C Lenski

467 total citations
7 papers, 286 citations indexed

About

C Lenski is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, C Lenski has authored 7 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Ophthalmology and 2 papers in Genetics. Recurrent topics in C Lenski's work include RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neurological Disease Mechanisms and Treatments (1 paper). C Lenski is often cited by papers focused on RNA modifications and cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Neurological Disease Mechanisms and Treatments (1 paper). C Lenski collaborates with scholars based in Germany, United States and Austria. C Lenski's co-authors include Juliane Ramser, Herbert A. Lubs, Céline Burcklé, Stefanie Engert, Alfons Meindl, Geneviève Nguyen, Charles E. Schwartz, Fatima Abidi, Gaiping Wen and Helga V. Toriello and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and American Journal of Medical Genetics.

In The Last Decade

C Lenski

6 papers receiving 282 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C Lenski Germany	4	196	79	61	60	59	7	286
Noriko Mutsuga United States	11	129 0.7×	19 0.2×	53 0.9×	49 0.8×	15 0.3×	16	331
Jens Schallner Germany	11	182 0.9×	34 0.4×	26 0.4×	120 2.0×	55 0.9×	15	324
Asma I. Tahir Saudi Arabia	11	129 0.7×	25 0.3×	20 0.3×	90 1.5×	14 0.2×	19	294
Delphine Dupin‐Deguine France	3	98 0.5×	53 0.7×	14 0.2×	63 1.1×	29 0.5×	7	208
Devon Lamb Thrush United States	10	218 1.1×	27 0.3×	14 0.2×	141 2.4×	25 0.4×	19	334
Judith López‐Fernández Spain	10	82 0.4×	24 0.3×	169 2.8×	47 0.8×	15 0.3×	15	309
Serge Clément Belgium	8	310 1.6×	25 0.3×	106 1.7×	25 0.4×	16 0.3×	10	459
Fılız Hazan Türkiye	10	183 0.9×	18 0.2×	23 0.4×	119 2.0×	18 0.3×	54	309
О. П. Рыжкова Russia	7	117 0.6×	30 0.4×	14 0.2×	51 0.8×	37 0.6×	74	216
Cristina Llombart Spain	8	169 0.9×	16 0.2×	35 0.6×	20 0.3×	10 0.2×	10	390

Countries citing papers authored by C Lenski

Since Specialization

Citations

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

Fields of papers citing papers by C Lenski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Lenski

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Feyen, Oliver, C Lenski, O. Schofer, et al.. (2009). ARDS as Presenting Symptom in an Infant with CD40L Deficiency (Hyper-IgM Syndrome Type 1). Klinische Pädiatrie. 221(5). 302–304. 1 indexed citations

2.

Ramser, Juliane, Mary Ellen Ahearn, C Lenski, et al.. (2008). Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy. The American Journal of Human Genetics. 82(1). 188–193. 124 indexed citations

3.

Ramser, Juliane, Fatima Abidi, Céline Burcklé, et al.. (2005). A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Human Molecular Genetics. 14(8). 1019–1027. 146 indexed citations

4.

Holinski‐Feder, Elke, Olaf Rittinger, Kerry Baldwin Jedele, et al.. (1999). Nonsyndromic X-linked mental retardation: Mapping of MRX58 to the pericentromeric region. American Journal of Medical Genetics. 86(2). 102–106. 9 indexed citations

5.

Lenski, C, et al.. (1986). [Choroidal hematoma in the development of malignant melanoma].. PubMed. 86(2). 211–2. 1 indexed citations

6.

Lenski, C, et al.. (1984). [Importance of hyperbaric oxygen therapy in poisoning caused by quinine].. PubMed. 83(6-7). 803–6. 4 indexed citations

7.

Lenski, C, et al.. (1982). [Vitelliform degeneration of the macula and neovascular choroidal membrane].. PubMed. 82(4). 587–90. 1 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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