Omran H - Search Results

1

Identification of the human CYS1 gene and candidate gene analysis in Boichis disease.

Fliegauf M, Fröhlich C, Horvath J, Olbrich H, Hildebrandt F, Omran H. Fliegauf M, et al. Among authors: omran h. Pediatr Nephrol. 2003 Jun;18(6):498-505. doi: 10.1007/s00467-003-1141-1. Epub 2003 May 6. Pediatr Nephrol. 2003. PMID: 12733055 Free 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. Among authors: omran h. Comput Biomed Res. 1993 Dec;26(6):592-9. doi: 10.1006/cbmr.1993.1042. Comput Biomed Res. 1993. PMID: 8112059

3

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. Among authors: omran h. Am J Hum Genet. 1993 Dec;53(6):1256-61. Am J Hum Genet. 1993. PMID: 8250041 Free PMC article.

4

Probable Opitz trigonocephaly C syndrome with medulloblastoma.

Omran H, Hildebrandt F, Korinthenberg R, Brandis M. Omran H, et al. Am J Med Genet. 1997 Apr 14;69(4):395-9. Am J Med Genet. 1997. PMID: 9098489

5

Two novel mutations of the gene for Kir 1.1 (ROMK) in neonatal Bartter syndrome.

Vollmer M, Koehrer M, Topaloglu R, Strahm B, Omran H, Hildebrandt F. Vollmer M, et al. Among authors: omran h. Pediatr Nephrol. 1998 Jan;12(1):69-71. doi: 10.1007/s004670050408. Pediatr Nephrol. 1998. PMID: 9502574

6

Exclusion of the candidate genes ACE and Bcl-2 for six families with nephronophthisis not linked to the NPH1 locus.

Omran H, Häffner K, Vollmer M, Pigulla J, Wagner G, Caridi G, Hildebrandt F. Omran H, et al. Nephrol Dial Transplant. 1999 Oct;14(10):2328-31. doi: 10.1093/ndt/14.10.2328. Nephrol Dial Transplant. 1999. PMID: 10528654

7

Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.

Omran H, Fernandez C, Jung M, Häffner K, Fargier B, Villaquiran A, Waldherr R, Gretz N, Brandis M, Rüschendorf F, Reis A, Hildebrandt F. Omran H, et al. Am J Hum Genet. 2000 Jan;66(1):118-27. doi: 10.1086/302705. Am J Hum Genet. 2000. PMID: 10631142 Free PMC article.

8

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. 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

9

Human adolescent nephronophthisis: gene locus synteny with polycystic kidney disease in pcy mice.

Omran H, Häffner K, Burth S, Fernandez C, Fargier B, Villaquiran A, Nothwang HG, Schnittger S, Lehrach H, Woo D, Brandis M, Sudbrak R, Hildebrandt F. Omran H, et al. J Am Soc Nephrol. 2001 Jan;12(1):107-113. doi: 10.1681/ASN.V121107. J Am Soc Nephrol. 2001. PMID: 11134256

10

Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis.

Hildebrandt F, Rensing C, Betz R, Sommer U, Birnbaum S, Imm A, Omran H, Leipoldt M, Otto E; Arbeitsgemeinschaft für Paediatrische Nephrologie (APN) Study Group. Hildebrandt F, et al. Among authors: omran h. Kidney Int. 2001 Feb;59(2):434-45. doi: 10.1046/j.1523-1755.2001.059002434.x. Kidney Int. 2001. PMID: 11168925 Free article.

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