Experiments

Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).

Publications 1.3k Datasets 392.5k Experiments 11

System / cell line: genetic ✕ Assay: health ✕ Clear

Negotiating the boundary between medicine and consumer culture: online marketing of nutrigenetic tests.

PMID 20022680 · PMC2824846 · Social science & medicine (1982) · 2010 · 8 claims · 3 setups

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Nutrigenetic testing companies create a new social/marketing space for their products positioned between medicine and consumer culture, rather than being simply delegitimized by boundary work.

webpages same fda qualitative framing document
Introduction: the challenge of incidental findings.

PMID 18547190 · PMC2587006 · The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2008 · 8 claims · 5 setups

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No consensus exists on how to handle incidental findings in human subjects research

publicly healthy asymptomatic families empirical functional colonography
GINA, genism, and civil rights.

PMID 18786085 · PMC2932647 · Bioethics · 2008 · 8 claims · 1 setups

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GINA prohibits health insurers and employers from collecting or using genetic information for underwriting, eligibility, premium-setting, or hiring/firing decisions.

american survey
Genomic medicine and developing countries: creating a room of their own.

PMID 18487990 · PMC7096950 · Nature reviews. Genetics · 2008 · 8 claims · 6 setups

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Developing countries can harness human genetic variation to benefit their populations and economies rather than only importing technology from developed nations.

key polio asthma patients in-depth viral genetic
Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

PMID 14735173 · PMC2410151 · British journal of cancer · 2004 · 6 claims · 3 setups

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The DA had no impact on well-being (anxiety, depression, cancer-related distress, general health)

women brca1 same randomised comparative validated
Putting science over supposition in the arena of personalized genomics.

PMID 18665132 · PMC2531214 · Nature genetics · 2008 · 6 claims · 3 setups

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There is a rapidly widening gap between gene-disease association discovery and research into the public health/clinical utility of that information.

adults same tested baseline multiplex telephone-based
The asthma consultative process: a collaborative approach to integrating genomics into public health practice.

PMID 15888238 · PMC1327721 · Preventing chronic disease · 2005 · 6 claims · 4 setups

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A collaborative process combining literature review, expert working group input, and professional/community consultations can synthesize asthma genomics knowledge for public health practice.

professionals community scientific key group literature
Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium.

PMID 20044523 · PMC2923092 · Stroke · 2010 · 8 claims · 6 setups

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SNP rs2208454 in intron 3 of MACROD2 (near FLRT3, chr20p12) is associated with lower risk of covert MRI-infarcts (OR=0.76, p=4.64x10-7)

stroke-free elderly african-american cardiovascular genome-wide direct expression
We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.

PMID 19998110 · PMC3749831 · The American journal of bioethics : AJOB · 2009 · 8 claims · 5 setups

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Medical establishment critics dismissed PGT information in 2008 as either not worth much or dangerous

social women relatives individuals survey epidemiological genetic
Systematic identification of ACE2 expression modulators reveals cardiomyopathy as a risk factor for mortality in COVID-19 patients.

PMID 35012625 · PMC8743438 · Genome biology · 2022 · 8 claims · 9 setups

Has reproduction · 68

GENEVA (Gene Expression Variance Analysis) is a semi-automated framework that mines large-scale public RNA-seq datasets to identify conditions associated with a gene's expression variance

gtex genetic lncap heart rna-seq meta-analysis electronic
Characterizing Neutrophil Subtypes in Cancer Using scRNA Sequencing Demonstrates the Importance of IL1β/CXCR2 Axis in Generation of Metastasis-specific Neutrophils.

PMID 38358352 · PMC10903300 · Cancer research communications · 2024 · 8 claims · 7 setups

Has reproduction · 64

Two main neutrophil subtypes exist in primary tumors: an activated subtype sharing transcriptomic signatures with healthy neutrophils, and a tumor-specific subtype.

colorectal sorted integrated neutrophil scrna-seq bulk immunohistochemistry

Experiments

Negotiating the boundary between medicine and consumer culture: online marketing of nutrigenetic tests.

Introduction: the challenge of incidental findings.

GINA, genism, and civil rights.

Genomic medicine and developing countries: creating a room of their own.

Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation.

Putting science over supposition in the arena of personalized genomics.

The asthma consultative process: a collaborative approach to integrating genomics into public health practice.

Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium.

We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.

Systematic identification of ACE2 expression modulators reveals cardiomyopathy as a risk factor for mortality in COVID-19 patients.

Characterizing Neutrophil Subtypes in Cancer Using scRNA Sequencing Demonstrates the Importance of IL1β/CXCR2 Axis in Generation of Metastasis-specific Neutrophils.