G. Wildhardt

826 total citations
17 papers, 460 citations indexed

About

G. Wildhardt is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, G. Wildhardt has authored 17 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in G. Wildhardt's work include Renal and related cancers (4 papers), Connective tissue disorders research (3 papers) and Developmental Biology and Gene Regulation (3 papers). G. Wildhardt is often cited by papers focused on Renal and related cancers (4 papers), Connective tissue disorders research (3 papers) and Developmental Biology and Gene Regulation (3 papers). G. Wildhardt collaborates with scholars based in Germany, Poland and Switzerland. G. Wildhardt's co-authors include Brigitte Royer‐Pokora, Susanne A. Schneider, R. Ludwig, Valerié Schumacher, Stefan G. R. Wirsel, Bernhard Zabel, Daniela Steinberger, Jochen Decker, D. Schmidt and B Weiss and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular Microbiology and Journal of Medical Genetics.

In The Last Decade

G. Wildhardt

17 papers receiving 451 citations

Peers

G. Wildhardt

GENET

PRM

BIOTE

PPCH

Temuujin Dansranjavin Germany

Ibrahim Khazaal France

Joyce Andrade Brazil

Sumiko Kurachi United States

Bisharah L. Libbus United States

Hisayo Nishida‐Fukuda Japan

Julien Nadjar France

Jeffrey Keenan United States

Katharina Walentin Germany

S. Fishel United Kingdom

Temuujin Dansranjavin Germany

G. Wildhardt

308 ×0.9

80 ×0.4

GENET

33 ×0.6

PRM

7 ×0.2

BIOTE

38 ×1.0

PPCH

Citations per year, relative to G. Wildhardt G. Wildhardt (= 1×) peers Temuujin Dansranjavin

Countries citing papers authored by G. Wildhardt

Since Specialization

Citations

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

Fields of papers citing papers by G. Wildhardt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Wildhardt

This figure shows the co-authorship network connecting the top 25 collaborators of G. Wildhardt. A scholar is included among the top collaborators of G. Wildhardt 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 G. Wildhardt. G. Wildhardt 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:

17 of 17 papers shown

Wildhardt, G., et al.. (2009). A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndrome. Rheumatology International. 30(6). 805–809. 3 indexed citations

Wildhardt, G., Zeyan Zhong, Rebecca Roth, et al.. (2009). Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain. Journal of Medical Genetics. 46(12). 834–839. 103 indexed citations

Forzano, Francesca, Mario Lituania, Valeria Viassolo, et al.. (2007). A familial case of achondrogenesis type II caused by a dominant COL2A1 mutation and “patchy” expression in the mosaic father. American Journal of Medical Genetics Part A. 143A(23). 2815–2820. 17 indexed citations

Wildhardt, G., et al.. (2005). Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications. Clinical & Laboratory Haematology. 27(5). 343–346. 5 indexed citations

Zankl, Andreas, Bernhard Zabel, Katja Hilbert, et al.. (2004). Spondyloperipheral dysplasia is caused by truncating mutations in the C‐propeptide of COL2A1. American Journal of Medical Genetics Part A. 129A(2). 144–148. 29 indexed citations

Kieslich, Matthias, et al.. (2001). Gegenwärtige Grenzen der molekularbiologischen Diagnostik bei Gillespie-Syndrom. Klinische Pädiatrie. 213(2). 47–49. 4 indexed citations

Drechsler, Matthias, Valerié Schumacher, Samantha R. Friedrich, et al.. (1999). Genomic structure, alternative transcripts and chromosome location of the human LIM domain binding protein 1 gene LDB1. Cytogenetic and Genome Research. 87(1-2). 119–124. 4 indexed citations

Wolf, Matthias T. F., Bernhard Zabel, Birgit Lorenz, et al.. (1998). Analysis of aniridia patients for mutations in the PAX6 gene. Der Ophthalmologe. 95(12). 828–830. 5 indexed citations

Wolf, Matthias T. F., Birgit Lorenz, Andreas Winterpacht, et al.. (1998). Ten novel mutations found in aniridia. Human Mutation. 12(5). 304–313. 5 indexed citations

10.

Spranger, J., et al.. (1998). Hypochondroplasie, Achondroplasie und thanatophore Dysplasie als Folge von Mutationen des Fibroblastenwachstumsfaktorrezeptor-3-Gens (FGFR3). Monatsschrift Kinderheilkunde. 146(7). 687–691. 4 indexed citations

11.

Wolf, Matthias T. F., Birgit Lorenz, Andreas Winterpacht, et al.. (1998). Ten novel mutations found in aniridia. Human Mutation. 12(5). 304–313. 41 indexed citations

12.

Pohlenz, Joachim, G. Wildhardt, Bernhard Zabel, & H Willgerodt. (1997). Resistance to Thyroid Hormone in a Family Caused by a New Point Mutation L330S in the Thyroid Receptor (TR) Beta Gene. Thyroid. 7(1). 39–41. 8 indexed citations

13.

Schumacher, Valerié, Susanne A. Schneider, G. Wildhardt, et al.. (1997). Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal–predominant histology. Proceedings of the National Academy of Sciences. 94(8). 3972–3977. 98 indexed citations

14.

Wildhardt, G., et al.. (1996). Two different PAX3 gene mutations causing Waardenburg syndrome type I. Molecular and Cellular Probes. 10(3). 229–231. 9 indexed citations

15.

Schneider, Susanne A., G. Wildhardt, R. Ludwig, & Brigitte Royer‐Pokora. (1993). Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations. Human Genetics. 91(6). 599–604. 39 indexed citations

16.

Brenner, Bernhard, G. Wildhardt, Susanne A. Schneider, & Brigitte Royer‐Pokora. (1992). RNA polymerase chain reaction detects different levels of four alternatively spliced WT1 transcripts in Wilms' tumors.. PubMed. 7(7). 1431–3. 30 indexed citations

17.

Wirsel, Stefan G. R., et al.. (1989). Three α‐amylase genes of Aspergillus oryzae exhibit identical intron‐exon organization. Molecular Microbiology. 3(1). 3–14. 56 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.

Explore authors with similar magnitude of impact