| Cloned transcription factor MTF‐1 activates the mouse metallothionein I promoter. F Radtke, R Heuchel, O Georgiev, M Hergersberg, M Gariglio, Z Dembic, ... The EMBO journal 12 (4), 1355-1362, 1993 | 463 | 1993 |
| Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation D Kotzot, S Schmitt, F Bernasconi, WP Robinson, IW Lurie, H Ilyina, ... Human molecular genetics 4 (4), 583-587, 1995 | 343 | 1995 |
| High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH CEG Bruder, C Hirvelä, I Tapia-Paez, I Fransson, R Segraves, ... Human molecular genetics 10 (3), 271-282, 2001 | 205 | 2001 |
| A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications PG Buckley, KK Mantripragada, M Benetkiewicz, I Tapia-Páez, ... Human Molecular Genetics 11 (25), 3221-3229, 2002 | 185 | 2002 |
| X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15 I Bader, O Brandau, H Achatz, E Apfelstedt-Sylla, M Hergersberg, ... Investigative ophthalmology & visual science 44 (4), 1458-1463, 2003 | 147 | 2003 |
| Biological aspects of cytosine methylation in eukaryotic cells M Hergersberg Experientia 47 (11), 1171-1185, 1991 | 121 | 1991 |
| Schizophrenia and smoking: evidence for a common neurobiological basis? HH Stassen, R Bridler, S Hägele, M Hergersberg, B Mehmann, A Schinzel, ... American journal of medical genetics 96 (2), 173-177, 2000 | 115 | 2000 |
| Tissue-specific expression of a FMR1/β-galactosidase fusion gene in transgenic mice M Hergersberg, K Matsuo, M Gassmann, W Schaffner, B Lüscher, ... Human molecular genetics 4 (3), 359-366, 1995 | 101 | 1995 |
| Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14 DM Brown, RA Graemiger, M Hergersberg, A Schinzel, EP Messmer, ... Archives of ophthalmology 113 (5), 671-675, 1995 | 100 | 1995 |
| Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product D Schindelhauer, M Weiss, H Hellebrand, A Golla, M Hergersberg, ... Human genetics 98, 68-76, 1996 | 99 | 1996 |
| McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings HH Jung, M Hergersberg, S Kneifel, H Alkadhi, R Schiess, ... Annals of neurology 49 (3), 384-392, 2001 | 98 | 2001 |
| Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina K Wutz, C Sauer, E Zrenner, B Lorenz, T Alitalo, M Broghammer, ... European Journal of Human Genetics 10 (8), 449-456, 2002 | 88 | 2002 |
| A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms A Baumer, U Wiedemann, M Hergersberg, A Schinzel Human mutation 17 (5), 423-430, 2001 | 85 | 2001 |
| Molecular cloning and partial characterization of the gene for granule-bound starch synthase from a wildtype and an amylose-free potato (Solanum tuberosum L.) RGF Visser, M Hergersberg, FR Van der Leij, E Jacobsen, B Witholt, ... Plant Science 64 (2), 185-192, 1989 | 83 | 1989 |
| McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement HH Jung, M Hergersberg, M Vogt, J Pahnke, V Treyer, B Röthlisberger, ... Transfusion 43 (7), 928-938, 2003 | 48 | 2003 |
| Codons 837 and 838 in the retinal guanylate cyclase gene on chromosome 17p: hot spots for mutations in autosomal dominant cone-rod dystrophy? M Weigell-Weber, S Fokstuen, B Török, G Niemeyer, A Schinzel, ... Archives of Ophthalmology 118 (2), 300-300, 2000 | 37 | 2000 |
| Phenotypic variability of a distinct deletion in McLeod syndrome M Miranda, C Castiglioni, BM Frey, M Hergersberg, A Danek, HH Jung Movement disorders: official journal of the Movement Disorder Society 22 (9 …, 2007 | 32 | 2007 |
| Thalassämie-Syndrome: Klinik und Diagnose Syndromes thalassémiques: clinique et diagnostic AR Huber, C Ottiger, L Risch, S Regenass, M Hergersberg, R Herklotz Schweiz Med Forum 4 (1), 947-52, 2004 | 32 | 2004 |
| Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy M Weigell-Weber, GM Sarra, D Kotzot, L Sandkuijl, E Messmer, ... Archives of ophthalmology 121 (8), 1184-1188, 2003 | 31 | 2003 |
| Expression in mammalian cells of a cloned gene encoding murine DNA methyltransferase A Czank, R Häuselmann, AW Page, H Leonhardt, TH Bestor, W Schaffner, ... Gene 109 (2), 259-263, 1991 | 31 | 1991 |
