A Prader

1.9k total citations
77 papers, 1.3k citations indexed

About

A Prader is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, A Prader has authored 77 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 20 papers in Molecular Biology and 18 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in A Prader's work include Digestive system and related health (13 papers), Sexual Differentiation and Disorders (13 papers) and Vitamin D Research Studies (9 papers). A Prader is often cited by papers focused on Digestive system and related health (13 papers), Sexual Differentiation and Disorders (13 papers) and Vitamin D Research Studies (9 papers). A Prader collaborates with scholars based in Switzerland, United States and Germany. A Prader's co-authors include R Illig, R. H. Largo, M. Zachmann, Salvatore Auricchio, Arne Dahlqvist, A Fanconi, A Giedion, Giorgio Semenza, D.H. Shmerling and G Stalder and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Gastroenterology.

In The Last Decade

A Prader

68 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A Prader Switzerland 22 438 412 294 231 148 77 1.3k
Anne P. Forbes United States 15 400 0.9× 355 0.9× 404 1.4× 162 0.7× 137 0.9× 27 1.3k
Philip H. Henneman United States 21 186 0.4× 344 0.8× 436 1.5× 163 0.7× 55 0.4× 40 1.7k
Patricia M. Crofton United Kingdom 28 282 0.6× 470 1.1× 562 1.9× 296 1.3× 377 2.5× 65 1.9k
Maurice D. Kogut United States 21 245 0.6× 325 0.8× 431 1.5× 116 0.5× 117 0.8× 51 1.2k
George Schneider United States 17 215 0.5× 361 0.9× 605 2.1× 148 0.6× 433 2.9× 59 1.6k
Linda Crofts Australia 11 687 1.6× 850 2.1× 251 0.9× 119 0.5× 34 0.2× 14 2.3k
Avraham Golander Israel 18 249 0.6× 187 0.5× 434 1.5× 95 0.4× 225 1.5× 36 1.4k
Akifumi Tokita Japan 14 490 1.1× 564 1.4× 264 0.9× 200 0.9× 33 0.2× 37 2.2k
Henning K. Nielsen Denmark 18 168 0.4× 248 0.6× 442 1.5× 66 0.3× 29 0.2× 27 1.1k
JohnC. Stevenson United Kingdom 12 151 0.3× 191 0.5× 246 0.8× 106 0.5× 53 0.4× 19 861

Countries citing papers authored by A Prader

Since Specialization
Citations

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

Fields of papers citing papers by A Prader

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Prader

This figure shows the co-authorship network connecting the top 25 collaborators of A Prader. A scholar is included among the top collaborators of A Prader 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 A Prader. A Prader 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.
Froesch, E. R., et al.. (1995). [Scientific raisins from 125 years SMW (Swiss Medical Weekly). Diagnostic use of a new adrenostatic agents. 1959].. PubMed. 125(48). 2359–61.
2.
Giedion, A, et al.. (1993). Angel‐shaped phalango‐epiphyseal dysplasia (ASPED): Identification of a new genetic bone marker. American Journal of Medical Genetics. 47(5). 765–771. 12 indexed citations
3.
Willi, Ulrich, et al.. (1991). Testicular adrenal-like tissue (TALT) in congenital adrenal hyperplasia: Detection by ultrasonography. Pediatric Radiology. 21(4). 284–287. 44 indexed citations
4.
Boltshauser, Eugen, Cengiz Yalçınkaya, W. Wichmann, et al.. (1989). MRI in Cockayne syndrome type I. Neuroradiology. 31(3). 276–277. 27 indexed citations
5.
Steinmann, B, et al.. (1984). Neonatal severe primary hyperparathyroidism and alkaptonuria in a boy born to related parents with familial hypocalciuric hypercalcemia.. PubMed. 39(2). 171–86. 31 indexed citations
6.
Largo, R. H., et al.. (1984). Menstrual patterns in adolescent Swiss girls: a longitudinal study. Annals of Human Biology. 11(6). 495–508. 102 indexed citations
7.
Giedion, A, et al.. (1982). Oto-spondylo-megaepiphyseal dysplasia (OSMED).. PubMed. 37(4). 361–80. 32 indexed citations
8.
Cacciari, E & A Prader. (1980). Pathophysiology of puberty. Academic Press eBooks. 27 indexed citations
9.
Exner, G. Ulrich, A Prader, U. Elsasser, et al.. (1980). Hypophosphatemic vitamin D resistant rickets (phosphate diabetes): bone mineral problems studied by 125I-computed tomography and microradiography.. PubMed. 35(1). 39–49. 9 indexed citations
10.
Werder, E A, R Illig, Toni Torresani, et al.. (1976). Gonadal function in young adults after surgical treatment of cryptorchidism.. BMJ. 2(6048). 1357–1359. 40 indexed citations
11.
Werder, E A, G. Mürset, R Illig, & A Prader. (1975). HYPOGONADISM AND PARATHYROID ADENOMA IN CONGENITAL POIKILODERMA (ROTHMUND‐THOMSON SYNDROME). Clinical Endocrinology. 4(1). 75–82. 17 indexed citations
12.
Brook, C. G. D., H Wagner, M. Zachmann, et al.. (1973). Familial Occurrence of Persistent Müllerian Structures in Otherwise Normal Males. BMJ. 1(5856). 771–773. 91 indexed citations
13.
Fanconi, A & A Prader. (1969). [Hereditary pseudo-vitamin D deficiency rickets].. PubMed. 24(5). 423–47. 6 indexed citations
14.
Zoppi, G, et al.. (1968). Protein content and pancreatic enzyme activities of duodenal juice in normal children and in children with exocrine pancreatic insufficiency.. PubMed. 23(6). 577–90. 6 indexed citations
15.
Fanconi, A & A Prader. (1967). Transient congenital idiopathic hypoparathyroidism.. PubMed. 22(4). 342–59. 21 indexed citations
16.
Fanconi, A, et al.. (1964). [CLINICAL AND BIOCHEMICAL HYPOPARATHYROIDISM WITH RADIOLOGIC SIGNS OF HYPERPARATHYROIDISM].. PubMed. 19. 181–206.
17.
Fanconi, A, et al.. (1963). [ADDISON'S DISEASE WITH CEREBRAL SCLEROSIS IN CHILDHOOD. A HEREDITARY SYNDROME TRANSMITTED THROUGH CHROMOSOME X?].. PubMed. 18. 480–501. 16 indexed citations
18.
Prader, A, et al.. (1961). [Diarrhea due to hereditary deficiency of intestinal saccharase activity (saccharose intolerance)].. PubMed. 91. 465–8. 21 indexed citations
19.
Illig, R & A Prader. (1959). [Casuistic contributions to idiopathic hypercalcemia and vitamin D intoxication].. PubMed. 14. 618–46.
20.
Prader, A, R Illig, E. Uehlinger, & G Stalder. (1959). [Rickets following bone tumor].. PubMed. 14. 554–65. 91 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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