Hildebrandt F - Search Results

1

HomozygosityMapper--an interactive approach to homozygosity mapping.

Seelow D, Schuelke M, Hildebrandt F, Nürnberg P. Seelow D, et al. Among authors: hildebrandt f. Nucleic Acids Res. 2009 Jul;37(Web Server issue):W593-9. doi: 10.1093/nar/gkp369. Epub 2009 May 21. Nucleic Acids Res. 2009. PMID: 19465395 Free PMC article.

2

LODVIEW: a computer program for the graphical evaluation of lod score results in exclusion mapping of human disease genes.

Hildebrandt F, Pohlmann A, Omran H. Hildebrandt F, et al. Comput Biomed Res. 1993 Dec;26(6):592-9. doi: 10.1006/cbmr.1993.1042. Comput Biomed Res. 1993. PMID: 8112059

3

Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene.

Omran H, Häffner K, Völkel A, Kuehr J, Ketelsen UP, Ross UH, Konietzko N, Wienker T, Brandis M, Hildebrandt F. Omran H, et al. Among authors: hildebrandt f. Am J Respir Cell Mol Biol. 2000 Nov;23(5):696-702. doi: 10.1165/ajrcmb.23.5.4257. Am J Respir Cell Mol Biol. 2000. PMID: 11062149

4

Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36.

Schuermann MJ, Otto E, Becker A, Saar K, Rüschendorf F, Polak BC, Ala-Mello S, Hoefele J, Wiedensohler A, Haller M, Omran H, Nürnberg P, Hildebrandt F. Schuermann MJ, et al. Among authors: hildebrandt f. Am J Hum Genet. 2002 May;70(5):1240-6. doi: 10.1086/340317. Epub 2002 Mar 27. Am J Hum Genet. 2002. PMID: 11920287 Free PMC article.

5

Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mapping.

Harville HM, Held S, Diaz-Font A, Davis EE, Diplas BH, Lewis RA, Borochowitz ZU, Zhou W, Chaki M, MacDonald J, Kayserili H, Beales PL, Katsanis N, Otto E, Hildebrandt F. Harville HM, et al. Among authors: hildebrandt f. J Med Genet. 2010 Apr;47(4):262-7. doi: 10.1136/jmg.2009.071365. Epub 2009 Sep 24. J Med Genet. 2010. PMID: 19797195 Free PMC article.

6

Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data.

Zhang L, Yang W, Ying D, Cherny SS, Hildebrandt F, Sham PC, Lau YL. Zhang L, et al. Among authors: hildebrandt f. Hum Mutat. 2011 Mar;32(3):345-53. doi: 10.1002/humu.21432. Hum Mutat. 2011. PMID: 21309031 Free PMC article.

7

[Hereditary diseases of the kidney].

Hildebrandt F, Weber M, Brandis M. Hildebrandt F, et al. Internist (Berl). 1995 Mar;36(3):254-62. Internist (Berl). 1995. PMID: 7737818 Review. German. No abstract available.

8

Genetic renal diseases in children.

Hildebrandt F. Hildebrandt F. Curr Opin Pediatr. 1995 Apr;7(2):182-91. doi: 10.1097/00008480-199504000-00012. Curr Opin Pediatr. 1995. PMID: 7787935 Review.

9

Mapping of a gene for familial juvenile nephronophthisis: refining the map and defining flanking markers on chromosome 2. APN Study Group.

Hildebrandt F, Singh-Sawhney I, Schnieders B, Centofante L, Omran H, Pohlmann A, Schmaltz C, Wedekind H, Schubotz C, Antignac C, et al. Hildebrandt F, et al. Am J Hum Genet. 1993 Dec;53(6):1256-61. Am J Hum Genet. 1993. PMID: 8250041 Free PMC article.

10

Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13.

Hildebrandt F, Cybulla M, Strahm B, Nothwang HG, Singh-Sawhney I, Berz K, Nicklin M, Reiner O, Brandis M. Hildebrandt F, et al. Cytogenet Cell Genet. 1996;73(3):235-9. doi: 10.1159/000134346. Cytogenet Cell Genet. 1996. PMID: 8697815

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