PubMed Clinical Queries for "Personal genomics"

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 "Personal genomics" 

Results: 5 of 138

• Aminoglycoside-associated nonsyndromic deafness and speech disorder in mitochondrial A1555G mutation in a family: A case report.
  Ou YH, Chen AW, Fan JY, Cheng WL, Lin TT, Chen MK, Liu CS.Medicine (Baltimore). 2018 Oct; 97(42):e12878.
• Increasing genomic literacy among adolescents.
  Sabatello M, Chen Y, Sanderson SC, Chung WK, Appelbaum PS.Genet Med. 2018 Sep 14; . Epub 2018 Sep 14.
• The melanoma genomics managing your risk study: A protocol for a randomized controlled trial evaluating the impact of personal genomic risk information on skin cancer prevention behaviors.
  Smit AK, Newson AJ, Morton RL, Kimlin M, Keogh L, Law MH, Kirk J, Dobbinson S, Kanetsky PA, Fenton G, et al.Contemp Clin Trials. 2018 Jul; 70:106-116. Epub 2018 May 23.
• Distress, uncertainty, and positive experiences associated with receiving information on personal genomic risk of melanoma.
  Smit AK, Newson AJ, Best M, Badcock CA, Butow PN, Kirk J, Dunlop K, Fenton G, Cust AE.Eur J Hum Genet. 2018 Aug; 26(8):1094-1100. Epub 2018 Apr 30.
• Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.
  Shickh S, Clausen M, Mighton C, Casalino S, Joshi E, Glogowski E, Schrader KA, Scheer A, Elser C, Panchal S, et al.BMJ Open. 2018 Apr 26; 8(4):e021876. Epub 2018 Apr 26.

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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 41

• Malaria in Meghalaya: a systematic literature review and analysis of data from the National Vector-Borne Disease Control Programme.
  Kessler A, van Eijk AM, Jamir L, Walton C, Carlton JM, Albert S.Malar J. 2018 Nov 6; 17(1):411. Epub 2018 Nov 6.
• Clinical implications of APOE genotyping for late-onset Alzheimer's disease (LOAD) risk estimation: a review of the literature.
  Marshe VS, Gorbovskaya I, Kanji S, Kish M, Müller DJ.J Neural Transm (Vienna). 2018 Oct 31; . Epub 2018 Oct 31.
• The first competency based framework in genetics/genomics specifically for midwifery education and practice.
  Tonkin ET, Skirton H, Kirk M.Nurse Educ Pract. 2018 Nov; 33:133-140. Epub 2018 Sep 14.
• Epidemiology of allergic rhinitis and associated risk factors in Asia.
  Chong SN, Chew FT.World Allergy Organ J. 2018; 11(1):17. Epub 2018 Aug 6.
• Optimising experimental research in respiratory diseases: an ERS statement.
  Bonniaud P, Fabre A, Frossard N, Guignabert C, Inman M, Kuebler WM, Maes T, Shi W, Stampfli M, Uhlig S, et al.Eur Respir J. 2018 May; 51(5). Epub 2018 May 17.

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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 1029

• Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia.
  Newson AJ, Ayres S, Boyle J, Gabbett MT, Nisselle A.Twin Res Hum Genet. 2018 Nov 21; :1-5. Epub 2018 Nov 21.
• Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study.
  Metcalfe SA, Hickerton C, Savard J, Stackpoole E, Tytherleigh R, Tutty E, Terrill B, Turbitt E, Gray K, Middleton A, et al.Eur J Med Genet. 2018 Nov 12; . Epub 2018 Nov 12.
• Perceptions of students in health and molecular life sciences regarding pharmacogenomics and personalized medicine.
  Mahmutovic L, Akcesme B, Durakovic C, Akcesme FB, Maric A, Adilovic M, Hamad N, Wjst M, Feeney O, Semiz S.Hum Genomics. 2018 Nov 14; 12(1):50. Epub 2018 Nov 14.
• Reclassification of <i>BRCA1</i> and <i>BRCA2</i> variants of uncertain significance: a multifactorial analysis of multicentre prospective cohort.
  Lee JS, Oh S, Park SK, Lee MH, Lee JW, Kim SW, Son BH, Noh DY, Lee JE, Park HL, et al.J Med Genet. 2018 Dec; 55(12):794-802. Epub 2018 Nov 10.
• Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.
  John SE, Antony D, Eaaswarkhanth M, Hebbar P, Channanath AM, Thomas D, Devarajan S, Tuomilehto J, Al-Mulla F, Alsmadi O, et al.Sci Rep. 2018 Nov 8; 8(1):16583. Epub 2018 Nov 8.

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