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 *

174 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. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Understanding Language from a Genomic Perspective.
    Graham SA; Fisher SE
    Annu Rev Genet; 2015; 49():131-60. PubMed ID: 26442845
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.