New Genetics and Society

Papers
(The median citation count of New Genetics and Society is 0. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
The pathos of precision16
Conviction: the making and unmaking of the violent brain11
Donors: curious connections in donor conception Donors: curious connections in donor conception , by P. Nordqvist and L. Gilman, Bingley, Emerald Group Publishing, 2022,8
Human heritable genome editing and its governance: views of scientists and governance professionals7
The salience of genomic information to reproductive autonomy: Australian healthcare professionals’ views on a changing prenatal testing landscape7
Governance through scientism: Taiwan Biobank and public controversy7
Capitalization and the production of value at the nexus of academia and industry: the case of a microbiome startup6
Editorial: themed issue: understanding the technical and social landscape of gene editing5
“I am happy to be alive, but I prefer to have children without my chronic disease”: chronically ill persons’ views on reproduction and genetic testing for their own condition5
Expanding the notion of “benefit”: comparing public, parent, and professional attitudes towards whole genome sequencing in newborns5
Correction5
The color of creatorship: intellectual property, race, and the making of Americans5
The Muslim genome: postcolonial nation-building through genomics in Pakistan5
Ancestry reimagined: dismantling the myth of genetic ethnicities4
Recoding the gift relationship: views on introducing genomic testing to blood donation4
Are we ready for the genomic era? Insights from judges and lawyers3
Exploring “quality” in cord blood transfusion: uncertainties, bionetworks, and collaborations3
Mitochondrial replacement in the English-language print media: continuity and change in metaphors and social representations2
The matrix of stem cell research: an approach to rethinking science in society2
“It’s personalized, but it’s still bucket based”: the promise of personalized medicine vs. the reality of genomic risk stratification in a breast cancer screening trial2
Freezing fertility: oocyte cryopreservation and the gender politics of aging2
The unexpected and unanticipated announcement of the “world’s first” gene edited babies: breaching, repairing and strengthening community boundaries2
“Idealists and capitalists”: ownership attitudes and preferences in genomic citizen science2
“Doing Good” in U.S. Cancer Genomics? Valuation practices across the boundaries of research and care in rural community oncology2
“Law at the frontiers of biomedicine”1
Reinterpreting “genetic identity” in the regulatory and ethical context of heritable genome editing1
Constructing maternal responsibility: narratives of “motherly love” and maternal blame in epigenetics research1
Many thanks for New Genetics and Society reviewers1
Public concerns about direct-to-consumer DNA test kits: the evidence from survey and social media data1
Being Human during COVID-19 Being Human during COVID-19 , edited by Paul Martin, Stevienna de Saille, Kirsty Liddiard and Warren Pearce, Bristol University Press, 2022, 1
Use of tissue and health data: attachments and detachments among an enabling public1
“Doing genetic literacy”: a discourse-oriented approach to literacy in genetic contexts0
The omics of our lives: practices and policies of direct-to-consumer epigenetic and microbiomic testing companies0
Healthcare activism: markets, morals, and the collective good Healthcare activism: markets, morals, and the collective good , edited by Susi Geiger, Oxford, Oxford Unive0
Consensus too soon: judges’ and lawyers’ views on genetic information use0
The platforming of human embryo editing: prospecting “disease free” futures0
Safe and purposeful genome editing under harmonized regulation for responsible use: views of research experts0
Vaccine court – the law and politics of injury0
Genetics and the Politics of Security: a social science perspective0
Navigating narratives of genetic categorization at the frayed edges of identity0
Laboring bodies and the quantified self0
Gene drive communication: exploring experts’ lived experience of metaphor use0
Goffman against DNA: genetic stigma and the use of genetic ancestry tests by white nationalists0
Toxic disruptions: polycystic ovary syndrome in urban India0
The challenge of recruiting diverse populations into health research: an embedded social science perspective0
The new stage of public engagement with science in the digital media environment: citizen science communicators in the discussion of GMOs on Zhihu0
Applying a risk governance approach to examine how professionals perceive the benefits and risks of clinical genomics in Australian healthcare0
Thinking the unthinkable: how did human germline genome editing become ethically acceptable?0
“It didn’t mean anything” – moving within a landscape of knowledge to interpret genetics and genetic test results within familial cancer concerns0
Intrinsic responsible innovation in a synthetic biology research project0
Promising precision medicine: how patients, clinicians and caregivers work to realize the potential of genomics-informed cancer care0
Embodiment and everyday cyborgs Embodiment and everyday cyborgs , by Gill Haddow, Manchester, Manchester University Press, 2021, 216 pp., $36.95 (hardback), ISBN-13: 9780
A place for science and technology studies. Observation, collaboration and intervention0
Siloed discourses: a year-long study of twitter engagement on the use of CRISPR in food and agriculture0
Genetic subjectivities of prospective fathers: men’s attitudes toward epigenetics0
“If relatives inherited the gene, they should inherit the data.” Bringing the family into the room where bioethics happens0
The rise of the biocyborg: synthetic biology, artificial chimerism and human enhancement0
Bio-imperialism. Disease, terror and the construction of national fragility0
Building the airplane while flying it: tracking the transformation of novel sequencing practices into clinical services0
Environmental sustainability and biobanking: a pilot study of the field0
How we get Mendel wrong, and why it matters: challenging the narrative of Mendelian genetics0
“We are all cousins.” Belgian ancestry and genomic testing in a close-knit community in Northeastern Wisconsin0
“Donating with eyes shut”: attitudes regarding DNA donation to a large-scale biobank in Israel0
In Memoriam of Andrew Webster0
Strategies on personalized medicine and the power of the imagined public0
Ancestral genomics: African American health in the age of precision medicine0
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