A. Kuechler

924 total citations
18 papers, 502 citations indexed

About

A. Kuechler is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, A. Kuechler has authored 18 papers receiving a total of 502 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Plant Science. Recurrent topics in A. Kuechler's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Chromatin Dynamics (4 papers). A. Kuechler is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Chromatin Dynamics (4 papers). A. Kuechler collaborates with scholars based in Germany, Poland and United States. A. Kuechler's co-authors include Thomas Liehr, Anja Weise, U. Claussen, Kristin Mrasek, Anita Heller, Heike Starke, Olaf Hiort, Susanne Ledig, G. Wolff and Gerd Scherer and has published in prestigious journals such as Human Reproduction, Food and Chemical Toxicology and Toxicological Sciences.

In The Last Decade

A. Kuechler

17 papers receiving 472 citations

Peers

A. Kuechler

GENET

PPCH

Ron Hochstenbach Netherlands

Sophie Tourpin France

Elisabeth Syk Lundberg Sweden

Jaime Garcia‐Heras United States

N. A. Skryabin Russia

Buhe Nashun China

Hiba Risheg United States

Sophie Brisset France

Nicholas M. Robert Canada

Shinsuke Ninomiya Japan

Ron Hochstenbach Netherlands

A. Kuechler

340 ×1.2

GENET

306 ×1.1

162 ×1.2

87 ×1.0

PPCH

47 ×0.9

Citations per year, relative to A. Kuechler A. Kuechler (= 1×) peers Ron Hochstenbach

Countries citing papers authored by A. Kuechler

Since Specialization

Citations

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

Fields of papers citing papers by A. Kuechler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Kuechler

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

All Works

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18 of 18 papers shown

Theurer, Sarah, Eva Biewald, K. Kuchelmeister, et al.. (2018). Primäres Meningeom des Nervus opticus im Säuglingsalter als Erstmanifestation einer Neurofibromatose Typ 2. Der Pathologe. 40(2). 179–184.

Kölbel, Heike, et al.. (2017). DYT16 mimics metabolic disease with fever associated beginning of dystonia and MRI abnormalities. European Journal of Paediatric Neurology. 21. e177–e177. 2 indexed citations

Revençu, Nicole, Laurence M. Boon, A. Dompmartin, et al.. (2013). Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. Molecular Syndromology. 4(4). 173–178. 29 indexed citations

Kuechler, A., Julia Hentschel, Ingo Kurth, et al.. (2012). A Novel Homozygous <b><i>WDR72</i></b> Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature. Molecular Syndromology. 3(5). 223–229. 13 indexed citations

Kuechler, A., Berthold P. Hauffa, Angela Köninger, et al.. (2010). An unbalanced translocation unmasks a recessive mutation in the follicle-stimulating hormone receptor (FSHR) gene and causes FSH resistance. European Journal of Human Genetics. 18(6). 656–661. 56 indexed citations

Ledig, Susanne, Olaf Hiort, Gerd Scherer, et al.. (2010). Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci. Human Reproduction. 25(10). 2637–2646. 72 indexed citations

Najm, Juliane, A.M.A. Lachmeijer, László Sztriha, et al.. (2008). Refining the phenotype of α‐1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. Clinical Genetics. 74(5). 425–433. 67 indexed citations

Liehr, Thomas, Gülen Eda Ütine, Udo Trautmann, et al.. (2007). Neocentric small supernumerary marker chromosomes (sSMC) – three more cases and review of the literature. Cytogenetic and Genome Research. 118(1). 31–37. 41 indexed citations

Glei, Michael, U. Claussen, A. Kuechler, et al.. (2006). Comet Fluorescence in situ Hybridization Analysis for Oxidative Stress-Induced DNA Damage in Colon Cancer Relevant Genes. Toxicological Sciences. 96(2). 279–284. 28 indexed citations

10.

Liehr, Thomas, Heike Starke, Anita Heller, et al.. (2006). Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding. Cytogenetic and Genome Research. 114(3-4). 240–244. 38 indexed citations

11.

Keller, Ulrike, Gerhard G. Grabenbauer, A. Kuechler, Rolf Sauer, & Luitpold Distel. (2004). Technical report: Radiation sensitivity testing by fluorescencein‐situhybridization: how many metaphases have to be analysed?. International Journal of Radiation Biology. 80(8). 615–620. 10 indexed citations

12.

Lehrer, Harold, Anja Weise, S. Michel, et al.. (2004). The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB). Cytogenetic and Genome Research. 105(1). 25–28. 7 indexed citations

13.

Weise, Anja, Anita Heller, Heike Starke, et al.. (2003). Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding method. Cytogenetic and Genome Research. 103(1-2). 34–39. 32 indexed citations

14.

Sendt, Wolfgang, J. Scheele, A. Kuechler, et al.. (2003). Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples. Food and Chemical Toxicology. 41(5). 655–664. 33 indexed citations

15.

Liehr, Thomas, Angela Nietzel, Heike Starke, et al.. (2003). Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches.. PubMed. 29(1). 5–10. 8 indexed citations

16.

Weise, Anja, Thomas Liehr, Thomas Efferth, A. Kuechler, & E. Gebhart. (2002). Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines. Cytogenetic and Genome Research. 98(2-3). 118–125. 8 indexed citations

17.

Liehr, Thomas, Anja Weise, Anita Heller, et al.. (2002). Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries. Cytogenetic and Genome Research. 97(1-2). 43–50. 51 indexed citations

18.

Kuechler, A., C R Mueller, Thomas Liehr, & U. Claussen. (2001). Detection of microdeletions in the short arm of the X chromosome by chromosome stretching. Cytogenetic and Genome Research. 95(1-2). 12–16. 7 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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