Similar articles for PMID: 10856193

Year	Number of Results
1995	2
1996	3
1997	1
1998	5
1999	7
2000	8
2001	10
2002	7
2003	6
2004	4
2005	3
2006	4
2007	7
2008	6
2009	7
2010	5
2011	3
2012	5
2013	3
2014	4
2015	2
2016	1
2017	1
2019	1
2020	3
2021	1
2024	0

1

Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome.

Yoshihashi H, Maeyama K, Kosaki R, Ogata T, Tsukahara M, Goto Y, Hata J, Matsuo N, Smith RJ, Kosaki K. Yoshihashi H, et al. Am J Hum Genet. 2000 Aug;67(2):476-82. doi: 10.1086/302997. Epub 2000 Jun 12. Am J Hum Genet. 2000. PMID: 10856193 Free PMC article.

2

Recombinant Chromosome 7 Driven by Maternal Chromosome 7 Pericentric Inversion in a Girl with Features of Silver-Russell Syndrome.

Catusi I, Bonati MT, Mainini E, Russo S, Orlandini E, Larizza L, Recalcati MP. Catusi I, et al. Int J Mol Sci. 2020 Nov 11;21(22):8487. doi: 10.3390/ijms21228487. Int J Mol Sci. 2020. PMID: 33187293 Free PMC article.

3

Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.

Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M. Yamazawa K, et al. J Med Genet. 2021 Jun;58(6):427-432. doi: 10.1136/jmedgenet-2020-107019. Epub 2020 Jun 23. J Med Genet. 2021. PMID: 32576657 Free PMC article.

4

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients.

Inoue T, Nakamura A, Iwahashi-Odano M, Tanase-Nakao K, Matsubara K, Nishioka J, Maruo Y, Hasegawa Y, Suzumura H, Sato S, Kobayashi Y, Murakami N, Nakabayashi K, Yamazawa K, Fuke T, Narumi S, Oka A, Ogata T, Fukami M, Kagami M. Inoue T, et al. Clin Epigenetics. 2020 Jun 16;12(1):86. doi: 10.1186/s13148-020-00865-x. Clin Epigenetics. 2020. PMID: 32546215 Free PMC article.

5

Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations.

Eggermann T, Begemann M, Kurth I, Elbracht M. Eggermann T, et al. Eur J Med Genet. 2019 Jul;62(7):103671. doi: 10.1016/j.ejmg.2019.103671. Epub 2019 May 14. Eur J Med Genet. 2019. PMID: 31100449

6

Imprinted disorders and growth.

Giabicani É, Brioude F, Le Bouc Y, Netchine I. Giabicani É, et al. Ann Endocrinol (Paris). 2017 Jun;78(2):112-113. doi: 10.1016/j.ando.2017.04.010. Epub 2017 May 4. Ann Endocrinol (Paris). 2017. PMID: 28478949

7

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Yuan H, Huang L, Hu X, Li Q, Sun X, Xie Y, Kong S, Wang X. Yuan H, et al. Orphanet J Rare Dis. 2016 Jul 2;11(1):89. doi: 10.1186/s13023-016-0465-4. Orphanet J Rare Dis. 2016. PMID: 27370225 Free PMC article.

8

Monoallelic loss of the imprinted gene Grb10 promotes tumor formation in irradiated Nf1+/- mice.

Mroue R, Huang B, Braunstein S, Firestone AJ, Nakamura JL. Mroue R, et al. PLoS Genet. 2015 May 22;11(5):e1005235. doi: 10.1371/journal.pgen.1005235. eCollection 2015 May. PLoS Genet. 2015. PMID: 26000738 Free PMC article.

9

Tissue-specific regulation and function of Grb10 during growth and neuronal commitment.

Plasschaert RN, Bartolomei MS. Plasschaert RN, et al. Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):6841-7. doi: 10.1073/pnas.1411254111. Epub 2014 Nov 3. Proc Natl Acad Sci U S A. 2015. PMID: 25368187 Free PMC article. Review.

10

Clinical characteristics and chromosome 11p15 imprinting analysis of Silver-Russell syndrome - a Chinese experience.

Wu D, Gong C, Zheng H, Saenger P, Zhao Y, Gu Y, Cao B, Li W, Su C. Wu D, et al. J Pediatr Endocrinol Metab. 2014 Nov;27(11-12):1113-20. doi: 10.1515/jpem-2013-0490. J Pediatr Endocrinol Metab. 2014. PMID: 24945423

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