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  1. Last 7 days
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    Personalized ctDNA detection and genomic profiling in the NeoRHEA Study
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    nature.com/articles/s41523-025-00852-6
  3. Dec 2025
  4. www.sciencedirect.com:5037 www.sciencedirect.com:5037
    Early lymph node T follicular helper cell signalling hub drives influenza vaccine response in an ancestrally diverse cohort
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    sciencedirect.com:5037/science/article/pii/S2352396425004803
  5. Aug 2025
  6. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    CYP2D6 Phenotype and Breast Cancer Outcomes: A Bias Analysis and Meta-Analysis
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    pmc.ncbi.nlm.nih.gov/articles/PMC11802319/
  7. Jun 2025
  8. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Spatial–Temporal Diversity of Extrachromosomal DNA Shapes Urothelial Carcinoma Evolution and the Tumor Immune Microenvironment
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    pmc.ncbi.nlm.nih.gov/articles/PMC12130809/
  9. May 2025
  10. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Tumor ploidy determination in low-pass whole genome sequencing and allelic copy number visualization using the Constellation Plot
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    pmc.ncbi.nlm.nih.gov/articles/PMC12090563/
  11. Apr 2025
  12. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Germline variants in patients from the Iranian hereditary colorectal cancer registry
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    pmc.ncbi.nlm.nih.gov/articles/PMC11995590/
  13. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Follow-up Analysis Enhances Understanding of Molecular Residual Disease in Localized Non–Small Cell Lung Cancer
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  14. Feb 2025
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    Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
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    sciencedirect.com/science/article/pii/S2666979X2500031X
  16. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Mendelian randomization analysis reveals genetic evidence for a causal link between inflammatory bowel disease and uterine cervical neoplasms
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    pmc.ncbi.nlm.nih.gov/articles/PMC11810950/
  17. Oct 2024
  18. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Causal relationship between genetic-predicted uric acid and cervical cancer risk: evidence for nutritional intervention on cervical cancer prevention
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    ncbi.nlm.nih.gov/pmc/articles/PMC11449874/
  19. aacrjournals.org aacrjournals.org
    Clinical Outcome–Related Mutational Signatures Identified by Integrative Genomic Analysis in Nasopharyngeal Carcinoma
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    aacrjournals.org/clincancerres/article/26/24/6494/82920/Clinical-Outcome-Related-Mutational-Signatures
  20. Aug 2024
  21. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors
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    ncbi.nlm.nih.gov/pmc/articles/PMC11294819/
  22. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Causal effect of COVID-19 on optic nerve and visual pathway disorders: genetic evidence of lung-brain axis
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    ncbi.nlm.nih.gov/pmc/articles/PMC11286426/
  23. May 2024
  24. aacrjournals.org aacrjournals.org
    Negative hyperselection of resistance mutations for panitumumab maintenance in RAS wild-type metastatic colorectal cancer (PanaMa phase II trial, AIO KRK 0212)
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    aacrjournals.org/clincancerres/article/30/7/1256/741834/Negative-Hyperselection-of-Resistance-Mutations
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    Integrative molecular analyses of the MD Anderson prostate cancer patient-derived xenograft (MDA PCa PDX) series
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    aacrjournals.org/clincancerres/article/30/10/2272/745168/Integrative-Molecular-Analyses-of-the-MD-Anderson
  26. Mar 2024
  27. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Predicted proteome association studies of breast, prostate, ovarian, and endometrial cancers implicate plasma protein regulation in cancer susceptibility
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    ncbi.nlm.nih.gov/pmc/articles/PMC10528410/
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    Follicular lymphoma B cells exhibit heterogeneous transcriptional states with associated somatic alterations and tumor microenvironments
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    sciencedirect.com/science/article/pii/S2666379124000661
  29. Jul 2023
  30. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A
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    ncbi.nlm.nih.gov/pmc/articles/PMC10319579/
  31. May 2023
  32. www.nature.com www.nature.com
    Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response
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    nature.com/articles/s41467-023-38271-5
  33. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Multiple germline events contribute to cancer development in patients with Li-Fraumeni syndrome
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    ncbi.nlm.nih.gov/pmc/articles/PMC10150777/
  34. Mar 2023
  35. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach
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    ncbi.nlm.nih.gov/pmc/articles/PMC10032232/
  36. Feb 2023
  37. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Breast Cancer Patients
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    ncbi.nlm.nih.gov/pmc/articles/PMC9357161/
  38. Jan 2023
  39. www.nature.com www.nature.com
    Germline rare deleterious variant load alters cancer risk, age of onset and tumor characteristics
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    nature.com/articles/s41698-023-00354-3
  40. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Circulating Tumor DNA in Stage III Colorectal Cancer, beyond Minimal Residual Disease Detection, toward Assessment of Adjuvant Therapy Efficacy and Clinical Behavior of Recurrences
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    ncbi.nlm.nih.gov/pmc/articles/PMC9401484/
  41. Dec 2022
  42. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    PRState: Incorporating genetic ancestry in prostate cancer risk scores for men of African ancestry
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    ncbi.nlm.nih.gov/pmc/articles/PMC9733391/
  43. Jul 2022
  44. 52.53.155.43 52.53.155.43
    ccr-20-4774-html.html
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  45. www.medrxiv.org www.medrxiv.org
    PRState: Incorporating Genetic Ancestry in Prostate Cancer Risk scores for African American Men
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    medrxiv.org/content/10.1101/2022.03.12.22271020v1
  46. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia–Related Infertility in Three Chinese Families
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    ncbi.nlm.nih.gov/pmc/articles/PMC9257073/
  47. May 2022
  48. aacrjournals.org aacrjournals.org
    Single cell characterization of the cellular landscape of acral melanoma identifies novel targets for immunotherapy
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    aacrjournals.org/clincancerres/article/28/10/2131/694823/Single-cell-Characterization-of-the-Cellular
  49. aacrjournals.org aacrjournals.org
    A Phenogenetic Axis that Modulates Clinical Manifestation and Predicts Treatment Outcome in Primary Myeloid NeoplasmsLandscape of Myeloid Neoplasms in a Chinese Cohort
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    aacrjournals.org/cancerrescommun/article/2/4/258/694752/A-Phenogenetic-Axis-that-Modulates-Clinical
  50. Apr 2022
  51. journals.physiology.org journals.physiology.org
    Whole genome sequencing identifies a deletion mutation in the unknown-functional KCNG2 from familial sick sinus syndrome
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    journals.physiology.org/doi/full/10.1152/physiolgenomics.00132.2021
  52. Feb 2022
  53. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Single-cell analysis of human glioma and immune cells identifies S100A4 as an immunotherapy target
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    ncbi.nlm.nih.gov/pmc/articles/PMC8828877/
  54. Nov 2021
  55. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Apolipoprotein E Genetic Variation and Its Association With Cognitive Function in Rural-Dwelling Older South Africans
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    ncbi.nlm.nih.gov/pmc/articles/PMC8551631/
  56. Sep 2021
  57. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Gene expression imputation across multiple tissue types provides insight into the genetic architecture of frontotemporal dementia and its clinical subtypes: A transcriptome-wide analysis on frontotemporal dementia
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    ncbi.nlm.nih.gov/pmc/articles/PMC8415425/
  58. Aug 2021
  59. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Studying immunotherapy resistance in a melanoma autologous humanized mouse xenograft.
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    ncbi.nlm.nih.gov/pmc/articles/PMC7864867/
  60. Jul 2021
  61. onlinelibrary.wiley.com onlinelibrary.wiley.com
    Functional analysis of novel RUNX2 mutations identified in patients with Cleidocranial dysplasia
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    onlinelibrary.wiley.com/doi/10.1111/cge.13610
  62. europepmc.org europepmc.org
    A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.
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    europepmc.org/articles/PMC5764568/
  63. May 2021
  64. cancerres.aacrjournals.org cancerres.aacrjournals.org
    Tumor mutational burden is polygenic and genetically associated with complex traits and diseases
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    cancerres.aacrjournals.org/content/81/5/1230
  65. Feb 2021
  66. www.sciencedirect.com www.sciencedirect.com
    Cell Type-Specific Intralocus Interactions Reveal Oligodendrocyte Mechanisms in MS
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    sciencedirect.com/science/article/pii/S0092867420302646
  67. Jan 2020
  68. www.sciencedirect.com www.sciencedirect.com
    Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks
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    sciencedirect.com/science/article/pii/S0092867419307809
  69. Nov 2017
  70. www.sciencedirect.com www.sciencedirect.com
    40,000-Year-Old Individual from Asia Provides Insight into Early Population Structure in Eurasia
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    sciencedirect.com/science/article/pii/S0960982217311958