Genetic testing [NEW TOPIC PAGE]

PubMed Clinical Queries





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 "Genetic testing" 

Results: 5 of 10426

• Pharmacogenetic testing among patients with mood and anxiety disorders is associated with decreased utilization and cost: A propensity-score matched study.
  Perlis RH, Mehta R, Edwards AM, Tiwari A, Imbens GW.Depress Anxiety. 2018 May 7; . Epub 2018 May 7.
• A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics.
  Su YR, Di C, Bien S, Huang L, Dong X, Abecasis G, Berndt S, Bezieau S, Brenner H, Caan B, et al.Am J Hum Genet. 2018 May 3; 102(5):904-919.
• Chromosomal barcoding as a tool for multiplexed phenotypic characterization of laboratory evolved lineages.
  Jahn LJ, Porse A, Munck C, Simon D, Volkova S, Sommer MOA.Sci Rep. 2018 May 3; 8(1):6961. Epub 2018 May 3.
• Optimal nonvitamin K antagonist oral anticoagulant therapy in a warfarin-sensitive patient after left atrial appendage closure: A case report.
  Shen L, Fang SS, Ge H, Qiao ZQ, Gu ZC.Medicine (Baltimore). 2018 May; 97(18):e0683.
• Fatal familial insomnia presenting with agrypnia excitata and very low atonia index level: A case report and literature review.
  Yang TW, Park B, Kim KT, Jun JS, Kim YS, Lee ST, Jung KH, Chu K, Lee SK, Jung KY.Medicine (Baltimore). 2018 May; 97(18):e0646.

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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 2088

• Expanded criteria for active surveillance in prostate cancer: a review of the current data.
  Jones C, Fam MM, Davies BJ.Transl Androl Urol. 2018 Apr; 7(2):221-227.
• An evidence-based approach to globally assess the covariate-dependent effect of the MTHFR single nucleotide polymorphism rs1801133 on blood homocysteine: a systematic review and meta-analysis.
  Jin H, Cheng H, Chen W, Sheng X, Levy MA, Brown MJ, Tian J.Am J Clin Nutr. 2018 May 1; 107(5):817-825.
• Mild ventriculomegaly from fetal consultation to neurodevelopmental assessment: A single center experience and review of the literature.
  Scelsa B, Rustico M, Righini A, Parazzini C, Balestriero MA, Introvini P, Spaccini L, Mastrangelo M, Lista G, Zuccotti GV, et al.Eur J Paediatr Neurol. 2018 Apr 12; . Epub 2018 Apr 12.
• First and Second Trimester Prenatal Screening Update
  Institute of Health Economics.2014 Aug.
• First and Second Trimester Prenatal Screening for Trisomies 13, 18, and 21 and Open Neural Tube Defects
  Institute of Health Economics.2012 Sep.

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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 69620

• CE: Understanding the Nurse's Role in Managing Gaucher Disease.
  Vucko ER.Am J Nurs. 2018 May 11; . Epub 2018 May 11.
• Holoprosencephaly: A clinical genomics perspective.
  Solomon BD, Retterer K, Juusola J.Am J Med Genet C Semin Med Genet. 2018 May 11; . Epub 2018 May 11.
• Classical fragile-X phenotype in a female infant disclosed by comprehensive genomic studies.
  Jorge P, Garcia E, Gonçalves A, Marques I, Maia N, Rodrigues B, Santos H, Fonseca J, Soares G, Correia C, et al.BMC Med Genet. 2018 May 10; 19(1):74. Epub 2018 May 10.
• Recently evolved human-specific methylated regions are enriched in schizophrenia signals.
  Banerjee N, Polushina T, Bettella F, Giddaluru S, Steen VM, Andreassen OA, Le Hellard S.BMC Evol Biol. 2018 May 11; 18(1):63. Epub 2018 May 11.
• Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt.
  Balasubramanian M, Jenkins TM, Kirk RJ, Nesbitt IM, Olpin SE, Hill M, Gillett GT.Mol Genet Metab Rep. 2018 Jun; 15:69-70. Epub 2018 Mar 6.

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