E. Bühler

996 total citations
34 papers, 722 citations indexed

About

E. Bühler is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, E. Bühler has authored 34 papers receiving a total of 722 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in E. Bühler's work include Genomic variations and chromosomal abnormalities (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Chromosomal and Genetic Variations (6 papers). E. Bühler is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Chromosomal and Genetic Variations (6 papers). E. Bühler collaborates with scholars based in Switzerland, Germany and Italy. E. Bühler's co-authors include U. Bühler, G. R. Stalder, G. Winkler, Katharina Schlegel, M. Fraccaro, Dirk W. Lachenmeier, Orsetta Zuffardi, G. Stalder, Pierre Ferrier and David C. Klein and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

E. Bühler

34 papers receiving 620 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. Bühler Switzerland	17	414	201	166	113	71	34	722
M. A. C. Ridler United States	17	328 0.8×	183 0.9×	153 0.9×	100 0.9×	40 0.6×	36	572
J Lejeune France	14	328 0.8×	202 1.0×	163 1.0×	99 0.9×	9 0.1×	50	576
Susan H. Black United States	20	505 1.2×	275 1.4×	632 3.8×	47 0.4×	69 1.0×	41	1.2k
J Lafourcade France	16	476 1.1×	216 1.1×	188 1.1×	174 1.5×	27 0.4×	57	698
Helene Stroh United States	14	170 0.4×	244 1.2×	251 1.5×	24 0.2×	40 0.6×	20	671
Gabriel S. Khodr United States	17	330 0.8×	173 0.9×	383 2.3×	44 0.4×	14 0.2×	29	1.1k
Jean‐Pierre Frijns Belgium	17	328 0.8×	300 1.5×	138 0.8×	34 0.3×	17 0.2×	23	670
Helen S. Baillie United Kingdom	10	129 0.3×	385 1.9×	60 0.4×	17 0.2×	18 0.3×	12	801
Dolores Saavedra Mexico	10	163 0.4×	123 0.6×	45 0.3×	6 0.1×	39 0.5×	17	435
Francisco I. Reyes Canada	15	217 0.5×	314 1.6×	206 1.2×	8 0.1×	16 0.2×	30	1.2k

Countries citing papers authored by E. Bühler

Since Specialization

Citations

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

Fields of papers citing papers by E. Bühler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Bühler

This figure shows the co-authorship network connecting the top 25 collaborators of E. Bühler. A scholar is included among the top collaborators of E. Bühler 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. Bühler. E. Bühler 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

Bühler, E., et al.. (2006). Ethical and Legal Aspects of Enteral Nutrition. Clinical Nutrition. 25(2). 196–202. 42 indexed citations

Bühler, E., et al.. (2004). Leitlinie Enterale Ernährung der DGEM und DGG:Ethische und rechtliche Gesichtpunkte. Aktuelle Ernährungsmedizin. 29(4). 226–230. 4 indexed citations

Rutishauser, Markus, et al.. (1995). Lung hypoplasia and severe pulmonary hypertension in an infant with double heterozygosity for spondyloepiphyseal dysplasia congenita and achondroplasia. Clinical Genetics. 48(1). 35–40. 9 indexed citations

Alkan, M., et al.. (1992). Arrangement of DYZ1 and DYZ2 repeats on the human Y-chromosome: a case with presence of DYZ1 and absence of DYZ2. Molecular and Cellular Probes. 6(3). 257–259. 9 indexed citations

Tupler, Rossella, E. Bühler, M. Alkan, et al.. (1992). Paternal origin of the de novo deleted chromosome 4 in Wolf-Hirschhorn syndrome.. Journal of Medical Genetics. 29(1). 53–55. 26 indexed citations

Bode, Hans R., et al.. (1990). [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].. PubMed. 138(11). 763–6. 1 indexed citations

Birkhäuser, M., et al.. (1989). Fertilität und Turner-Mosaik-Syndrom. Geburtshilfe und Frauenheilkunde. 49(9). 825–829. 6 indexed citations

Alkan, M., Stephen Wood, U. V. Borer, Sandra L. Hofmann, & E. Bühler. (1989). Physical mapping of D8S7 and D8S11 to the band 8p23.1 of the short arm of chromosome 8. Nucleic Acids Research. 17(20). 8395–8395. 1 indexed citations

Bühler, E., et al.. (1983). Expression of H-Y antigen in the sex-change fishCoris julis. Cellular and Molecular Life Sciences. 39(7). 767–769. 11 indexed citations

10.

Fraccaro, M., A Mayerová, U. Wolf, et al.. (1982). Correlation between the number of sex chromosomes and the H-Y antigen titer. Human Genetics. 61(2). 135–140. 34 indexed citations

11.

Zuffardi, Orsetta, E. Bühler, & M. Fraccaro. (1978). Chromosome 15 and Prader‐Willi Syndrome. Clinical Genetics. 14(5). 315–316. 21 indexed citations

12.

Fraccaro, M., et al.. (1977). 15/15 translocation in Prader-Willi syndrome.. Journal of Medical Genetics. 14(4). 275–276. 42 indexed citations

13.

Bühler, E., et al.. (1975). 45,X/46,XYq dic-Geschlechtschromosomenmosaik. PubMed. 27(2). 81–90. 39 indexed citations

14.

Bühler, E., György Kosztolányi, & G. R. Stalder. (1975). POSSIBLE MOSAIC XXX-XXY MARRIAGE WITH ABNORMAL OFFSPRING. The Lancet. 305(7902). 334–334. 2 indexed citations

15.

Müller, Hansjakob, et al.. (1972). Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.. Journal of Medical Genetics. 9(4). 462–467. 26 indexed citations

16.

Stalder, G. R., E. Bühler, & U. Bühler. (1965). Possible role of heterochromatin in human aneuploidy. Human Genetics. 1(3). 307–310. 10 indexed citations

17.

Ferrier, Pierre, et al.. (1964). CONGENITAL ASYMMETRY ASSOCIATED WITH DIPLOID-TRIPLOID MOSAICISM AND LARGE SATELLITES. The Lancet. 283(7324). 80–82. 92 indexed citations

18.

Bühler, E., U. Bühler, & G. R. Stalder. (1964). PARTIAL MONOSOMY 18 AND ANOMALY OF THYROXINE SYNTHESIS. The Lancet. 283(7325). 170–171. 26 indexed citations

19.

Bühler, E., et al.. (1963). Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism. Acta Paediatrica. 52(2). 177–182. 28 indexed citations

20.

Bühler, E. & R. Witmer. (1959). Immun-Elektrophorese kataraktöser Linsen. Ophthalmologica. 137(3). 188–193. 6 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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