Barbara Lucke

1.3k total citations
10 papers, 875 citations indexed

About

Barbara Lucke is a scholar working on Molecular Biology, Genetics and Small Animals. According to data from OpenAlex, Barbara Lucke has authored 10 papers receiving a total of 875 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Small Animals. Recurrent topics in Barbara Lucke's work include Mitochondrial Function and Pathology (2 papers), Molecular Biology Techniques and Applications (2 papers) and Genomics and Phylogenetic Studies (2 papers). Barbara Lucke is often cited by papers focused on Mitochondrial Function and Pathology (2 papers), Molecular Biology Techniques and Applications (2 papers) and Genomics and Phylogenetic Studies (2 papers). Barbara Lucke collaborates with scholars based in Germany, United Kingdom and United States. Barbara Lucke's co-authors include Markus Schuelke, Dominik Seelow, Ellen Knierim, Jana Marie Schwarz, Katrin Hoffmann, Tom H. Lindner, André Reis, Russell E. Ware, Ada L. Olins and Donald E. Olins and has published in prestigious journals such as Nature Genetics, PLoS ONE and Stroke.

In The Last Decade

Barbara Lucke

10 papers receiving 861 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Barbara Lucke Germany	9	649	189	163	102	95	10	875
Ana Lía Taratuto Argentina	19	402 0.6×	278 1.5×	112 0.7×	189 1.9×	73 0.8×	42	1.1k
Isabelle Nelson France	24	1.3k 2.0×	100 0.5×	53 0.3×	249 2.4×	113 1.2×	49	1.5k
Ryan E. Lamont Canada	16	611 0.9×	58 0.3×	148 0.9×	133 1.3×	165 1.7×	35	850
Katrin Koehler Germany	19	873 1.3×	132 0.7×	148 0.9×	123 1.2×	333 3.5×	52	1.3k
Haike Reznik‐Wolf Israel	15	554 0.9×	33 0.2×	118 0.7×	95 0.9×	171 1.8×	39	888
Pagon Ra United States	6	450 0.7×	70 0.4×	44 0.3×	82 0.8×	260 2.7×	291	791
Bianca Miterski Germany	14	299 0.5×	48 0.3×	160 1.0×	201 2.0×	90 0.9×	19	778
M Schmidt United States	14	233 0.4×	70 0.4×	93 0.6×	89 0.9×	149 1.6×	28	559
Emmanuelle Lacène France	17	1.3k 1.9×	356 1.9×	370 2.3×	212 2.1×	101 1.1×	32	1.5k
Maja Hempel Germany	19	511 0.8×	50 0.3×	68 0.4×	90 0.9×	342 3.6×	58	855

Countries citing papers authored by Barbara Lucke

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Lucke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Lucke

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

All Works

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10 of 10 papers shown

Knierim, Ellen, Barbara Lucke, Jana Marie Schwarz, Markus Schuelke, & Dominik Seelow. (2011). Systematic Comparison of Three Methods for Fragmentation of Long-Range PCR Products for Next Generation Sequencing. PLoS ONE. 6(11). e28240–e28240. 90 indexed citations

Knierim, Ellen, Lilia Leisle, C. N. J. Wagner, et al.. (2010). Recurrent Stroke Due to a Novel Voltage Sensor Mutation in Ca _v 2.1 Responds to Verapamil. Stroke. 42(2). e14–7. 36 indexed citations

Rajab, Anna, Volker Straub, Liza McCann, et al.. (2010). Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations. PLoS Genetics. 6(3). e1000874–e1000874. 181 indexed citations

Hoffmann, Katrin, Franz Rüschendorf, Bertram Müller‐Myhsok, et al.. (2009). A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany*. Journal of Hypertension. 27(5). 983–990. 8 indexed citations

Janssen, A.J.M., Markus Schuelke, Jan Smeıtınk, et al.. (2008). Muscle 3243A→G mutation load and capacity of the mitochondrial energy‐generating system. Annals of Neurology. 63(4). 473–481. 20 indexed citations

Rüther, Klaus, Kathleen A. Williamson, Birgit Lorenz, et al.. (2006). De novo double mutation in PAX6 and mtDNA tRNA Lys associated with atypical aniridia and mitochondrial disease. Journal of Molecular Medicine. 85(2). 163–168. 9 indexed citations

Wolf, Matthias T. F., Isabella Zalewski, Félix Claverie-Martı́n, et al.. (2005). Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2–q34.2 by total genome search for linkage. Nephrology Dialysis Transplantation. 20(5). 909–914. 20 indexed citations

Ruf, Rainer, Matthias T. F. Wolf, Hans Christian Hennies, et al.. (2003). A Gene Locus for Steroid-Resistant Nephrotic Syndrome with Deafness Maps to Chromosome 14q24.2. Journal of the American Society of Nephrology. 14(6). 1519–1522. 6 indexed citations

Hoffmann, Katrin, Ada L. Olins, Donald E. Olins, et al.. (2002). Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly). Nature Genetics. 31(4). 410–414. 261 indexed citations

10.

Grohmann, Katja, Markus Schuelke, Alexander Diers, et al.. (2001). Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1. Nature Genetics. 29(1). 75–77. 244 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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