Martina Broghammer

716 total citations
20 papers, 310 citations indexed

About

Martina Broghammer is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Martina Broghammer has authored 20 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Martina Broghammer's work include Retinal Development and Disorders (9 papers), Forensic and Genetic Research (7 papers) and Molecular Biology Techniques and Applications (4 papers). Martina Broghammer is often cited by papers focused on Retinal Development and Disorders (9 papers), Forensic and Genetic Research (7 papers) and Molecular Biology Techniques and Applications (4 papers). Martina Broghammer collaborates with scholars based in Germany, United States and Switzerland. Martina Broghammer's co-authors include Carsten M. Pusch, Frank Jacobi, Nikolaus Blin, E. Zrenner, Eberhart Zrenner, Bernd Wissinger, Michael Scholz, Alfons Meindl, Tiina Alitalo and Christian Sauer and has published in prestigious journals such as Analytical Biochemistry, Molecular Biology and Evolution and Cellular and Molecular Life Sciences.

In The Last Decade

Martina Broghammer

20 papers receiving 303 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Martina Broghammer Germany 8 204 115 71 70 63 20 310
Matthew Carrigan Ireland 10 334 1.6× 125 1.1× 36 0.5× 31 0.4× 117 1.9× 18 401
Taro Kominami Japan 13 290 1.4× 253 2.2× 108 1.5× 65 0.9× 35 0.6× 41 395
Danping Zhu United States 8 323 1.6× 198 1.7× 116 1.6× 61 0.9× 98 1.6× 8 471
Ruth L. Pickett Seltner Canada 9 187 0.9× 143 1.2× 113 1.6× 67 1.0× 11 0.2× 10 313
Fernanda Belga Ottoni Porto Brazil 12 284 1.4× 157 1.4× 43 0.6× 54 0.8× 82 1.3× 19 351
Shinichi Yamade Japan 10 184 0.9× 102 0.9× 19 0.3× 62 0.9× 23 0.4× 26 297
S.F. Webb United Kingdom 8 191 0.9× 173 1.5× 83 1.2× 28 0.4× 70 1.1× 14 427
Chiara O. Pierrottet Italy 7 205 1.0× 207 1.8× 121 1.7× 28 0.4× 37 0.6× 12 317
Simone Schaich Germany 5 242 1.2× 123 1.1× 21 0.3× 34 0.5× 29 0.5× 6 260
Samantha Johnson United Kingdom 8 216 1.1× 108 0.9× 32 0.5× 37 0.5× 34 0.5× 10 265

Countries citing papers authored by Martina Broghammer

Since Specialization
Citations

This map shows the geographic impact of Martina Broghammer's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Martina Broghammer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martina Broghammer more than expected).

Fields of papers citing papers by Martina Broghammer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martina Broghammer. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Martina Broghammer. The network helps show where Martina Broghammer may publish in the future.

Co-authorship network of co-authors of Martina Broghammer

This figure shows the co-authorship network connecting the top 25 collaborators of Martina Broghammer. A scholar is included among the top collaborators of Martina Broghammer based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Martina Broghammer. Martina Broghammer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Jacobi, Frank, Martina Broghammer, Christian Becker, et al.. (2008). Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping. International Journal of Molecular Medicine. 21(4). 429–38. 27 indexed citations
2.
Karra, Daniela, Frank Jacobi, Martina Broghammer, Nikolaus Blin, & Carsten M. Pusch. (2006). Population Haplotypes of Exon ORF15 of the Retinitis Pigmentosa GTPase Regulator Gene in Germany. Molecular Diagnosis & Therapy. 10(2). 115–123. 7 indexed citations
3.
Jacobi, Frank, Daniela Karra, Martina Broghammer, Nikolaus Blin, & Carsten M. Pusch. (2005). Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background. International Journal of Molecular Medicine. 16(6). 1175–8. 6 indexed citations
4.
Jacobi, Frank, E. Zrenner, Martina Broghammer, & Carsten M. Pusch. (2005). A genetic perspective on myopia. Cellular and Molecular Life Sciences. 62(7-8). 800–808. 43 indexed citations
5.
Pusch, Carsten M., Martina Broghammer, Graeme Nicholson, et al.. (2004). PCR-Induced Sequence Alterations Hamper the Typing of Prehistoric Bone Samples for Diagnostic Achondroplasia Mutations. Molecular Biology and Evolution. 21(11). 2005–2011. 18 indexed citations
6.
Broghammer, Martina, et al.. (2004). Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations. Cancer Letters. 214(2). 225–229. 5 indexed citations
7.
Jacobi, Frank, Christian Hamel, Bernard Arnaud, et al.. (2003). A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. American Journal of Ophthalmology. 135(5). 733–736. 20 indexed citations
8.
Pusch, Carsten M., Martina Broghammer, & Nikolaus Blin. (2003). Molecular phylogenetics employing modern and ancient DNA.. PubMed. 44(3). 269–90. 5 indexed citations
9.
Pusch, Carsten M., Martina Broghammer, Bernhard Jurklies, Dorothea Besch, & Frank Jacobi. (2002). Ten novel ORF15 mutations confirm mutational hot spot in theRPGR gene in European patients with X-linked retinitis pigmentosa. Human Mutation. 20(5). 405–405. 24 indexed citations
10.
Sauer, Christian, Eberhart Zrenner, Birgit Lorenz, et al.. (2002). Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. European Journal of Human Genetics. 10(8). 449–456. 66 indexed citations
11.
Pusch, Carsten M., Martina Broghammer, & Alfred Czarnetzki. (2001). Molekulare Paläobiologie: Ancient DNA und Authentizität. Germania: Anzeiger der Römisch-Germanischen Kommission des Deutschen Archäologischen Instituts. 79(1). 121–141. 1 indexed citations
12.
Broghammer, Martina, Eberhart Zrenner, E Apfelstedt-Sylla, et al.. (2001). Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders. International Journal of Molecular Medicine. 8(1). 53–8. 1 indexed citations
13.
Scholz, Michael, et al.. (2001). Intrapopulational Relationships in Ancient Societies: A multidisciplinary Study.. Zeitschrift für Morphologie und Anthropologie. 83(1). 5–21. 5 indexed citations
14.
Pusch, Carsten M., Lutz Bachmann, Martina Broghammer, & Michael Scholz. (2000). Internal Alu-Polymerase Chain Reaction: A Sensitive Contamination Monitoring Protocol for DNA Extracted from Prehistoric Animal Bones. Analytical Biochemistry. 284(2). 408–411. 7 indexed citations
15.
Jacobi, Frank, et al.. (2000). Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1. Human Genetics. 107(1). 89–91. 5 indexed citations
16.
Bachmann, Lutz, Michael Scholz, Martina Broghammer, Ian Giddings, & Carsten M. Pusch. (2000). Voltage-induced release of nucleic acids from palaeontological samples. Electrophoresis. 21(8). 1488–1492. 6 indexed citations
17.
Pusch, Carsten M., Martina Broghammer, & Michael Scholz. (2000). Cremation practices and the survival of ancient DNA: burnt bone analyses via RAPD-mediated PCR. Anthropologischer Anzeiger. 58(3). 237–251. 7 indexed citations
18.
Jacobi, Frank, et al.. (2000). Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1. Human Genetics. 107(1). 89–91. 2 indexed citations
19.
Blin, Nathalie, et al.. (2000). Adaptor-mediated amplification of minute amounts of severely fragmented ancient nucleic acids.. PubMed. 41(4). 303–15. 2 indexed citations
20.
Wissinger, Bernd, Herbert Jägle, Susanne Kohl, et al.. (1998). Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11. Genomics. 51(3). 325–331. 53 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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