Schuster H - Search Results

1

Relating two deep-rooted pedigrees from Central Germany by high-resolution Y-STR haplotyping.

Kayser M, Vermeulen M, Knoblauch H, Schuster H, Krawczak M, Roewer L. Kayser M, et al. Among authors: schuster h. Forensic Sci Int Genet. 2007 Jun;1(2):125-8. doi: 10.1016/j.fsigen.2007.02.004. Epub 2007 Mar 13. Forensic Sci Int Genet. 2007. PMID: 19083742

2

DNA testing for familial hypercholesterolemia: improving disease recognition and patient care.

Vergopoulos A, Knoblauch H, Schuster H. Vergopoulos A, et al. Among authors: schuster h. Am J Pharmacogenomics. 2002;2(4):253-62. doi: 10.2165/00129785-200202040-00005. Am J Pharmacogenomics. 2002. PMID: 12421096 Review.

3

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol.

Knoblauch H, Bauerfeind A, Toliat MR, Becker C, Luganskaja T, Günther UP, Rohde K, Schuster H, Junghans C, Luft FC, Nürnberg P, Reich JG. Knoblauch H, et al. Among authors: schuster h. Hum Mol Genet. 2004 May 15;13(10):993-1004. doi: 10.1093/hmg/ddh119. Epub 2004 Mar 25. Hum Mol Genet. 2004. PMID: 15044381

4

A cholesterol-lowering gene maps to chromosome 13q.

Knoblauch H, Müller-Myhsok B, Busjahn A, Ben Avi L, Bähring S, Baron H, Heath SC, Uhlmann R, Faulhaber HD, Shpitzen S, Aydin A, Reshef A, Rosenthal M, Eliav O, Mühl A, Lowe A, Schurr D, Harats D, Jeschke E, Friedlander Y, Schuster H, Luft FC, Leitersdorf E. Knoblauch H, et al. Among authors: schuster h. Am J Hum Genet. 2000 Jan;66(1):157-66. doi: 10.1086/302704. Am J Hum Genet. 2000. PMID: 10631147 Free PMC article.

5

Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families.

Pei W, Baron H, Müller-Myhsok B, Knoblauch H, Al-Yahyaee SA, Hui R, Wu X, Liu L, Busjahn A, Luft FC, Schuster H. Pei W, et al. Among authors: schuster h. Clin Genet. 2000 Jan;57(1):29-34. doi: 10.1034/j.1399-0004.2000.570105.x. Clin Genet. 2000. PMID: 10733233

6

Single nucleotide polymorphism haplotypes in the cholesteryl-ester transfer protein (CETP) gene and lipid phenotypes.

Bauerfeind A, Knoblauch H, Schuster H, Luft FC, Reich JG. Bauerfeind A, et al. Among authors: schuster h. Hum Hered. 2002;54(4):166-73. doi: 10.1159/000070662. Hum Hered. 2002. PMID: 12771549

7

A region on chromosome 3 is linked to dizygotic twinning.

Busjahn A, Knoblauch H, Faulhaber HD, Aydin A, Uhlmann R, Tuomilehto J, Kaprio J, Jedrusik P, Januszewicz A, Strelau J, Schuster H, Luft FC, Müller-Myhsok B. Busjahn A, et al. Among authors: schuster h. Nat Genet. 2000 Dec;26(4):398-9. doi: 10.1038/82515. Nat Genet. 2000. PMID: 11101833 No abstract available.

8

Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population.

Knoblauch H, Bauerfeind A, Krähenbühl C, Daury A, Rohde K, Bejanin S, Essioux L, Schuster H, Luft FC, Reich JG. Knoblauch H, et al. Among authors: schuster h. Hum Mol Genet. 2002 Jun 1;11(12):1477-85. doi: 10.1093/hmg/11.12.1477. Hum Mol Genet. 2002. PMID: 12023990

9

A pathway model of lipid metabolism to predict the effect of genetic variability on lipid levels.

Knoblauch H, Schuster H, Luft FC, Reich J. Knoblauch H, et al. Among authors: schuster h. J Mol Med (Berl). 2000;78(9):507-15. doi: 10.1007/s001090000156. J Mol Med (Berl). 2000. PMID: 11140376

10

QT interval is linked to 2 long-QT syndrome loci in normal subjects.

Busjahn A, Knoblauch H, Faulhaber HD, Boeckel T, Rosenthal M, Uhlmann R, Hoehe M, Schuster H, Luft FC. Busjahn A, et al. Among authors: schuster h. Circulation. 1999 Jun 22;99(24):3161-4. doi: 10.1161/01.cir.99.24.3161. Circulation. 1999. PMID: 10377080

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