BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 36421837)

  • 1. Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying
    Ferilli M; Ciolfi A; Pedace L; Niceta M; Radio FC; Pizzi S; Miele E; Cappelletti C; Mancini C; Galluccio T; Andreani M; Iascone M; Chiriatti L; Novelli A; Micalizzi A; Matraxia M; Menale L; Faletra F; Prontera P; Pilotta A; Bedeschi MF; Capolino R; Baban A; Seri M; Mammì C; Zampino G; Digilio MC; Dallapiccola B; Priolo M; Tartaglia M
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421837
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations.
    Grand K; Gonzalez-Gandolfi C; Ackermann AM; Aljeaid D; Bedoukian E; Bird LM; De Leon DD; Diaz J; Hopkin RJ; Kadakia SP; Keena B; Klein KO; Krantz I; Leon E; Lord K; McDougall C; Medne L; Skraban CM; Stanley CA; Tarpinian J; Zackai E; Deardorff MA; Kalish JM
    Am J Med Genet A; 2019 Apr; 179(4):542-551. PubMed ID: 30719864
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NSD1 mutations generate a genome-wide DNA methylation signature.
    Choufani S; Cytrynbaum C; Chung BH; Turinsky AL; Grafodatskaya D; Chen YA; Cohen AS; Dupuis L; Butcher DT; Siu MT; Luk HM; Lo IF; Lam ST; Caluseriu O; Stavropoulos DJ; Reardon W; Mendoza-Londono R; Brudno M; Gibson WT; Chitayat D; Weksberg R
    Nat Commun; 2015 Dec; 6():10207. PubMed ID: 26690673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A boy with Silver-Russell syndrome and Sotos syndrome.
    Schwaibold EMC; Beygo J; Obeid K; Jauch A; Hinderhofer K; Moog U
    Am J Med Genet A; 2021 Feb; 185(2):549-554. PubMed ID: 33191647
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1.
    Oishi S; Zalucki O; Vega MS; Harkins D; Harvey TJ; Kasherman M; Davila RA; Hale L; White M; Piltz S; Thomas P; Burne THJ; Harris L; Piper M
    Genes Brain Behav; 2020 Apr; 19(4):e12637. PubMed ID: 31909872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.
    Conteduca G; Testa B; Baldo C; Arado A; Malacarne M; Candiano G; Garbarino A; Coviello DA; Cantoni C
    Gene; 2023 Jan; 851():146970. PubMed ID: 36261088
    [TBL] [Abstract][Full Text] [Related]  

  • 7. NSD1 mutations deregulate transcription and DNA methylation of bivalent developmental genes in Sotos syndrome.
    Brennan K; Zheng H; Fahrner JA; Shin JH; Gentles AJ; Schaefer B; Sunwoo JB; Bernstein JA; Gevaert O
    Hum Mol Genet; 2022 Jul; 31(13):2164-2184. PubMed ID: 35094088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The first pineoblastoma case report of a patient with Sotos syndrome harboring NSD1 germline mutation.
    Yue X; Liu B; Han T; Guo D; Ding R; Wang G
    BMC Pediatr; 2024 Mar; 24(1):166. PubMed ID: 38459438
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sotos syndrome with marked overgrowth in three Japanese patients with heterozygous likely pathogenic NSD1 variants: case reports with review of literature.
    Masunaga Y; Ono H; Fujisawa Y; Taniguchi K; Saitsu H; Ogata T
    Endocr J; 2024 Jan; 71(1):75-81. PubMed ID: 37989294
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations.
    Tatton-Brown K; Douglas J; Coleman K; Baujat G; Cole TR; Das S; Horn D; Hughes HE; Temple IK; Faravelli F; Waggoner D; Turkmen S; Cormier-Daire V; Irrthum A; Rahman N;
    Am J Hum Genet; 2005 Aug; 77(2):193-204. PubMed ID: 15942875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.
    Watanabe H; Higashimoto K; Miyake N; Morita S; Horii T; Kimura M; Suzuki T; Maeda T; Hidaka H; Aoki S; Yatsuki H; Okamoto N; Uemura T; Hatada I; Matsumoto N; Soejima H
    FASEB J; 2020 Jan; 34(1):960-973. PubMed ID: 31914674
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Epigenetic inactivation of the Sotos overgrowth syndrome gene histone methyltransferase NSD1 in human neuroblastoma and glioma.
    Berdasco M; Ropero S; Setien F; Fraga MF; Lapunzina P; Losson R; Alaminos M; Cheung NK; Rahman N; Esteller M
    Proc Natl Acad Sci U S A; 2009 Dec; 106(51):21830-5. PubMed ID: 20018718
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sotos syndrome in two children from India.
    Panigrahi I; Chaudhry C
    Am J Med Genet A; 2020 Sep; 182(9):2181-2183. PubMed ID: 32677741
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of Novel NSD1 variations in four Pediatric cases with sotos Syndrome.
    Ren Z; Yue L; Hu HY; Hou XL; Chen WQ; Tan Y; Dong Z; Zhang J
    BMC Med Genomics; 2024 Apr; 17(1):116. PubMed ID: 38684994
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome.
    Testa B; Conteduca G; Grasso M; Cecconi M; Lantieri F; Baldo C; Arado A; Andraghetti L; Malacarne M; Milani D; Coviello D; Sotos Collaborative Group
    Genes (Basel); 2023 Jan; 14(2):. PubMed ID: 36833222
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients.
    Machida M; Katoh H; Machida M; Miyake A; Taira K; Ohashi H
    Spine (Phila Pa 1976); 2021 Jul; 46(13):E726-E733. PubMed ID: 33332788
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reversal of Clinical Phenotype of Sotos Syndrome Due to Microduplication of NSD1 Gene.
    Takkar A; Arora V; Saxena R; Kumar P; Verma IC
    Indian J Pediatr; 2022 Nov; 89(11):1137-1139. PubMed ID: 35925544
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in SETD2 cause a novel overgrowth condition.
    Luscan A; Laurendeau I; Malan V; Francannet C; Odent S; Giuliano F; Lacombe D; Touraine R; Vidaud M; Pasmant E; Cormier-Daire V
    J Med Genet; 2014 Aug; 51(8):512-7. PubMed ID: 24852293
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.
    Castro MAA; Dos Santos JHV; Honjo RS; Yamamoto GL; Bertola DR; Hurst AC; Chorich LP; Layman LC; Kim CA; Kim HG
    Am J Med Genet A; 2021 Dec; 185(12):3916-3923. PubMed ID: 34405946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disrupted epigenetics in the Sotos syndrome neurobehavioral phenotype.
    Harris JR; Fahrner JA
    Curr Opin Psychiatry; 2019 Mar; 32(2):55-59. PubMed ID: 30601169
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.