Jürgen Herrmann

1.4k total citations
30 papers, 984 citations indexed

About

Jürgen Herrmann is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jürgen Herrmann has authored 30 papers receiving a total of 984 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Jürgen Herrmann's work include Nail Diseases and Treatments (5 papers), Plant Pathogens and Fungal Diseases (5 papers) and Connective tissue disorders research (4 papers). Jürgen Herrmann is often cited by papers focused on Nail Diseases and Treatments (5 papers), Plant Pathogens and Fungal Diseases (5 papers) and Connective tissue disorders research (4 papers). Jürgen Herrmann collaborates with scholars based in United States, Germany and Switzerland. Jürgen Herrmann's co-authors include John M. Opitz, Pietro Nenoff, Yvonne Gräser, JohnM. Opitz, Enid F. Gilbert, Marcel Erhard, Mark Lubinsky, James G. Coldwell, Giovanni Neri and John C. Carey and has published in prestigious journals such as The Lancet, The Journal of Pediatrics and Pediatric Research.

In The Last Decade

Jürgen Herrmann

29 papers receiving 911 citations

Peers

Jürgen Herrmann

GENET

EPIDE

PPCH

Michael J. Lyons United States

Gerald Α. Hegreberg United States

Fulvia Baldinotti Italy

Wilson H.Y. Lo China

Michael V. Zaragoza United States

Chiara Di Bella Italy

K. Fried Israel

I. T. Thomas United States

Petra Werner United States

E Haan Australia

Michael J. Lyons United States

Jürgen Herrmann

302 ×0.7

GENET

301 ×0.7

133 ×0.5

EPIDE

29 ×0.1

53 ×0.4

PPCH

Citations per year, relative to Jürgen Herrmann Jürgen Herrmann (= 1×) peers Michael J. Lyons

Countries citing papers authored by Jürgen Herrmann

Since Specialization

Citations

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

Fields of papers citing papers by Jürgen Herrmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jürgen Herrmann

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

All Works

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20 of 20 papers shown

Nenoff, Pietro, Silke Uhrlaß, Constanze Krüger, et al.. (2014). Trichophyton species of Arthroderma benhamiae – a new infectious agent in dermatology. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 12(7). 571–581. 65 indexed citations

Nenoff, Pietro, et al.. (2012). MALDI-TOF mass spectrometry – a rapid method for the identification of dermatophyte species. Medical Mycology. 51(1). 17–24. 110 indexed citations

Gerlach, Christina, et al.. (2010). Biochirurgisches Débridement mittels Lucilia sericata-Maden – ein Update. Wiener Medizinische Wochenschrift. 160(21-22). 578–585. 1 indexed citations

Nenoff, Pietro, Jürgen Herrmann, & Yvonne Gräser. (2007). Trichophyton mentagrophytes sive interdigitale? A dermatophyte in the course of time. JDDG Journal der Deutschen Dermatologischen Gesellschaft. 5(3). 198–202. 98 indexed citations

Opitz, John M., Jürgen Herrmann, Enid F. Gilbert, & Reuben Matalon. (1988). Simpson‐Golabi‐Behmel syndrome: Follow‐up of the michigan family. American Journal of Medical Genetics. 30(1-2). 301–308. 28 indexed citations

Garruto, Ralph M., Chris C. Plato, Ntinos C. Myrianthopoulos, et al.. (1983). Blood groups, immunoglobulin allotypes and dermatoglyphic features of patients with amyotrophic lateral sclerosis and parkinsonism‐dementia of guam. American Journal of Medical Genetics. 14(2). 289–298. 12 indexed citations

Freire‐Maia, N., Marta Pinheiro, John M. Opitz, & Jürgen Herrmann. (1982). The neurofaciodigitorenal (NFDR) syndrome. American Journal of Medical Genetics. 11(3). 329–336. 10 indexed citations

Herbst, Diana S., Patricia A. Baird, & Jürgen Herrmann. (1982). Sib risks for nonspecific mental retardation in British Columbia. American Journal of Medical Genetics. 13(2). 197–208. 15 indexed citations

Sommer, Annemarie, et al.. (1981). Neurofibromatosis in monozygotic twins: A case report of spontaneous mutation. American Journal of Medical Genetics. 8(2). 155–158. 14 indexed citations

10.

Puck, Mary & Jürgen Herrmann. (1981). Some considerations bearing on the doctrine of self‐fulfilling prophecy in sex chromosome aneuploidy. American Journal of Medical Genetics. 9(2). 129–137. 24 indexed citations

11.

Matsunaga, Ei, Jürgen Herrmann, & John M. Opitz. (1981). Retinoblastoma: Mutational mosaicism or host resistance?. American Journal of Medical Genetics. 8(4). 375–387. 10 indexed citations

12.

Herrmann, Jürgen & John M. Opitz. (1979). Syndrome delineation 1. Malformations and dysplasias. Postgraduate Medicine. 65(1). 207–214. 1 indexed citations

13.

Opitz, John M., et al.. (1979). Terminological, Diagnostic, Nosological, and Anatomical-Developmental Aspects of Developmental Defects in Man. PubMed. 9. 71–164. 44 indexed citations

14.

Herrmann, Jürgen & John M. Opitz. (1979). Syndrome delineation 2. Inborn errors of metabolism, deformities, and variant familial developmental patterns. Postgraduate Medicine. 65(2). 231–237. 1 indexed citations

15.

Herrmann, Jürgen & John M. Opitz. (1977). Genetic patient evaluation. Postgraduate Medicine. 62(5). 191–203. 1 indexed citations

16.

Herrmann, Jürgen, et al.. (1976). Studies of malformation syndromes of man XXIX: The Wiedemann-Beckwith syndrome. European Journal of Pediatrics. 123(3). 139–166. 48 indexed citations

17.

Gilbert, Enid F., et al.. (1974). Studies of malformation syndromes VID: The G syndrome. Further observations. PubMed. 118(2). 81–85. 16 indexed citations

18.

Lubinsky, Mark, et al.. (1974). AUTOSOMAL-DOMINANT SEX-DEPENDENT TRANSMISSION OF THE WIEDEMANN-BECKWITH SYNDROME. The Lancet. 303(7863). 932–932. 56 indexed citations

19.

Herrmann, Jürgen, et al.. (1974). THE STICKLER SYNDROME. Pediatric Research. 8(4). 440–440. 1 indexed citations

20.

Herrmann, Jürgen, et al.. (1972). THE WIEDEMANN-BECKWITH SYNDROME: GENETIC CONSIDERATIONS AND A DIAGNOSTIC SIGN. The Lancet. 299(7755). 844–844. 37 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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