Genetic counseling

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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 1694

• Genetic Risk of Alzheimer's Disease: Three Wishes Now That the Genie is Out of the Bottle.
  Frank L, Wesson Ashford J, Bayley P, 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.
• Electronically ascertained extended pedigrees in breast cancer genetic counseling.
  Stefansdottir V, Skirton H, Johannsson OT, Olafsdottir H, Olafsdottir GH, Tryggvadottir L, Jonsson JJ.Fam Cancer. 2018 Sep 24; . Epub 2018 Sep 24.
• Promoting guideline-based cancer genetic risk assessment for hereditary breast and ovarian cancer in ethnically and geographically diverse cancer survivors: Rationale and design of a 3-arm randomized controlled trial.
  Kinney AY, Howell R, Ruckman R, McDougall JA, Boyce TW, Vicuña B, Lee JH, Guest DD, Rycroft R, Valverde PA, et al.Contemp Clin Trials. 2018 Oct; 73:123-135. Epub 2018 Sep 18.
• Implementing Precision Medicine Programs and Clinical Trials in the Community-Based Oncology Practice: Barriers and Best Practices.
  Ersek JL, Black LJ, Thompson MA, Kim ES.Am Soc Clin Oncol Educ Book. 2018 May 23; (38):188-196.

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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 603

• 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.
• The utility of Leventhal's model in the analysis of the psycho-behavioral implications of familial cancer - a literature review.
  Postolica R, Iorga M, Savin M, Azoicai D, Enea V.Arch Med Sci. 2018 Aug; 14(5):1144-1154. Epub 2016 Oct 19.
• A survey study with assessment of esophageal screening and genetic counseling in patients with Howel-Evans syndrome.
  Jenkins LE, Abner S, Schadt C.Dermatol Online J. 2018 Jun 15; 24(6). Epub 2018 Jun 15.
• Consensus Statement of the Indian Academy of Pediatrics in Diagnosis and Management of Hemophilia.
  Sachdeva A, Gunasekaran V, Ramya HN, Dass J, Kotwal J, Seth T, Das S, Garg K, Kalra M, Sirisha RS, et al.Indian Pediatr. 2018 Jul 15; 55(7):582-590.

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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 23254

• The Global State of the Genetic Counseling Profession.
  Abacan M, Alsubaie L, Barlow-Stewart K, Caanen B, Cordier C, Courtney E, Davoine E, Edwards J, Elackatt NJ, Gardiner K, et al.Eur J Hum Genet. 2018 Oct 5; . Epub 2018 Oct 5.
• Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis.
  Wu-Chou YH, Hung TC, Lin YT, Cheng HW, Lin JL, Lin CH, Yu CC, Chen KT, Yeh TH, Chen YR.J Biomed Sci. 2018 Oct 5; 25(1):72. Epub 2018 Oct 5.
• Prenatal profile of Pallister-Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis.
  Salzano E, Raible SE, Kaur M, Wilkens A, Sperti G, Tilton RK, Bettini LR, Rocca A, Cocchi G, Selicorni A, et al.Am J Med Genet A. 2018 Oct 5; . Epub 2018 Oct 5.
• Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.
  Moufid FZ, Bouguenouch L, El Bouchikhi I, Houssaini MI, Ouldim K.Turk J Gastroenterol. 2018 Oct 5; . Epub 2018 Oct 5.
• 16p13.11 microduplication in 45 new patients: refined clinical significance and genotype-phenotype correlations.
  Allach El Khattabi L, Heide S, Caberg JH, Andrieux J, Doco Fenzy M, Vincent-Delorme C, Callier P, Chantot-Bastaraud S, Afenjar A, Boute-Benejean O, et al.J Med Genet. 2018 Oct 4; . Epub 2018 Oct 4.

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