BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 34897852)

  • 1. BGvar: A comprehensive resource for blood group immunogenetics.
    Rophina M; Pandhare K; Jadhao S; Nagaraj SH; Scaria V
    Transfus Med; 2022 Jun; 32(3):229-236. PubMed ID: 34897852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. BGMUT: NCBI dbRBC database of allelic variations of genes encoding antigens of blood group systems.
    Patnaik SK; Helmberg W; Blumenfeld OO
    Nucleic Acids Res; 2012 Jan; 40(Database issue):D1023-9. PubMed ID: 22084196
    [TBL] [Abstract][Full Text] [Related]  

  • 3. WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson's Disease.
    Kumar M; Gaharwar U; Paul S; Poojary M; Pandhare K; Scaria V; Bk B
    Sci Rep; 2020 Jun; 10(1):9037. PubMed ID: 32493955
    [TBL] [Abstract][Full Text] [Related]  

  • 4. International Society of Blood Transfusion Working Party on Red Cell Immunogenetics and Blood Group Terminology Report of Basel and three virtual business meetings: Update on blood group systems.
    Gassner C; Castilho L; Chen Q; Clausen FB; Denomme GA; Flegel WA; Gleadall N; Hellberg Å; Ji Y; Keller MA; Lane WJ; Ligthart P; Lomas-Francis C; Nogues N; Olsson ML; Peyrard T; Storry JR; Tani Y; Thornton N; van der Schoot E; Veldhuisen B; Wagner F; Weinstock C; Wendel S; Westhoff C; Yahalom V; Hyland CA
    Vox Sang; 2022 Nov; 117(11):1332-1344. PubMed ID: 36121188
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation databases and other online sites as a resource for transfusion medicine: history and attributes.
    Blumenfeld OO
    Transfus Med Rev; 2002 Apr; 16(2):103-14. PubMed ID: 11941573
    [TBL] [Abstract][Full Text] [Related]  

  • 6. tbvar: A comprehensive genome variation resource for Mycobacterium tuberculosis.
    Joshi KR; Dhiman H; Scaria V
    Database (Oxford); 2014; 2014():bat083. PubMed ID: 24408216
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants.
    Han Q; Yang Y; Wu S; Liao Y; Zhang S; Liang H; Cram DS; Zhang Y
    BMC Genomics; 2021 Jun; 22(1):407. PubMed ID: 34082700
    [TBL] [Abstract][Full Text] [Related]  

  • 8. International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Cancun report (2012).
    Storry JR; Castilho L; Daniels G; Flegel WA; Garratty G; de Haas M; Hyland C; Lomas-Francis C; Moulds JM; Nogues N; Olsson ML; Poole J; Reid ME; Rouger P; van der Schoot E; Scott M; Tani Y; Yu LC; Wendel S; Westhoff C; Yahalom V; Zelinski T
    Vox Sang; 2014 Jul; 107(1):90-6. PubMed ID: 24372289
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A community-based resource for automatic exome variant-calling and annotation in Mendelian disorders.
    Mutarelli M; Marwah V; Rispoli R; Carrella D; Dharmalingam G; Oliva G; di Bernardo D
    BMC Genomics; 2014; 15 Suppl 3(Suppl 3):S5. PubMed ID: 25078076
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database.
    Blumenfeld OO; Patnaik SK
    Hum Mutat; 2004 Jan; 23(1):8-16. PubMed ID: 14695527
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Circad: a comprehensive manually curated resource of circular RNA associated with diseases.
    Rophina M; Sharma D; Poojary M; Scaria V
    Database (Oxford); 2020 Jan; 2020():. PubMed ID: 32219412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The role of genomics in transfusion medicine.
    Wheeler MM; Johnsen JM
    Curr Opin Hematol; 2018 Nov; 25(6):509-515. PubMed ID: 30138126
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AnnTools: a comprehensive and versatile annotation toolkit for genomic variants.
    Makarov V; O'Grady T; Cai G; Lihm J; Buxbaum JD; Yoon S
    Bioinformatics; 2012 Mar; 28(5):724-5. PubMed ID: 22257670
    [TBL] [Abstract][Full Text] [Related]  

  • 14. IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes.
    Jain A; Bhoyar RC; Pandhare K; Mishra A; Sharma D; Imran M; Senthivel V; Divakar MK; Rophina M; Jolly B; Batra A; Sharma S; Siwach S; Jadhao AG; Palande NV; Jha GN; Ashrafi N; Mishra PK; A K V; Jain S; Dash D; Kumar NS; Vanlallawma A; Sarma RJ; Chhakchhuak L; Kalyanaraman S; Mahadevan R; Kandasamy S; B M P; Rajagopal RE; J ER; P ND; Bajaj A; Gupta V; Mathew S; Goswami S; Mangla M; Prakash S; Joshi K; S S; Gajjar D; Soraisham R; Yadav R; Devi YS; Gupta A; Mukerji M; Ramalingam S; B K B; Scaria V; Sivasubbu S
    Nucleic Acids Res; 2021 Jan; 49(D1):D1225-D1232. PubMed ID: 33095885
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Patterns of human genetic variation inferred from comparative analysis of allelic mutations in blood group antigen genes.
    Patnaik SK; Blumenfeld OO
    Hum Mutat; 2011 Mar; 32(3):263-71. PubMed ID: 21312314
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants.
    Patel RY; Shah N; Jackson AR; Ghosh R; Pawliczek P; Paithankar S; Baker A; Riehle K; Chen H; Milosavljevic S; Bizon C; Rynearson S; Nelson T; Jarvik GP; Rehm HL; Harrison SM; Azzariti D; Powell B; Babb L; Plon SE; Milosavljevic A;
    Genome Med; 2017 Jan; 9(1):3. PubMed ID: 28081714
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic Variants Within the Erythroid Transcription Factor, KLF1, and Reduction of the Expression of Lutheran and Other Blood Group Antigens: Review of the In(Lu) Phenotype.
    Fraser NS; Knauth CM; Moussa A; Dean MM; Hyland CA; Perkins AC; Flower RL; Schoeman EM
    Transfus Med Rev; 2019 Apr; 33(2):111-117. PubMed ID: 31023581
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
    Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
    Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations.
    K S; Jalali S; Scaria V; Bhardwaj A
    PLoS One; 2013; 8(4):e60066. PubMed ID: 23585830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evolutionary divergence of the ABO and GBGT1 genes specifying the ABO and FORS blood group systems through chromosomal rearrangements.
    Yamamoto F
    Sci Rep; 2017 Aug; 7(1):9375. PubMed ID: 28839219
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.