Grzeschik Kh

494 total citations
9 papers, 268 citations indexed

About

Grzeschik Kh is a scholar working on Molecular Biology, Genetics and Dermatology. According to data from OpenAlex, Grzeschik Kh has authored 9 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Dermatology. Recurrent topics in Grzeschik Kh's work include Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and rare skin diseases. (2 papers). Grzeschik Kh is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genetic and rare skin diseases. (2 papers). Grzeschik Kh collaborates with scholars based in Germany, Switzerland and Greece. Grzeschik Kh's co-authors include Konrad Beyreuther, Axel Unterbeck, J. Michael Salbaum, CL Masters, Gerd Multhaup, Klaus Willecke, Edgar Dahl, Stefan Jungbluth, Hanjo Hennemann and Manuel Buchwald and has published in prestigious journals such as International Journal of Obesity, Journal of the European Academy of Dermatology and Venereology and Alzheimer Disease & Associated Disorders.

In The Last Decade

Grzeschik Kh

9 papers receiving 261 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Grzeschik Kh Germany	6	166	107	52	26	26	9	268
Christina Looße Germany	9	156 0.9×	128 1.2×	29 0.6×	21 0.8×	42 1.6×	13	259
Shelly Whelan United States	5	143 0.9×	86 0.8×	105 2.0×	24 0.9×	33 1.3×	7	250
Sara C. Domingues Portugal	13	242 1.5×	128 1.2×	42 0.8×	23 0.9×	41 1.6×	14	355
Antonio S. Tutor Spain	8	244 1.5×	57 0.5×	28 0.5×	17 0.7×	80 3.1×	14	377
Zhouxian Bai China	9	134 0.8×	101 0.9×	39 0.8×	10 0.4×	18 0.7×	22	255
Elaine Gower United Kingdom	4	116 0.7×	116 1.1×	14 0.3×	34 1.3×	65 2.5×	6	215
Jiahui Xia China	8	165 1.0×	76 0.7×	54 1.0×	16 0.6×	58 2.2×	20	272
Tsz Hang Wong Netherlands	10	146 0.9×	145 1.4×	37 0.7×	22 0.8×	37 1.4×	13	308
Rosa Ferrando-Miguel Austria	9	254 1.5×	83 0.8×	45 0.9×	9 0.3×	64 2.5×	12	420
Daniel Militz United States	5	221 1.3×	185 1.7×	35 0.7×	20 0.8×	78 3.0×	6	383

Countries citing papers authored by Grzeschik Kh

Since Specialization

Citations

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

Fields of papers citing papers by Grzeschik Kh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Grzeschik Kh

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

All Works

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9 of 9 papers shown

1.

Katsambas, A., et al.. (2009). CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder. Journal of the European Academy of Dermatology and Venereology. 24(6). 733–736. 14 indexed citations

2.

Kolb‐Mäurer, Annette, Grzeschik Kh, Daniel A. Haas, E.-B. Bröcker, & Heidi E. Hamm. (2008). Conradi-Hünermann-Happle Syndrome (X-linked Dominant Chondrodysplasia Punctata) Confirmed by Plasma Sterol and Mutation Analysis. Acta Dermato Venereologica. 88(1). 47–51. 10 indexed citations

3.

García‐Bravo, B., Antonio Rodríguez‐Pichardo, Arne König, et al.. (2002). Un nuevo caso de síndrome CHILD diagnosticado previamente como nevo epidérmico verrugoso inflamatorio lineal (NEVIL). 30(3). 120–125. 4 indexed citations

4.

Oeffner, Frank, Thomas Korn, Helmut Roth, et al.. (2001). Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. International Journal of Obesity. 25(6). 767–769. 6 indexed citations

5.

Schäfer, Reinhold, et al.. (1991). Evidence for human DNA-mediated transfer of the suppressed phenotype into malignant Chinese hamster cells.. PubMed. 6(12). 2221–8. 3 indexed citations

6.

Willecke, Klaus, et al.. (1990). Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes.. PubMed. 53(2). 275–80. 71 indexed citations

7.

Unterbeck, Axel, J. Michael Salbaum, CL Masters, et al.. (1987). The precursor of Alzheimer??s disease amyloid A4 protein resembles a cell-surface receptor. Alzheimer Disease & Associated Disorders. 1(3). 206–207. 127 indexed citations

8.

Kh, Grzeschik, et al.. (1987). Mapping of DNA markers linked to the cystic fibrosis locus on the long arm of chromosome 7.. PubMed. 40(3). 228–36. 32 indexed citations

9.

Schwinger, E., et al.. (1980). Assignment of the gene locus for human phosphoglucomutase 3 to chromosome 6q12-qter.. PubMed. 23(1). 12–4. 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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