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Martina Broghammer

Observed names: M Broghammer, M. Broghammer
OpenAlex ID: A5085735985
CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders
2001 · Bernd Wissinger, Daphne Gamer, et al. · The American Journal of Human Genetics · 331
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Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina
2002 · Krisztina Wutz, Christian Sauer, et al. · European Journal of Human Genetics · 87
Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11
1998 · Bernd Wissinger, Herbert Jägle, et al. · Genomics · 70
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A genetic perspective on myopia
2005 · F. K. Jacobi, E. Zrenner, et al. · Cellular and Molecular Life Sciences · 45
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping
2008 · Felix Jacobi, Martina Broghammer, et al. · International Journal of Molecular Medicine · 38
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Ten novel ORF15 mutations confirm mutational hot spot in theRPGR gene in European patients with X-linked retinitis pigmentosa
2002 · Carsten M. Pusch, Martina Broghammer, et al. · Human Mutation · 32
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A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness
2003 · Felix Karl Jacobi, Christian P. Hamel, et al. · American Journal of Ophthalmology · 23
PCR-Induced Sequence Alterations Hamper the Typing of Prehistoric Bone Samples for Diagnostic Achondroplasia Mutations
2004 · C. M. Pusch, M. Broghammer, et al. · Molecular Biology and Evolution · 22
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Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1
2000 · Felix K. Jacobi, Martina Broghammer, et al. · Human Genetics · 14
Cremation practices and the survival of ancient DNA: burnt bone analyses via RAPD-mediated PCR
2000 · Carsten M. Pusch, Martina Broghammer, et al. · Anthropologischer Anzeiger · 11
Population Haplotypes of Exon ORF15 of the Retinitis Pigmentosa GTPase Regulator Gene in Germany
2006 · Daniela Karra, Felix K. Jacobi, et al. · Molecular Diagnosis & Therapy · 10
Intrapopulational Relationships in Ancient Societies: A multidisciplinary Study.
2001 · M. Scholz, S. Hengst, et al. · Zeitschrift für Morphologie und Anthropologie · 10
Internal Alu-Polymerase Chain Reaction: A Sensitive Contamination Monitoring Protocol for DNA Extracted from Prehistoric Animal Bones
2000 · Carsten M. Pusch, Lutz Bachmann, et al. · Analytical Biochemistry · 9
Voltage-induced release of nucleic acids from palaeontological samples
2000 · Lutz Bachmann, Michael Scholz, et al. · Electrophoresis · 8
Molecular phylogenetics employing modern and ancient DNA.
2003 · Carsten M Pusch, Martina Broghammer, et al. · PubMed · 7
Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background
2005 · Felix Jacobi, Daniela Karra, et al. · International Journal of Molecular Medicine · 6
Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations
2004 · Martina Broghammer, Peter Leistenschneider, et al. · Cancer Letters · 6
Adaptor-mediated amplification of minute amounts of severely fragmented ancient nucleic acids.
2000 · C M Pusch, N Blin, et al. · PubMed · 2
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders
2001 · K. Pesch, J. Tomiuk, et al. · International Journal of Molecular Medicine · 1
Molekulare Paläobiologie: Ancient DNA und Authentizität
2001 · Carsten M. Pusch, Martina Broghammer, et al. · Germania: Anzeiger der Römisch-Germanischen Kommission des Deutschen Archäologischen Instituts · 1
Achromatopsia on chromosome 8q21 is caused by mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP gated channel
2000 · Susanne Kohl, Britta Baumann, et al.
Works count: 21
Citation count: 733
H-index: 10
I10-index: 12
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