Karl Hackmann

3.1k total citations
54 papers, 1.3k citations indexed

About

Karl Hackmann is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Karl Hackmann has authored 54 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 28 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Karl Hackmann's work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (8 papers) and BRCA gene mutations in cancer (7 papers). Karl Hackmann is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (8 papers) and BRCA gene mutations in cancer (7 papers). Karl Hackmann collaborates with scholars based in Germany, United States and France. Karl Hackmann's co-authors include Evelin Schröck, Feng Qian, Gregory G. Germino, Hangxue Xu, Andreas Rump, Nataliya Di Donato, Barbara Klink, Andreas Schlösser, Hildgund Schrempf and Sigrid Tinschert and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Oncology.

In The Last Decade

Karl Hackmann

53 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karl Hackmann Germany 19 739 614 128 121 110 54 1.3k
Lingqian Wu China 24 1.2k 1.6× 865 1.4× 170 1.3× 83 0.7× 124 1.1× 186 2.4k
Lalitha R. Belur United States 17 715 1.0× 485 0.8× 95 0.7× 38 0.3× 108 1.0× 35 1.1k
Walter Tsark United States 19 1.1k 1.4× 273 0.4× 58 0.5× 57 0.5× 142 1.3× 33 1.4k
Jan Blancato United States 22 943 1.3× 454 0.7× 142 1.1× 108 0.9× 254 2.3× 47 1.7k
Mark T. Ross United Kingdom 17 699 0.9× 403 0.7× 144 1.1× 131 1.1× 120 1.1× 35 1.2k
Gurbax S. Sekhon United States 17 596 0.8× 522 0.9× 102 0.8× 61 0.5× 85 0.8× 42 1.1k
Antoaneta Mincheva Germany 21 992 1.3× 380 0.6× 68 0.5× 72 0.6× 192 1.7× 41 1.5k
Ilse Wieland Germany 23 1.3k 1.8× 391 0.6× 46 0.4× 159 1.3× 237 2.2× 81 1.9k
Cole Ferguson United States 17 616 0.8× 365 0.6× 248 1.9× 59 0.5× 228 2.1× 28 1.3k
Karl‐Heinz Grzeschik Germany 17 1.4k 1.9× 542 0.9× 52 0.4× 67 0.6× 158 1.4× 25 1.9k

Countries citing papers authored by Karl Hackmann

Since Specialization
Citations

This map shows the geographic impact of Karl Hackmann'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 Karl Hackmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karl Hackmann more than expected).

Fields of papers citing papers by Karl Hackmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karl Hackmann. 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 Karl Hackmann. The network helps show where Karl Hackmann may publish in the future.

Co-authorship network of co-authors of Karl Hackmann

This figure shows the co-authorship network connecting the top 25 collaborators of Karl Hackmann. A scholar is included among the top collaborators of Karl Hackmann 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 Karl Hackmann. Karl Hackmann 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.
Rump, Andreas, et al.. (2018). PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome. European Journal of Medical Genetics. 62(12). 103587–103587. 7 indexed citations
2.
Porrmann, Joseph, Martin Smitka, Evelin Schröck, et al.. (2018). Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion. Ophthalmic Genetics. 39(5). 645–647. 1 indexed citations
3.
Porrmann, Joseph, Andreas Rump, Karl Hackmann, et al.. (2018). Novel truncating PPM1D mutation in a patient with intellectual disability. European Journal of Medical Genetics. 62(1). 70–72. 6 indexed citations
4.
Penkert, Judith, Gunnar Schmidt, Winfried Hofmann, et al.. (2018). Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast Cancer Research. 20(1). 87–87. 6 indexed citations
5.
Gieldon, Laura, Luisa Mackenroth, Anne‐Karin Kahlert, et al.. (2018). Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE. 13(8). e0201041–e0201041. 29 indexed citations
6.
Hackmann, Karl, Ida Paris, Angelo Minucci, et al.. (2018). Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients. Molecular Diagnosis & Therapy. 23(1). 121–126. 8 indexed citations
7.
Concolino, Paola, Karl Hackmann, Ida Paris, et al.. (2017). Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome. Breast Cancer Research and Treatment. 164(2). 497–503. 15 indexed citations
8.
Hauber, Ilona, Jan Chemnitz, Carola Schäfer, et al.. (2016). Directed evolution of a recombinase that excises the provirus of most HIV-1 primary isolates with high specificity. Nature Biotechnology. 34(4). 401–409. 95 indexed citations
9.
Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations
10.
Papuc, Sorina Mihaela, Karl Hackmann, Joris Andrieux, et al.. (2015). Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalities. European Journal of Medical Genetics. 58(5). 319–323. 6 indexed citations
11.
Donato, Nataliya Di, C. Le Caignec, Barbara Klink, et al.. (2014). Distinct phenotype of PHF6 deletions in females. European Journal of Medical Genetics. 57(2-3). 85–89. 15 indexed citations
12.
Donato, Nataliya Di, Barbara Klink, Gabriele Hahn, Evelin Schröck, & Karl Hackmann. (2014). Interstitial deletion 1p36.32 in two brothers with a distinct phenotype – Overgrowth, macrocephaly and nearly normal intellectual function. European Journal of Medical Genetics. 57(9). 494–497. 3 indexed citations
13.
Hackmann, Karl, Jens Schallner, Evelin Schröck, et al.. (2013). Severe intellectual disability, West syndrome, Dandy–Walker malformation, and syndactyly in a patient with partial tetrasomy 17q25.3. American Journal of Medical Genetics Part A. 161(12). 3144–3149. 13 indexed citations
14.
Hauber, Ilona, Jan Chemnitz, Janet Chusainow, et al.. (2013). Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice. PLoS Pathogens. 9(9). e1003587–e1003587. 47 indexed citations
15.
Abou‐El‐Ardat, Khalil, Karol Szafranski, Andreas Rump, et al.. (2013). Novel CIC Point Mutations and an Exon-Spanning, Homozygous Deletion Identified in Oligodendroglial Tumors by a Comprehensive Genomic Approach Including Transcriptome Sequencing. PLoS ONE. 8(9). e76623–e76623. 15 indexed citations
16.
Michaelis, Martin, Stefan Barth, Rainer Breitling, et al.. (2012). Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection. Oncogenesis. 1(4). e10–e10. 5 indexed citations
17.
18.
Yu, Shengqiang, Karl Hackmann, Jiangang Gao, et al.. (2007). Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure. Proceedings of the National Academy of Sciences. 104(47). 18688–18693. 136 indexed citations
19.
Hackmann, Karl, et al.. (2007). Characterization of cis-Autoproteolysis of Polycystin-1, the Product of Human Polycystic Kidney Disease 1 Gene. Journal of Biological Chemistry. 282(30). 21729–21737. 86 indexed citations
20.
Hackmann, Karl, Arseni Markoff, Feng Qian, et al.. (2005). A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1. Human Molecular Genetics. 14(21). 3249–3262. 12 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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