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 *

149 related articles for article (PubMed ID: 34009343)

  • 1. Finding commonalities in rare diseases through the undiagnosed diseases network.
    Yates J; Gutiérrez-Sacristán A; Jouhet V; LeBlanc K; Esteves C; ; DeSain TN; Benik N; Stedman J; Palmer N; Mellon G; Kohane I; Avillach P
    J Am Med Inform Assoc; 2021 Jul; 28(8):1694-1702. PubMed ID: 34009343
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Machine Learning of Patient Characteristics to Predict Admission Outcomes in the Undiagnosed Diseases Network.
    Amiri H; Kohane IS;
    JAMA Netw Open; 2021 Feb; 4(2):e2036220. PubMed ID: 33630084
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Accelerating rare disease detection: an experience of multidisciplinary team model in undiagnosed diseases program in a children's hospital.
    Shi Y; Miao S; Yuan Y; Fu Y; Sun C; Wang H; Ge M; Li D; Shen G; Gao X; Zhai X
    Front Public Health; 2024; 12():1373649. PubMed ID: 39354993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure.
    Kim SY; Lee S; Woo H; Han J; Ko YJ; Shim Y; Park S; Jang SS; Lim BC; Ko JM; Kim KJ; Cho A; Kim H; Hwang H; Choi JE; Kim MJ; Moon J; Seong MW; Park SS; Choi SA; Lee JE; Kwon YS; Sohn YB; Kim JS; Kim WS; Lee YJ; Kwon S; Kim YO; Kook H; Cho YG; Cheon CK; Kang KS; Song MR; Kim YJ; Cha HJ; Choi HJ; Kee Y; Park SG; Baek ST; Choi M; Ryu DS; Chae JH
    Orphanet J Rare Dis; 2022 Oct; 17(1):372. PubMed ID: 36209187
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network.
    Mukherjee S; Cogan JD; Newman JH; Phillips JA; Hamid R; ; Meiler J; Capra JA
    Am J Hum Genet; 2021 Oct; 108(10):1946-1963. PubMed ID: 34529933
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reported environmental exposures are inversely associated with obtaining a genetic diagnosis in the Undiagnosed Diseases Network.
    Silverman EK; Allard P; Loscalzo J; Mulvihill JJ; Korrick SA;
    Am J Med Genet A; 2019 Jun; 179(6):958-965. PubMed ID: 30903737
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.
    Salvatore M; Polizzi A; De Stefano MC; Floridia G; Baldovino S; Roccatello D; Sciascia S; Menegatti E; Remuzzi G; Daina E; Iatropoulos P; Bembi B; Da Riol RM; Ferlini A; Neri M; Novelli G; Sangiuolo F; Brancati F; Taruscio D
    Ital J Pediatr; 2020 Sep; 46(1):130. PubMed ID: 32928283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.
    Harnish JM; Li L; Rogic S; Poirier-Morency G; Kim SY; ; Boycott KM; Wangler MF; Bellen HJ; Hieter P; Pavlidis P; Liu Z; Yamamoto S
    Hum Mutat; 2022 Jun; 43(6):743-759. PubMed ID: 35224820
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
    Moynihan D; Monaco S; Ting TW; Narasimhalu K; Hsieh J; Kam S; Lim JY; Lim WK; Davila S; Bylstra Y; Balakrishnan ID; Heng M; Chia E; Yeo KK; Goh BK; Gupta R; Tan T; Baynam G; Jamuar SS
    Sci Rep; 2024 Mar; 14(1):5056. PubMed ID: 38424111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Undiagnosed Diseases: Italy-US Collaboration and International Efforts to Tackle Rare and Common Diseases Lacking a Diagnosis.
    Taruscio D; Floridia G; Salvatore M; Groft SC; Gahl WA
    Adv Exp Med Biol; 2017; 1031():25-38. PubMed ID: 29214564
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Undiagnosed Diseases Network International: Five years and more!
    Taruscio D; Baynam G; Cederroth H; Groft SC; Klee EW; Kosaki K; Lasko P; Melegh B; Riess O; Salvatore M; Gahl WA
    Mol Genet Metab; 2020 Apr; 129(4):243-254. PubMed ID: 32033911
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases.
    Kyle JE; Stratton KG; Zink EM; Kim YM; Bloodsworth KJ; Monroe ME; ; Waters KM; Webb-Robertson BM; Koeller DM; Metz TO
    Sci Data; 2021 Apr; 8(1):114. PubMed ID: 33883556
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision.
    Baldridge D; Wangler MF; Bowman AN; Yamamoto S; ; Schedl T; Pak SC; Postlethwait JH; Shin J; Solnica-Krezel L; Bellen HJ; Westerfield M
    Orphanet J Rare Dis; 2021 May; 16(1):206. PubMed ID: 33962631
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich node embeddings for the Human Phenotype Ontology.
    Shen F; Peng S; Fan Y; Wen A; Liu S; Wang Y; Wang L; Liu H
    J Biomed Inform; 2019 Aug; 96():103246. PubMed ID: 31255713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Six years' accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures.
    Takahashi Y; Date H; Oi H; Adachi T; Imanishi N; Kimura E; Takizawa H; Kosugi S; Matsumoto N; Kosaki K; Matsubara Y; ; Mizusawa H
    J Hum Genet; 2022 Sep; 67(9):505-513. PubMed ID: 35318459
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Italian cancer figures--Report 2015: The burden of rare cancers in Italy.
    ; Busco S; Buzzoni C; Mallone S; Trama A; Castaing M; Bella F; Amodio R; Bizzoco S; Cassetti T; Cirilli C; Cusimano R; De Angelis R; Fusco M; Gatta G; Gennaro V; Giacomin A; Giorgi Rossi P; Mangone L; Mannino S; Rossi S; Pierannunzio D; Tavilla A; Tognazzo S; Tumino R; Vicentini M; Vitale MF; Crocetti E; Dal Maso L
    Epidemiol Prev; 2016; 40(1 Suppl 2):1-120. PubMed ID: 26951748
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant.
    Ezell KM; Tinker RJ; Furuta Y; Gulsevin A; Bastarache L; Hamid R; Cogan JD; Rives L; Neumann S; Corner B; Kozuria M; Phillips JA;
    Am J Med Genet A; 2024 Jul; 194(7):e63597. PubMed ID: 38511854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. SpainUDP: The Spanish Undiagnosed Rare Diseases Program.
    López-Martín E; Martínez-Delgado B; Bermejo-Sánchez E; Alonso J; ; Posada M
    Int J Environ Res Public Health; 2018 Aug; 15(8):. PubMed ID: 30110963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Initiative on Rare and Undiagnosed Diseases: Achievements and Future Prospects].
    Suzuki H
    Brain Nerve; 2023 Sep; 75(9):1065-1070. PubMed ID: 37691248
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.