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 *

82 related articles for article (PubMed ID: 30140248)

  • 1. Novel Variants Identified in Multiple Sclerosis Patients From Southern China.
    Wang H; Pardeshi LA; Rong X; Li E; Wong KH; Peng Y; Xu RH
    Front Neurol; 2018; 9():582. PubMed ID: 30140248
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Variants of CYP27B1 are associated with both multiple sclerosis and neuromyelitis optica patients in Han Chinese population.
    Zhuang JC; Huang ZY; Zhao GX; Yu H; Li ZX; Wu ZY
    Gene; 2015 Feb; 557(2):236-9. PubMed ID: 25542806
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Ziliotto N; Marchetti G; Scapoli C; Bovolenta M; Meneghetti S; Benazzo A; Lunghi B; Balestra D; Laino LA; Bozzini N; Guidi I; Salvi F; Straudi S; Gemmati D; Menegatti E; Zamboni P; Bernardi F
    Front Genet; 2019; 10():573. PubMed ID: 31297130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.
    Cardinale CJ; Li D; Tian L; Connolly JJ; March ME; Hou C; Wang F; Snyder J; Kim CE; Chiavacci RM; Sleiman PM; Burnham JM; Hakonarson H
    BMC Musculoskelet Disord; 2016 Nov; 17(1):462. PubMed ID: 27829420
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing.
    Heo WI; Park KY; Jin T; Lee MK; Kim M; Choi EH; Kim HS; Bae JM; Moon NJ; Seo SJ
    BMC Med Genet; 2017 Jan; 18(1):8. PubMed ID: 28125976
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity.
    Jiao H; Arner P; Gerdhem P; Strawbridge RJ; Näslund E; Thorell A; Hamsten A; Kere J; Dahlman I
    Eur J Hum Genet; 2015 Sep; 23(9):1216-22. PubMed ID: 25406998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.
    Zaragoza MV; Fung L; Jensen E; Oh F; Cung K; McCarthy LA; Tran CK; Hoang V; Hakim SA; Grosberg A
    PLoS One; 2016; 11(5):e0155421. PubMed ID: 27182706
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.
    Kelsen JR; Dawany N; Moran CJ; Petersen BS; Sarmady M; Sasson A; Pauly-Hubbard H; Martinez A; Maurer K; Soong J; Rappaport E; Franke A; Keller A; Winter HS; Mamula P; Piccoli D; Artis D; Sonnenberg GF; Daly M; Sullivan KE; Baldassano RN; Devoto M
    Gastroenterology; 2015 Nov; 149(6):1415-24. PubMed ID: 26193622
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.
    Lin D; Wang D; Li P; Deng L; Zhang Z; Zhang Y; Zhang M; Zhang N
    BMC Med Genomics; 2023 Jan; 16(1):13. PubMed ID: 36703207
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epstein-Barr virus genetic variants are associated with multiple sclerosis.
    Mechelli R; Manzari C; Policano C; Annese A; Picardi E; Umeton R; Fornasiero A; D'Erchia AM; Buscarinu MC; Agliardi C; Annibali V; Serafini B; Rosicarelli B; Romano S; Angelini DF; Ricigliano VA; Buttari F; Battistini L; Centonze D; Guerini FR; D'Alfonso S; Pesole G; Salvetti M; Ristori G
    Neurology; 2015 Mar; 84(13):1362-8. PubMed ID: 25740864
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population.
    Clarelli F; Barizzone N; Mangano E; Zuccalà M; Basagni C; Anand S; Sorosina M; Mascia E; Santoro S; ; ; Guerini FR; Virgilio E; Gallo A; Pizzino A; Comi C; Martinelli V; Comi G; De Bellis G; Leone M; Filippi M; Esposito F; Bordoni R; Martinelli Boneschi F; D'Alfonso S
    Front Genet; 2021; 12():800262. PubMed ID: 35047017
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Brief Report: Whole-Exome Sequencing for Identification of Potential Causal Variants for Diffuse Cutaneous Systemic Sclerosis.
    Mak AC; Tang PL; Cleveland C; Smith MH; Kari Connolly M; Katsumoto TR; Wolters PJ; Kwok PY; Criswell LA
    Arthritis Rheumatol; 2016 Sep; 68(9):2257-62. PubMed ID: 27111861
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.
    Li J; Jiang D; Xiao X; Li S; Jia X; Sun W; Guo X; Zhang Q
    Invest Ophthalmol Vis Sci; 2015 Jan; 56(2):722-9. PubMed ID: 25587058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients.
    Lim EC; Brett M; Lai AH; Lee SP; Tan ES; Jamuar SS; Ng IS; Tan EC
    Hum Genomics; 2015 Dec; 9():33. PubMed ID: 26666243
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Using Whole Exome Sequencing to Identify Candidate Genes With Rare Variants In Nonsyndromic Cleft Lip and Palate.
    Aylward A; Cai Y; Lee A; Blue E; Rabinowitz D; Haddad J;
    Genet Epidemiol; 2016 Jul; 40(5):432-41. PubMed ID: 27229527
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exome sequencing in families with severe mental illness identifies novel and rare variants in genes implicated in Mendelian neuropsychiatric syndromes.
    Ganesh S; Ahmed P H; Nadella RK; More RP; Seshadri M; Viswanath B; Rao M; Jain S; ; Mukherjee O
    Psychiatry Clin Neurosci; 2019 Jan; 73(1):11-19. PubMed ID: 30367527
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
    Sadovnick AD; Traboulsee AL; Bernales CQ; Ross JP; Forwell AL; Yee IM; Guillot-Noel L; Fontaine B; Cournu-Rebeix I; Alcina A; Fedetz M; Izquierdo G; Matesanz F; Hilven K; Dubois B; Goris A; Astobiza I; Alloza I; Antigüedad A; Vandenbroeck K; Akkad DA; Aktas O; Blaschke P; Buttmann M; Chan A; Epplen JT; Gerdes LA; Kroner A; Kubisch C; Kümpfel T; Lohse P; Rieckmann P; Zettl UK; Zipp F; Bertram L; Lill CM; Fernandez O; Urbaneja P; Leyva L; Alvarez-Cermeño JC; Arroyo R; Garagorri AM; García-Martínez A; Villar LM; Urcelay E; Malhotra S; Montalban X; Comabella M; Berger T; Fazekas F; Reindl M; Schmied MC; Zimprich A; Vilariño-Güell C
    G3 (Bethesda); 2016 Jul; 6(7):2073-9. PubMed ID: 27194806
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.