Lotte Henke

2.6k total citations
44 papers, 1.1k citations indexed

About

Lotte Henke is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Lotte Henke has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 22 papers in Genetics and 6 papers in Hematology. Recurrent topics in Lotte Henke's work include Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (13 papers) and RNA and protein synthesis mechanisms (6 papers). Lotte Henke is often cited by papers focused on Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (13 papers) and RNA and protein synthesis mechanisms (6 papers). Lotte Henke collaborates with scholars based in Germany, Japan and Netherlands. Lotte Henke's co-authors include Jürgen Henke, Manfred Kayser, Lutz Roewer, Tadeusz Dobosz, Silke Brauer, R. Szibor, Marion Nagy, Michael Krawczak, Peter de Knijff and Mark Stoneking and has published in prestigious journals such as Ophthalmology, The American Journal of Human Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Lotte Henke

43 papers receiving 1.1k citations

Peers

Lotte Henke

GENET

ARCHE

Jürgen Henke Germany

K Omoto Japan

Abra Brisbin United States

E. Dietzsch South Africa

Jake Byrnes United States

Mark Vermeulen Netherlands

William Beggs United States

Aavo‐Valdur Mikelsaar Estonia

Brian K. Maples United States

Sofia B. Zuniga Netherlands

Jürgen Henke Germany

Lotte Henke

761 ×1.0

GENET

612 ×1.1

255 ×1.7

89 ×0.9

ARCHE

37 ×0.5

Citations per year, relative to Lotte Henke Lotte Henke (= 1×) peers Jürgen Henke

Countries citing papers authored by Lotte Henke

Since Specialization

Citations

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

Fields of papers citing papers by Lotte Henke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lotte Henke

This figure shows the co-authorship network connecting the top 25 collaborators of Lotte Henke. A scholar is included among the top collaborators of Lotte Henke 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 Lotte Henke. Lotte Henke is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ralf, Arwin, Lutz Roewer, Josephine Purps, et al.. (2020). Identification and characterization of novel rapidly mutating Y‐chromosomal short tandem repeat markers. Human Mutation. 41(9). 1680–1696. 36 indexed citations

Yuasa, Isao, Hiroaki Nishimukai, Yasuo Fukumori, et al.. (2009). A hypervariable STR polymorphism in the complement factor I (CFI) gene: Asian-specific alleles. International Journal of Legal Medicine. 125(1). 121–125. 6 indexed citations

Yuasa, Isao, Mayumi Nakagawa, Kazuo Umetsu, et al.. (2008). Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific. Journal of Human Genetics. 53(11-12). 1016–1021. 10 indexed citations

Mansuet‐Lupo, Audrey, Jürgen Henke, Lotte Henke, et al.. (2008). A paternity case with three genetic incompatibilities between father and child due to maternal uniparental disomy 21 and a mutation at the Y chromosome. Forensic Science International Genetics. 3(2). 141–143. 26 indexed citations

Yuasa, Isao, K. Umetsu, Shinji Harihara, et al.. (2007). Distribution of Two Asian-Related Coding SNPs in the MC1R and OCA2 Genes. Biochemical Genetics. 45(7-8). 535–542. 26 indexed citations

Bender, Klaus, Jeanett Edelmann, Frank Götz, et al.. (2007). New alleles and mutational events at 14 STR loci from different German populations. Forensic Science International Genetics. 1(3-4). 232–237. 16 indexed citations

Nagy, Melinda, Lotte Henke, Jürgen Henke, et al.. (2006). Searching for the origin of Romanies: Slovakian Romani, Jats of Haryana and Jat Sikhs Y-STR data in comparison with different Romani populations. Forensic Science International. 169(1). 19–26. 36 indexed citations

Yuasa, Isao, K. Umetsu, Shinji Harihara, et al.. (2006). Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis. Annals of Human Genetics. 70(6). 802–811. 29 indexed citations

Henke, Lotte & Jürgen Henke. (2006). Supplemented Data on Mutation Rates in 33 Autosomal Short Tandem Repeat Polymorphisms. Journal of Forensic Sciences. 51(2). 446–447. 12 indexed citations

10.

Henke, Lotte, et al.. (2001). Sequence analysis and population data on the ‘new’ short tandem repeat locus D5S2360. Forensic Science International. 116(1). 55–58. 2 indexed citations

11.

Yuasa, Isao, et al.. (2001). Characterization of genomic rearrangements of the α1-acid glycoprotein/orosomucoid gene in Ghanaians. Journal of Human Genetics. 46(10). 572–578. 8 indexed citations

12.

Nakamura, Hiroaki, Isao Yuasa, K. Umetsu, et al.. (2000). Molecular analysis of the human orosomucoid gene ORM1*Q0 köln responsible for incompatibility in a German paternity case. International Journal of Legal Medicine. 114(1-2). 114–117. 5 indexed citations

13.

Kayser, Manfred, Lutz Roewer, Minttu Hedman, et al.. (2000). Characteristics and Frequency of Germline Mutations at Microsatellite Loci from the Human Y Chromosome, as Revealed by Direct Observation in Father/Son Pairs. The American Journal of Human Genetics. 66(5). 1580–1588. 295 indexed citations

14.

Henke, Lotte, et al.. (1999). Usefulness of conventional blood groups, DNA-minisatellites, and short tandem repeat polymorphisms in paternity testing: a comparison. Forensic Science International. 103(2). 133–142. 7 indexed citations

15.

Henke, Lotte, et al.. (1996). Population genetic and family data for the human minisatellite locus D16S309 (MS205) in Germans. International Journal of Legal Medicine. 109(4). 178–180. 1 indexed citations

16.

Suzuki, Koichi, J. Henke, Lotte Henke, et al.. (1996). Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene. Human Genetics. 98(4). 393–395. 42 indexed citations

17.

Schneider, Peter M., Rolf Fimmers, Jörg Bertrams, et al.. (1992). Biostatistical basis of individualisation and segregation analysis using the multilocus DNA probe MZ 1.3: Results of a collaborative study. Forensic Science International. 55(1). 45–58. 5 indexed citations

18.

Henke, Lotte, et al.. (1991). Population Genetic Data Determined For Five Different Single Locus Minisatellite Probes. Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions. 58. 144–153. 13 indexed citations

19.

Henke, Lotte, et al.. (1991). Size calculation of restriction enzyme HaeIII-generated fragments detected by probe YNH24 by comparison of data from two laboratories: The generation of fragment-size frequencies. Forensic Science International. 49(1). 21–31. 1 indexed citations

20.

Henke, Lotte, et al.. (1990). BamHI polymorphism of locus D2S44 in a West German population as revealed by VNTR probe YNH24. International Journal of Legal Medicine. 104(1). 33–38. 2 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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