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 *

200 related articles for article (PubMed ID: 24449059)

  • 1. Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.
    Hitch K; Joseph G; Guiltinan J; Kianmahd J; Youngblom J; Blanco A
    J Genet Couns; 2014 Aug; 23(4):539-51. PubMed ID: 24449059
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
    Rosell AM; Pena LD; Schoch K; Spillmann R; Sullivan J; Hooper SR; Jiang YH; Mathey-Andrews N; Goldstein DB; Shashi V
    J Genet Couns; 2016 Oct; 25(5):1019-31. PubMed ID: 26868367
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
    Levenseller BL; Soucier DJ; Miller VA; Harris D; Conway L; Bernhardt BA
    J Genet Couns; 2014 Aug; 23(4):552-65. PubMed ID: 23846343
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Oncologists' and cancer patients' views on whole-exome sequencing and incidental findings: results from the CanSeq study.
    Gray SW; Park ER; Najita J; Martins Y; Traeger L; Bair E; Gagne J; Garber J; Jänne PA; Lindeman N; Lowenstein C; Oliver N; Sholl L; Van Allen EM; Wagle N; Wood S; Garraway L; Joffe S
    Genet Med; 2016 Oct; 18(10):1011-9. PubMed ID: 26866579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
    Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
    Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Investigating barriers to genetic counseling and germline mutation testing in women with suspected hereditary breast and ovarian cancer syndrome and Lynch syndrome.
    Shaw J; Bulsara C; Cohen PA; Gryta M; Nichols CB; Schofield L; O'Sullivan S; Pachter N; Hardcastle SJ
    Patient Educ Couns; 2018 May; 101(5):938-944. PubMed ID: 29273311
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.
    Solomon I; Harrington E; Hooker G; Erby L; Axilbund J; Hampel H; Semotiuk K; Blanco A; Klein WMP; Giardiello F; Leonard L
    J Genet Couns; 2017 Aug; 26(4):866-877. PubMed ID: 28127677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Genetic counseling and cascade genetic testing in Lynch syndrome.
    Hampel H
    Fam Cancer; 2016 Jul; 15(3):423-7. PubMed ID: 26969309
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis.
    Petersen J; Koptiuch C; Wu YP; Mooney R; Elrick A; Szczotka K; Keener M; Pappas L; Kanth P; Soisson A; Kohlmann W; Kaphingst KA
    Patient Educ Couns; 2018 Nov; 101(11):2011-2017. PubMed ID: 30097381
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic counselors' views and experiences with the clinical integration of genome sequencing.
    Machini K; Douglas J; Braxton A; Tsipis J; Kramer K
    J Genet Couns; 2014 Aug; 23(4):496-505. PubMed ID: 24671342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death.
    Amendola LM; Horike-Pyne M; Trinidad SB; Fullerton SM; Evans BJ; Burke W; Jarvik GP
    J Law Med Ethics; 2015; 43(3):476-85. PubMed ID: 26479557
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Targeted Next-Generation Sequencing for Hereditary Cancer Syndromes: A Focus on Lynch Syndrome and Associated Endometrial Cancer.
    Tafe LJ
    J Mol Diagn; 2015 Sep; 17(5):472-82. PubMed ID: 26162329
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results.
    Matias M; Wusik K; Neilson D; Zhang X; Valencia CA; Collins K
    J Genet Couns; 2019 Apr; 28(2):182-193. PubMed ID: 30648779
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.
    Maradiegue A; Jasperson K; Edwards QT; Lowstuter K; Weitzel J
    J Am Acad Nurse Pract; 2008 Feb; 20(2):76-84. PubMed ID: 18271762
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice.
    Cohen SA; Laurino M; Bowen DJ; Upton MP; Pritchard C; Hisama F; Jarvik G; Fichera A; Sjoding B; Bennett RL; Naylor L; Jacobson A; Burke W; Grady WM
    Cancer; 2016 Feb; 122(3):393-401. PubMed ID: 26480326
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience.
    Lazaridis KN; Schahl KA; Cousin MA; Babovic-Vuksanovic D; Riegert-Johnson DL; Gavrilova RH; McAllister TM; Lindor NM; Abraham RS; Ackerman MJ; Pichurin PN; Deyle DR; Gavrilov DK; Hand JL; Klee EW; Stephens MC; Wick MJ; Atkinson EJ; Linden DR; Ferber MJ; Wieben ED; Farrugia G;
    Mayo Clin Proc; 2016 Mar; 91(3):297-307. PubMed ID: 26944241
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Increasing Lynch syndrome identification through establishment of a hereditary colorectal cancer registry.
    Sturgeon D; McCutcheon T; Geiger TM; Muldoon RL; Herline AJ; Wise PE
    Dis Colon Rectum; 2013 Mar; 56(3):308-14. PubMed ID: 23392144
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Outcomes of screening endometrial cancer patients for Lynch syndrome by patient-administered checklist.
    Daniels MS; Urbauer DL; Zangeneh A; Batte BA; Dempsey KM; Lu KH
    Gynecol Oncol; 2013 Dec; 131(3):619-23. PubMed ID: 24141004
    [TBL] [Abstract][Full Text] [Related]  

  • 20. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing.
    Jamal L; Robinson JO; Christensen KD; Blumenthal-Barby J; Slashinski MJ; Perry DL; Vassy JL; Wycliff J; Green RC; McGuire AL
    AJOB Empir Bioeth; 2017; 8(2):82-88. PubMed ID: 28949844
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.