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Dec 2025
www.nature.com www.nature.com

Personalized ctDNA detection and genomic profiling in the NeoRHEA Study

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1. scibot 11 Dec 2025
  
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  DOI: 10.1038/s41523-025-00852-6
  
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nature.com/articles/s41523-025-00852-6
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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
Aug 2025
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CYP2D6 Phenotype and Breast Cancer Outcomes: A Bias Analysis and Meta-Analysis

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pmc.ncbi.nlm.nih.gov/articles/PMC11802319/
Jun 2025
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Spatial–Temporal Diversity of Extrachromosomal DNA Shapes Urothelial Carcinoma Evolution and the Tumor Immune Microenvironment

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1. scibot 12 Jun 2025
  
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pmc.ncbi.nlm.nih.gov/articles/PMC12130809/
May 2025
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Tumor ploidy determination in low-pass whole genome sequencing and allelic copy number visualization using the Constellation Plot

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1. scibot 22 May 2025
  
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pmc.ncbi.nlm.nih.gov/articles/PMC12090563/
Apr 2025
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Germline variants in patients from the Iranian hereditary colorectal cancer registry

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  DOI: 10.1186/s12935-025-03773-3
  
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pmc.ncbi.nlm.nih.gov/articles/PMC11995590/
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Follow-up Analysis Enhances Understanding of Molecular Residual Disease in Localized Non–Small Cell Lung Cancer

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pmc.ncbi.nlm.nih.gov/articles/PMC11959268/
Feb 2025
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Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants

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  DOI: 10.1016/j.xgen.2025.100775
  
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sciencedirect.com/science/article/pii/S2666979X2500031X
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Mendelian randomization analysis reveals genetic evidence for a causal link between inflammatory bowel disease and uterine cervical neoplasms

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  DOI: 10.3389/fgene.2024.1436512
  
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pmc.ncbi.nlm.nih.gov/articles/PMC11810950/
Oct 2024
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Causal relationship between genetic-predicted uric acid and cervical cancer risk: evidence for nutritional intervention on cervical cancer prevention

1
1. scibot 08 Oct 2024
  
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  DOI: 10.3389/fnut.2024.1464046
  
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ncbi.nlm.nih.gov/pmc/articles/PMC11449874/
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Clinical Outcome–Related Mutational Signatures Identified by Integrative Genomic Analysis in Nasopharyngeal Carcinoma

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1. scibot 02 Oct 2024
  
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  DOI: 10.1158/1078-0432.CCR-20-2854
  
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aacrjournals.org/clincancerres/article/26/24/6494/82920/Clinical-Outcome-Related-Mutational-Signatures
Aug 2024
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St. Jude Survivorship Portal: Sharing and Analyzing Large Clinical and Genomic Datasets from Pediatric Cancer Survivors

1
1. scibot 19 Aug 2024
  
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  DOI: 10.1158/2159-8290.CD-23-1441
  
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ncbi.nlm.nih.gov/pmc/articles/PMC11294819/
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Causal effect of COVID-19 on optic nerve and visual pathway disorders: genetic evidence of lung-brain axis

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1. scibot 01 Aug 2024
  
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  DOI: 10.3389/fimmu.2024.1440262
  
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ncbi.nlm.nih.gov/pmc/articles/PMC11286426/
May 2024
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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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1. scibot 23 May 2024
  
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  DOI: 10.1158/1078-0432.CCR-23-3023
  
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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

1
1. scibot 17 May 2024
  
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  DOI: 10.1158/1078-0432.CCR-23-2438
  
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aacrjournals.org/clincancerres/article/30/10/2272/745168/Integrative-Molecular-Analyses-of-the-MD-Anderson
Mar 2024
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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  DOI: 10.1158/1055-9965.EPI-23-0309
  
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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

2
1. scibot 01 Mar 2024
  
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  DOI: 10.1016/j.xcrm.2024.101443
  
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  DOI: 10.1016/j.xcrm.2024.101443
  
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sciencedirect.com/science/article/pii/S2666379124000661
Jul 2023
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Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A

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1. scibot 08 Jul 2023
  
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  DOI: 10.3389/fgene.2023.1158350
  
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ncbi.nlm.nih.gov/pmc/articles/PMC10319579/
May 2023
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Germline modifiers of the tumor immune microenvironment implicate drivers of cancer risk and immunotherapy response

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  DOI: 10.1038/s41467-023-38271-5
  
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nature.com/articles/s41467-023-38271-5
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Multiple germline events contribute to cancer development in patients with Li-Fraumeni syndrome

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  DOI: 10.1158/2767-9764.CRC-22-0402
  
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ncbi.nlm.nih.gov/pmc/articles/PMC10150777/
Mar 2023
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Predicting Cancer Risk from Germline Whole-exome Sequencing Data Using a Novel Context-based Variant Aggregation Approach

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  DOI: 10.1158/2767-9764.CRC-22-0355
  
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ncbi.nlm.nih.gov/pmc/articles/PMC10032232/
Feb 2023
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Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Breast Cancer Patients

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  DOI: 10.1158/1078-0432.CCR-20-4774
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9357161/
Jan 2023
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Germline rare deleterious variant load alters cancer risk, age of onset and tumor characteristics

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  DOI: 10.1038/s41698-023-00354-3
  
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nature.com/articles/s41698-023-00354-3
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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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1. scibot 12 Jan 2023
  
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  DOI: 10.1158/1078-0432.CCR-21-2404
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9401484/
Dec 2022
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PRState: Incorporating genetic ancestry in prostate cancer risk scores for men of African ancestry

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  DOI: 10.1186/s12885-022-10258-3
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9733391/
Jul 2022
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ccr-20-4774-html.html

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52.53.155.43/d17a03e1a46f7a33fcad5a11f782a83d59ae6739/ccr-20-4774-html.html
www.medrxiv.org www.medrxiv.org

PRState: Incorporating Genetic Ancestry in Prostate Cancer Risk scores for African American Men

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1. scibot 15 Jul 2022
  
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  DOI: 10.1101/2022.03.12.22271020
  
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medrxiv.org/content/10.1101/2022.03.12.22271020v1
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Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia–Related Infertility in Three Chinese Families

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1. scibot 09 Jul 2022
  
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  DOI: 10.3389/fgene.2022.922287
  
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ncbi.nlm.nih.gov/pmc/articles/PMC9257073/
May 2022
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Single cell characterization of the cellular landscape of acral melanoma identifies novel targets for immunotherapy

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  DOI: 10.1158/1078-0432.CCR-21-3145
  
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aacrjournals.org/clincancerres/article/28/10/2131/694823/Single-cell-Characterization-of-the-Cellular
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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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  DOI: 10.1158/2767-9764.CRC-21-0194
  
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aacrjournals.org/cancerrescommun/article/2/4/258/694752/A-Phenogenetic-Axis-that-Modulates-Clinical
Apr 2022
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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1. scibot 29 Apr 2022
  
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  DOI: 10.1152/physiolgenomics.00132.2021
  
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journals.physiology.org/doi/full/10.1152/physiolgenomics.00132.2021
Feb 2022
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Single-cell analysis of human glioma and immune cells identifies S100A4 as an immunotherapy target

1
1. scibot 17 Feb 2022
  
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  DOI: 10.1038/s41467-022-28372-y
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8828877/
Nov 2021
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Apolipoprotein E Genetic Variation and Its Association With Cognitive Function in Rural-Dwelling Older South Africans

1
1. scibot 05 Nov 2021
  
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  DOI: 10.3389/fgene.2021.689756
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8551631/
Sep 2021
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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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1. scibot 09 Sep 2021
  
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  RRID:SCR_008801
  
  DOI: 10.1016/j.biopsych.2020.12.023
  
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ncbi.nlm.nih.gov/pmc/articles/PMC8415425/
Aug 2021
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Studying immunotherapy resistance in a melanoma autologous humanized mouse xenograft.

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1. scibot 06 Aug 2021
  
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  RRID:SCR_008801
  
  DOI: 10.1158/1541-7786.MCR-20-0686
  
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ncbi.nlm.nih.gov/pmc/articles/PMC7864867/
Jul 2021
onlinelibrary.wiley.com onlinelibrary.wiley.com

Functional analysis of novel RUNX2 mutations identified in patients with Cleidocranial dysplasia

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1. scibot 29 Jul 2021
  
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  1000 Genomes Project
  
  DOI: 10.1111/cge.13610
  
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  Curator: @Naa003
  
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onlinelibrary.wiley.com/doi/10.1111/cge.13610
europepmc.org europepmc.org

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

2
1. scibot 29 Jul 2021
  
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  RRID:SCR_008801
  
  DOI: 10.7554/eLife.30490
  
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  Curator: @evieth
  
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2. scibot 29 Jul 2021
  
  in Public
  
  RRID:SCR_008801
  
  DOI: 10.7554/eLife.30490
  
  Resource: 1000 Genomes Project and AWS (RRID:SCR_008801)
  
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europepmc.org/articles/PMC5764568/
May 2021
cancerres.aacrjournals.org cancerres.aacrjournals.org

Tumor mutational burden is polygenic and genetically associated with complex traits and diseases

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1. scibot 10 May 2021
  
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  RRID:SCR_008801
  
  DOI: 10.1158/0008-5472.CAN-20-3459
  
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cancerres.aacrjournals.org/content/81/5/1230
Feb 2021
www.sciencedirect.com www.sciencedirect.com

Cell Type-Specific Intralocus Interactions Reveal Oligodendrocyte Mechanisms in MS

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1. scibot 25 Feb 2021
  
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  RRID:SCR_008801
  
  DOI: 10.1016/j.cell.2020.03.002
  
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sciencedirect.com/science/article/pii/S0092867420302646
Jan 2020
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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

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1. scibot 13 Jan 2020
  
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  RRID:SCR_008801
  
  DOI: 10.1016/j.cell.2019.07.015
  
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  Curator: @ethanbadger
  
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sciencedirect.com/science/article/pii/S0092867419307809
Nov 2017
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40,000-Year-Old Individual from Asia Provides Insight into Early Population Structure in Eurasia

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1. scibot 08 Nov 2017
  
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  RRID:SCR_008801
  
  Curator: @Jmenke
  
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sciencedirect.com/science/article/pii/S0960982217311958