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From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Genomic medicine" 

Results: 5 of 6489

• Therapeutic Strategies in EGFR Mutant Non-Small Cell Lung Cancer.
  Loong HH, Kwan SS, Mok TS, Lau YM.Curr Treat Options Oncol. 2018 Sep 29; 19(11):58. Epub 2018 Sep 29.
• Telomere length measurement as a clinical biomarker of aging and disease.
  Fasching CL.Crit Rev Clin Lab Sci. 2018 Sep 28; :1-23. Epub 2018 Sep 28.
• Modeling methylation data as an additional genetic variance component.
  Almeida M, Peralta J, Garcia J, Diego V, Goring H, Williams-Blangero S, Blangero J.BMC Proc. 2018; 12(Suppl 9):29. Epub 2018 Sep 17.
• Guidelines for Diagnosis and Treatment of Chronic Lymphocytic Leukemia. Krohem B-Cll 2017.
  Jakšić B, Pejša V, Ostojić-Kolonić S, Kardum-Skelin I, Bašić-Kinda S, Coha B, Gverić-Krečak V, Vrhovac R, Jakšić O, Aurer I, et al.Acta Clin Croat. 2018 Mar; 57(1):190-215.
• Causal modeling in a multi-omic setting: insights from GAW20.
  Auerbach J, Howey R, Jiang L, Justice A, Li L, Oualkacha K, Sayols-Baixeras S, Aslibekyan SW.BMC Genet. 2018 Sep 17; 19(Suppl 1):74. Epub 2018 Sep 17.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 1213

• Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain.
  Suri P, Palmer MR, Tsepilov YA, Freidin MB, Boer CG, Yau MS, Evans DS, Gelemanovic A, Bartz TM, Nethander M, et al.PLoS Genet. 2018 Sep; 14(9):e1007601. Epub 2018 Sep 27.
• Guidelines for Diagnosis and Treatment of Chronic Lymphocytic Leukemia. Krohem B-Cll 2017.
  Jakšić B, Pejša V, Ostojić-Kolonić S, Kardum-Skelin I, Bašić-Kinda S, Coha B, Gverić-Krečak V, Vrhovac R, Jakšić O, Aurer I, et al.Acta Clin Croat. 2018 Mar; 57(1):190-215.
• The Patient in Precision Medicine: A Systematic Review Examining Evaluations of Patient-Facing Materials.
  Wynn RM, Adams KT, Kowalski RL, Shivega WG, Ratwani RM, Miller KE.J Healthc Eng. 2018; 2018:9541621. Epub 2018 Sep 3.
• Defective (interfering) viral genomes re-explored: impact on antiviral immunity and virus persistence.
  Manzoni TB, López CB.Future Virol. 2018 Jul; 13(7):493-503. Epub 2018 Jun 12.
• Genomic Subtypes of GISTs for Stratifying Patient Response to Sunitinib following Imatinib Resistance: A Pooled Analysis and Systematic Review.
  Tan S, Chen P, Ji J, Guo S, Yu D, Asakawa T, Zhou Y, Abe M, Zong L.Dis Markers. 2018; 2018:1368617. Epub 2018 Aug 26.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 48357

• NBEA: developmental disease gene with early generalized epilepsy phenotypes.
  Mulhern MS, Stumpel C, Stong N, Brunner HG, Bier L, Lippa N, Riviello J, Rouhl RPW, Kempers M, Pfundt R, et al.Ann Neurol. 2018 Sep 30; . Epub 2018 Sep 30.
• Monogenic diabetes mellitus in cystic fibrosis.
  Gan HW, Bhatt JM, Denvir L, Randell T, Sachdev P.Arch Dis Child. 2018 Sep 29; . Epub 2018 Sep 29.
• Towards broadening Forensic DNA Phenotyping beyond pigmentation: Improving the prediction of head hair shape from DNA.
  Pośpiech E, Chen Y, Kukla-Bartoszek M, Breslin K, Aliferi A, Andersen JD, Ballard D, Chaitanya L, Freire-Aradas A, van der Gaag KJ, et al.Forensic Sci Int Genet. 2018 Aug 29; 37:241-251. Epub 2018 Aug 29.
• Highlights of the 14th international mesothelioma interest group meeting: Pathologic separation of benign from malignant mesothelial proliferations and histologic/molecular analysis of malignant mesothelioma subtypes.
  Churg A, Nabeshima K, Ali G, Bruno R, Fernandez-Cuesta L, Galateau-Salle F.Lung Cancer. 2018 Oct; 124:95-101. Epub 2018 Jul 30.
• Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.
  Tester DJ, Wong LCH, Chanana P, Gray B, Jaye A, Evans JM, Evans M, Fleming P, Jeffrey I, Cohen M, et al.J Pediatr. 2018 Sep 26; . Epub 2018 Sep 26.

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This column displays citations pertaining to topics in medical genetics. See more filter information.