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 *

183 related articles for article (PubMed ID: 28595269)

  • 21. Whole exome sequencing identifies PLEC, EXO5 and DNAH7 as novel susceptibility genes in testicular cancer.
    Paumard-Hernández B; Calvete O; Inglada Pérez L; Tejero H; Al-Shahrour F; Pita G; Barroso A; Carlos Triviño J; Urioste M; Valverde C; González Billalabeitia E; Quiroga V; Francisco Rodríguez Moreno J; Fernández Aramburo A; López C; Maroto P; Sastre J; José Juan Fita M; Duran I; Lorenzo-Lorenzo I; Iranzo P; García Del Muro X; Ros S; Zambrana F; María Autran A; Benítez J
    Int J Cancer; 2018 Oct; 143(8):1954-1962. PubMed ID: 29761480
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke.
    Ilinca A; Martinez-Majander N; Samuelsson S; Piccinelli P; Truvé K; Cole J; Kittner S; Soller M; Kristoffersson U; Tatlisumak T; Puschmann A; Putaala J; Lindgren A
    Stroke; 2020 Apr; 51(4):1056-1063. PubMed ID: 32172663
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
    Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
    World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Candidate variants in TUB are associated with familial tremor.
    Sailani MR; Jahanbani F; Abbott CW; Lee H; Zia A; Rego S; Winkelmann J; Hopfner F; Khan TN; Katsanis N; Müller SH; Berg D; Lyman KM; Mychajliw C; Deuschl G; Bernstein JA; Kuhlenbäumer G; Snyder MP
    PLoS Genet; 2020 Sep; 16(9):e1009010. PubMed ID: 32956375
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
    Braun DA; Warejko JK; Ashraf S; Tan W; Daga A; Schneider R; Hermle T; Jobst-Schwan T; Widmeier E; Majmundar AJ; Nakayama M; Schapiro D; Rao J; Schmidt JM; Hoogstraten CA; Hugo H; Bakkaloglu SA; Kari JA; El Desoky S; Daouk G; Mane S; Lifton RP; Shril S; Hildebrandt F
    Nephrol Dial Transplant; 2019 Mar; 34(3):485-493. PubMed ID: 29534211
    [TBL] [Abstract][Full Text] [Related]  

  • 26. COL4A5 and LAMA5 variants co-inherited in familial hematuria: digenic inheritance or genetic modifier effect?
    Voskarides K; Papagregoriou G; Hadjipanagi D; Petrou I; Savva I; Elia A; Athanasiou Y; Pastelli A; Kkolou M; Hadjigavriel M; Stavrou C; Pierides A; Deltas C
    BMC Nephrol; 2018 May; 19(1):114. PubMed ID: 29764427
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.
    Guo MH; Plummer L; Chan YM; Hirschhorn JN; Lippincott MF
    Am J Hum Genet; 2018 Oct; 103(4):522-534. PubMed ID: 30269813
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole exome sequencing in familial isolated primary hyperparathyroidism.
    Cetani F; Pardi E; Aretini P; Saponaro F; Borsari S; Mazoni L; Apicella M; Civita P; La Ferla M; Caligo MA; Lessi F; Mazzanti CM; Torregossa L; Oppo A; Marcocci C
    J Endocrinol Invest; 2020 Feb; 43(2):231-245. PubMed ID: 31486992
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genome-wide linkage and exome analyses identify variants of HMCN1 for splenic epidermoid cyst.
    Omer WH; Narita A; Hosomichi K; Mitsunaga S; Hayashi Y; Yamashita A; Krasniqi A; Iwasaki Y; Kimura M; Inoue I
    BMC Med Genet; 2014 Oct; 15():115. PubMed ID: 25338956
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
    Wang H; Wang X; He C; Li H; Qing J; Grati M; Hu Z; Li J; Hu Y; Xia K; Mei L; Wang X; Yu J; Chen H; Jiang L; Liu Y; Men M; Zhang H; Guan L; Xiao J; Zhang J; Liu X; Feng Y
    J Hum Genet; 2015 Mar; 60(3):119-126. PubMed ID: 25589040
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole exome sequencing identified genetic variations in Chinese hemangioblastoma patients.
    Ma D; Yang J; Wang Y; Huang X; Du G; Zhou L
    Am J Med Genet A; 2017 Oct; 173(10):2605-2613. PubMed ID: 28742274
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy.
    Norton N; Li D; Rampersaud E; Morales A; Martin ER; Zuchner S; Guo S; Gonzalez M; Hedges DJ; Robertson PD; Krumm N; Nickerson DA; Hershberger RE;
    Circ Cardiovasc Genet; 2013 Apr; 6(2):144-53. PubMed ID: 23418287
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in
    Robyns T; Willems R; Van Cleemput J; Jhangiani S; Muzny D; Gibbs R; Lupski JR; Breckpot J; Devriendt K; Corveleyn A
    Acta Cardiol; 2020 Dec; 75(8):748-753. PubMed ID: 31583969
    [No Abstract]   [Full Text] [Related]  

  • 34. Challenges in whole exome sequencing: an example from hereditary deafness.
    Sirmaci A; Edwards YJ; Akay H; Tekin M
    PLoS One; 2012; 7(2):e32000. PubMed ID: 22363784
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnosing rare diseases after the exome.
    Frésard L; Montgomery SB
    Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559314
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole exome sequencing identifies multiple, complex etiologies in an idiopathic hereditary pancreatitis kindred.
    LaRusch J; Barmada MM; Solomon S; Whitcomb DC
    JOP; 2012 May; 13(3):258-62. PubMed ID: 22572128
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification of rare missense mutations in
    Lee HS; Jeong HR; Rho JG; Kum CD; Kim KH; Kim DW; Cheong JY; Jeong SY; Hwang JS
    Gynecol Endocrinol; 2020 Aug; 36(8):682-686. PubMed ID: 32400230
    [No Abstract]   [Full Text] [Related]  

  • 38. Novel genes and variants associated with IgA nephropathy by co-segregating with the disease phenotypes in 10 IgAN families.
    Liu R; Hu B; Li Q; Jing X; Zhong C; Chang Y; Liao Q; Lam MF; Leung JC; Lai KN; Wang Y
    Gene; 2015 Oct; 571(1):43-51. PubMed ID: 26095808
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy.
    Wells QS; Becker JR; Su YR; Mosley JD; Weeke P; D'Aoust L; Ausborn NL; Ramirez AH; Pfotenhauer JP; Naftilan AJ; Markham L; Exil V; Roden DM; Hong CC
    Circ Cardiovasc Genet; 2013 Aug; 6(4):317-26. PubMed ID: 23861363
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PCR-free whole exome sequencing: Cost-effective and efficient in detecting rare mutations.
    Yamaguchi I; Watanabe T; Ohara O; Hasegawa Y
    PLoS One; 2019; 14(9):e0222562. PubMed ID: 31518370
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.