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1.
Dong, X.* et al.: Evaluating coverage of exons by HapMap SNPs. Genomics 101, 20-23 (2013)
2.
Pfeiffer, F.* et al.: Genome sequences of Halobacterium salinarum: A reply. Genomics 91, 553-554 (2008)
3.
Pfeiffer, F.* et al.: Evolution in the laboratory: The genome of Halobacterium salinarum strain R1 compared to that of strain NRC-1. Genomics 91, 335-346 (2008)
4.
Nag, N.* et al.: Endogenous retroviral insertion in Cryge in the mouse No3 cataract mutant. Genomics 89, 512-520 (2007)
5.
Zebhauser, R.* et al.: Identification of a novel group of evolutionarily conserved members within the rapidly diverging murine Cea family. Genomics 86, 566-580 (2005)
6.
Hahn, H.* et al.: Genetic mapping of a Ptch1-associated rhabdomyosarcoma susceptibility locus on mouse chromosome 2. Genomics 84, 853-858 (2004)
7.
Hansdottir, A.G.* et al.: The novel mouse microphthalmia mutations Mitfmi-enu5 and Mitfmi-bcc2 produce dominant negative Mitf proteins. Genomics 83, 932-935 (2004)
8.
Huang, K.M.* et al.: Organization and annotation of the Xcat critical region: Elimination of seven positional candidate genes. Genomics 83, 893-901 (2004)
9.
Ihalmo, P.* et al.: Molecular cloning and characterization of an endogenous antisense transcript of Nphs1*. Genomics 83, 1134-1140 (2004)
10.
Müller, S.* ; Finelli, P.* ; Neusser, M.* & Wienberg, J.: The evolutionary history of human chromosome 7. Genomics 84, 458-467 (2004)
11.
Runkel, F.* et al.: The dominant alopecia phenotypes Bareskin, Rex-denuded and recuced coat 2 are caused by mutations in gasdermin 3. Genomics 84, 824-835 (2004)
12.
Wahl, M. et al.: Transcriptome analysis of early chondrogenesis in ATDC5 cells induced by bone morphogenetic protein 4. Genomics 83, 45-58 (2004)
13.
Herbon, N. et al.: High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases. Genomics 81, 510-518 (2003)
14.
Berti, L. et al.: Isolation and Characterization of a Novel Gene from the DiGeorge Chromosomal Region That Encodes for a Mediator Subunit. Genomics 74, 320-332 (2001)
15.
Baust, C.* ; Seifarth, W.* ; Germaier, H. ; Hehlmann, R.* & Leib-Mösch, C.: HERV-K-T47D-Related Long Terminal Repeats Mediate Polyadenylation of Cellular Transcripts. Genomics 66, 98-103 (2000)
16.
Graw, J. et al.: Mutation in the ßA3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse. Genomics 62, 67-73 (1999)
17.
Wjst, M. et al.: A genome-wide search for linkage to asthma. Genomics 58, 1-8 (1999)
18.
Leib-Mösch, C. et al.: Genomic distribution and transcription of solitary HERV-K LTRs. Genomics 18, 261-269 (1993)
19.
Morris, D.J. ; Adler, I.-D. & Robinson, T.J.: Somatic Cell Hybrid Mapping on Mouse Chromosome 11 (MMU11): Assignment of 21 Markers Relative to two Breakpoints in band D. Genomics 15, 323-331 (1993)
20.
Brack-Werner, R. et al.: Human SSAV-related endogenous retroviral element: LTR-like sequence and chromosomal localization to 18q21. Genomics 4, 68-75 (1989)
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