Diaz-Lacava A - Search Results

1

VEGF gene haplotypes are associated with sarcoidosis.

Pabst S, Karpushova A, Diaz-Lacava A, Herms S, Walier M, Zimmer S, Cichon S, Nickenig G, Nöthen MM, Wienker TF, Grohé C. Pabst S, et al. Chest. 2010 Jan;137(1):156-63. doi: 10.1378/chest.09-1003. Epub 2009 Sep 9. Chest. 2010. PMID: 19741061

2

Caspase recruitment domain 15 gene haplotypes in sarcoidosis.

Pabst S, Golebiewski M, Herms S, Karpushova A, Díaz-Lacava A, Walier M, Zimmer S, Cichon S, Wienker TF, Nöthen MM, Nickenig G, Meyer R, Skowasch D, Grohé C. Pabst S, et al. Tissue Antigens. 2011 Apr;77(4):333-7. doi: 10.1111/j.1399-0039.2010.01628.x. Tissue Antigens. 2011. PMID: 21388357

3

IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.

Birnbaum S, Ludwig KU, Reutter H, Herms S, de Assis NA, Diaz-Lacava A, Barth S, Lauster C, Schmidt G, Scheer M, Saffar M, Martini M, Reich RH, Schiefke F, Hemprich A, Pötzsch S, Pötzsch B, Wienker TF, Hoffmann P, Knapp M, Kramer FJ, Nöthen MM, Mangold E. Birnbaum S, et al. Eur J Oral Sci. 2009 Dec;117(6):766-9. doi: 10.1111/j.1600-0722.2009.00680.x. Eur J Oral Sci. 2009. PMID: 20121942

4

Spatial assessment of Argentinean genetic admixture with geographical information systems.

Diaz-Lacava A, Walier M, Penacino G, Wienker TF, Baur MP. Diaz-Lacava A, et al. Forensic Sci Int Genet. 2011 Aug;5(4):297-302. doi: 10.1016/j.fsigen.2010.05.003. Epub 2010 Jun 19. Forensic Sci Int Genet. 2011. PMID: 20646980

5

Geostatistical inference of main Y-STR-haplotype groups in Europe.

Diaz-Lacava A, Walier M, Willuweit S, Wienker TF, Fimmers R, Baur MP, Roewer L. Diaz-Lacava A, et al. Forensic Sci Int Genet. 2011 Mar;5(2):91-4. doi: 10.1016/j.fsigen.2010.09.010. Forensic Sci Int Genet. 2011. PMID: 20970399

6

Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.

Birnbaum S, Reutter H, Mende M, de Assis NA, Diaz-Lacava A, Herms S, Scheer M, Lauster C, Braumann B, Schmidt G, Martini M, Hemprich A, Pötzsch S, Knapp M, Nöthen MM, Kramer FJ, Mangold E. Birnbaum S, et al. Eur J Oral Sci. 2009 Apr;117(2):200-3. doi: 10.1111/j.1600-0722.2008.00604.x. Eur J Oral Sci. 2009. PMID: 19320731

7

Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin.

Mangold E, Reutter H, Birnbaum S, Walier M, Mattheisen M, Henschke H, Lauster C, Schmidt G, Schiefke F, Reich RH, Scheer M, Hemprich A, Martini M, Braumann B, Krimmel M, Opitz C, Lenz JH, Kramer FJ, Wienker TF, Nöthen MM, Diaz Lacava A. Mangold E, et al. Am J Med Genet A. 2009 Dec;149A(12):2680-94. doi: 10.1002/ajmg.a.33136. Am J Med Genet A. 2009. PMID: 19938073

8

Increased frequency of the CTLA-4 49 A/G polymorphism in patients with acquired haemophilia A compared to healthy controls.

Pavlova A, Diaz-Lacava A, Zeitler H, Satoguina J, Niemann B, Krause M, Scharrer I, Hoerauf A, Wienker T, Oldenburg J. Pavlova A, et al. Haemophilia. 2008 Mar;14(2):355-60. doi: 10.1111/j.1365-2516.2007.01618.x. Epub 2007 Dec 10. Haemophilia. 2008. PMID: 18081831

9

Methylation at global LINE-1 repeats in human blood are affected by gender but not by age or natural hormone cycles.

El-Maarri O, Walier M, Behne F, van Üüm J, Singer H, Diaz-Lacava A, Nüsgen N, Niemann B, Watzka M, Reinsberg J, van der Ven H, Wienker T, Stoffel-Wagner B, Schwaab R, Oldenburg J. El-Maarri O, et al. PLoS One. 2011 Jan 19;6(1):e16252. doi: 10.1371/journal.pone.0016252. PLoS One. 2011. PMID: 21311577 Free PMC article.

10

A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation.

El-Maarri O, Kareta MS, Mikeska T, Becker T, Diaz-Lacava A, Junen J, Nüsgen N, Behne F, Wienker T, Waha A, Oldenburg J, Chédin F. El-Maarri O, et al. Hum Mol Genet. 2009 May 15;18(10):1755-68. doi: 10.1093/hmg/ddp088. Epub 2009 Feb 26. Hum Mol Genet. 2009. PMID: 19246518 Free article.

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