PERSONAL GENOMICS [NEW TOPIC PAGE]

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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 "Personal genomics" 

Results: 5 of 140

• Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment.
  Sliz E, Kettunen J, Holmes MV, Williams CO, Boachie C, Wang Q, Männikkö M, Sebert S, Walters R, Lin K, et al.Circulation. 2018 Nov 27; 138(22):2499-2512. Epub 2018 Aug 15.
• 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.
• Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: a population-based exome-wide association study.
  Li Z, Zhu M, Du J, Ma H, Jin G, Dai J.BMC Genomics. 2018 Oct 16; 19(1):752. Epub 2018 Oct 16.
• 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.

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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: 4 of 4

• 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.
• Global trends on fears and concerns of genetic discrimination: a systematic literature review.
  Wauters A, Van Hoyweghen I.J Hum Genet. 2016 Apr; 61(4):275-82. Epub 2016 Jan 7.
• Attitudes of research participants and the general public towards genomic data sharing: a systematic literature review.
  Shabani M, Bezuidenhout L, Borry P.Expert Rev Mol Diagn. 2014 Nov; 14(8):1053-65. Epub 2014 Sep 26.
• Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected?
  Groisman IJ, Mathieu G, Godard B.BMC Med Ethics. 2012 Dec 20; 13:36. Epub 2012 Dec 20.

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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 1048

• Insertional translocation involving an additional nonchromothriptic chromosome in constitutional chromothripsis: Rule or exception?
  Kurtas NE, Xumerle L, Giussani U, Pansa A, Cardarelli L, Bertini V, Valetto A, Liehr T, Clara Bonaglia M, Errichiello E, et al.Mol Genet Genomic Med. 2018 Dec 18; . Epub 2018 Dec 18.
• Yield of peripheral sodium channels gene screening in pure small fibre neuropathy.
  Eijkenboom I, Sopacua M, Hoeijmakers JGJ, de Greef BTA, Lindsey P, Almomani R, Marchi M, Vanoevelen J, Smeets HJM, Waxman SG, et al.J Neurol Neurosurg Psychiatry. 2018 Dec 15; . Epub 2018 Dec 15.
• Alkylphenolic compounds and risk of breast and prostate cancer in the MCC-Spain study.
  Peremiquel-Trillas P, Benavente Y, Martín-Bustamante M, Casabonne D, Pérez-Gómez B, Gómez-Acebo I, Oliete-Canela A, Diéguez-Rodríguez M, Tusquets I, Amiano P, et al.Environ Int. 2018 Dec 12; . Epub 2018 Dec 12.
• Genetics and genomics of pulmonary arterial hypertension.
  Morrell NW, Aldred MA, Chung WK, Elliott CG, Nichols WC, Soubrier F, Trembath RC, Loyd JE.Eur Respir J. 2018 Dec 13; . Epub 2018 Dec 13.
• How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family HealthLink.
  Thomas SN, Hovick SR, Tan N, Sturm AC, Sweet K.Public Health Genomics. 2018 Dec 12; :1-14. Epub 2018 Dec 12.

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