BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

192 related articles for article (PubMed ID: 23750647)

  • 1. Genes, assisted reproductive technology and trans-illumination.
    Dias RP; Maher ER
    Epigenomics; 2013 Jun; 5(3):331-40. PubMed ID: 23750647
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.
    Eggermann T; Yapici E; Bliek J; Pereda A; Begemann M; Russo S; Tannorella P; Calzari L; de Nanclares GP; Lombardi P; Temple IK; Mackay D; Riccio A; Kagami M; Ogata T; Lapunzina P; Monk D; Maher ER; Tümer Z
    Clin Epigenetics; 2022 Mar; 14(1):41. PubMed ID: 35296332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide allelic methylation analysis reveals disease-specific susceptibility to multiple methylation defects in imprinting syndromes.
    Court F; Martin-Trujillo A; Romanelli V; Garin I; Iglesias-Platas I; Salafsky I; Guitart M; Perez de Nanclares G; Lapunzina P; Monk D
    Hum Mutat; 2013 Apr; 34(4):595-602. PubMed ID: 23335487
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human imprinting syndromes.
    Lim DH; Maher ER
    Epigenomics; 2009 Dec; 1(2):347-69. PubMed ID: 22122706
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.
    Hiura H; Okae H; Miyauchi N; Sato F; Sato A; Van De Pette M; John RM; Kagami M; Nakai K; Soejima H; Ogata T; Arima T
    Hum Reprod; 2012 Aug; 27(8):2541-8. PubMed ID: 22674207
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.
    Docherty LE; Rezwan FI; Poole RL; Turner CL; Kivuva E; Maher ER; Smithson SF; Hamilton-Shield JP; Patalan M; Gizewska M; Peregud-Pogorzelski J; Beygo J; Buiting K; Horsthemke B; Soellner L; Begemann M; Eggermann T; Baple E; Mansour S; Temple IK; Mackay DJ
    Nat Commun; 2015 Sep; 6():8086. PubMed ID: 26323243
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic imprinting syndromes and cancer.
    Lim DH; Maher ER
    Adv Genet; 2010; 70():145-75. PubMed ID: 20920748
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genomic imprinting and its relevance to congenital disease, infertility, molar pregnancy and induced pluripotent stem cell.
    Tomizawa S; Sasaki H
    J Hum Genet; 2012 Feb; 57(2):84-91. PubMed ID: 22237588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.
    Fontana L; Bedeschi MF; Maitz S; Cereda A; Faré C; Motta S; Seresini A; D'Ursi P; Orro A; Pecile V; Calvello M; Selicorni A; Lalatta F; Milani D; Sirchia SM; Miozzo M; Tabano S
    Epigenetics; 2018; 13(9):897-909. PubMed ID: 30221575
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Epigenetics, genomic imprinting and assisted reproductive technology.
    Le Bouc Y; Rossignol S; Azzi S; Steunou V; Netchine I; Gicquel C
    Ann Endocrinol (Paris); 2010 May; 71(3):237-8. PubMed ID: 20362968
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders.
    Soejima H; Higashimoto K
    J Hum Genet; 2013 Jul; 58(7):402-9. PubMed ID: 23719190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Maternal variants in
    Begemann M; Rezwan FI; Beygo J; Docherty LE; Kolarova J; Schroeder C; Buiting K; Chokkalingam K; Degenhardt F; Wakeling EL; Kleinle S; González Fassrainer D; Oehl-Jaschkowitz B; Turner CLS; Patalan M; Gizewska M; Binder G; Bich Ngoc CT; Chi Dung V; Mehta SG; Baynam G; Hamilton-Shield JP; Aljareh S; Lokulo-Sodipe O; Horton R; Siebert R; Elbracht M; Temple IK; Eggermann T; Mackay DJG
    J Med Genet; 2018 Jul; 55(7):497-504. PubMed ID: 29574422
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
    Meyer E; Lim D; Pasha S; Tee LJ; Rahman F; Yates JR; Woods CG; Reik W; Maher ER
    PLoS Genet; 2009 Mar; 5(3):e1000423. PubMed ID: 19300480
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes.
    Demars J; Gicquel C
    Clin Genet; 2012 Apr; 81(4):350-61. PubMed ID: 22150955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?
    Ulker V; Gurkan H; Tozkir H; Karaman V; Ozgur H; Numanoglu C; Gedikbasi A; Akbayir O; Uyguner ZO
    Eur J Obstet Gynecol Reprod Biol; 2013 Sep; 170(1):188-92. PubMed ID: 23880596
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of four imprinting disorders and ART.
    Hattori H; Hiura H; Kitamura A; Miyauchi N; Kobayashi N; Takahashi S; Okae H; Kyono K; Kagami M; Ogata T; Arima T
    Clin Epigenetics; 2019 Feb; 11(1):21. PubMed ID: 30732658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. NLRP7 or KHDC3L genes and the etiology of molar pregnancies and recurrent miscarriage.
    Andreasen L; Christiansen OB; Niemann I; Bolund L; Sunde L
    Mol Hum Reprod; 2013 Nov; 19(11):773-81. PubMed ID: 23963444
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders.
    Aref-Eshghi E; Schenkel LC; Lin H; Skinner C; Ainsworth P; Paré G; Siu V; Rodenhiser D; Schwartz C; Sadikovic B
    J Mol Diagn; 2017 Nov; 19(6):848-856. PubMed ID: 28807811
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Imprinted anomalies in fetal and childhood growth disorders: the model of Russell-Silver and Beckwith-Wiedemann syndromes.
    Netchine I; Rossignol S; Azzi S; Brioude F; Le Bouc Y
    Endocr Dev; 2012; 23():60-70. PubMed ID: 23182821
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Epigenetics, genomic imprinting and developmental disorders].
    Le Bouc Y; Rossignol S; Azzi S; Brioude F; Cabrol S; Gicquel C; Netchine I
    Bull Acad Natl Med; 2010 Feb; 194(2):287-97; discussion 297-300. PubMed ID: 21166119
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.