I. Willers

727 total citations
25 papers, 497 citations indexed

About

I. Willers is a scholar working on Molecular Biology, Epidemiology and Infectious Diseases. According to data from OpenAlex, I. Willers has authored 25 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 8 papers in Epidemiology and 4 papers in Infectious Diseases. Recurrent topics in I. Willers's work include Biochemical and Molecular Research (13 papers), Cytomegalovirus and herpesvirus research (4 papers) and HIV/AIDS drug development and treatment (4 papers). I. Willers is often cited by papers focused on Biochemical and Molecular Research (13 papers), Cytomegalovirus and herpesvirus research (4 papers) and HIV/AIDS drug development and treatment (4 papers). I. Willers collaborates with scholars based in Germany, Poland and United States. I. Willers's co-authors include Andreas Gal, Catharina Whybra, Michael Beck, Joanna P. Davies, Bryan Winchester, Bengt Lindblad, Surjit Singh, C. Kampmann, Susanna Bunge and Jörg Kriegsmann and has published in prestigious journals such as Journal of the Neurological Sciences, Pediatric Research and Advances in experimental medicine and biology.

In The Last Decade

I. Willers

24 papers receiving 470 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I. Willers Germany 8 366 197 146 129 106 25 497
Petersen Ee Germany 4 389 1.1× 207 1.1× 134 0.9× 74 0.6× 95 0.9× 10 452
C. Robinson United States 8 454 1.2× 208 1.1× 170 1.2× 77 0.6× 123 1.2× 12 534
Masahisa Kobayashi Japan 15 427 1.2× 212 1.1× 114 0.8× 113 0.9× 131 1.2× 38 564
H.C. Janse Netherlands 11 268 0.7× 96 0.5× 61 0.4× 127 1.0× 84 0.8× 17 404
Ya. V. Voznyi Russia 12 592 1.6× 248 1.3× 105 0.7× 206 1.6× 171 1.6× 19 685
Karen M. Ashe United States 8 308 0.8× 122 0.6× 50 0.3× 151 1.2× 122 1.2× 9 390
Josanne Cox‐Brinkman Netherlands 9 886 2.4× 375 1.9× 200 1.4× 242 1.9× 285 2.7× 11 991
W.P. de Groot Netherlands 15 217 0.6× 63 0.3× 84 0.6× 154 1.2× 143 1.3× 25 494
Matthew J. Elrick United States 12 322 0.9× 183 0.9× 35 0.2× 135 1.0× 82 0.8× 16 575
Sabrina Eichler Germany 10 251 0.7× 94 0.5× 30 0.2× 111 0.9× 87 0.8× 15 324

Countries citing papers authored by I. Willers

Since Specialization
Citations

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

Fields of papers citing papers by I. Willers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Willers

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

All Works

20 of 20 papers shown
1.
Willers, I.. (2004). Germline mosaicism complicates molecular diagnosis of Lesch–Nyhan syndrome. Prenatal Diagnosis. 24(9). 737–740. 4 indexed citations
2.
Ries, Markus, Uma Ramaswami, Rossella Parini, et al.. (2003). The early clinical phenotype of Fabry disease: a study on 35 European children and adolescents. European Journal of Pediatrics. 162(11). 767–772. 164 indexed citations
3.
Whybra, Catharina, C. Kampmann, I. Willers, et al.. (2001). Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes. Journal of Inherited Metabolic Disease. 24(7). 715–724. 209 indexed citations
4.
Willers, I., Hanno J. Bolz, Manfred Wehnert, & Andreas Gal. (1999). Eighteen novel mutations in patients with Lesch–Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiency. Journal of Inherited Metabolic Disease. 22(7). 845–846. 7 indexed citations
5.
Willers, I., et al.. (1993). Immunocytochemical studies on the vimentin distribution and cell proliferation of fibroblasts in patients with Friedreich's ataxia. Journal of the Neurological Sciences. 117(1-2). 159–163. 4 indexed citations
6.
Willers, I., et al.. (1991). Growth Studies on Fibroblasts of Patients with Autosomal Recessive Friedreich’s Ataxia. Pathobiology. 59(5). 357–360. 3 indexed citations
7.
Willers, I., et al.. (1990). Characterization of long-term cell cultures of human chorion villi and fibroblasts using antibodies to cytoskeletal proteins. Archives of Gynecology and Obstetrics. 248(2). 87–92. 2 indexed citations
8.
Singh, Surjit, et al.. (1989). Lesch-Nyhan Syndrome and HPRT Variants: Study of Heterogeneity at the Gene Level. Advances in experimental medicine and biology. 253A. 145–150. 1 indexed citations
9.
10.
11.
Willers, I., Surjit Singh, & H. W. Goedde. (1984). Studies in Fibroblasts of Patients with the Lesch-NyhanSyndrome and HPRT Variants. Enzyme. 32(4). 241–247. 4 indexed citations
12.
Klose, J., I. Willers, Surjit Singh, & H. W. Goedde. (1983). Two-dimensional electrophoresis of soluble and structure-bound proteins from cultured human fibroblasts and hair root cells: Qualitative and quantitative variation. Human Genetics. 63(3). 262–7. 19 indexed citations
13.
Willers, I., et al.. (1982). Purine Metabolism in Fibroblasts of Patients with Duchenne’s Muscular Dystrophy. Human Heredity. 32(4). 233–239. 3 indexed citations
14.
Singh, Surjit, I. Willers, H. W. Goedde, & J. Klose. (1981). Analysis of inborn errors of metabolism and other genetic defects in human fibroblasts using two‐dimensional polypeptide mapping. Journal of Inherited Metabolic Disease. 4(1). 97–98. 1 indexed citations
15.
Singh, Surjit, I. Willers, J. Klose, & H. W. Goedde. (1981). High-resolution protein mapping of human fibroblasts and hair root cells: A standardized reproducible procedure considering the effect of cell culture parameters. Biochemical Genetics. 19(9-10). 871–880. 8 indexed citations
16.
Willers, I., Surjit Singh, K. R. Held, & H. W. Goedde. (1980). High HPRT Activity in Fibroblasts from Patients with Lesch-Nyhan Syndrome Due to Bacterial “L-Form” Contamination. Advances in experimental medicine and biology. 122A. 327–331. 2 indexed citations
17.
Willers, I., K. R. Held, Surjit Singh, & H. W. Goedde. (1977). Genetic heterogeneity of hypoxanthine‐phosphoribosyl transferase in human fibroblasts of 3 families*. Clinical Genetics. 11(2). 193–200. 3 indexed citations
18.
Singh, Surjit, I. Willers, & H. W. Goedde. (1976). A rapid micromethod for prenatal diagnosis of Lesch Nyhan syndrome*. Clinical Genetics. 10(1). 12–15. 6 indexed citations
19.
Singh, Surjit, I. Willers, W. Schloot, & H. W. Goedde. (1975). A rapid micro culture method of chromosome preparations from fibroblasts and amniotic cells*. Clinical Genetics. 8(1). 18–19. 1 indexed citations
20.
Willers, I., D. P. Agarwal, Surjit Singh, W. Schloot, & H. W. Goedde. (1975). Rapid determination of hypoxanthine-guanine-phosphoribosyl transferase in human fibroblasts and amniotic cells. PubMed. 27(4). 323–328. 10 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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