Binder G - Search Results

1

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring.

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. Begemann M, et al. Among authors: binder g. J Med Genet. 2018 Jul;55(7):497-504. doi: 10.1136/jmedgenet-2017-105190. Epub 2018 Mar 24. J Med Genet. 2018. PMID: 29574422 Free PMC article.

2

Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely.

Eggermann K, Wollmann HA, Binder G, Kaiser P, Ranke MB, Eggermann T. Eggermann K, et al. Among authors: binder g. Ann Genet. 1999;42(2):117-21. Ann Genet. 1999. PMID: 10434128

3

Tall stature, gonadal dysgenesis, and stigmata of Turner's syndrome caused by a structurally altered X chromosome.

Binder G, Eggermann T, Enders H, Ranke MB, Dufke A. Binder G, et al. J Pediatr. 2001 Feb;138(2):285-7. doi: 10.1067/mpd.2001.110277. J Pediatr. 2001. PMID: 11174634

4

Screening for insulin-like growth factor-I receptor mutations in patients with Silver-Russell syndrome.

Binder G, Mavridou K, Wollmann HA, Eggermann T, Ranke MB. Binder G, et al. J Pediatr Endocrinol Metab. 2002 Sep-Oct;15(8):1167-71. doi: 10.1515/jpem.2002.15.8.1167. J Pediatr Endocrinol Metab. 2002. PMID: 12387515

5

Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome.

Eggermann T, Schönherr N, Eggermann K, Buiting K, Ranke MB, Wollmann HA, Binder G. Eggermann T, et al. Among authors: binder g. Clin Genet. 2008 Jan;73(1):79-84. doi: 10.1111/j.1399-0004.2007.00930.x. Epub 2007 Dec 7. Clin Genet. 2008. PMID: 18070127

6

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. Zeschnigk M, et al. Among authors: binder g. Eur J Hum Genet. 2008 Mar;16(3):328-34. doi: 10.1038/sj.ejhg.5201974. Epub 2008 Jan 9. Eur J Hum Genet. 2008. PMID: 18159214

7

The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration.

Binder G, Seidel AK, Martin DD, Schweizer R, Schwarze CP, Wollmann HA, Eggermann T, Ranke MB. Binder G, et al. J Clin Endocrinol Metab. 2008 Apr;93(4):1402-7. doi: 10.1210/jc.2007-1897. Epub 2008 Jan 29. J Clin Endocrinol Metab. 2008. PMID: 18230663

8

Search for subtelomeric imbalances by multiplex ligation-dependent probe amplification in Silver-Russell syndrome.

Eggermann K, Schönherr N, Ranke MB, Wollmann HA, Binder G, Eggermann T. Eggermann K, et al. Among authors: binder g. Genet Test. 2008 Mar;12(1):111-3. doi: 10.1089/gte.2007.0075. Genet Test. 2008. PMID: 18307383

9

No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.

Schönherr N, Meyer E, Binder G, Wollmann HA, Eggermann T. Schönherr N, et al. Among authors: binder g. J Pediatr Endocrinol Metab. 2007 Dec;20(12):1329-31. doi: 10.1515/jpem.2007.20.12.1329. J Pediatr Endocrinol Metab. 2007. PMID: 18341093

10

No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patients.

Schöherr N, Jäger S, Ranke MB, Wollmann HA, Binder G, Eggermann T. Schöherr N, et al. Among authors: binder g. Eur J Med Genet. 2008 Jul-Aug;51(4):322-4. doi: 10.1016/j.ejmg.2008.05.001. Epub 2008 May 23. Eur J Med Genet. 2008. PMID: 18585117

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