Boemers TM - Search Results

1

First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.

Gehlen J, Giel AS, Köllges R, Haas SL, Zhang R, Trcka J, Sungur AÖ, Renziehausen F, Bornholdt D, Jung D, Hoyer PD, Nordenskjöld A, Tibboel D, Vlot J, Spaander MCW, Smigiel R, Patkowski D, Roeleveld N, van Rooij IA, de Blaauw I, Hölscher A, Pauly M, Leutner A, Fuchs J, Niethammer J, Melissari MT, Jenetzky E, Zwink N, Thiele H, Hilger AC, Hess T, Trautmann J, Marks M, Baumgarten M, Bläss G, Landén M, Fundin B, Bulik CM, Pennimpede T, Ludwig M, Ludwig KU, Mangold E, Heilmann-Heimbach S, Moebus S, Herrmann BG, Alsabeah K, Burgos CM, Lilja HE, Azodi S, Stenström P, Arnbjörnsson E, Frybova B, Lebensztejn DM, Debek W, Kolodziejczyk E, Kozera K, Kierkus J, Kaliciński P, Stefanowicz M, Socha-Banasiak A, Kolejwa M, Piaseczna-Piotrowska A, Czkwianianc E, Nöthen MM, Grote P, Rygl M, Reinshagen K, Spychalski N, Ludwikowski B, Hubertus J, Heydweiller A, Ure B, Muensterer OJ, Aubert O, Gosemann JH, Lacher M, Degenhardt P, Boemers TM, Mokrowiecka A, Małecka-Panas E, Wöhr M, Knapp M, Seitz G, de Klein A, Oracz G, Brosens E, Reutter H, Schumacher J. Gehlen J, et al. Among authors: boemers tm. HGG Adv. 2022 Jan 25;3(2):100093. doi: 10.1016/j.xhgg.2022.100093. eCollection 2022 Apr 14. HGG Adv. 2022. PMID: 35199045 Free PMC article.

2

MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?

Reutter H, Betz RC, Ludwig M, Boemers TM. Reutter H, et al. Among authors: boemers tm. Eur J Pediatr. 2006 Aug;165(8):566-8. doi: 10.1007/s00431-006-0116-1. Epub 2006 Apr 7. Eur J Pediatr. 2006. PMID: 16602006

3

Bladder exstrophy-epispadias complex: Investigation of suppressor of variegation, enhancer of zeste and Trithorax (SET) as a candidate gene in a large cohort of patients.

Reutter H, Thauvin-Robinet C, Boemers TM, Rösch WH, Ludwig M. Reutter H, et al. Among authors: boemers tm. Scand J Urol Nephrol. 2006;40(3):221-4. doi: 10.1080/00365590600621204. Scand J Urol Nephrol. 2006. PMID: 16809264

4

Dynamic magnetic resonance imaging of the pelvic floor in children and adolescents with vesical and anorectal malformations.

Boemers TM, Ludwikowski B, Forstner R, Schimke C, Ardelean MA. Boemers TM, et al. J Pediatr Surg. 2006 Jul;41(7):1267-71. doi: 10.1016/j.jpedsurg.2006.03.006. J Pediatr Surg. 2006. PMID: 16818061

5

Family-based association study of the MTHFR polymorphism C677T in the bladder-exstrophy-epispadias-complex.

Reutter H, Becker T, Ludwig M, Schäfer N, Detlefsen B, Beaudoin S, Fisch M, Ebert AK, Rösch W, Nöthen MM, Boemers TM, Betz RC. Reutter H, et al. Among authors: boemers tm. Am J Med Genet A. 2006 Nov 15;140(22):2506-9. doi: 10.1002/ajmg.a.31484. Am J Med Genet A. 2006. PMID: 17041930 No abstract available.

6

Concordance analyses of twins with bladder exstrophy-epispadias complex suggest genetic etiology.

Reutter H, Qi L, Gearhart JP, Boemers T, Ebert AK, Rösch W, Ludwig M, Boyadjiev SA. Reutter H, et al. Am J Med Genet A. 2007 Nov 15;143A(22):2751-6. doi: 10.1002/ajmg.a.31975. Am J Med Genet A. 2007. PMID: 17937426 No abstract available.

7

Investigation of FGF10 as a candidate gene in patients with anorectal malformations and exstrophy of the cloaca.

Krüger V, Khoshvaghti M, Reutter H, Vogt H, Boemers TM, Ludwig M. Krüger V, et al. Among authors: boemers tm. Pediatr Surg Int. 2008 Aug;24(8):893-7. doi: 10.1007/s00383-008-2193-x. Epub 2008 Jun 28. Pediatr Surg Int. 2008. PMID: 18587586

8

Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.

Reutter H, Bökenkamp A, Ebert AK, Rösch W, Boemers TM, Nöthen MM, Ludwig M. Reutter H, et al. Among authors: boemers tm. Eur J Pediatr. 2009 Jul;168(7):881-3. doi: 10.1007/s00431-008-0852-5. Epub 2008 Oct 16. Eur J Pediatr. 2009. PMID: 18923839 Review.

9

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.

Draaken M, Reutter H, Schramm C, Bartels E, Boemers TM, Ebert AK, Rösch W, Schröder A, Stein R, Moebus S, Stienen D, Hoffmann P, Nöthen MM, Ludwig M. Draaken M, et al. Among authors: boemers tm. Eur J Med Genet. 2010 Mar-Apr;53(2):55-60. doi: 10.1016/j.ejmg.2009.12.005. Epub 2010 Jan 10. Eur J Med Genet. 2010. PMID: 20060941

10

De novo microduplication at 22q11.21 in a patient with VACTERL association.

Schramm C, Draaken M, Bartels E, Boemers TM, Aretz S, Brockschmidt FF, Nöthen MM, Ludwig M, Reutter H. Schramm C, et al. Among authors: boemers tm. Eur J Med Genet. 2011 Jan-Feb;54(1):9-13. doi: 10.1016/j.ejmg.2010.09.001. Epub 2010 Sep 16. Eur J Med Genet. 2011. PMID: 20849991

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