Nadine Kluck

1.3k total citations
5 papers, 296 citations indexed

About

Nadine Kluck is a scholar working on Genetics, Molecular Biology and Dermatology. According to data from OpenAlex, Nadine Kluck has authored 5 papers receiving a total of 296 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Dermatology. Recurrent topics in Nadine Kluck's work include RNA modifications and cancer (1 paper), Hair Growth and Disorders (1 paper) and Genetic Associations and Epidemiology (1 paper). Nadine Kluck is often cited by papers focused on RNA modifications and cancer (1 paper), Hair Growth and Disorders (1 paper) and Genetic Associations and Epidemiology (1 paper). Nadine Kluck collaborates with scholars based in Germany, Sweden and United Kingdom. Nadine Kluck's co-authors include Markus M. Nöthen, Sven Cichon, Peter Propping, Yun Freudenberg‐Hua, Jan Freudenberg, Ellen Plume, Andreas Warnke, Helmut Remschmidt, Andreas Ziegler and Myriam Peyrard‐Janvid and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and British Journal of Dermatology.

In The Last Decade

Nadine Kluck

5 papers receiving 288 citations

Peers

Nadine Kluck

GENET

DEP

MB

SP

CN

F.F. Brockschmidt Germany

Satu Massinen Sweden

Natalie R. Powers United States

James H. Schick United States

Mark Lathrop France

Diana J. Slater United States

Gérald Bussy France

Yixun Li China

Avinash M. Veerappa India

Alejandro Q. Nato United States

F.F. Brockschmidt Germany

Nadine Kluck

61 ×0.4

GENET

57 ×0.4

DEP

73 ×0.8

MB

27 ×0.5

SP

30 ×0.7

CN

Citations per year, relative to Nadine Kluck Nadine Kluck (= 1×) peers F.F. Brockschmidt

Countries citing papers authored by Nadine Kluck

Since Specialization

Citations

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

Fields of papers citing papers by Nadine Kluck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadine Kluck

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

All Works

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5 of 5 papers shown

1.

Redler, Silke, F.F. Brockschmidt, Rachid Tazi‐Ahnini, et al.. (2012). Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss. British Journal of Dermatology. 166(6). 1314–1318. 36 indexed citations

2.

Assis, Nilma Almeida de, Stefanie Nowak, Kerstin U. Ludwig, et al.. (2010). SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients. International Journal of Pediatric Otorhinolaryngology. 75(1). 49–52. 9 indexed citations

3.

Schumacher, Johannes, Heidi Anthoni, Inke R. König, et al.. (2005). Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia. The American Journal of Human Genetics. 78(1). 52–62. 180 indexed citations

4.

Freudenberg‐Hua, Yun, Jan Freudenberg, Nadine Kluck, et al.. (2005). Systematic investigation of genetic variability in 111 human genes—implications for studying variable drug response. The Pharmacogenomics Journal. 5(3). 183–192. 12 indexed citations

5.

Freudenberg‐Hua, Yun, Jan Freudenberg, Nadine Kluck, et al.. (2003). Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population. Genome Research. 13(10). 2271–2276. 59 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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