BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 32414353)

  • 1. Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.
    Savatt JM; Wagner JK; Joffe S; Rahm AK; Williams MS; Bradbury AR; Davis FD; Hergenrather J; Hu Y; Kelly MA; Kirchner HL; Meyer MN; Mozersky J; O'Dell SM; Pervola J; Seeley A; Sturm AC; Buchanan AH
    BMC Pediatr; 2020 May; 20(1):222. PubMed ID: 32414353
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
    Manickam K; Buchanan AH; Schwartz MLB; Hallquist MLG; Williams JL; Rahm AK; Rocha H; Savatt JM; Evans AE; Butry LM; Lazzeri AL; Lindbuchler DM; Flansburg CN; Leeming R; Vogel VG; Lebo MS; Mason-Suares HM; Hoskinson DC; Abul-Husn NS; Dewey FE; Overton JD; Reid JG; Baras A; Willard HF; McCormick CZ; Krishnamurthy SB; Hartzel DN; Kost KA; Lavage DR; Sturm AC; Frisbie LR; Person TN; Metpally RP; Giovanni MA; Lowry LE; Leader JB; Ritchie MD; Carey DJ; Justice AE; Kirchner HL; Faucett WA; Williams MS; Ledbetter DH; Murray MF
    JAMA Netw Open; 2018 Sep; 1(5):e182140. PubMed ID: 30646163
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
    Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
    Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort.
    Savatt JM; Ortiz NM; Thone GM; McDonald WS; Kelly MA; Berry ASF; Alvi MM; Hallquist MLG; Malinowski J; Purdy NC; Williams MS; Sturm AC; Buchanan AH
    BMC Med; 2022 Jun; 20(1):205. PubMed ID: 35668420
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
    Patel AP; Wang M; Fahed AC; Mason-Suares H; Brockman D; Pelletier R; Amr S; Machini K; Hawley M; Witkowski L; Koch C; Philippakis A; Cassa CA; Ellinor PT; Kathiresan S; Ng K; Lebo M; Khera AV
    JAMA Netw Open; 2020 Apr; 3(4):e203959. PubMed ID: 32347951
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Parental attitudes and expectations towards receiving genomic test results in healthy children.
    Kulchak Rahm A; Bailey L; Fultz K; Fan A; Williams JL; Buchanan A; Davis FD; Murray MF; Williams MS
    Transl Behav Med; 2018 Jan; 8(1):44-53. PubMed ID: 29385584
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results.
    Schwartz MLB; McDonald WS; Hallquist MLG; Hu Y; McCormick CZ; Walters NL; Tsun J; Zimmerman K; Decker A; Gray C; Malinowski J; Sturm AC; Buchanan AH
    JAMA Netw Open; 2024 Mar; 7(3):e242388. PubMed ID: 38488794
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Engaging Adolescents and Young Adults in Decisions About Return of Genomic Research Results: a mixed-methods longitudinal clinical trial protocol.
    Blumling A; McGowan M; Prows C; Childers-Buschle K; Martin L; Lynch J; Dufendach K; Lipstein E; Kovacic MB; Brinkman B; Myers M
    Res Sq; 2023 Apr; ():. PubMed ID: 37162875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Testing and Management of Iron Overload After Genetic Screening-Identified Hemochromatosis.
    Savatt JM; Johns A; Schwartz MLB; McDonald WS; Salvati ZM; Oritz NM; Masnick M; Hatchell K; Hao J; Buchanan AH; Williams MS
    JAMA Netw Open; 2023 Oct; 6(10):e2338995. PubMed ID: 37870835
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Parental Decision Making Regarding the Disclosure or Nondisclosure of a Mutation-Positive BRCA1/2 Test Result to Minors.
    Seenandan-Sookdeo KA; Hack TF; Lobchuk M; Murphy L; Marles S
    Oncol Nurs Forum; 2016 May; 43(3):330-41. PubMed ID: 27105194
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
    Martin CL; Wain KE; Oetjens MT; Tolwinski K; Palen E; Hare-Harris A; Habegger L; Maxwell EK; Reid JG; Walsh LK; Myers SM; Ledbetter DH
    JAMA Psychiatry; 2020 Dec; 77(12):1276-1285. PubMed ID: 32697297
    [TBL] [Abstract][Full Text] [Related]  

  • 12. At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children.
    Balciuniene J; Liu R; Bean L; Guo F; Nallamilli BRR; Guruju N; Chen-Deutsch X; Yousaf R; Fura K; Chin E; Mathur A; Ma Z; Carmichael J; da Silva C; Collins C; Hegde M
    JAMA Netw Open; 2023 Jul; 6(7):e2326445. PubMed ID: 37523181
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.
    Pereira S; Smith HS; Frankel LA; Christensen KD; Islam R; Robinson JO; Genetti CA; Blout Zawatsky CL; Zettler B; Parad RB; Waisbren SE; Beggs AH; Green RC; Holm IA; McGuire AL;
    JAMA Pediatr; 2021 Nov; 175(11):1132-1141. PubMed ID: 34424265
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Returning individual genomic results to population-based cohort study participants with BRCA1/2 pathogenic variants.
    Ohneda K; Hamanaka Y; Kawame H; Fuse N; Nagami F; Suzuki Y; Yamaguchi-Kabata Y; Shimada M; Masamune A; Aoki Y; Ishida T; Yamamoto M
    Breast Cancer; 2023 Jan; 30(1):110-120. PubMed ID: 36161580
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.
    Buchanan AH; Manickam K; Meyer MN; Wagner JK; Hallquist MLG; Williams JL; Rahm AK; Williams MS; Chen ZE; Shah CK; Garg TK; Lazzeri AL; Schwartz MLB; Lindbuchler DM; Fan AL; Leeming R; Servano PO; Smith AL; Vogel VG; Abul-Husn NS; Dewey FE; Lebo MS; Mason-Suares HM; Ritchie MD; Davis FD; Carey DJ; Feinberg DT; Faucett WA; Ledbetter DH; Murray MF
    Genet Med; 2018 Apr; 20(5):554-558. PubMed ID: 29261187
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical outcomes of a genomic screening program for actionable genetic conditions.
    Buchanan AH; Lester Kirchner H; Schwartz MLB; Kelly MA; Schmidlen T; Jones LK; Hallquist MLG; Rocha H; Betts M; Schwiter R; Butry L; Lazzeri AL; Frisbie LR; Rahm AK; Hao J; Willard HF; Martin CL; Ledbetter DH; Williams MS; Sturm AC
    Genet Med; 2020 Nov; 22(11):1874-1882. PubMed ID: 32601386
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leveraging population-based exome screening to impact clinical care: The evolution of variant assessment in the Geisinger MyCode research project.
    Kelly MA; Leader JB; Wain KE; Bodian D; Oetjens MT; Ledbetter DH; Martin CL; Strande NT
    Am J Med Genet C Semin Med Genet; 2021 Mar; 187(1):83-94. PubMed ID: 33576083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol.
    Milko LV; Rini C; Lewis MA; Butterfield RM; Lin FC; Paquin RS; Powell BC; Roche MI; Souris KJ; Bailey DB; Berg JS; Powell CM
    Trials; 2018 Jun; 19(1):344. PubMed ID: 29950170
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The BabySeq project: implementing genomic sequencing in newborns.
    Holm IA; Agrawal PB; Ceyhan-Birsoy O; Christensen KD; Fayer S; Frankel LA; Genetti CA; Krier JB; LaMay RC; Levy HL; McGuire AL; Parad RB; Park PJ; Pereira S; Rehm HL; Schwartz TS; Waisbren SE; Yu TW; ; Green RC; Beggs AH
    BMC Pediatr; 2018 Jul; 18(1):225. PubMed ID: 29986673
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
    Anderson JA; Meyn MS; Shuman C; Zlotnik Shaul R; Mantella LE; Szego MJ; Bowdin S; Monfared N; Hayeems RZ
    J Med Ethics; 2017 Aug; 43(8):535-539. PubMed ID: 27888232
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.