These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 27811861)

  • 21. Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants.
    Jarvik GP; Browning BL
    Am J Hum Genet; 2016 Jun; 98(6):1077-1081. PubMed ID: 27236918
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing.
    Amor DJ; Chitty LS; Van den Veyver IB
    Prenat Diagn; 2020 Dec; 40(12):1508-1514. PubMed ID: 32091628
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The future of Cochrane Neonatal.
    Soll RF; Ovelman C; McGuire W
    Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
    Vears DF; Niemiec E; Howard HC; Borry P
    Eur J Hum Genet; 2018 Dec; 26(12):1743-1751. PubMed ID: 30143804
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Medical genetics and the genome].
    Gerdes AM; Vogel I
    Ugeskr Laeger; 2014 Nov; 176(46):. PubMed ID: 25394930
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Practical considerations in the clinical application of whole-exome sequencing.
    Shashi V; McConkie-Rosell A; Schoch K; Kasturi V; Rehder C; Jiang YH; Goldstein DB; McDonald MT
    Clin Genet; 2016 Feb; 89(2):173-81. PubMed ID: 25678066
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The Somatic Curation and Interpretation Across Laboratories (SOCIAL) project-current state of solid-tumour variant interpretation for molecular pathology in Canada.
    Spence T; Sukhai MA; Kamel-Reid S; Stockley TL
    Curr Oncol; 2019 Dec; 26(6):353-360. PubMed ID: 31896933
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
    Amendola LM; Muenzen K; Biesecker LG; Bowling KM; Cooper GM; Dorschner MO; Driscoll C; Foreman AKM; Golden-Grant K; Greally JM; Hindorff L; Kanavy D; Jobanputra V; Johnston JJ; Kenny EE; McNulty S; Murali P; Ou J; Powell BC; Rehm HL; Rolf B; Roman TS; Van Ziffle J; Guha S; Abhyankar A; Crosslin D; Venner E; Yuan B; Zouk H; ; Jarvik GP
    Am J Hum Genet; 2020 Nov; 107(5):932-941. PubMed ID: 33108757
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genomic testing: the clinical laboratory perspective.
    Faruki H
    Clin Pharmacol Ther; 2013 Aug; 94(2):190-2. PubMed ID: 23872833
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Laboratory testing for heparin-induced thrombocytopenia is inconsistent in North America: a survey of North American specialized coagulation laboratories.
    Price EA; Hayward CP; Moffat KA; Moore JC; Warkentin TE; Zehnder JL
    Thromb Haemost; 2007 Dec; 98(6):1357-61. PubMed ID: 18064336
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The link between providers and patients: how laboratories can ensure quality results with genetic testing.
    Quillin JM; Jackson-Cook C; Bodurtha J
    Clin Leadersh Manag Rev; 2003; 17(6):351-7. PubMed ID: 14692080
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
    Hegde M; Santani A; Mao R; Ferreira-Gonzalez A; Weck KE; Voelkerding KV
    Arch Pathol Lab Med; 2017 Jun; 141(6):798-805. PubMed ID: 28362156
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Personnel standards and quality assurance practices of biochemical genetic testing laboratories in the United States.
    McGovern MM; Benach M; Wallenstein S; Boone J; Lubin IM
    Arch Pathol Lab Med; 2003 Jan; 127(1):71-6. PubMed ID: 12521371
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling.
    Smith LA; Douglas J; Braxton AA; Kramer K
    J Genet Couns; 2015 Aug; 24(4):654-62. PubMed ID: 25403901
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.
    Tudini E; Andrews J; Lawrence DM; King-Smith SL; Baker N; Baxter L; Beilby J; Bennetts B; Beshay V; Black M; Boughtwood TF; Brion K; Cheong PL; Christie M; Christodoulou J; Chong B; Cox K; Davis MR; Dejong L; Dinger ME; Doig KD; Douglas E; Dubowsky A; Ellul M; Fellowes A; Fisk K; Fortuno C; Friend K; Gallagher RL; Gao S; Hackett E; Hadler J; Hipwell M; Ho G; Hollway G; Hooper AJ; Kassahn KS; Krishnaraj R; Lau C; Le H; San Leong H; Lundie B; Lunke S; Marty A; McPhillips M; Nguyen LT; Nones K; Palmer K; Pearson JV; Quinn MCJ; Rawlings LH; Sadedin S; Sanchez L; Schreiber AW; Sigalas E; Simsek A; Soubrier J; Stark Z; Thompson BA; U J; Vakulin CG; Wells AV; Wise CA; Woods R; Ziolkowski A; Brion MJ; Scott HS; Thorne NP; Spurdle AB;
    Am J Hum Genet; 2022 Nov; 109(11):1960-1973. PubMed ID: 36332611
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A comparison of genomic laboratory reports and observations that may enhance their clinical utility for providers and patients.
    Davis KW; Hamby Erby L; Fiallos K; Martin M; Wassman ER
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00551. PubMed ID: 31115190
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Misattributed parentage identified through diagnostic exome sequencing: Frequency of detection and reporting practices.
    Stefka J; El-Khechen D; Cain T; Blanco K; Feldmann B; Towne MC; Hagman KDF
    J Genet Couns; 2022 Jun; 31(3):631-640. PubMed ID: 34826357
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Secondary findings: How did we get here, and where are we going?
    Ormond KE; O'Daniel JM; Kalia SS
    J Genet Couns; 2019 Apr; 28(2):326-333. PubMed ID: 30821867
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Reporting clinically relevant genetic variants unrelated to genomic test requests: a survey of Australian clinical laboratory policies and practices.
    Tudini E; Haas MA; Mattiske T; Spurdle AB
    J Med Genet; 2023 Jun; 60(6):609-614. PubMed ID: 36604177
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
    Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
    Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.