OOIR: Observatory of International Research

Papers

(The median citation count of New Genetics and Society is 1. 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 2022-05-01 to 2026-05-01.)

Article	Citations
Governance through scientism: Taiwan Biobank and public controversy	10
Donors: curious connections in donor conception Donors: curious connections in donor conception , by P. Nordqvist and L. Gilman, Bingley, Emerald Group Publishing, 2022,	9
The commercial dynamics of direct-to-consumer genome testing and law enforcement cooperation	6
Human heritable genome editing and its governance: views of scientists and governance professionals	6
The matrix of stem cell research: an approach to rethinking science in society	5
Capitalization and the production of value at the nexus of academia and industry: the case of a microbiome startup	5
Safe and purposeful genome editing under harmonized regulation for responsible use: views of research experts	4
The unexpected and unanticipated announcement of the “world’s first” gene edited babies: breaching, repairing and strengthening community boundaries	4
Healthcare activism: markets, morals, and the collective good Healthcare activism: markets, morals, and the collective good , edited by Susi Geiger, Oxford, Oxford Unive	4
Public concerns about direct-to-consumer DNA test kits: the evidence from survey and social media data	4
Commoning contingent resources: constructing an Australian stem cell registry	3
Goffman against DNA: genetic stigma and the use of genetic ancestry tests by white nationalists	3
Consensus too soon: judges’ and lawyers’ views on genetic information use	3
“We are all cousins.” Belgian ancestry and genomic testing in a close-knit community in Northeastern Wisconsin	3
Toxic disruptions: polycystic ovary syndrome in urban India	3
“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 trial	3
Building the airplane while flying it: tracking the transformation of novel sequencing practices into clinical services	3
How we get Mendel wrong, and why it matters: challenging the narrative of Mendelian genetics	2
Recoding the gift relationship: views on introducing genomic testing to blood donation	2
Mitochondrial replacement in the English-language print media: continuity and change in metaphors and social representations	2
Acid Revival: The psychedelic renaissance and the quest for medical legitimacy	2
“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 condition	2
Siloed discourses: a year-long study of twitter engagement on the use of CRISPR in food and agriculture	2
Genetic subjectivities of prospective fathers: men’s attitudes toward epigenetics	1
Repoliticizing heritable human genome editing: discursive narrowing and technomoral change in the international debate on human germline modification	1

The challenge of recruiting diverse populations into health research: an embedded social science perspective	1
Capitalizing a cure: how finance controls the price and value of medicines	1
“Law at the frontiers of biomedicine”	1
Constructing maternal responsibility: narratives of “motherly love” and maternal blame in epigenetics research	1
A History of Genomics Across Species, Communities and Projects	1
Use of tissue and health data: attachments and detachments among an enabling public	1