BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 27016271)

  • 1. Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
    Kornilov SA; Rakhlin N; Koposov R; Lee M; Yrigollen C; Caglayan AO; Magnuson JS; Mane S; Chang JT; Grigorenko EL
    Pediatrics; 2016 Apr; 137(4):. PubMed ID: 27016271
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Candidate gene variant effects on language disorders in Robinson Crusoe Island.
    Mountford HS; Villanueva P; Fernández MA; Barbieri Z; Cazier JB; Newbury DF
    Ann Hum Biol; 2019 Mar; 46(2):109-119. PubMed ID: 31132892
    [No Abstract]   [Full Text] [Related]  

  • 4. Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways.
    Cappi C; Brentani H; Lima L; Sanders SJ; Zai G; Diniz BJ; Reis VN; Hounie AG; Conceição do Rosário M; Mariani D; Requena GL; Puga R; Souza-Duran FL; Shavitt RG; Pauls DL; Miguel EC; Fernandez TV
    Transl Psychiatry; 2016 Mar; 6(3):e764. PubMed ID: 27023170
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family-based exome-wide assessment of maternal genetic effects on susceptibility to childhood B-cell acute lymphoblastic leukemia in hispanics.
    Archer NP; Perez-Andreu V; Scheurer ME; Rabin KR; Peckham-Gregory EC; Plon SE; Zabriskie RC; De Alarcon PA; Fernandez KS; Najera CR; Yang JJ; Antillon-Klussmann F; Lupo PJ
    Cancer; 2016 Dec; 122(23):3697-3704. PubMed ID: 27529658
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cohesion of Cortical Language Networks During Word Processing Is Predicted by a Common Polymorphism in the SETBP1 Gene.
    Rakhlin N; Landi N; Lee M; Magnuson JS; Naumova OY; Ovchinnikova IV; Grigorenko EL
    New Dir Child Adolesc Dev; 2020 Jan; 2020(169):131-155. PubMed ID: 32324324
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.
    Sabo A; Mishra P; Dugan-Perez S; Voruganti VS; Kent JW; Kalra D; Cole SA; Comuzzie AG; Muzny DM; Gibbs RA; Butte NF
    Obesity (Silver Spring); 2017 Jul; 25(7):1270-1276. PubMed ID: 28508493
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis.
    Grauers A; Wang J; Einarsdottir E; Simony A; Danielsson A; Åkesson K; Ohlin A; Halldin K; Grabowski P; Tenne M; Laivuori H; Dahlman I; Andersen M; Christensen SB; Karlsson MK; Jiao H; Kere J; Gerdhem P
    Spine J; 2015 Oct; 15(10):2239-46. PubMed ID: 25987191
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome Sequencing and the Management of Neurometabolic Disorders.
    Tarailo-Graovac M; Shyr C; Ross CJ; Horvath GA; Salvarinova R; Ye XC; Zhang LH; Bhavsar AP; Lee JJ; Drögemöller BI; Abdelsayed M; Alfadhel M; Armstrong L; Baumgartner MR; Burda P; Connolly MB; Cameron J; Demos M; Dewan T; Dionne J; Evans AM; Friedman JM; Garber I; Lewis S; Ling J; Mandal R; Mattman A; McKinnon M; Michoulas A; Metzger D; Ogunbayo OA; Rakic B; Rozmus J; Ruben P; Sayson B; Santra S; Schultz KR; Selby K; Shekel P; Sirrs S; Skrypnyk C; Superti-Furga A; Turvey SE; Van Allen MI; Wishart D; Wu J; Wu J; Zafeiriou D; Kluijtmans L; Wevers RA; Eydoux P; Lehman AM; Vallance H; Stockler-Ipsiroglu S; Sinclair G; Wasserman WW; van Karnebeek CD
    N Engl J Med; 2016 Jun; 374(23):2246-55. PubMed ID: 27276562
    [TBL] [Abstract][Full Text] [Related]  

  • 10. New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.
    Pronicka E; Piekutowska-Abramczuk D; Ciara E; Trubicka J; Rokicki D; Karkucińska-Więckowska A; Pajdowska M; Jurkiewicz E; Halat P; Kosińska J; Pollak A; Rydzanicz M; Stawinski P; Pronicki M; Krajewska-Walasek M; Płoski R
    J Transl Med; 2016 Jun; 14(1):174. PubMed ID: 27290639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics in disorders of language.
    Gilger JW
    Clin Commun Disord; 1992; 2(4):35-47. PubMed ID: 1284525
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome versus transcriptome sequencing in identifying coding region variants.
    Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
    Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities.
    Cipriani V; Kalhoro A; Arno G; Silva RS; Pontikos N; Puech V; McClements ME; Hunt DM; van Heyningen V; Michaelides M; Webster AR; Moore AT; Puech B
    Ophthalmic Genet; 2017 Dec; 38(6):511-519. PubMed ID: 28635424
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data.
    Saad M; Brkanac Z; Wijsman EM
    Genes Brain Behav; 2015 Nov; 14(8):607-17. PubMed ID: 26394601
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of Exome Variants and Their Metabolic Impact in 6,716 American Indians from the Southwest US.
    Kim HI; Ye B; Gosalia N; ; Köroğlu Ç; Hanson RL; Hsueh WC; Knowler WC; Baier LJ; Bogardus C; Shuldiner AR; Van Hout CV
    Am J Hum Genet; 2020 Aug; 107(2):251-264. PubMed ID: 32640185
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
    Hollegaard MV; Grauholm J; Nielsen R; Grove J; Mandrup S; Hougaard DM
    Mol Genet Metab; 2013; 110(1-2):65-72. PubMed ID: 23830478
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies.
    Beryozkin A; Shevah E; Kimchi A; Mizrahi-Meissonnier L; Khateb S; Ratnapriya R; Lazar CH; Blumenfeld A; Ben-Yosef T; Hemo Y; Pe'er J; Averbuch E; Sagi M; Boleda A; Gieser L; Zlotogorski A; Falik-Zaccai T; Alimi-Kasem O; Jacobson SG; Chowers I; Swaroop A; Banin E; Sharon D
    Sci Rep; 2015 Aug; 5():13187. PubMed ID: 26306921
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.
    Leu C; Balestrini S; Maher B; Hernández-Hernández L; Gormley P; Hämäläinen E; Heggeli K; Schoeler N; Novy J; Willis J; Plagnol V; Ellis R; Reavey E; O'Regan M; Pickrell WO; Thomas RH; Chung SK; Delanty N; McMahon JM; Malone S; Sadleir LG; Berkovic SF; Nashef L; Zuberi SM; Rees MI; Cavalleri GL; Sander JW; Hughes E; Helen Cross J; Scheffer IE; Palotie A; Sisodiya SM
    EBioMedicine; 2015 Sep; 2(9):1063-70. PubMed ID: 26501104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome-Wide Association Study Identifies Low-Frequency Coding Variants in 2p23.2 and 7p11.2 Associated with Survival of Non-Small Cell Lung Cancer Patients.
    Zhu M; Geng L; Shen W; Wang Y; Liu J; Cheng Y; Wang C; Dai J; Jin G; Hu Z; Ma H; Shen H
    J Thorac Oncol; 2017 Apr; 12(4):644-656. PubMed ID: 28104536
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.
    Funayama M; Ohe K; Amo T; Furuya N; Yamaguchi J; Saiki S; Li Y; Ogaki K; Ando M; Yoshino H; Tomiyama H; Nishioka K; Hasegawa K; Saiki H; Satake W; Mogushi K; Sasaki R; Kokubo Y; Kuzuhara S; Toda T; Mizuno Y; Uchiyama Y; Ohno K; Hattori N
    Lancet Neurol; 2015 Mar; 14(3):274-82. PubMed ID: 25662902
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.