Gromoll J - Search Results

1

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: gromoll j. 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

2

An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance.

Kuechler A, Hauffa BP, Köninger A, Kleinau G, Albrecht B, Horsthemke B, Gromoll J. Kuechler A, et al. Among authors: gromoll j. Eur J Hum Genet. 2010 Jun;18(6):656-61. doi: 10.1038/ejhg.2009.244. Epub 2010 Jan 20. Eur J Hum Genet. 2010. PMID: 20087398 Free PMC article.

3

The origin of the RB1 imprint.

Kanber D, Buiting K, Roos C, Gromoll J, Kaya S, Horsthemke B, Lohmann D. Kanber D, et al. Among authors: gromoll j. PLoS One. 2013 Nov 25;8(11):e81502. doi: 10.1371/journal.pone.0081502. eCollection 2013. PLoS One. 2013. PMID: 24282601 Free PMC article.

4

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1.

Poplinski A, Tüttelmann F, Kanber D, Horsthemke B, Gromoll J. Poplinski A, et al. Among authors: gromoll j. Int J Androl. 2010 Aug 1;33(4):642-9. doi: 10.1111/j.1365-2605.2009.01000.x. Int J Androl. 2010. PMID: 19878521

5

Epigenetic germline mosaicism in infertile men.

Laurentino S, Beygo J, Nordhoff V, Kliesch S, Wistuba J, Borgmann J, Buiting K, Horsthemke B, Gromoll J. Laurentino S, et al. Among authors: gromoll j. Hum Mol Genet. 2015 Mar 1;24(5):1295-304. doi: 10.1093/hmg/ddu540. Epub 2014 Oct 21. Hum Mol Genet. 2015. PMID: 25336341

6

Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome.

Poplinski A, Wieacker P, Kliesch S, Gromoll J. Poplinski A, et al. Among authors: gromoll j. Eur J Endocrinol. 2010 Jan;162(1):169-75. doi: 10.1530/EJE-09-0768. Epub 2009 Oct 7. Eur J Endocrinol. 2010. PMID: 19812237

7

A germ cell-specific ageing pattern in otherwise healthy men.

Laurentino S, Cremers JF, Horsthemke B, Tüttelmann F, Czeloth K, Zitzmann M, Pohl E, Rahmann S, Schröder C, Berres S, Redmann K, Krallmann C, Schlatt S, Kliesch S, Gromoll J. Laurentino S, et al. Among authors: gromoll j. Aging Cell. 2020 Oct;19(10):e13242. doi: 10.1111/acel.13242. Epub 2020 Sep 20. Aging Cell. 2020. PMID: 32951333 Free PMC article.

8

No correlation between androgen receptor CAG and GGN repeat length and the degree of genital virilization in females with 21-hydroxylase deficiency.

Welzel M, Schwarz HP, Hedderich J, Dörr HG, Binder G, Brämswig JH, Krude H, Richter-Unruh A, Niedziela M, Gromoll J, Krone N, Riepe FG, Holterhus PM. Welzel M, et al. Among authors: gromoll j. J Clin Endocrinol Metab. 2010 May;95(5):2443-50. doi: 10.1210/jc.2009-1338. Epub 2010 Mar 16. J Clin Endocrinol Metab. 2010. PMID: 20233785

9

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.

Röpke A, Tewes AC, Gromoll J, Kliesch S, Wieacker P, Tüttelmann F. Röpke A, et al. Among authors: gromoll j. Eur J Hum Genet. 2013 Sep;21(9):1012-5. doi: 10.1038/ejhg.2012.290. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299922 Free PMC article.

10

The FSHB -211G>T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndrome.

Busch AS, Tüttelmann F, Zitzmann M, Kliesch S, Gromoll J. Busch AS, et al. Among authors: gromoll j. Eur J Hum Genet. 2015 May;23(5):700-3. doi: 10.1038/ejhg.2014.142. Epub 2014 Jul 23. Eur J Hum Genet. 2015. PMID: 25052309 Free PMC article.

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