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10 merged results for "Genetic Variants"

Partial results: at least one source did not answer. Available results are shown rather than treating an upstream outage as zero matches.

Source status
  1. Family screening and genetic testing in transthyretin cardiac amyloidosis : Changing (not only) variant transthyretin cardiac amyloidosis.

    Muller SA, Kieviet LC, van Tintelen JP, Zwetsloot PP · 2026 · Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1007/s12471-026-02088-w

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    • not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  2. Mitochondrial DNA in cardiovascular disease.

    Koller A, Weissensteiner H · 2026 · Atherosclerosis

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.atherosclerosis.2026.121952

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  3. Prostaglandin-Endoperoxide Synthase 1 Regulatory Variants Link Aspirin-Treated Cardiovascular Outcomes to Multicellular Cyclooxygenase-1 Expression and Activity Beyond Platelet-Derived Cyclooxygenase-1 Inhibition.

    Li XL, Wang YZ, Wang Q, Hu XX · 2026 · European journal of pharmacology

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.ejphar.2026.179548

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  4. Exome-wide characterization of genetic diversity and population-specific functional variants in indigenous tribal populations of India.

    Datta S, Jena D, Ghosh A, Biswas VK · 2026 · Journal of genetics and genomics = Yi chuan xue bao

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.jgg.2026.11.002

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    • not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  5. Characterization of EHV-1 viral genes at the respiratory tract using a tracheal explant culture model.

    Vázquez GB, Giessler KS, Sharma S, Osterrieder N · 2026 · Virus research

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.virusres.2026.199831

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    • not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  6. Waardenburg-anophthalmia syndrome associated with an SMOC1 start- loss variant: a case report.

    Pawar N, Krishna S, Ravindran M · 2026 · Ophthalmic genetics

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1080/13816810.2026.2743066

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    • not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
    • not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  7. Cancer Risks Associated With Germline BARD1 Pathogenic/Likely Pathogenic Variants: A Multicenter Study of 445 Families.

    Homer JP, Demeure MJ, Yao Y, Hanson K · 2026 · JCO precision oncology

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1200/po-26-00417

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  8. Polygenic Risk Scores for Kidney Function Decline in Japanese Population-Based Cohorts: A Validation Study.

    Oshima M, Toyama T, Hara A, Asayama A · 2026 · Kidney360

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.34067/kid.0000001444

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  9. A Data-Driven Approach to Polygenic Risk Scoring: Combining Support Vector Machine and Ridge Regression in Diseases Lacking GWAS Data Utilizing Lipedema as a Model.

    Ferrari L, Gordani O, Macchia A, Feizyab S · 2026 · Lymphology

    limited evidence Transparent signal score 48/100 · policy 1.0.0

    Found in pubmed · no DOI

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  10. Early-Onset Primary Lymphedema as The Initial Manifestation of GATA2 Deficiency: A Case Report.

    Palero SR, Carrion SC, Mancilla LCC, Gonda EMS · 2026 · Lymphology

    limited evidence Transparent signal score 48/100 · policy 1.0.0

    Found in pubmed · no DOI

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer