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SNP-Based analysis of genetic substructure in the German population.
Steffens, M. and Lamina, C. and Illig, T. and Bettecken, T. and Vogler, R. and Entz, P. and Suk, E.K. and Toliat, M.R. and Klopp, N. and Caliebe, A. and Koenig, I.R. and Koehler, K. and Luedemann, J. and Lacava, A.D. and Fimmers, R. and Lichtner, P. and Ziegler, A. and Wolf, A. and Krawczak, M. and Nuernberg, P. and Hampe, J. and Schreiber, S. and Meitinger, T. and Wichmann, H.E. and Roeder, K. and Wienker, T.F. and Baur, M.P.
Human Heredity 62 (1): 20-29. October 2006

Concordant association of lipid gene variation with a combined HDL/LDL-cholesterol phenotype in two European populations.
Bauerfeind, A. and Knoblauch, H. and Costanza, M.C. and Luganskaja, T. and Toliat, M.R. and Nuernberg, P. and Luft, F.C. and Reich, J.G. and Morabia, A.
Human Heredity 61 (3): 123-131. August 2006

Single nucleotide polymorphism haplotypes in the cholesteryl-ester transfer protein (CETP) gene and lipid phenotypes.
Bauerfeind, A. and Knoblauch, H. and Schuster, H. and Luft, F.C. and Reich, J.G.
Human Heredity 54 (4): 166-173. May 2003

Entropy as a Measure for Linkage Disequilibrium over Multilocus Haplotype Blocks.
Nothnagel, M. and Fuerst, R. and Rohde, K.
Human Heredity 54 (4): 186-198. May 2003

Association of genetic traits to estimated haplotypes from SNP genotypes using EM algorithm and Markov chain Monte Carlo techniques.
Rohde, K. and Fuerst, R.
Human Heredity 56 (1-3): 41-47. 1 January 2003

Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms.
Gordon, D. and Finch, S.J. and Nothnagel, M. and Ott, J.
Human Heredity 54 (1): 22-33. November 2002

Statistical considerations for genome-wide scans: design and application of a novel software package POLYMORPHISM.
Niu, T. and Struk, B. and Lindpaintner, K.
Human Heredity 52 (2): 102-109. July 2001

A complete enumeration and classification of two-locus disease models.
Li, W.T. and Reich, J.
Human Heredity 50 (6): 334-349. 1 November 2000

Mapping genes for polygenic disorders: considerations for study design in the complex trait of inflammatory bowel disease.
Hampe, J. and Wienker, T. and Nuernberg, P. and Schreiber, S.
Human Heredity 50 : 91-101. 1 March 2000

Multi-locus nonparametric linkage analysis of complex trait loci with neural networks.
Lucek, P. and Hanke, J. and Reich, J. and Solla, S.A. and Ott, J.
Human Heredity 48 : 275-284. 1 September 1998

Microsatellite haplotypes of Polish cystic fibrosis alleles: deltaF508 chromosomes demonstrate a North-South haplotype frequency gradient.
Witt, M. and Reis, A. and Cichy, W. and Dziechciowska, K.
Human Heredity 46 : 310-314. 1 January 1996

A program using loss-of-constitutional- heterozygosity data to ascertain the location of predisposing genes in cancer families.
Rohde, K. and Teare, M.D. and Scherneck, S. and Santibanez-Koref, M.F.
Human Heredity 45 : 337-345. 1 January 1995

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