Search Results - "Amberger JS"

A genomic-led strategy to anticipate drug safety effects.

Authors: Ferolito, Brian R. Horimoto, Andrea R. V. R. Gravel-Pucillo, Kai et al.

Source: PLoS Genetics. 7/16/2026, Vol. 22 Issue 7, p1-22. 22p.

Genome sequencing for the diagnosis of intellectual disability as a paradigm for rare diseases in the French healthcare setting: the prospective DEFIDIAG study.

Authors: El Chehadeh, Salima Heide, Solveig Quélin, Chloé et al.

Source: Genome Medicine. 10/3/2025, Vol. 17 Issue 1, p1-28. 28p.

Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network.

Authors: de Oliveira, Bibiana Mello Bernardi, Filipe Andrade Baiochi, João Francisco et al.

Source: Orphanet Journal of Rare Diseases. 10/30/2024, Vol. 19 Issue 1, p1-13. 13p.

VUStruct: A compute pipeline for high throughput and personalized structural biology.

Authors: Moth, Christopher W. Sheehan, Jonathan H. Al Mamun, Abdullah et al.

Source: PLoS Computational Biology. 5/4/2026, Vol. 22 Issue 5, p1-15. 15p.

An integrative analysis reveals the mechanism of plastic stabilizers inducing breast cancer.

Authors: Huo, Xingfa Duan, Xueqin Huang, Xiaojuan et al.

Source: PLoS Computational Biology. 3/6/2026, Vol. 22 Issue 3, p1-22. 22p.

iCRCexp: An Integrative Database for Colorectal Cancer-Associated Gene Expression Profiles.

Authors: Yuan, Yan Cao, Bi-Jin Qian, Zhi-Kai et al.

Source: Cancer Informatics. 5/30/2026, Vol. 25, p1-11. 11p.

Whole exome sequencing reveals DNA repair gene variants in women exposed to chronic arsenic poisoning.

Authors: Agarwal, Radhika Kumar, Arun Pandey, Tejasvi et al.

Source: Discover Toxicology. 7/1/2026, Vol. 3 Issue 1, p1-16. 16p.

Exploring the mechanism of ursodeoxycholic acid in the treatment of osteoarthritis based on network pharmacology, molecular docking, and molecular dynamics simulations.

Authors: Li, Xin Xiong, Jinhe

Source: European Journal of Inflammation. 6/15/2026, Vol. 24, p1-22. 22p.

Exploring the toxicological mechanisms of Benzo[a]anthracene (BaA) exposure in lung adenocarcinoma (LUAD) via network toxicology, machine learning, and multi-dimensional bioinformatics analysis.

Authors: Shi, Zhiyao Fang, Zhiyong Qin, Qiang et al.

Source: PLoS ONE. 2/11/2026, Vol. 21 Issue 2, p1-21. 21p.

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Cornea Arcus and Dyslipidemia in Unrelated Adults With Monoallelic Germline Variants in the Glucokinase Regulator Gene.

Authors: Olarewaju, Bukola A. Trujillo, Ileana Osundiji, Mayowa A.

Source: Clinical Medicine Insights: Endocrinology & Diabetes. 5/6/2026, Vol. 19, p1-4. 4p.

Elucidating the potential carcinogenic molecular mechanisms of parabens in head and neck squamous cell carcinoma through network toxicology and molecular docking.

Authors: Zhao, Lei Yang, Jianwang Liu, Tao et al.

Source: PLoS ONE. 3/23/2026, Vol. 21 Issue 3, p1-22. 22p.

Integrative network pharmacology and machine learning identify potential targets of indole-3-lactic acid in colorectal cancer.

Authors: Li, Jie Zhang, Jian Ke, Jun et al.

Source: PLoS ONE. 3/9/2026, Vol. 21 Issue 3, p1-25. 25p.

Human genetic evidence enriched for side effects of approved drugs.

Authors: Minikel, Eric Vallabh Nelson, Matthew R.

Source: PLoS Genetics. 3/31/2025, Vol. 21 Issue 3, p1-13. 13p.

Revisiting Minamata disease through computational phenotypic similarity analysis.

Authors: Marchi, Edoardo Boldi, Paolo Casiraghi, Elena et al.

Source: PLoS ONE. 2/26/2026, Vol. 21 Issue 2, p1-13. 13p.

Analysis of potential targets of 20S-protopanaxadiol on diabetic nephropathy based on network pharmacology, molecular docking, and experimental validation.

Authors: Li, Chenfei Ma, Chifa Zhao, Ruxuan et al.

Source: Renal Failure. Dec2025, Vol. 47 Issue 1, p1-15. 15p.

Understanding the prevalence of germline oncogenic biomarker variants across the Indian population.

Authors: Vatsyayan, Aastha Bhoyar, Rahul C. Imran, Mohamed et al.

Source: Journal of Genetics. Dec2025, Vol. 104 Issue 2, p1-8. 8p.

Face-based machine learning diagnostics: applications, challenges and opportunities.

Authors: Song, Jie He, Mengqiao Zheng, Xin et al.

Source: Artificial Intelligence Review; Aug2025, Vol. 58 Issue 8, p1-71, 71p

Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants.

Authors: Haque, Bushra Cheerie, David Pan, Amy et al.

Source: PLoS Genetics. 1/6/2025, Vol. 21 Issue 1, p1-21. 21p.

Clinical and biochemical features of atherogenic hyperlipidemias with different genetic basis: A comprehensive comparative study.

Authors: Blokhina, Anastasia V. Ershova, Alexandra I. Kiseleva, Anna V. et al.

Source: PLoS ONE. 12/20/2024, Vol. 19 Issue 12, p1-22. 22p.