E Plöchl

697 total citations
34 papers, 325 citations indexed

About

E Plöchl is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, E Plöchl has authored 34 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 12 papers in Genetics. Recurrent topics in E Plöchl's work include Metabolism and Genetic Disorders (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Amino Acid Enzymes and Metabolism (6 papers). E Plöchl is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Amino Acid Enzymes and Metabolism (6 papers). E Plöchl collaborates with scholars based in Austria, Switzerland and United States. E Plöchl's co-authors include Peter Blümel, Klaus Schmitt, H Frisch, G. Haeusler, Thomas Waldhör, A. Behmel, W Rosenkranz, Olaf Rittinger, M. Schemper and Georg F. Hoffmann and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Clinical Chemistry.

In The Last Decade

E Plöchl

32 papers receiving 307 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E Plöchl Austria 11 205 159 110 60 51 34 325
Junko Muroi Japan 12 228 1.1× 172 1.1× 168 1.5× 79 1.3× 58 1.1× 19 439
W Zaleski Canada 12 206 1.0× 182 1.1× 105 1.0× 84 1.4× 8 0.2× 29 449
Jean‐Paul Harpey France 7 137 0.7× 63 0.4× 104 0.9× 37 0.6× 19 0.4× 7 253
James R. Bonham United Kingdom 9 171 0.8× 42 0.3× 180 1.6× 36 0.6× 25 0.5× 20 302
Jaina Patel Canada 8 118 0.6× 193 1.2× 125 1.1× 37 0.6× 16 0.3× 17 389
Dimitar N. Azmanov Australia 12 191 0.9× 122 0.8× 26 0.2× 53 0.9× 10 0.2× 23 336
Daniela Buti Italy 6 112 0.5× 179 1.1× 78 0.7× 136 2.3× 8 0.2× 8 428
Sandra Sabbagh Lebanon 11 118 0.6× 68 0.4× 84 0.8× 153 2.5× 19 0.4× 30 369
Radha Rama Devi Akella India 8 84 0.4× 97 0.6× 56 0.5× 32 0.5× 15 0.3× 14 252
J E Toublanc France 10 174 0.8× 106 0.7× 20 0.2× 107 1.8× 212 4.2× 27 378

Countries citing papers authored by E Plöchl

Since Specialization
Citations

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

Fields of papers citing papers by E Plöchl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E Plöchl

This figure shows the co-authorship network connecting the top 25 collaborators of E Plöchl. A scholar is included among the top collaborators of E Plöchl 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 E Plöchl. E Plöchl 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.
Plöchl, Walter, E Plöchl, H. Pokorny, et al.. (2001). Multiorgan donation from a donor with unrecognized ornithine transcarbamylase deficiency. Transplant International. 14(3). 196–201. 11 indexed citations
2.
Plöchl, E, Walter Plöchl, Bendicht Wermuth, & A. Roscher. (2001). Varianten angeborener Stoffwechselstörungen mit spätem Beginn, aber bedrohlichem Verlauf. Klinische Pädiatrie. 213(5). 261–265. 1 indexed citations
3.
Plöchl, E, et al.. (1999). Clinical, Cytogenetic and Molecular Analysis of Three 46,XX Males. Journal of Pediatric Endocrinology and Metabolism. 12(3). 389–95. 4 indexed citations
4.
Forstner, Rosemarie, et al.. (1999). Glutaric aciduria type I: ultrasonographic demonstration of early signs. Pediatric Radiology. 29(2). 138–143. 41 indexed citations
5.
Plöchl, E, Olaf Rittinger, Klaus Schmitt, et al.. (1999). Screening of patients with Turner Syndrome for "hidden" Y-mosaicism. Klinische Pädiatrie. 211(1). 30–34. 13 indexed citations
6.
Mitchell, Grant A., Pinar T. Ozand, Marie‐France Robert, et al.. (1998). HMG CoA Lyase Deficiency: Identification of Five Causal Point Mutations in Codons 41 and 42, Including a Frequent Saudi Arabian Mutation, R41Q. The American Journal of Human Genetics. 62(2). 295–300. 32 indexed citations
7.
Plöchl, E, et al.. (1997). A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism. Klinische Pädiatrie. 209(3). 133–136. 15 indexed citations
8.
9.
Plöchl, E, et al.. (1996). Carnitinmangel und Carnitintherapie bei einer Patientin mit Rett-Syndrom. Klinische Pädiatrie. 208(3). 129–134. 8 indexed citations
10.
11.
12.
Plöchl, E, et al.. (1992). Retrospektive Studie bei 160 Kindern mit Fieberkrämpfen. Klinische Pädiatrie. 204(1). 16–20. 5 indexed citations
13.
Haeusler, G., M. Schemper, H Frisch, et al.. (1992). Spontaneous growth in turner syndrome: Evidence for a minor pubertal growth spurt. European Journal of Pediatrics. 151(4). 283–287. 26 indexed citations
14.
Schmidtke, Klaus, W. Endres, A. Roscher, et al.. (1992). Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. European Journal of Pediatrics. 151(12). 899–903. 8 indexed citations
15.
Plöchl, E, J. P. Colombo, Bendicht Wermuth, & K. Michael Gibson. (1992). Increased plasma amylase in the family of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency. Clinical Chemistry. 38(2). 307–309. 2 indexed citations
16.
Plöchl, E, Cornelius G. Bachmann, Joseph Colombo, & K Gibson. (1990). 3-Hydroxy-3-Methyl-Glutaraturie - Klinik, Verlauf und Therapie bei einem Kleinkind. Klinische Pädiatrie. 202(2). 76–80. 3 indexed citations
17.
Christensen, Erik, et al.. (1990). Ultraschall, Computertomographie und Magnetresonanztomographie bei einem Kind mit Makrozephalie und Glutarazidurie Typ I. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 153(12). 683–687. 1 indexed citations
18.
Behmel, A., E Plöchl, & W Rosenkranz. (1988). A new X‐linked dysplasia gigantism syndrome: Follow up in the first family and report on a second Austrian family. American Journal of Medical Genetics. 30(1-2). 275–285. 34 indexed citations
19.
Plöchl, E, Olaf Rittinger, Christian Bachmann, et al.. (1986). Die kraniale Computertomographie bei der Ahornsiruperkrankung. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 144(4). 413–417. 2 indexed citations
20.
Plöchl, E & H. H. Klein. (1974). [Neuroblastoma of both adrenal glands in a newborn infant].. PubMed. 92(7). 259–62. 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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