Elke Botzenhart

837 total citations
8 papers, 331 citations indexed

About

Elke Botzenhart is a scholar working on Molecular Biology, Rheumatology and Biochemistry. According to data from OpenAlex, Elke Botzenhart has authored 8 papers receiving a total of 331 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Rheumatology and 3 papers in Biochemistry. Recurrent topics in Elke Botzenhart's work include Amino Acid Enzymes and Metabolism (3 papers), Folate and B Vitamins Research (3 papers) and Metabolism and Genetic Disorders (2 papers). Elke Botzenhart is often cited by papers focused on Amino Acid Enzymes and Metabolism (3 papers), Folate and B Vitamins Research (3 papers) and Metabolism and Genetic Disorders (2 papers). Elke Botzenhart collaborates with scholars based in Germany, Australia and Poland. Elke Botzenhart's co-authors include Klaus Zerres, Shireen R. Lamandé, David J. Amor, Yuan Yuan, Peter McIntyre, William G. Cole, Christopher B. Little, Irma Gresshoff, Lynn Rowley and Daniele Belluoccio and has published in prestigious journals such as Nature Genetics, Kidney International and Human Mutation.

In The Last Decade

Elke Botzenhart

8 papers receiving 325 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elke Botzenhart Germany	7	175	77	64	55	50	8	331
Triantafyllos Paparountas Greece	6	222 1.3×	19 0.2×	170 2.7×	16 0.3×	18 0.4×	6	445
Mengping Jia China	10	281 1.6×	14 0.2×	53 0.8×	14 0.3×	19 0.4×	12	361
Laura González Spain	13	313 1.8×	11 0.1×	27 0.4×	80 1.5×	33 0.7×	23	441
Kaplan Jc France	12	185 1.1×	7 0.1×	167 2.6×	36 0.7×	67 1.3×	50	405
Chiyoko N. Inoue Japan	12	292 1.7×	4 0.1×	42 0.7×	14 0.3×	45 0.9×	24	426
Chaoxia He United States	9	399 2.3×	6 0.1×	63 1.0×	53 1.0×	60 1.2×	11	574
Mohammad Miryounesi Iran	10	191 1.1×	8 0.1×	8 0.1×	28 0.5×	83 1.7×	70	337
Saori Miwa Japan	9	265 1.5×	8 0.1×	37 0.6×	18 0.3×	44 0.9×	12	462
Eva M. Pastor‐Arroyo Switzerland	12	156 0.9×	5 0.1×	50 0.8×	32 0.6×	112 2.2×	15	456
Most. Nahid Parvin Japan	12	297 1.7×	27 0.4×	83 1.3×	9 0.2×	34 0.7×	15	362

Countries citing papers authored by Elke Botzenhart

Since Specialization

Citations

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

Fields of papers citing papers by Elke Botzenhart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elke Botzenhart

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

All Works

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8 of 8 papers shown

Lamandé, Shireen R., Yuan Yuan, Irma Gresshoff, et al.. (2011). Mutations in TRPV4 cause an inherited arthropathy of hands and feet. Nature Genetics. 43(11). 1142–1146. 120 indexed citations

Ala‐Mello, Sirpa, Carola Saloranta, Maila Penttinen, et al.. (2007). Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions. Genetics in Medicine. 9(10). 690–694. 38 indexed citations

Borozdin, Wiktor, Michael J. Bamshad, Elke Botzenhart, et al.. (2006). Expanding the spectrum ofTBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations. Human Mutation. 27(9). 975–976. 33 indexed citations

Rudnik‐Schöneborn, Sabine, Elke Botzenhart, Thomas Eggermann, et al.. (2006). Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy. Neurogenetics. 8(2). 137–142. 27 indexed citations

Botzenhart, Elke, Andrew Green, Helena G. Ilyina, et al.. (2005). SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype. Human Mutation. 26(3). 282–282. 48 indexed citations

Botzenhart, Elke, Udo Vester, Albrecht Hesse, et al.. (2003). Genetic variations of the SLC7A9 gene: allele distribution of 13 polymorphic sites in German cystinuria patients and controls.. PubMed. 59(5). 353–9. 17 indexed citations

Botzenhart, Elke, Udo Vester, Christa K. Schmidt, et al.. (2002). Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes. Kidney International. 62(4). 1136–1142. 2 indexed citations

Botzenhart, Elke, Udo Vester, Albrecht Hesse, et al.. (2002). Cystinuria in children: Distribution and frequencies of mutations in the SLC3A1 and SLC7A9 genes. Kidney International. 62(4). 1136–1142. 46 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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