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 *

314 related articles for article (PubMed ID: 30193136)

  • 1. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
    Amendola LM; Berg JS; Horowitz CR; Angelo F; Bensen JT; Biesecker BB; Biesecker LG; Cooper GM; East K; Filipski K; Fullerton SM; Gelb BD; Goddard KAB; Hailu B; Hart R; Hassmiller-Lich K; Joseph G; Kenny EE; Koenig BA; Knight S; Kwok PY; Lewis KL; McGuire AL; Norton ME; Ou J; Parsons DW; Powell BC; Risch N; Robinson M; Rini C; Scollon S; Slavotinek AM; Veenstra DL; Wasserstein MP; Wilfond BS; Hindorff LA; ; Plon SE; Jarvik GP
    Am J Hum Genet; 2018 Sep; 103(3):319-327. PubMed ID: 30193136
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
    Green RC; Goddard KAB; Jarvik GP; Amendola LM; Appelbaum PS; Berg JS; Bernhardt BA; Biesecker LG; Biswas S; Blout CL; Bowling KM; Brothers KB; Burke W; Caga-Anan CF; Chinnaiyan AM; Chung WK; Clayton EW; Cooper GM; East K; Evans JP; Fullerton SM; Garraway LA; Garrett JR; Gray SW; Henderson GE; Hindorff LA; Holm IA; Lewis MH; Hutter CM; Janne PA; Joffe S; Kaufman D; Knoppers BM; Koenig BA; Krantz ID; Manolio TA; McCullough L; McEwen J; McGuire A; Muzny D; Myers RM; Nickerson DA; Ou J; Parsons DW; Petersen GM; Plon SE; Rehm HL; Roberts JS; Robinson D; Salama JS; Scollon S; Sharp RR; Shirts B; Spinner NB; Tabor HK; Tarczy-Hornoch P; Veenstra DL; Wagle N; Weck K; Wilfond BS; Wilhelmsen K; Wolf SM; Wynn J; Yu JH;
    Am J Hum Genet; 2016 Jun; 98(6):1051-1066. PubMed ID: 27181682
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium.
    Suckiel SA; O'Daniel JM; Donohue KE; Gallagher KM; Gilmore MJ; Hendon LG; Joseph G; Lianoglou BR; Mathews JM; Norton ME; Odgis JA; Poss AF; Rego S; Scollon S; Yip T; Amendola LM
    J Pers Med; 2021 Mar; 11(3):. PubMed ID: 33805616
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Examining access to care in clinical genomic research and medicine: Experiences from the CSER Consortium.
    Gutierrez AM; Robinson JO; Outram SM; Smith HS; Kraft SA; Donohue KE; Biesecker BB; Brothers KB; Chen F; Hailu B; Hindorff LA; Hoban H; Hsu RL; Knight SJ; Koenig BA; Lewis KL; Lich KH; O'Daniel JM; Okuyama S; Tomlinson GE; Waltz M; Wilfond BS; Ackerman SL; Majumder MA
    J Clin Transl Sci; 2021; 5(1):e193. PubMed ID: 34888063
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience.
    Kraft SA; Russell H; Bensen JT; Bonini KE; Robinson JO; Sahin-Hodoglugil N; Renna K; Hindorff LA; Kaufman D; Horowitz CR; Waltz M; Zepp JM; Knight SJ
    Am J Med Genet A; 2023 Feb; 191(2):391-399. PubMed ID: 36341765
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
    Gottesman O; Kuivaniemi H; Tromp G; Faucett WA; Li R; Manolio TA; Sanderson SC; Kannry J; Zinberg R; Basford MA; Brilliant M; Carey DJ; Chisholm RL; Chute CG; Connolly JJ; Crosslin D; Denny JC; Gallego CJ; Haines JL; Hakonarson H; Harley J; Jarvik GP; Kohane I; Kullo IJ; Larson EB; McCarty C; Ritchie MD; Roden DM; Smith ME; Böttinger EP; Williams MS;
    Genet Med; 2013 Oct; 15(10):761-71. PubMed ID: 23743551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
    Berg JS; Amendola LM; Eng C; Van Allen E; Gray SW; Wagle N; Rehm HL; DeChene ET; Dulik MC; Hisama FM; Burke W; Spinner NB; Garraway L; Green RC; Plon S; Evans JP; Jarvik GP;
    Genet Med; 2013 Nov; 15(11):860-7. PubMed ID: 24195999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
    Sperber NR; Carpenter JS; Cavallari LH; J Damschroder L; Cooper-DeHoff RM; Denny JC; Ginsburg GS; Guan Y; Horowitz CR; Levy KD; Levy MA; Madden EB; Matheny ME; Pollin TI; Pratt VM; Rosenman M; Voils CI; W Weitzel K; Wilke RA; Ryanne Wu R; Orlando LA
    BMC Med Genomics; 2017 May; 10(1):35. PubMed ID: 28532511
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Implementing genomics and pharmacogenomics in the clinic: The National Human Genome Research Institute's genomic medicine portfolio.
    Manolio TA
    Atherosclerosis; 2016 Oct; 253():225-236. PubMed ID: 27612677
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.
    Odgis JA; Gallagher KM; Suckiel SA; Donohue KE; Ramos MA; Kelly NR; Bertier G; Blackburn C; Brown K; Fielding L; Lopez J; Aguiniga KL; Maria E; Rodriguez JE; Sebastin M; Teitelman N; Watnick D; Yelton NM; Abhyankar A; Abul-Husn NS; Baum A; Bauman LJ; Beal JC; Bloom T; Cunningham-Rundles C; Diaz GA; Dolan S; Ferket BS; Jobanputra V; Kovatch P; McDonald TV; McGoldrick PE; Rhodes R; Rinke ML; Robinson M; Rubinstein A; Shulman LH; Stolte C; Wolf SM; Yozawitz E; Zinberg RE; Greally JM; Gelb BD; Horowitz CR; Wasserstein MP; Kenny EE
    Trials; 2021 Jan; 22(1):56. PubMed ID: 33446240
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
    McCarty CA; Chisholm RL; Chute CG; Kullo IJ; Jarvik GP; Larson EB; Li R; Masys DR; Ritchie MD; Roden DM; Struewing JP; Wolf WA;
    BMC Med Genomics; 2011 Jan; 4():13. PubMed ID: 21269473
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Toward health technology assessment of whole-genome sequencing diagnostic tests: challenges and solutions.
    Payne K; Eden M; Davison N; Bakker E
    Per Med; 2017 May; 14(3):235-247. PubMed ID: 29767583
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.
    Sebastin M; Odgis JA; Suckiel SA; Bonini KE; Di Biase M; Brown K; Marathe P; Kelly NR; Ramos MA; Rodriguez JE; Aguiñiga KL; Lopez J; Maria E; Rodriguez MA; Yelton NM; Cunningham-Rundles C; Gallagher K; McDonald TV; McGoldrick PE; Robinson M; Rubinstein A; Shulman LH; Wolf SM; Yozawitz E; Zinberg RE; Abul-Husn NS; Bauman LJ; Diaz GA; Ferket BS; Greally JM; Jobanputra V; Gelb BD; Horowitz CR; Kenny EE; Wasserstein MP
    Pilot Feasibility Stud; 2023 Mar; 9(1):47. PubMed ID: 36949526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial.
    Staley BS; Milko LV; Waltz M; Griesemer I; Mollison L; Grant TL; Farnan L; Roche M; Navas A; Lightfoot A; Foreman AKM; O'Daniel JM; O'Neill SC; Lin FC; Roman TS; Brandt A; Powell BC; Rini C; Berg JS; Bensen JT
    Trials; 2021 Jun; 22(1):395. PubMed ID: 34127041
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Improving access to exome sequencing in a medically underserved population through the Texome Project.
    Vuocolo B; German RJ; Lalani SR; Murali CN; Bacino CA; Baskin S; Littlejohn R; Odom JD; McLean S; Schmid C; Nutter M; Stuebben M; Magness E; Juarez O; El Achi D; Mitchell B; Glinton KE; Robak L; Nagamani SCS; Saba L; Ritenour A; Zhang L; Streff H; Chan K; Kemere KJ; Carter K; ; Owen N; Vossaert L; Liu P; Bellen H; Wangler MF
    Genet Med; 2024 Jun; 26(6):101102. PubMed ID: 38431799
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing.
    Bowling KM; Thompson ML; Kelly MA; Scollon S; Slavotinek AM; Powell BC; Kirmse BM; Hendon LG; Brothers KB; Korf BR; Cooper GM; Greally JM; Hurst ACE
    Genome Med; 2022 Nov; 14(1):131. PubMed ID: 36414972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.
    Smith HS; Swint JM; Lalani SR; Yamal JM; de Oliveira Otto MC; Castellanos S; Taylor A; Lee BH; Russell HV
    Genet Med; 2019 Jan; 21(1):3-16. PubMed ID: 29760485
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.
    Amendola LM; Robinson JO; Hart R; Biswas S; Lee K; Bernhardt BA; East K; Gilmore MJ; Kauffman TL; Lewis KL; Roche M; Scollon S; Wynn J; Blout C
    J Genet Couns; 2018 Sep; 27(5):1220-1227. PubMed ID: 29497922
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER Consortium.
    O'Daniel JM; Ackerman S; Desrosiers LR; Rego S; Knight SJ; Mollison L; Byfield G; Anderson KP; Danila MI; Horowitz CR; Joseph G; Lamoure G; Lindberg NM; McMullen CK; Mittendorf KF; Ramos MA; Robinson M; Sillari C; Madden EB;
    Genet Med; 2022 May; 24(5):1108-1119. PubMed ID: 35227608
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study.
    Shickh S; Gutierrez Salazar M; Zakoor KR; Lázaro C; Gu J; Goltz J; Kleinman D; Noor A; Khalouei S; Mighton C; Reble E; Kodida R; Bombard Y; DiTroia S; Baxter S; Watkins N; Care M; Adler A; Horsburgh S; Morar O; Murphy J; Nevay DL; Szybowska M; Aronson M; Panchal S; Godoy R; Holter S; Randall Armel S; Semotiuk K; Elser C; Kim RH; Chitayat D; So J; Faghfoury H; Silver J; Morel CF; Lerner-Ellis J
    J Med Genet; 2021 Apr; 58(4):275-283. PubMed ID: 32581083
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.