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 *

121 related articles for article (PubMed ID: 31475197)

  • 1. Whole exome sequencing identifies a rare variant in
    Sun SW; Zhou M; Chen L; Wu JH; Meng ZJ; Miao SY; Han HL; Zhu CC; Xiong XZ
    Ann Transl Med; 2019 Jul; 7(14):327. PubMed ID: 31475197
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of a novel candidate HSD3B2 gene variant for familial hypospadias by whole-exome sequencing.
    Almaramhy HH; Abdul Samad F; Al-Harbi G; Zaytuni D; Imam SN; Masoodi T; Shamsi MB
    Front Genet; 2023; 14():1106933. PubMed ID: 37384334
    [No Abstract]   [Full Text] [Related]  

  • 4. Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot.
    Pan Y; Liu M; Zhang S; Mei H; Wu J
    J Thorac Dis; 2022 Aug; 14(8):3008-3015. PubMed ID: 36071769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer.
    O'Brien TD; Jia P; Xia J; Saxena U; Jin H; Vuong H; Kim P; Wang Q; Aryee MJ; Mino-Kenudson M; Engelman JA; Le LP; Iafrate AJ; Heist RS; Pao W; Zhao Z
    Methods; 2015 Jul; 83():118-27. PubMed ID: 25913717
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A practical method to detect SNVs and indels from whole genome and exome sequencing data.
    Shigemizu D; Fujimoto A; Akiyama S; Abe T; Nakano K; Boroevich KA; Yamamoto Y; Furuta M; Kubo M; Nakagawa H; Tsunoda T
    Sci Rep; 2013; 3():2161. PubMed ID: 23831772
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies.
    Sun D; Liu Y; Cai W; Ma J; Ni K; Chen M; Wang C; Liu Y; Zhu Y; Liu Z; Zhu F
    Front Pediatr; 2021; 9():635703. PubMed ID: 34055682
    [No Abstract]   [Full Text] [Related]  

  • 8. Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
    Dong C; Wei P; Jian X; Gibbs R; Boerwinkle E; Wang K; Liu X
    Hum Mol Genet; 2015 Apr; 24(8):2125-37. PubMed ID: 25552646
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole-exome sequencing analysis in twin sibling males with an anterior cruciate ligament rupture.
    Caso E; Maestro A; Sabiers CC; Godino M; Caracuel Z; Pons J; Gonzalez FJ; Bautista R; Claros MG; Caso-Onzain J; Viejo-Allende E; Giannoudis PV; Alvarez S; Maietta P; Guerado E
    Injury; 2016 Sep; 47 Suppl 3():S41-S50. PubMed ID: 27692106
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole exome sequencing identifies multiple novel candidate genes in familial gastroschisis.
    Salinas-Torres VM; Gallardo-Blanco HL; Salinas-Torres RA; Cerda-Flores RM; Lugo-Trampe JJ; Villarreal-Martínez DZ; Ibarra-Ramírez M; Martínez de Villarreal LE
    Mol Genet Genomic Med; 2020 May; 8(5):e1176. PubMed ID: 32163230
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diffuse pulmonary ossification: A case report unveiling clinical and histopathological challenges.
    Polit F; Alloush F; Espinosa C; Bahmad HF; Gill A; Mendez L; Urdaneta G; Poppiti R; Recine M; Garcia H
    Respir Med Case Rep; 2023; 42():101815. PubMed ID: 36712477
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Increased dishevelled associated activator of morphogenesis 2, a new podocyte-associated protein, in diabetic nephropathy.
    Qi C; Alsomali F; Zhong J; Harris RC; Kon V; Yang H; Fogo AB
    Nephrol Dial Transplant; 2021 May; 36(6):1006-1016. PubMed ID: 33544843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Three Cases of Idiopathic Diffuse Pulmonary Ossification.
    Edahiro R; Kurebe H; Nakatsubo S; Hosono Y; Sawa N; Nishida K; Ohara Y; Oshitani Y; Kagawa H; Tsujino K; Yoshimura K; Miki K; Miki M; Kitada S; Mori M
    Intern Med; 2019 Feb; 58(4):545-551. PubMed ID: 30333390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analytical validation of whole exome and whole genome sequencing for clinical applications.
    Linderman MD; Brandt T; Edelmann L; Jabado O; Kasai Y; Kornreich R; Mahajan M; Shah H; Kasarskis A; Schadt EE
    BMC Med Genomics; 2014 Apr; 7():20. PubMed ID: 24758382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Using whole-exome sequencing to identify variants inherited from mosaic parents.
    Rios JJ; Delgado MR
    Eur J Hum Genet; 2015 Apr; 23(4):547-50. PubMed ID: 24986828
    [TBL] [Abstract][Full Text] [Related]  

  • 16.
    Zhang X; Zhen D; Li X; Yi F; Zhang Z; Yang W; Li X; Sheng Y; Liu X; Jin T; He Y
    Pharmgenomics Pers Med; 2023; 16():389-400. PubMed ID: 37138656
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diffuse Pulmonary Ossification in Fibrosing Interstitial Lung Diseases: Prevalence and Associations.
    Egashira R; Jacob J; Kokosi MA; Brun AL; Rice A; Nicholson AG; Wells AU; Hansell DM
    Radiology; 2017 Jul; 284(1):255-263. PubMed ID: 28182861
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Global inference of disease-causing single nucleotide variants from exome sequencing data.
    Wu M; Chen T; Jiang R
    BMC Bioinformatics; 2016 Dec; 17(Suppl 17):468. PubMed ID: 28155632
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular characterization of known and novel ACVR1 variants in phenotypes of aberrant ossification.
    Gupta A; Zimmermann MT; Wang H; Broski SM; Sigafoos AN; Macklin SK; Urrutia RA; Clark KJ; Atwal PS; Pignolo RJ; Klee EW
    Am J Med Genet A; 2019 Sep; 179(9):1764-1777. PubMed ID: 31240838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned.
    Almoguera B; Li J; Fernandez-San Jose P; Liu Y; March M; Pellegrino R; Golhar R; Corton M; Blanco-Kelly F; López-Molina MI; García-Sandoval B; Guo Y; Tian L; Liu X; Guan L; Zhang J; Keating B; Xu X; Hakonarson H; Ayuso C
    PLoS One; 2015; 10(7):e0133624. PubMed ID: 26197217
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.