Sociology of Health & Illness

Papers
(The TQCC of Sociology of Health & Illness is 4. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-04-01 to 2024-04-01.)
ArticleCitations
Beyond deficit: ‘strengths‐based approaches’ in Indigenous health research63
Health inequalities, fundamental causes and power: towards the practice of good theory38
Understanding and managing uncertainty in health care: revisiting and advancing sociological contributions36
Gender, socioeconomic status, and COVID‐19 vaccine hesitancy in the US: An intersectionality approach33
Can digital data diagnose mental health problems? A sociological exploration of ‘digital phenotyping’31
Towards a sociological understanding of medical gaslighting in western health care29
Social networks and health in later life: a state of the literature29
Masculinities, emotions and men’s suicide28
“No one associates alcohol with being in good health”: Health and wellbeing as imperatives to manage alcohol use for young people28
Populism and health policy: three international case studies of right‐wing populist policy frames25
Media framing of fighting COVID‐19 in China22
Exclusion and hospitality: the subtle dynamics of stigma in healthcare access for people emerging from alcohol and other drug treatment22
Coronavirus (COVID‐19), pandemic psychology and the fractured society: a sociological case for critique, foresight and action20
Trust, affect, and choice in parents’ vaccination decision‐making and health‐care provider selection in Switzerland20
Feeding inequality: food insecurity, social status and college student health19
Emerging contaminants, coerced ignorance and environmental health concerns: The case of per‐ and polyfluoroalkyl substances (PFAS)18
Race/ethnicity, gender and the SES gradient in BMI: The diminishing returns of SES for racial/ethnic minorities18
Patient data work: filtering and sensing patient‐reported outcomes18
Fertility and digital technology: narratives of using smartphone app ‘Natural Cycles’ while trying to conceive17
Intersectional analysis of cannabis use, stigma and health among marginalized Nigerian women16
What does the literature mean by social prescribing? A critical review using discourse analysis16
The diffusion of innovative diabetes technologies as a fundamental cause of social inequalities in health. The Nord‐Trøndelag Health Study, Norway16
‘Willy nilly’ doctors, bad patients, and resistant bodies in general public explanations of antimicrobial resistance16
Re‐ordering connections: UK healthcare workers' experiences of emotion management during the COVID‐19 pandemic15
What would it take to meaningfully attend to ethnicity and race in health research? Learning from a trial intervention development study15
‘That thing in his head’: Aboriginal and non‐Aboriginal Australian caregiver responses to neurodevelopmental disability diagnoses15
Implications of internalised ableism for the health and wellbeing of disabled young people15
Non‐human matter, health disparities and a thousand tiny dis/advantages15
The violence of narrative: embodying responsibility for poverty‐related stress15
Children's active outdoor play: ‘good’ mothering and the organisation of children's free time15
Why doesn’t integrated care work? Using Strong Structuration Theory to explain the limitations of an English case14
How men step back – and recover – from suicide attempts: A relational and gendered account14
Destabilising social inclusion and recovery, and pursuing 'lines of flight' in the mental health sector14
‘And breathe…’? The sociology of health and illness in COVID‐19 time13
Air care: an ‘aerography’ of breath, buildings and bugs in the cystic fibrosis clinic13
The COVID‐19 pandemic and cause of death13
Social vulnerability and the impact of policy responses to COVID‐19 on disabled people13
A sociology of precision‐in‐practice: The affective and temporal complexities of everyday clinical care13
Place of alcohol in the ‘wellness toolkits’ of midlife women in different social classes: A qualitative study in South Australia13
‘You're just a locum’: professional identity and temporary workers in the medical profession13
‘You Have to Withstand That Because You Have Come for What You Have Come for’: Barriers and facilitators to antiretroviral treatment access among older South Africans living with HIV12
Frailty as biographical disruption12
Women’s empowerment and their experience to food security in rural Bangladesh12
Body mass index is just a number: Conflating riskiness and unhealthiness in discourse on body size12
Essentially invisible: risk and personal support workers in the time of COVID‐1912
Universal HIV testing and treatment and HIV stigma reduction: a comparative thematic analysis of qualitative data from the HPTN 071 (PopART) trial in South Africa and Zambia11
Obese societies: Reconceptualising the challenge for public health11
Negotiating identities of ‘responsible drinking’: Exploring accounts of alcohol consumption of working mothers in their early parenting period11
Delivering healthcare’s ‘triple aim’: electronic health records and the health research participant in the UK National Health Service11
Tracking towards care: Relational affordances of self‐tracking in gym culture11
In a vigilant state of chronic disruption: how parents with a young child with type 1 diabetes negotiate events and moments of uncertainty11
Material Citizenship: An ethnographic study exploring object–person relations in the context of people with dementia in care homes10
A delicate balance between control and flexibility: Experiences of care and support among pre‐teenage children with type 1 diabetes and their families10
Discussing the effects of prostate cancer beyond biographical disruption and new normalcy: the experiences of men with prostate cancer in Germany10
How does cultural capital keep you thin? Exploring unique aspects of cultural class that link social advantage to lower body mass index10
Excitable models: Projections, targets, and the making of futures without disease9
Biological costs and benefits of social relationships for men and women in adulthood: The role of partner, family and friends9
“We’re just stuck in a daily routine”: Implications of the temporal dimensions, demands and dispositions of mothering for leisure time physical activity9
Desynchronised times? Chronobiology, (bio)medicalisation and the rhythms of life itself9
The impossibility of engaged research: Complicity and accountability between researchers, ‘publics’ and institutions9
Hepatitis C cure as a ‘gathering’: Attending to the social and material relations of hepatitis C treatment9
Assembling care: How nurses organise care in uncharted territory and in times of pandemic9
Wild data: how front‐line hospital staff make sense of patients’ experiences9
Shame in a post‐socialist society: a qualitative study of healthcare seeking and utilisation in common mental disorders9
Feeling less alone online: patients’ ambivalent engagements with digital media9
Is the end in sight? A study of how and why services are decommissioned in the English National Health Service8
Structuring unequal relations: role trajectories in informal dementia care8
Community pharmacy and public health: preserving professionalism by extending the pharmacy gaze?8
Family imaginaries in the disclosure of a blood‐borne virus8
Triage as an infrastructure of care: The intimate work of redistributing medical care in nursing homes8
Ambivalent anticipation: How people with Alzheimer’s disease value diagnosis in current and envisioned future practices8
Attending to child agency in paediatric palliative care consultations: Adults’ use of tag questions directed to the child8
Exploring the relevance of intersectionality in Australian dietetics: Issues of diversity and representation8
‘A holistic approach’: incorporating sustainability into biopedagogies of healthy eating in Sweden’s dietary guidelines8
Managing death: navigating divergent logics in end‐of‐life care8
Experiential expertise in the co‐development of social and health‐care services: Self‐promotion and self‐dismissal as interactional strategies8
Managing (im) patience of nurses and nurse's aides: Emotional labour and normalizing practices at geriatric facilities8
Professional boundary struggles in the context of healthcare change: the relational and symbolic constitution of nursing ethos in the space of possible professionalisation8
Obligatory medical prescription of antibiotics in Russia: Navigating formal and informal health‐care infrastructures7
The ‘normality’ of living as a gay serodiscordant couple in Sydney, Australia7
Forms of resistance in people with severe and profound intellectual disabilities7
Intra‐familial health polarisation: how diverse health concerns become barriers to health behaviour change in families with preschool children and emerging obesity7
Drug fatalities and treatment fatalism: Complicating the ageing cohort theory7
Sitting as a moral practice: Older adults’ accounts from qualitative interviews on sedentary behaviours7
Platform encounters: A study of digitised patient follow‐up in HIV care7
Health consequences of child removal among Indigenous and non‐Indigenous sex workers: Examining trajectories, mechanisms and resiliencies7
The social meanings of PrEP use – A mixed‐method study of PrEP use disclosure in Antwerp and Amsterdam7
Mindfulness and the ‘psychological imagination’7
Enacting evidence‐based medicine in fertility care: Tensions between commercialisation and knowledge standardisation7
‘You're only there on the phone’? A qualitative exploration of community, affect and agential capacity in HIV self‐testing using a smartphone app7
Depressive symptoms and perception of risk during the first wave of the COVID‐19 pandemic: A web‐based cross‐country comparative survey7
The impact of financialisation on public health in times of COVID‐19 and beyond7
Effect of caste on health, independent of economic disparity: evidence from school children of two rural districts of India7
Frying eggs or making a treatment plan? Frictions between different modes of caring in a community mental health team7
How companions speak on patients’ behalf without undermining their autonomy: Findings from a conversation analytic study of palliative care consultations7
“They created a team of almost entirely the people who work and are like them”: A qualitative study of organisational culture and racialised inequalities among healthcare staff7
Making sense of experiences in suicide helpline calls: Offering empathy without endorsing suicidal ideation7
Impact of COVID‐19 inequalities on children: An intersectional analysis7
Searching for diagnostic certainty, governing risk: Patients' ambivalent experiences of medical testing7
Linking socioeconomic disadvantage to healthiness of food practices: Can a practice‐theoretical perspective sharpen everyday life analysis?7
Uncomfortable science: How mathematical models, and consensus, come to be in public policy7
‘Your wealth is your health’: the fundamental causes of inequalities in diabetes management outcomes: a qualitative analysis7
The mask trap: from symbol of preparation to symbol of negligence—understanding the ambiguous relationships between face masks and the French public decision‐makers17
Men, suicide, and family and interpersonal violence: A mixed methods exploratory study7
Precision patients: Selection practices and moral pathfinding in experimental oncology7
Knowing (with) the body: Sensory knowing in contraceptive self‐tracking6
An ethnocultural perspective on loneliness in young adulthood: A population‐based study in Israel6
Constituting link working through choice and care: An ethnographic account of front‐line social prescribing6
Mapping mental health inequalities: The intersecting effects of gender, race, class, and ethnicity on ADHD diagnosis6
Experiences of face mask use during the COVID‐19 pandemic: A qualitative study6
Black knowledges matter: How the suppression of non‐white understandings of dementia harms us all and how we can combat it6
COVID‐19, public health, and the politics of prevention6
Overdiagnosis and overtreatment: a sociological perspective on tackling a contemporary healthcare issue6
In their own words: A narrative analysis of illness memoirs written by men with prostate cancer6
From ‘dirty wound care’ to ‘woundology’: A professional project for wound healing clinicians6
Interrogating inclusion with youths who use augmentative and alternative communication6
Epistemic injustices in clinical communication: the example of narrative elicitation in person‐centred care6
Performing care: emotion work and ‘dignity work’ – a joint autoethnography of caring for our mum at the end of life6
The health effects of wage setting institutions: How collective bargaining improves health but not because it reduces inequality6
Is it an issue before it’s a problem? Investigating men’s talk about fertility6
Men, chronic illness and healthwork: accounts from male partners of women with endometriosis6
Prescribing as affective clinical practice: Transformations in sexual health consultations through HIV pre‐exposure prophylaxis6
Burnout as an identity rupture in the life course: a longitudinal narrative method6
A ‘patient–industry complex’? Investigating the financial dependency of UK patient organisations on drug company funding6
‘My relationships have changed because I’ve changed’: biographical disruption, personal relationships and the formation of an early menopausal subjectivity6
From more‐than‐human solidarity to multi‐species biographical value: insights from a veterinary school about ethical dilemmas in One Health promotion6
Vaccine hesitancy and emerging parental norms: A qualitative study in Taiwan6
Moral barriers to HIV prevention and care for gay and bisexual men: Challenges in times of conservatism in Brazil6
Risk, trust and patients’ strategic choices of healthcare practitioners6
Biologically infallible? Men’s views on male age‐related fertility decline and sperm freezing5
Unpacking ‘patient‐centredness’: how knowledge is negotiated dialogically in the interweaving of genres and voices in counselling conversations5
Getting back to normal? Identity and role disruptions among adults with Long COVID5
Fat shaming under neoliberalism and COVID‐19: Examining the UK’s Tackling Obesity campaign5
‘I just don’t think it’s that natural’: adolescent mothers’ constructions of breastfeeding as deviant5
Theorising rehabilitation: Actors and parameters shaping normality, liminality and depersonalisation in a UK hospital5
The practice of participatory action research: Complicity, power and prestige in dialogue with the ‘racialised mad’5
‘Who cares if you're poz right now?’: Barebackers, HIV and COVID‐195
Physician dominance in the 21st century: Examining the rise of non‐physician autonomy through prevailing theoretical lenses5
Inter‐professional practice in the prevention and management of child and adolescent self‐harm: foster carers’ and residential carers’ negotiation of expertise and professional identity5
‘Black African’ identification and the COVID‐19 pandemic in Britain: A site for sociological, ethical and policy debate5
Stigma, mental illness & ethnicity: Time to centre racism and structural stigma5
Experiences and meaning of loneliness beyond age and group identity5
Defining patient’s experiential knowledge: Who, what and how patients know. A narrative critical review5
An incongruous intervention: Exploring the role of anti‐institutionalism in less‐educated individual’s limited uptake of nutrition information5
Post‐place care: disrupting place‐care ontologies5
Compulsory separation of women prisoners from their babies following childbirth: Uncertainty, loss and disenfranchised grief5
Appraising screening, making risk in/visible. The medical debate over Non‐Rare Thrombophilia (NRT) testing before prescribing the pill5
Patient experience data as enacted: Sociomaterial perspectives and ‘singular‐multiples’ in health care quality improvement research5
Troubling content: Guiding discussion of death by suicide on social media5
The exchange and use of cultural and social capital among community health workers in the United States5
Advising without personalising: how a helpline may satisfy callers without giving medical advice beyond its remit5
Parents' management of alcohol in the context of discourses of ‘competent’ parenting: A qualitative analysis5
Reordering the machinery of participation with young people5
Integrating fundamental cause theory and Bourdieu to explain pathways between socioeconomic status and health: the case of health insurance denials for genetic testing5
Can HIV‐positive gay men become parents? How men living with HIV and HIV clinicians talk about the possibility of having children5
‘We're responsible for the diagnosis and for finding help’. The help‐seeking trajectories of families of children on the autism spectrum5
Epistemic in/justice in patient participation. A discourse analysis of the Dutch ME/CFS Health Council advisory process5
Interrogating the promise of technology in epilepsy care: systematic, hermeneutic review4
Theorising health professionals’ prevention and management practices with children and young people experiencing self‐harm: a qualitative hospital‐based case study4
Biographical accounts of the impact of fatigue in young people with sickle cell disease4
The different facets of ‘experiential knowledge’ in Swedish women’s claims about systemic side effects of the copper intrauterine device4
Valuing Black lives and the ‘Good Death’ in the United States4
Data protection, information governance and the potential erosion of ethnographic methods in health care?4
Digital health: A sociomaterial approach4
Paradoxes of professional autonomy: a qualitative study of U.S. neonatologists from 1978‐20174
Overcoming adversity: a grounded theory of health management among middle‐aged and older gay men4
Gendered social practices in reproductive health: A qualitative study exploring lived experiences of unwed single mothers in China4
At the limits of “capability”: The sexual and reproductive health of women migrant workers in Malaysia4
Desire over damage: Epistemological shifts and anticolonial praxis from an indigenous‐led community health project4
Maintaining ordinariness in dementia care4
Psychosocial resilience among left‐behind adolescents in rural Thailand: A qualitative exploration4
Understanding adolescent health risk behaviour and socioeconomic position: A grounded theory study of UK young adults4
‘So just to go through the options…’: patient choice in the telephone delivery of the NHS Improving Access to Psychological Therapies services4
Off the record: The invisibility work of doctors in a patient‐accessible electronic health record information service4
‘I am just a shadow of who I used to be’—Exploring existential loss of identity among people living with chronic conditions of Long COVID4
From community of practice to epistemic community – law, discipline and security in the battle for the legalisation of medical cannabis in Poland4
Running out of time: The case of patient advocacy for ovarian cancer patients' access to PARP inhibitors4
Can a disability studies‐medical sociology rapprochement help re‐value the work disabled people do within their rehabilitation?4
Off‐label prescribing of stimulant medication to students: a qualitative study on the general practitioner perspective4
Disease surveillance infrastructure and the economisation of public health4
Experiential knowledge in mental health services: Analysing the enactment of expertise in peer support4
Researching the health and social inequalities experienced by European Roma populations: Complicity, oppression and resistance4
The costs of care: An ethnography of care work in residential homes for older people4
From knowledge to a gendered event and trustful ties: HPV vaccine framings of eligible Finnish girls and school nurses4
Struggling, helping and adapting: Crowdfunding motivations and outcomes during the early US COVID‐19 pandemic4
The muddle of institutional racism in mental health4
Affect, dis/ability and the pandemic4
Risk work in dental practices: an ethnographic study of how risk is managed in NHS dental appointments4
‘They don't know themselves, so how can they tell us?’: parents navigating uncertainty at the frontiers of neonatal surgery4
Disaggregating inequalities in the career outcomes of international medical graduates in the United States4
Sociological contributions to race and health: Diversifying the ontological and methodological agenda4
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