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 *

256 related articles for article (PubMed ID: 28832569)

  • 1. SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.
    Ameur A; Dahlberg J; Olason P; Vezzi F; Karlsson R; Martin M; Viklund J; Kähäri AK; Lundin P; Che H; Thutkawkorapin J; Eisfeldt J; Lampa S; Dahlberg M; Hagberg J; Jareborg N; Liljedahl U; Jonasson I; Johansson Å; Feuk L; Lundeberg J; Syvänen AC; Lundin S; Nilsson D; Nystedt B; Magnusson PK; Gyllensten U
    Eur J Hum Genet; 2017 Nov; 25(11):1253-1260. PubMed ID: 28832569
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new Swedish twin registry containing environmental and medical base line data from about 14,000 same-sexed pairs born 1926-58.
    Medlund P; Cederlöf R; Flodérus-Myrhed B; Friberg L; Sörensen S
    Acta Med Scand Suppl; 1976; 600():1-111. PubMed ID: 16995293
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A whole-genome sequenced control population in northern Sweden reveals subregional genetic differences.
    Svensson D; Rentoft M; Dahlin AM; Lundholm E; Olason PI; Sjödin A; Nylander C; Melin BS; Trygg J; Johansson E
    PLoS One; 2020; 15(9):e0237721. PubMed ID: 32915809
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Similarity Assessment of Twin-Family Populations by Custom-Designed Genotyping Array.
    Beck JJ; Hottenga JJ; Mbarek H; Finnicum CT; Ehli EA; Hur YM; Martin NG; de Geus EJC; Boomsma DI; Davies GE
    Twin Res Hum Genet; 2019 Aug; 22(4):210-219. PubMed ID: 31379313
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals.
    Teo SM; Ku CS; Naidoo N; Hall P; Chia KS; Salim A; Pawitan Y
    J Hum Genet; 2011 Jul; 56(7):524-33. PubMed ID: 21633363
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-Genome Sequencing of 502 Individuals from Latvia: The First Step towards a Population-Specific Reference of Genetic Variation.
    Reščenko R; Brīvība M; Atava I; Rovīte V; Pečulis R; Silamiķelis I; Ansone L; Megnis K; Birzniece L; Leja M; Xu L; Shi X; Zhou Y; Slaitas A; Hou Y; Kloviņš J
    Int J Mol Sci; 2023 Oct; 24(20):. PubMed ID: 37895026
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quality control metrics improve repeatability and reproducibility of single-nucleotide variants derived from whole-genome sequencing.
    Zhang W; Soika V; Meehan J; Su Z; Ge W; Ng HW; Perkins R; Simonyan V; Tong W; Hong H
    Pharmacogenomics J; 2015 Aug; 15(4):298-309. PubMed ID: 25384574
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy number variations in the genome of the Qatari population.
    Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
    BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loqusdb: added value of an observations database of local genomic variation.
    Magnusson M; Eisfeldt J; Nilsson D; Rosenbaum A; Wirta V; Lindstrand A; Wedell A; Stranneheim H
    BMC Bioinformatics; 2020 Jul; 21(1):273. PubMed ID: 32611382
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree.
    Eberle MA; Fritzilas E; Krusche P; Källberg M; Moore BL; Bekritsky MA; Iqbal Z; Chuang HY; Humphray SJ; Halpern AL; Kruglyak S; Margulies EH; McVean G; Bentley DR
    Genome Res; 2017 Jan; 27(1):157-164. PubMed ID: 27903644
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assessing single nucleotide variant detection and genotype calling on whole-genome sequenced individuals.
    Cheng AY; Teo YY; Ong RT
    Bioinformatics; 2014 Jun; 30(12):1707-13. PubMed ID: 24558117
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Discovery of Novel Sequences in 1,000 Swedish Genomes.
    Eisfeldt J; Mårtensson G; Ameur A; Nilsson D; Lindstrand A
    Mol Biol Evol; 2020 Jan; 37(1):18-30. PubMed ID: 31560401
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SWEDEGENE-a Swedish nation-wide DNA sample collection for pharmacogenomic studies of serious adverse drug reactions.
    Hallberg P; Yue QY; Eliasson E; Melhus H; Ås J; Wadelius M
    Pharmacogenomics J; 2020 Aug; 20(4):579-585. PubMed ID: 31949290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.
    Salmela E; Lappalainen T; Liu J; Sistonen P; Andersen PM; Schreiber S; Savontaus ML; Czene K; Lahermo P; Hall P; Kere J
    PLoS One; 2011 Feb; 6(2):e16747. PubMed ID: 21347369
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance.
    Kumar P; Al-Shafai M; Al Muftah WA; Chalhoub N; Elsaid MF; Aleem AA; Suhre K
    BMC Res Notes; 2014 Oct; 7():747. PubMed ID: 25339461
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cancer in twins: genetic and nongenetic familial risk factors.
    Ahlbom A; Lichtenstein P; Malmström H; Feychting M; Hemminki K; Pedersen NL
    J Natl Cancer Inst; 1997 Feb; 89(4):287-93. PubMed ID: 9048832
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Positional bias in variant calls against draft reference assemblies.
    Briskine RV; Shimizu KK
    BMC Genomics; 2017 Mar; 18(1):263. PubMed ID: 28351369
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis.
    Rentoft M; Svensson D; Sjödin A; Olason PI; Sjöström O; Nylander C; Osterman P; Sjögren R; Netotea S; Wibom C; Cederquist K; Chabes A; Trygg J; Melin BS; Johansson E
    PLoS One; 2019; 14(3):e0213350. PubMed ID: 30917156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis.
    Meltz Steinberg K; Nicholas TJ; Koboldt DC; Yu B; Mardis E; Pamphlett R
    Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(5-6):385-92. PubMed ID: 25960086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic and environmental factors in conjunctival UV autofluorescence.
    Yazar S; Cuellar-Partida G; McKnight CM; Quach-Thanissorn P; Mountain JA; Coroneo MT; Pennell CE; Hewitt AW; MacGregor S; Mackey DA
    JAMA Ophthalmol; 2015 Apr; 133(4):406-12. PubMed ID: 25590795
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.