits. There is no theoretical reason to think that autistic traits function differently based on whether someone has a family member with autism, though that remains an empirical question. Population research has shown that autistic traits are widespread beyond families with diagnosed autism and remain consistent over time (Hoekstra et al., 2007; Robinson et al., 2011). How people are perceived as “different” in social settings (e.g., social exclusion, misunderstanding, stigma) depends not on genetic background but on observable behaviors and interaction styles that suggest atypicality (Sasson & Morrison, 2019; Sasson et al., 2017). Limiting studies to family environments likely means overlooking most people with these traits.
Diagnostic disparities compound this sampling problem. Diagnostic practices have historically been normed on white, male, middle-class children (Begeer et al., 2013; Mandell et al., 2009), leading to substantial underdiagnosis in women (Hull et al., 2020; Loomes et al., 2017), people of color (Durkin et al., 2017; Mandell et al., 2009), individuals from lower socioeconomic backgrounds (Rai et al., 2012), and adults who developed effective compensatory strategies in childhood (Lai & Baron-Cohen, 2015). Geographic access, insurance coverage, cultural factors, and clinician bias all create barriers to diagnosis unrelated to trait presence (Bishop-Fitzpatrick & Kind, 2017). Individuals who are autistic and LGBTQ+ face particular barriers to diagnosis, compounding the underrepresentation of already marginalized groups in both clinical and research samples (Ardeleanu et al., 2025). Thus, many individuals with high autistic traits exist outside the “autism family” sampling frame entirely, and our understanding of BAP may be disproportionately based on white, middle-class families with the resources to obtain a diagnosis (Fountain et al., 2011).
To be clear, these gaps are not failures of the heritability research program. They reflect questions it was never designed to answer. That program accomplished what it set out to do, but in doing so, produced an imbalance. Clinicians encounter high-BAP individuals who are struggling but do not meet diagnostic criteria. Researchers using the BAPQ gather rich data on trait levels but rarely ask about daily functioning or subjective experience. And the individuals themselves have few frameworks for making sense of their experiences beyond either minimization or pathologization. The key question is not whether the heritability paradigm was valuable (it undoubtedly was) but whether we are prepared to expand our approach.
A related terminological issue deserves explicit attention before moving forward. Throughout this paper, “BAP” is used as the organizing construct, reflecting the specific research lineage from which the paper departs. However, a growing body of population-level research uses “autistic traits” rather than BAP to describe elevated autistic characteristics in non-diagnosed individuals. These terms do not always measure the same thing, nor are they theoretically equivalent. BAP carries the implication of a phenotypic shadow of diagnosed autism, tied to familial genetic research and specific instruments like the BAPQ. “Autistic traits” is broader and more atheoretical, encompassing population studies that make no claims about heritability or family history. Much of the more recent literature this paper draws on, including work on camouflaging, internalized stigma, and mental health outcomes in non-diagnosed individuals, uses the autistic traits framing rather than BAP (Ai et al., 2024; Milner et al., 2023; Somerville et al., 2024). Sasson and Bottema-Beutel (2022) have argued precisely that studies of autistic traits in the general population are not straightforwardly studies of autism, and that treating them as such risks theoretical confusion. The social-relational framework proposed here is agnostic on this question. Its logic applies wherever individuals carry elevated autistic traits that generate a habitus–field mismatch, whether those traits are framed through the BAP construct or through the broader autistic traits literature. Future work should attend more carefully to whether these two research traditions are studying the same population, using compatible methods, and producing commensurable findings, or whether the apparent convergence obscures important differences.
From Pathology to Neurodivergence
The neurodiversity paradigm, emerging from autistic self-advocacy and disability studies, redefines autism as a natural variation in human cognition rather than a disorder to be cured (Botha et al., 2024; Walker, 2014). Autistic cognition is seen as different rather than deficient, marked by specific perception, processing, and social interaction patterns in a world mainly designed for neurotypical people. This shift aligns with broader psychology trends away from deficit framing: recognition of sensory specificities as natural variation (Little et al., 2017), emphasis on person–environment fit over individual remediation (Armstrong, 2015), and growing attention to well-being and quality of life as primary outcomes rather than behavioral normalization (Sedgwick et al., 2019). However, whether strengths-based framings risk importing neoliberal productivity logics remains a live debate within neurodiversity scholarship (Chapman, 2023; Runswick-Cole, 2014).
The term “neurodiversity” is itself contested. Critics have questioned whether it glosses over genuine impairment, whether its non-disorder claims are defensible across the full range of autistic experience, and whether it functions more as a political framework than an empirical one (Hughes, 2021; Jaarsma & Welin, 2012). This paper does not adopt neurodiversity as a settled framework but draws on its structural insights—specifically, the challenge to deficit-based accounts of neurocognitive difference—while remaining attentive to its limits, which are addressed more fully in the theoretical implications section.
High-BAP individuals are not subclinical cases awaiting a diagnosis; they are people whose neurocognitive style generates real differences in how social interaction is experienced and processed (Chapman, 2020; Walker, 2014). The challenge is not individuals’ capacity but the dominance of neurotypical interaction styles as the standard, placing the burden on high-BAP people to translate their ways of engaging, not because they are inferior but because social norms favor a different approach (Crompton et al., 2021; Milton, 2012). Milton’s (2012) double empathy problem offers a direct theoretical grounding for this claim. Milton argued that the difficulty in social interaction between autistic and non-autistic people is not a one-sided deficit in the autistic person but a bidirectional breakdown arising from divergent dispositions, values, and ways of engaging with the world. Neurotypical individuals are no more naturally equipped to understand autistic communication than autistic individuals are to understand neurotypical communication; the asymmetry lies not in competence but in power—whose interactional style is treated as the standard against which the other is measured. Empirical support for this account has since accumulated. Autistic people communicate effectively with other autistic people, with information transfer and rapport comparable to those in neurotypical dyads, while cross-neurotype interactions reveal breakdowns typically attributed solely to autism (Crompton et al., 2021). For high-BAP individuals, the double empathy framework reframes the experience of social difficulty as the friction of cross-neurotype interaction in a world that assigns the interpretive burden asymmetrically rather than as a personal inadequacy.
The neurodiversity paradigm’s structural critique of clinical framing finds its most radical expression in emic perspectives that reframe autism not as a trait profile but as a culture. Jim Sinclair’s foundational autistic self-advocacy work argued that autism is not a deviation from a human norm but a different way of being human, one with its own forms of perception, communication, and community (Sinclair, 1993). From this perspective, the problem with terms like “subclinical” is not only that they imply diluted pathology but that they impose a clinical frame on what might be better understood as cultural difference: autism and high-BAP experience as subcultural rather than subclinical dimensions of human variation. This reframing has direct implications for what high-BAP individuals lack. The argument throughout this paper is that the absence of community, shared language, and explanatory frameworks leaves high-BAP individuals without resources to contest the field’s verdict. The cultural framing names that absence as a form of cultural displacement, not merely a diagnostic gap, inhabiting a social world organized by and for a different culture, without access to one’s own. The distress this produces is real, but its source is not the traits themselves; it is the structural condition of cultural foreignness without cultural recognition.
That cultural foreignness is not merely an internal experience; it is legible to others, and consistently evaluated. Research shows that neurotypical observers form negative first impressions of autistic adults within seconds based on nonverbal behavior and interaction style (Morrison et al., 2019; Sasson et al., 2017), judgments that likely extend to high-BAP individuals who display similar but more subtle differences. These are not simply social miscommunications. They are evaluations in which the social field appraises whether someone possesses the interactional style it recognizes as competent, trustworthy, and appropriately socialized. Where diagnosed individuals may disclose their diagnosis to contextualize their interaction style (Cage et al., 2019), high-BAP individuals lack this resource, leaving them not only vulnerable to misattribution but without any mechanism for contesting the field’s judgment. The evaluation stands, and without a framework to name it as structural, it becomes, over time, self-understanding.
Disability, Field, and Habitus: A Bourdieusian Account
The social model of disability argues that disability arises not from bodily or cognitive difference per se but from social barriers, attitudes, and structures that exclude or disadvantage people with particular characteristics (Kafer, 2013; Oliver, 1990). A wheelchair user is disabled by stairs and narrow doorways, not by their mobility difference itself. Similarly, an autistic person may be disabled by overwhelming sensory environments, unspoken social expectations, and demands for constant social performance, not by their neurology per se.
Bourdieu’s account of social practice offers a theoretical framework for understanding precisely why this happens, and why its consequences are so effectively naturalized (Bourdieu, 1977, 1990). For Bourdieu, social life is structured around fields, or organized areas of activity like workplaces, schools, or social events, each with its own unwritten rules, values, and rankings. Success in a field depends on having the right habitus: a system of lasting dispositions, instincts, and embodied tendencies that people develop through socialization and that give them an intuitive sense of how to act. Someone with the right habitus moves smoothly through the field—they know when to speak or stay silent, how to control eye contact, when a joke fits, and how to interpret unspoken social signals. This knowledge is not consciously taught; it becomes part of the body as a kind of social skill. Importantly, fields also confer cultural capital, or the social skills, credentials, and behavioral styles valued and rewarded in that field. People whose habitus matches the field’s needs gain this capital; those whose habitus does not can find themselves at a structural disadvantage that might be invisible to others, including themselves.
Bourdieu developed these concepts to explain how dominant, class-based groups maintain advantage by naturalizing their own dispositions as universal competence. Extending this framework to neurocognitive differences requires modification. The habitus of high-BAP individuals is not acquired primarily through socialization in a particular class position; it is shaped, at least in part, by how a particular nervous system perceives and responds to the social world. But the structural logic Bourdieu identified, that dominant norms become naturalized as the standard against which all participation is measured, that costs fall asymmetrically on those whose dispositions diverge, and that those costs are effectively internalized as personal inadequacy, operates across multiple axes of difference, not only class. Others have extended Bourdieu’s framework to gender, race, and disability on precisely these grounds, and to psychological research specifically (Wagner & McLaughlin, 2015). The extension proposed here follows the same logic.
The misrecognition mechanism that Bourdieu identifies, through which the dominated (in Bourdieu’s technical sense, those whose habitus diverges from field norms) come to experience their own domination as natural, even deserved, may require particular qualification here. For Bourdieu, misrecognition operates partly because dominated groups share, through socialization, enough of the dominant classificatory schema to evaluate themselves by its terms. High-BAP individuals may arrive at a similar outcome through a different route, not because they have fully internalized neurotypical norms as legitimate (although that may certainly play a role), but because those norms are so pervasively enforced, and so lacking in any alternative framework, that the field’s judgment has nowhere to land except as self-understanding. The absence of community, shared language, or diagnostic recognition means that the structural origin of the mismatch remains unnamed, and what remains unnamed tends to be absorbed as personal. The result is functionally similar to Bourdieusian misrecognition, even if the mechanism differs. The arbitrary becomes self-evident not through shared socialization but through the absence of any counter-narrative.
High-BAP individuals develop a habitus misaligned with the dominant social fields they must navigate, which are structured around neurotypical norms of interaction, conversation, emotional expression, and social reciprocity. This is not a minor incompatibility that can be fully overcome with effort. Habitus is acquired slowly, through years of socialization, and tends to persist; it cannot simply be exchanged for a more field-appropriate version at will. What neurotypical individuals experience as natural social fluency, the unreflective ease of everyday interaction, high-BAP individuals must approximate through conscious, deliberate effort. The asymmetry is structural: one group moves through the field; the other works to keep up. An example of this is camouflaging. From a Bourdieusian perspective, camouflaging is best understood as an attempt to acquire cultural capital that the dominant field systematically withholds from those whose habitus does not naturally conform. Radulski (2022), drawing on Ahmed and Fanon, theorizes this as the product of neurotypical hegemony and majority-group privilege operating as structural drivers of masking behavior, a formulation that converges with the Bourdieusian account from a different theoretical tradition.
What Bourdieu called symbolic violence, or the process by which dominant norms become naturalized, is where this dynamic becomes most damaging, rendering the arbitrary as self-evident and the structural as personal (Bourdieu & Wacquant, 1992). Symbolic violence does not require overt coercion; it operates through the internalization of the field’s judgments as one’s own. For high-BAP individuals, this manifests as the conviction that social difficulties reflect personal inadequacy rather than a structural mismatch. They do not think “the field is demanding a habitus I was not socialized into.” They think, “I am bad at people.” They do not recognize their exhaustion as the cost of sustained cultural labor. They experience it as failure. The absence of any explanatory framework, community, or language for neurodivergent experience means that symbolic violence operates largely unchallenged. That verdict becomes the individual’s self-understanding. Recent empirical work supports precisely this pathway. In a representative general population sample, internalized stigma predicted camouflaging through social anxiety, which in turn predicted adverse mental health outcomes—a chain of effects that maps closely onto the Bourdieusian account of how structural judgment becomes embodied as personal failure (Ai et al., 2024).
The clinical field provides a clear example of this dynamic. Women with high autistic traits who seek mental health support without a diagnosis are more often diagnosed with Borderline Personality Disorder rather than being recognized as neurodivergent (McQuaid et al., 2024). From a Bourdieusian perspective, this is not just misdiagnosis. It is the clinical field using its authority to label the mismatch, attributing it to the individual rather than the system. The traits that cause the mismatch, such as emotional intensity, challenges with reading implicit social cues, and exhaustion from ongoing social performance, are reinterpreted as symptoms of a disordered personality. The field’s verdict is then institutionalized in a diagnostic record, influencing future clinical interactions, treatment choices, and, importantly, how the individual understands herself. Symbolic violence here operates not through informal social judgment but through the concentrated authority of clinical practice. The woman who leaves a psychiatric appointment with a BPD diagnosis has not just been misunderstood; she has been given an authoritative label that makes it harder, not easier, to see the structural roots of her struggles. This illustrates how the arbitrary can be made self-evident by an institution with the power to enforce it.
The Bourdieusian account also clarifies the relational understanding of disability. Applied to BAP, high-BAP traits become disabling primarily in fields that demand neurotypical habitus and reward neurotypical cultural capital: open-plan offices, unstructured social gatherings, and workplaces that prize constant networking and improvisational social performance. A high-BAP individual might accumulate capital readily in a field structured around deep expertise, clear rules, and predictable interaction, but find themselves systematically disadvantaged in fields where social fluency is the primary currency. The traits themselves have not changed; what has changed is the degree of mismatch between the individual’s habitus and the field’s demands. “Impairment,” in this view, is not a fixed property of the individual but a relational outcome produced at the intersection of a particular habitus and a particular field (Anastasiou & Kauffman, 2013; Shakespeare, 2006).
This framework has a direct and uncomfortable implication for current clinical practice. Social skills training often aims to teach neurodivergent individuals to make more naturalistic eye contact, modulate their conversational style, and read implicit social cues more reliably. Within a deficit model, this is straightforwardly therapeutic, as it addresses the impairment. From within the Bourdieusian account, it looks quite different. If masking is cultural labor rather than symptom compensation, and if it is the labor of performance itself rather than the underlying trait profile that most directly predicts adverse mental health outcomes (Ai et al., 2024; Somerville et al., 2024), then training people to mask more effectively is not reducing harm. Rather, it is increasing the demand for the very expenditure that produces it. The clinical field, in this reading, is not helping high-BAP individuals adapt to their environment; it is recruiting them into greater performance of neurotypical capital at greater personal cost, while framing that recruitment as treatment.
This does not mean social skills training is never appropriate or wanted. Some individuals actively seek these skills, find them useful, and experience them as expanding rather than constraining their repertoire. The point is not that the intervention is always harmful but that its framing as therapeutic rather than adaptive is doing ideological work—naturalizing the neurotypical field’s demands as the fixed point around which the individual must reorganize, rather than asking whether those demands are themselves the problem. A socially relational approach would reorient clinical goals not toward helping high-BAP individuals more efficiently approximate a neurotypical habitus, but toward reducing the extent to which neurotypical capital is the only capital that counts, through environmental modification, advocacy for structural accommodation, and psychoeducation that names the mismatch as structural rather than personal.
The social-relational model clarifies diagnostic thresholds, with terms such as “subclinical” or “subthreshold” BAP implying a diluted pathology specific to the disorder (Kapp, 2020). Diagnostic thresholds are pragmatic, shaped by clinical consensus, culture, service access, and administration, rather than by natural neurobiological boundaries (Jutel, 2009; Rosenberg, 2002). No consistent biomarkers reliably distinguish autistic individuals from those without, and neurobiological heterogeneity within autism often exceeds inter-group differences, with studies showing substantial overlap around diagnostic cutoffs (Brunsdon & Happé, 2014; Ecker, 2017; Lai et al., 2014; Lombardo et al., 2019). Recent evidence suggests autism may be categorical at the diagnostic level, but quantitative symptom measures better explain relationships with other factors (Frazier et al., 2023). Whether BAP is a discrete pattern or part of a neurotypical spectrum remains unresolved. The pragmatic nature of thresholds and their impact on those below them are not settled by evidence of categorical structure.
None of this means that diagnosis is meaningless. Clinical criteria play important roles in organizing services and identifying those with the greatest support needs (Jutel, 2009). Diagnoses can offer validation, explanation, and community access, thereby substantially enhancing quality of life (Crane et al., 2021; Lewis, 2017). The neurodiversity paradigm and social model challenge the automatic equation of difference with deficit and criticize prioritizing conformity over well-being (Kapp, 2020; Pellicano & den Houting, 2022). Thus, the threshold or diagnostic function is less a marker of pathology and more a gatekeeper determining who receives recognition and support for their neurocognitive differences (Russell et al., 2019). The Bourdieusian perspective clarifies the costs of gatekeeping. It leaves high-BAP individuals without the key resource that might enable them to name and challenge the mismatch they experience.
A social-relational reframing understands high BAP as a site of structural mismatch: individuals carry a habitus, a genuine, coherent set of dispositions, perceptual tendencies, and ways of engaging with the world, that is systematically misaligned with the environments they are required to inhabit. These environments, built around neurotypical norms of interaction, communication, and social performance, normalize a particular interaction style as the standard against which competence, likability, and social fitness are measured. High-BAP individuals are not deficient versions of neurotypical people; they are people whose habitus generates real competencies and authentic ways of relating, but who must navigate fields that do not recognize or reward those competencies in the same way. The experience of high BAP, therefore, is not mainly about deficits but about structural foreignness: the ongoing, deliberate effort of inhabiting contexts designed for a different kind of mind. This foreignness is compounded by the absence of any framework to name it. Without community, shared language, or explanatory frameworks, high-BAP individuals have no grounds on which to contest the field’s verdict. The next section outlines what that experience should look like and identifies what research has not yet been designed to find.
Living the Mismatch: High-BAP Experience in Neurotypical Fields
The habitus–field account generates specific predictions about what high-BAP experience should look like, predictions that existing research has not been designed to test. This section derives those predictions from the framework, draws on adjacent literatures where evidence is suggestive, and identifies what each prediction requires empirically that we do not yet have. It is an account of the contours of high-BAP experience that a social-relational framework makes visible, not a summary of established findings. A further limitation applies throughout. The empirical sources drawn on here share many of the sampling biases previously identified—predominantly white, Western, and relatively well-resourced samples. The predictions should be understood as applying most directly to high-BAP individuals in similar demographic contexts, and as requiring intersectional extension before they can claim broader applicability.
The Cost of Cultural Labor: Masking and Social Exhaustion
A social-relational framework grounded in a Bourdieusian perspective predicts a persistent, largely invisible gap between how high-BAP individuals appear socially and the actual costs of social interaction. Someone who makes eye contact, contributes to conversation, and navigates workplace relationships adequately may be doing so through sustained deliberate effort—monitoring body language, planning conversational turns, suppressing responses that feel natural in favor of ones that will read as appropriate, reviewing interactions afterward for signs of failure. This is what cultural labor looks like at the level of experience, not compensation for a deficit, but the effort of performing fluency in a social language one was not raised to speak. Critically, because the performance often succeeds, the labor behind it goes unrecognized by interaction partners, employers, and, frequently, the individuals themselves. The framework predicts that this invisibility is structural rather than incidental. When habitus mismatch is unnamed, its costs have nowhere to land except as private experience.
Adjacent evidence is suggestive. Camouflaging is well documented in autistic populations (Cook et al., 2021), and Milner et al. (2023) found it occurs among individuals with high autistic traits who have not received a diagnosis. Preliminary findings in nonautistic adults indicate that camouflaging predicts mental health outcomes independently of trait levels, and more strongly in women (Ai et al., 2024; Somerville et al., 2024). But this literature cannot yet confirm the mechanism the framework specifies, that it is the labor of performance itself, rather than the underlying trait profile, that drives outcomes, and that this labor is experienced as ordinary social life rather than recognized as effortful. What is needed is research that captures the phenomenology of social interaction for high-BAP individuals in real time, including what it costs, how it varies by context, and whether its invisibility to others is matched by invisibility to the individuals themselves. The framework also predicts a substantial recovery time after social events, not from disinterest but from genuine depletion. This pattern is documented in autistic populations (Cage & Troxell-Whitman, 2019; Hull et al., 2017) but has not been examined in high-BAP samples. Whether the same dynamic operates below the diagnostic threshold and, if so, at what intensity, is an open empirical question.
Self-Attribution and the Internalization of Field Judgments
The symbolic violence mechanism generates a specific prediction about self-attribution such that high-BAP individuals should perceive themselves as different, without a framework to explain why. The field’s negative evaluation, delivered through social exclusion, professional setbacks, or the accumulated experience of interactions that feel slightly wrong, lands without any mechanism for contesting it. The framework predicts this produces a characteristic pattern of internalization: hypervigilance experienced as anxiety, interaction difficulty experienced as social incompetence, and habitus mismatch experienced as a personality flaw. The structural then becomes personal, not because high-BAP individuals are especially prone to self-blame, but because nothing in their environment names the mismatch as structural. That verdict, delivered repeatedly and absorbed without a counter-narrative, becomes self-understanding.
There is some evidence to support this prediction. Ai et al. (2024) found that internalized stigma predicted camouflaging through social anxiety, which in turn predicted adverse mental health outcomes in a general population sample, a chain that maps onto the Bourdieusian account of how structural judgment becomes embodied as personal failure. The clinical field offers the sharpest illustration of this dynamic, examined in the previous section. When the institutional verdict names habitus mismatch as personality disorder, symbolic violence operates with particular authority and leaves the individual with an account of themselves that makes the structural origin of their difficulties harder, not easier, to recognize. But confirming the framework’s prediction requires more than outcome data. What is needed is research that tracks the subjective experience of self-attribution in high-BAP individuals—whether and how they make sense of their social difficulties, whether neurodivergent frameworks alter that self-understanding when they become available, and what the lived difference is between having and lacking an explanatory account of one’s own experience.
The absence of community and shared language is predicted to be particularly consequential here. Unlike diagnosed autistic individuals, who may draw on their diagnosis and community membership to contest the field’s judgment (Cage et al., 2019; Lewis, 2017), high-BAP individuals typically lack this resource. The framework predicts that access to neurodivergent frameworks, whether through late diagnosis, community contact, or psychoeducation, should function as a counter to symbolic violence by naming the mismatch as structural. Whether this prediction holds, and under what conditions, is an unanswered empirical question.
Field-Dependent Disability: The Role of Context
One of the clearest predictions of the habitus–field theory is that the same person, with the same traits, should produce very different outcomes depending on the context, not because their traits change but because different fields demand different things from habitus. A high-BAP individual should be able to gather capital easily in a field structured around expertise, clear rules, and predictable interaction, while they may systematically struggle in fields where social fluency is the main currency (i.e., open-plan workplaces, informal networking, environments that value improvisational social skills, etc.). The point is that trait severity is a poor predictor of outcomes; the field’s demands should explain more.
This prediction is consistent with available evidence in autistic populations but has not yet been directly tested in high-BAP samples. In autistic populations, environmental demands rather than trait severity are among the primary determinants of functional outcomes (Kapp et al., 2013; Scott et al., 2019). Demizu et al. (2022) found that autistic traits predicted social but not occupational functioning in a general population sample, a domain specificity that makes sense if field demands, not traits per se, are driving the effect. But neither study was designed to test the field-dependence prediction directly, and neither examined high-BAP individuals as a distinct group. What is needed is research that systematically varies context—tracking the same individuals across fields with different neurotypical demands—to establish whether outcomes follow field structure as the framework predicts.
Life transitions are effective for testing this prediction because they reshape the environment, exposing habitus mismatches that were previously less noticeable. Moving from school to university, to work, or from contributor to manager, shifts which forms of capital are important, and the level of social fluency needed. The framework indicates high-BAP individuals will find these transitions especially disorienting, not because they are more difficult but because the changes challenge their habitus. Late-diagnosed autistic adults show this pattern (French & Cassidy, 2026), and the framework predicts that high-BAP individuals will experience it similarly, without any explanatory framework. Longitudinal research tracking high-BAP individuals during major life changes could test this.
Beyond the Social: Sensory, Executive, and Intersecting Dimensions
The habitus–field account extends beyond the social domain, generating parallel predictions about sensory and executive experience. Elevated sensory sensitivities are documented in high-BAP populations (Robertson & Simmons, 2013), and the framework predicts these represent an additional dimension of field mismatch. Environments designed for neurotypical sensory tolerances become dysregulating for those whose sensory habitus differs. Executive function differences are similarly documented in high-BAP samples (Losh et al., 2008), and the framework predicts that they should be experienced as mismatches between cognitive style and field expectations rather than as personal failings. Both sensory and executive function specificities are predicted to be interpreted, in the absence of any explanatory framework, as individual inadequacy: sensory overwhelm becomes oversensitivity; executive difficulty becomes laziness or disorganization. Whether this internalization follows the same symbolic violence pathway as social difficulties, and whether naming the mismatch as structural has the same counter-effect in these domains, are questions that remain entirely unexamined in high-BAP populations.
The framework also predicts that these experiences should be compounded by intersecting identities, and this is where the inferential distance from existing evidence is greatest. High-BAP individuals from marginalized racial, gender, or socioeconomic backgrounds should navigate compounded mismatches, contending simultaneously with the demands of neurotypical fields and with the additional labor of navigating fields structured around whiteness, cisnormativity, or class privilege (Crenshaw, 1989). The masking and code-switching required across these dimensions are predicted to compound one another in ways that single-axis accounts cannot capture. This prediction is theoretically derivable from the framework but, empirically, is almost entirely unexamined. Peer-reviewed work at the intersection of race and neurodivergence remains sparse (Pearson & Rose, 2021; Radulski, 2022), and high-BAP samples specifically have not been studied intersectionally at all. This is not a peripheral gap. If the framework is correct, that field demands and habitus mismatch are the primary drivers of outcome, then the most disadvantaged high-BAP individuals, those navigating multiple simultaneous mismatches, are precisely those most absent from existing research.
Implications and Future Directions
Before turning to the research, clinical, and theoretical implications of a social-relational reframing of BAP, it is worth addressing three objections that this framework predictably invites. The first is that applying neurodiversity scholarship’s structural insights to high-BAP individuals expands pathologization. This concern misreads the direction of the argument. Where the etiological model pathologizes, framing high BAP as a subclinical disorder and genetic liability, a social-relational reframing moves in the opposite direction, locating difficulties in structural mismatch rather than in individual deficit and proposing accommodation rather than treatment (Chapman, 2020; Walker, 2014).
The second objection is practical: without diagnostic thresholds, how do we determine who receives services? This critique assumes diagnosis should be the sole arbiter of support, an assumption disability rights frameworks have long questioned (Kafer, 2013). Much of what high-BAP individuals might benefit from requires no formal clinical infrastructure (e.g., psychoeducation about neurodivergence, validation of experience, permission to advocate for environmental adjustments). Where formal accommodations are relevant, the question should be whether functional need is present, not whether a diagnostic threshold has been crossed. Universal design principles benefit neurodivergent and neurotypical individuals alike and need not be rationed by diagnosis (Dolmage, 2017).
The third objection is that emphasizing dimensional traits risks trivializing narratives—“everyone’s a little autistic”—that dismiss genuine difficulty and undermine diagnosed communities. The argument here is not that autistic traits are universal. High BAP represents the upper end of trait distribution in non-diagnosed populations, approximately 15–20% of individuals, not average human experience (Sasson et al., 2013; Wainer et al., 2011). Recognizing meaningful neurocognitive differences below diagnostic thresholds does not flatten the spectrum; it extends recognition more accurately along it.
Research: New Questions and Methods
Standardized instruments like the BAPQ remain valuable for identifying individuals with elevated autistic traits, but the questions derived in the previous section require methods that capture how high-BAP traits are lived rather than merely measured. Several research directions follow directly from the proposed framework. First, ecological momentary assessment could track high-BAP experiences in real time, identifying which contexts generate the greatest habitus–field mismatch, how masking effort varies across settings, and whether recovery patterns follow the depletion the proposed framework predicts (Chen et al., 2025). Second, longitudinal studies are needed to examine how high-BAP traits interact with major life transitions—the moments when field demands shift suddenly and existing compensatory strategies may no longer suffice. Third, social perception research should examine how neurotypical others evaluate high-BAP individuals, whether information about neurodivergence alters these evaluations, and how the double empathy problem manifests in everyday interaction rather than laboratory settings (Crompton et al., 2021).
The familial sampling bias must be actively corrected. A growing body of research has examined BAP traits in community and college samples, documenting associations with loneliness, social difficulties, and internalizing symptoms (Jobe & White, 2007; Kurtz et al., 2023; Riccio et al., 2020), but this work remains largely quantitative and outcome-focused. Future research should recruit from diverse community contexts, ask qualitative experiential questions, and treat high-BAP individuals as collaborators rather than subjects—including neurodivergent researchers on teams and building in reflexivity about how researchers’ own neurotypes shape their understanding (Fletcher-Watson et al., 2019).
Intersectional research is particularly urgent. How is high-BAP experience shaped by gender identity, given emerging evidence of elevated autistic traits in gender-diverse populations (Warrier et al., 2020)? How do race, ethnicity, and culture affect the expression, recognition, and interpretation of BAP traits? How does socioeconomic position affect access to environments that accommodate neurocognitive difference? These questions are not peripheral to understanding high BAP. They are central to understanding whose experiences the current research paradigm has systematically failed to capture.
Theoretical Implications: Toward a Fuller Account of Neurocognitive Diversity
The reframing of BAP contributes to broader conversations in psychology about the limits of categorical diagnostic systems for capturing neurodevelopmental variation. If high-BAP individuals experience meaningful neurocognitive differences and face real challenges yet fall outside diagnostic boundaries, this reveals an inadequacy not only in BAP research but also in how psychology conceptualizes the relationship among traits, thresholds, and support needs. Diagnosis has served as a proxy for recognition, a gatekeeper determining whose difficulties count, in ways that reflect administrative convenience as much as neurobiological reality.
The Bourdieusian account of habitus and field offers psychology a more structurally sophisticated vocabulary for understanding neurocognitive diversity than person–environment fit models alone provide. It explains not just that mismatches exist but why they are systematically produced and maintained, why their costs fall asymmetrically on those whose habitus diverges from field norms, and why those costs are so reliably internalized as personal failure. This has implications beyond BAP. Wherever psychology studies dimensional traits that generate person–environment mismatches—such as ADHD, sensory processing differences, and personality variation at subdiagnostic levels—the same structural dynamics are likely at work. Importing sociological frameworks that can name those dynamics is not a departure from psychological science but an enrichment of it. This raises questions about neurodevelopmental research as a Bourdieusian field, focusing on what types of capital it distributes and to whom. Etiological research on BAP has gained prestige, funding, and legitimacy, not because genetic questions are inherently more important but because the field’s habitus favors them as more rigorous and publishable.
The reflexive perspective of the Bourdieusian approach to etiological research must be applied consistently, including in relation to the neurodiversity paradigm this paper discusses as a corrective. Neurodiversity scholarship is itself a field in Bourdieu’s sense. It has its own habitus, its own forms of legitimate capital, and its own mechanisms for deciding which voices and questions are important. Scholars within neurodiversity studies have identified several of these dynamics: the paradigm centers autism while leaving the boundaries of neurodivergence unexamined (Stenning & Bertilsdotter Rosqvist, 2021); its non-disorder claims are most defensible for high-functioning presentations, raising questions about whose experiences it represents (Hughes, 2021; Jaarsma & Welin, 2012); and it has largely overlooked Global Southern epistemologies and the intersectional experiences of racialized neurodivergent individuals, reproducing a predominantly white, Global Northern knowledge base (Nair et al., 2026). A Bourdieusian reframe that uncritically incorporates neurodiversity scholarship risks reproducing these dynamics rather than challenging them. The purpose is not to replace one field’s habitus with another’s but to use the framework’s structural logic to examine what any paradigm tends to naturalize, whose experiences it centers, and whose it makes invisible.
Conclusion
This paper has argued that the BAP, as currently understood, is an incomplete concept, not because heritability research is incorrect, but because it was designed to answer questions that are not the only important ones. This incompleteness is constitutive rather than contingent. There is no fully determinate biological BAP waiting to be uncovered, only shared biologies and forms of life embedded in social relations that any purely etiological account will systematically misread. By applying Bourdieu’s sociology of practice to the study of BAP, this paper has proposed an account capable of explaining not just the distribution of autistic traits but their social significance: why they lead to consistent disadvantages, why that disadvantage is experienced as personal failure, and why the research paradigm has been slow to recognize either.
These are not simply more empathic takes on existing deficit models; they are distinct claims with different implications. A deficit model asks what is wrong with the individual and how to fix it. A Bourdieusian view asks what is wrong with the field and who benefits from its current configuration. The former targets individual intervention, while the latter focuses on social structures creating disadvantage. Masking is not compensation but cultural labor. Social exhaustion is not a symptom but the cost of performing social fluency. Self-blame is not a cognitive distortion but symbolic violence, making the structural personal, as Bourdieu described.
The dominance of etiological research on BAP reflects more than scientific interest or feasibility. As Bourdieusian theory predicts, it results from a field organizing around a habitus that values genetic and neurobiological explanations as rigorous, viewing experiential and sociological questions as secondary. Funding, prestige, and careers have been built within an infrastructure that rewards etiological precision. Researchers within this field did not intentionally ignore human meaning; they were socialized into a set of dispositions that prioritized certain questions over others. This habitus explains the gap not as an oversight but as a structural outcome of 30 years of measuring traits with limited exploration of their human significance. This is not a critique of individual researchers but an application of the same analytical lens used throughout, now turned on the institution doing the analysis. If symbolic violence makes the arbitrary seem self-evident, then the key question is not just what research has found but what it has obscured. For high-BAP individuals, invisibility has been the cost: decades of measurement without a clear understanding of their lives. Whether the field is ready to ask this is not just an intellectual matter but a question of whose experiences are taken seriously and whose are excluded by the field’s own logic.
Footnotes
Ethical Considerations
This paper is a theoretical review and does not report empirical research involving human participants, human data, or human tissue. Ethical approval was not required.
Consent to Participate
Not applicable.
Consent for Publication
Not applicable.
Funding
The author received no financial support for the research, authorship, and/or publication of this article.
Declaration of Conflicting Interests
The author declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Data Availability Statement
Not applicable. This paper is a theoretical review, and no datasets were generated or analyzed.
