498 related articles for article (PubMed ID: 25395389)
1. Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.
Azzi S; Steunou V; Tost J; Rossignol S; Thibaud N; Das Neves C; Le Jule M; Habib WA; Blaise A; Koudou Y; Busato F; Le Bouc Y; Netchine I
J Med Genet; 2015 Jan; 52(1):53-60. PubMed ID: 25395389
[TBL] [Abstract][Full Text] [Related]
2. 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
Abi Habib W; Brioude F; Azzi S; Salem J; Das Neves C; Personnier C; Chantot-Bastaraud S; Keren B; Le Bouc Y; Harbison MD; Netchine I
Hum Mutat; 2017 Jan; 38(1):105-111. PubMed ID: 27701793
[TBL] [Abstract][Full Text] [Related]
3. Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation.
Azzi S; Blaise A; Steunou V; Harbison MD; Salem J; Brioude F; Rossignol S; Habib WA; Thibaud N; Neves CD; Jule ML; Brachet C; Heinrichs C; Bouc YL; Netchine I
Hum Mutat; 2014 Oct; 35(10):1211-20. PubMed ID: 25044976
[TBL] [Abstract][Full Text] [Related]
4. Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders.
Demars J; Shmela ME; Rossignol S; Okabe J; Netchine I; Azzi S; Cabrol S; Le Caignec C; David A; Le Bouc Y; El-Osta A; Gicquel C
Hum Mol Genet; 2010 Mar; 19(5):803-14. PubMed ID: 20007505
[TBL] [Abstract][Full Text] [Related]
5. A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient.
Higashimoto K; Jozaki K; Kosho T; Matsubara K; Fuke T; Yamada D; Yatsuki H; Maeda T; Ohtsuka Y; Nishioka K; Joh K; Koseki H; Ogata T; Soejima H
Clin Genet; 2014 Dec; 86(6):539-44. PubMed ID: 24299031
[TBL] [Abstract][Full Text] [Related]
6. Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome.
Kannenberg K; Urban C; Binder G
Clin Genet; 2012 Apr; 81(4):366-77. PubMed ID: 22248018
[TBL] [Abstract][Full Text] [Related]
7. Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci.
Azzi S; Rossignol S; Steunou V; Sas T; Thibaud N; Danton F; Le Jule M; Heinrichs C; Cabrol S; Gicquel C; Le Bouc Y; Netchine I
Hum Mol Genet; 2009 Dec; 18(24):4724-33. PubMed ID: 19755383
[TBL] [Abstract][Full Text] [Related]
8. Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.
Abi Habib W; Azzi S; Brioude F; Steunou V; Thibaud N; Das Neves C; Le Jule M; Chantot-Bastaraud S; Keren B; Lyonnet S; Michot C; Rossi M; Pasquier L; Gicquel C; Rossignol S; Le Bouc Y; Netchine I
Hum Mol Genet; 2014 Nov; 23(21):5763-73. PubMed ID: 24916376
[TBL] [Abstract][Full Text] [Related]
9. Epigenetic anomalies in childhood growth disorders.
Netchine I; Rossignol S; Azzi S; Le Bouc Y
Nestle Nutr Inst Workshop Ser; 2013; 71():65-73. PubMed ID: 23502140
[TBL] [Abstract][Full Text] [Related]
10. A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith-Wiedemann or Silver-Russell syndrome in a single family.
Jurkiewicz D; Kugaudo M; Skórka A; Śmigiel R; Smyk M; Ciara E; Chrzanowska K; Krajewska-Walasek M
Am J Med Genet A; 2017 Jan; 173(1):72-78. PubMed ID: 27612309
[TBL] [Abstract][Full Text] [Related]
11. IGF-I sensitivity in Silver-Russell syndrome with IGF2/H19 hypomethylation.
Iliev DI; Kannenberg K; Weber K; Binder G
Growth Horm IGF Res; 2014 Oct; 24(5):187-91. PubMed ID: 25066218
[TBL] [Abstract][Full Text] [Related]
12. Methylation profiling in individuals with Russell-Silver syndrome.
Peñaherrera MS; Weindler S; Van Allen MI; Yong SL; Metzger DL; McGillivray B; Boerkoel C; Langlois S; Robinson WP
Am J Med Genet A; 2010 Feb; 152A(2):347-55. PubMed ID: 20082469
[TBL] [Abstract][Full Text] [Related]
13. The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome.
Sun F; Higashimoto K; Awaji A; Ohishi K; Nishizaki N; Tanoue Y; Aoki S; Watanabe H; Yatsuki H; Soejima H
J Hum Genet; 2019 Sep; 64(9):937-943. PubMed ID: 31235774
[TBL] [Abstract][Full Text] [Related]
14. Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome.
Higashimoto K; Watanabe H; Tanoue Y; Tonoki H; Tokutomi T; Hara S; Yatsuki H; Soejima H
J Med Genet; 2021 Jun; 58(6):422-425. PubMed ID: 32447322
[TBL] [Abstract][Full Text] [Related]
15. Is ZFP57 binding to
Sparago A; Cerrato F; Riccio A
Clin Epigenetics; 2018; 10():23. PubMed ID: 29484033
[TBL] [Abstract][Full Text] [Related]
16. IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia.
Zeschnigk M; Albrecht B; Buiting K; Kanber D; Eggermann T; Binder G; Gromoll J; Prott EC; Seland S; Horsthemke B
Eur J Hum Genet; 2008 Mar; 16(3):328-34. PubMed ID: 18159214
[TBL] [Abstract][Full Text] [Related]
17. First report on concordant monozygotic twins with Silver-Russell syndrome and ICR1 hypomethylation.
Riess A; Binder G; Ziegler J; Begemann M; Soellner L; Eggermann T
Eur J Med Genet; 2016 Jan; 59(1):1-4. PubMed ID: 26691664
[TBL] [Abstract][Full Text] [Related]
18. Are H19 variants associated with Silver-Russell syndrome?
Schönherr N; Binder G; Korsch E; Kämmerer E; Wollmann HA; Eggermann T
J Pediatr Endocrinol Metab; 2008 Oct; 21(10):985-93. PubMed ID: 19209620
[TBL] [Abstract][Full Text] [Related]
19. Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation.
Grønskov K; Poole RL; Hahnemann JM; Thomson J; Tümer Z; Brøndum-Nielsen K; Murphy R; Ravn K; Melchior L; Dedic A; Dolmer B; Temple IK; Boonen SE; Mackay DJ
J Med Genet; 2011 May; 48(5):308-11. PubMed ID: 21278389
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]