W Isler

657 total citations
34 papers, 511 citations indexed

About

W Isler is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Neurology. According to data from OpenAlex, W Isler has authored 34 papers receiving a total of 511 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 7 papers in Molecular Biology and 6 papers in Neurology. Recurrent topics in W Isler's work include Neonatal and fetal brain pathology (5 papers), RNA regulation and disease (5 papers) and Metabolism and Genetic Disorders (4 papers). W Isler is often cited by papers focused on Neonatal and fetal brain pathology (5 papers), RNA regulation and disease (5 papers) and Metabolism and Genetic Disorders (4 papers). W Isler collaborates with scholars based in Switzerland and Ireland. W Isler's co-authors include Eugen Boltshauser, Neil F. Gordon, H Spiess, Edmund H. Burrows, Albert Bischoff, G. Dumermuth, J. Ulrich, R Hess, U. Redweik and W. Leimbacher and has published in prestigious journals such as The Lancet, Journal of Chromatography A and Journal of the Neurological Sciences.

In The Last Decade

W Isler

34 papers receiving 480 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
W Isler Switzerland	12	169	156	150	104	77	34	511
G. Gobbi Italy	14	191 1.1×	141 0.9×	86 0.6×	115 1.1×	403 5.2×	41	722
Rosario Berardi Italy	14	108 0.6×	146 0.9×	189 1.3×	36 0.3×	84 1.1×	29	422
N Pinsard France	15	302 1.8×	234 1.5×	84 0.6×	164 1.6×	476 6.2×	52	951
Patricia L. Hartlage United States	12	54 0.3×	161 1.0×	38 0.3×	63 0.6×	42 0.5×	24	451
N Heldt France	10	54 0.3×	145 0.9×	34 0.2×	126 1.2×	56 0.7×	27	488
G.C.Y. Fong China	10	56 0.3×	150 1.0×	142 0.9×	124 1.2×	129 1.7×	17	508
Ian J. Hopkins Australia	13	163 1.0×	109 0.7×	44 0.3×	58 0.6×	247 3.2×	18	472
Yoshihisa Higuchi Japan	14	163 1.0×	221 1.4×	42 0.3×	86 0.8×	66 0.9×	31	518
G.K. van Wijngaarden Netherlands	17	33 0.2×	563 3.6×	63 0.4×	149 1.4×	54 0.7×	24	959
Stanley D. Johnsen United States	13	217 1.3×	510 3.3×	36 0.2×	87 0.8×	45 0.6×	29	895

Countries citing papers authored by W Isler

Since Specialization

Citations

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

Fields of papers citing papers by W Isler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W Isler

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

20 of 20 papers shown

Gordon, Neil F. & W Isler. (1989). Childhood Moyamoya Disease. Developmental Medicine & Child Neurology. 31(1). 103–107. 40 indexed citations

Boltshauser, Eugen, Wilfried Lang, Robert C. Janzer, et al.. (1987). Computed Tomography in Hallervorden-Spatz Disease¹. Neuropediatrics. 18(2). 81–83. 12 indexed citations

Isler, W. (1984). Stroke in Childhood and Adolescence. European Neurology. 23(6). 421–424. 39 indexed citations

Keller, Heidi, Eugen Boltshauser, H. Imhof, A. Valavanis, & W Isler. (1982). Cerebrovascular Doppler-Ultrasound Examination in Children: Principle, Indication and Findings. Neuropediatrics. 13(3). 142–151. 2 indexed citations

Boltshauser, Eugen, et al.. (1981). Permanent flaccid paraplegia in children with thoracic spinal cord injury. Spinal Cord. 19(4). 227–234. 8 indexed citations

Boltshauser, Eugen, et al.. (1980). Intracranial haemorrhage in the term infant confirmed by computed tomography.. PubMed. 35(6). 531–44. 9 indexed citations

Boltshauser, Eugen, et al.. (1980). Hemiparesis - An Uncommon Symptom of Hydrocephalus or Shunt Dysfunction¹. European Journal of Pediatric Surgery. 30(7). 191–197. 1 indexed citations

Huber, A., W Isler, & H. W. Spieß. (1979). [Computertomography for diagnosis of optic nerve and chiasmal gliomas (author's transl)].. PubMed. 174(6). 833–42. 1 indexed citations

Boltshauser, Eugen, Albert Bischoff, & W Isler. (1977). Giant axonal neuropathy. Journal of the Neurological Sciences. 31(2). 269–278. 33 indexed citations

10.

Meier, C., et al.. (1976). Dynamic aspects of peripheral nerve changes in progressive neural muscular atrophy. Journal of Neurology. 211(2). 111–124. 7 indexed citations

11.

Boltshauser, Eugen & W Isler. (1976). Computerised Axial Tomography in Spongy Degeneration. The Lancet. 307(7969). 1123–1123. 9 indexed citations

12.

Curtius, H.‐Ch., et al.. (1975). Mass fragmentography of 5-hydroxytryptophol and 5-methoxytryptophol in human cerebrospinal fluid. Journal of Chromatography A. 112. 523–531. 21 indexed citations

13.

Rampini, Silvana K., et al.. (1970). [Combination of metachromatic leucodystrophy and mucopolysaccharidosis: a disease entity (mucosulfatidosis)].. PubMed. 25(5). 436–61. 6 indexed citations

14.

Isler, W. (1969). Akute Hemiplegien und Hemisyndrome im Kindesalter : unter besonderer Berücksichtigung des klinischen Bildes, der neuroradiologischen und EEG-Befunde und des Verlaufes. Biblioteca Digital (Real Academia Nacional de Medicina). 2 indexed citations

15.

Isler, W. (1966). [The neurological and neuroradiological diagnosis of cerebral tumors in children].. PubMed. 9(4). 229–36. 1 indexed citations

16.

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

17.

Isler, W, A. Bischoff, & E Esslen. (1963). [METACHROMATIC LEUKODYSTROPHY. DIAGNOSIS BY MEANS OF BIOPSY AND DEMONSTRATION OF A STRONG REDUCTION OF NERVE CONDUCTION VELOCITY IN A CASE IN EARLY INFANTILE FORM].. PubMed. 18. 107–19. 2 indexed citations

18.

Hess, R & W Isler. (1958). [Development of epileptic manifestations associated with the disease in children].. PubMed. 99(1). 138–43. 1 indexed citations

19.

Isler, W, et al.. (1957). [Complementary researches on subacute sclerosing leukoencephalitis. I. Anatomoclinical report on 3 new cases].. PubMed. 79(1). 73–112. 6 indexed citations

20.

Fanconi, G & W Isler. (1954). [Hereditary diseases in children].. PubMed. 43(42). 890–2. 3 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