Genetic counseling [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 "Genetic counseling" 

Results: 5 of 1702

• Disparities in genetic services utilization in a random sample of young breast cancer survivors.
  Nikolaidis C, Duquette D, Mendelsohn-Victor KE, Anderson B, Copeland G, Milliron KJ, Merajver SD, Janz NK, Northouse LL, Duffy SA, et al.Genet Med. 2018 Nov 2; . Epub 2018 Nov 2.
• Identifying patients with a history of ovarian cancer for referral for genetic counselling: non-randomised comparison of two case-finding strategies in primary care.
  Helsper CW, Van Vliet LM, Velthuizen ME, de Wit NJ, Beijaert RP, Butter E, van Gent-Wagemakers MP, Witteveen EO, Zweemer RP, van Dulmen SM, et al.Br J Gen Pract. 2018 Nov; 68(676):e750-e756.
• Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.
  Qian F, Wang S, Mitchell J, McGuffog L, Barrowdale D, Leslie G, Oosterwijk JC, Chung WK, Evans DG, Engel C, et al.J Natl Cancer Inst. 2018 Oct 12; . Epub 2018 Oct 12.
• Genetic Risk of Alzheimer's Disease: Three Wishes Now That the Genie is Out of the Bottle.
  Frank L, Wesson Ashford J, Bayley PJ, Borson S, Buschke H, Cohen D, Cummings JL, Davies P, Dean M, Finkel SI, et al.J Alzheimers Dis. 2018 Sep 27; . Epub 2018 Sep 27.
• Mutations of ARX and non-syndromic intellectual disability in Chinese population.
  Wu Y, Zhang H, Liu X, Shi Z, Li H, Wang Z, Jie X, Huang S, Zhang F, Li J, et al.Genes Genomics. 2018 Sep 25; . Epub 2018 Sep 25.

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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 608

• Clinical and Genetic Characteristics of BRCA1/2 Mutation in Korean Ovarian Cancer Patients: A Multicenter Study and Literature Review.
  Kwon BS, Byun JM, Lee HJ, Jeong DH, Lee TH, Shin KH, Suh DS, Kim KH.Cancer Res Treat. 2018 Oct 8; . Epub 2018 Oct 8.
• Dermatoglyphic Analysis in Parents with Cleft Children: A Comparative Study.
  Harika DJ, Sridevi E, Sai Sankar AJ, Pranitha K, Gosla SR, Kiran GB.Contemp Clin Dent. 2018 Sep; 9(Suppl 2):S291-S298.
• [The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition].
  Moretta J, Berthet P, Bonadona V, Caron O, Cohen-Haguenauer O, Colas C, Corsini C, Cusin V, De Pauw A, Delnatte C, et al.Bull Cancer. 2018 Oct; 105(10):907-917. Epub 2018 Sep 27.
• Management of congenital ichthyoses: European guidelines of care: Part One.
  Mazereeuw-Hautier J, Vahlquist A, Traupe H, Bygum A, Amaro C, Aldwin M, Audouze A, Bodemer C, Bourrat E, Diociaiuti A, et al.Br J Dermatol. 2018 Sep 14; . Epub 2018 Sep 14.
• Developing a genetic services assessment tool to inform quality improvement efforts in state genetic service delivery.
  Chou AF, Mulvihill J, Kaye C, Mann S, Williams MS, Williamson L.Genet Med. 2018 Sep 14; . Epub 2018 Sep 14.

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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 23346

• Parental Mosaicism in <i>PAX6</i> Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and Microphthalmia.
  Tarilonte M, Morín M, Ramos P, Galdós M, Blanco-Kelly F, Villaverde C, Rey-Zamora D, Rebolleda G, Muñoz-Negrete FJ, Tahsin-Swafiri S, et al.Front Genet. 2018; 9:479. Epub 2018 Oct 17.
• [Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients].
  Aalfs CM, Westermann AM, van El CG.Ned Tijdschr Geneeskd. 2017; 161(0):D1525.
• Translating genomic risk into an early detection strategy for sarcoma.
  Ballinger ML, Pinese M, Thomas DM.Genes Chromosomes Cancer. 2018 Nov 1; . Epub 2018 Nov 1.
• 22q11.2 deletion syndrome: A tiny piece leading to a big picture.
  McDonald-McGinn DM.Am J Med Genet A. 2018 Oct; 176(10):2055-2057.
• The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome.
  Grand K, Levitt Katz LE, Crowley TB, Moss E, Lessig M, Bamba V, Lord K, Zackai EH, Emanuel BS, Valverde K, et al.Am J Med Genet A. 2018 Oct; 176(10):2167-2171.

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