W Kühl

3.1k total citations
65 papers, 2.5k citations indexed

About

W Kühl is a scholar working on Physiology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, W Kühl has authored 65 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Physiology, 31 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in W Kühl's work include Lysosomal Storage Disorders Research (29 papers), Neonatal Health and Biochemistry (17 papers) and Glycosylation and Glycoproteins Research (15 papers). W Kühl is often cited by papers focused on Lysosomal Storage Disorders Research (29 papers), Neonatal Health and Biochemistry (17 papers) and Glycosylation and Glycoproteins Research (15 papers). W Kühl collaborates with scholars based in United States, Spain and Israel. W Kühl's co-authors include Ernest Beutler, Terri Gelbart, Carol West, Joseph A. Sorge, JT Prchal, Linda Forman, George L. Dale, Beryl Westwood, Ari Zimran and Ari Zimran and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

W Kühl

65 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
W Kühl United States 31 1.4k 957 717 527 480 65 2.5k
Carol West United States 33 2.0k 1.4× 1.4k 1.5× 361 0.5× 526 1.0× 961 2.0× 76 4.4k
G. W. Löhr Germany 20 622 0.4× 631 0.7× 464 0.6× 58 0.1× 244 0.5× 68 2.2k
J. G. M. Huijmans Netherlands 26 555 0.4× 867 0.9× 257 0.4× 132 0.3× 207 0.4× 72 2.1k
J C Dreyfus France 24 368 0.3× 674 0.7× 304 0.4× 89 0.2× 212 0.4× 80 1.6k
A L Miller United States 23 566 0.4× 614 0.6× 107 0.1× 242 0.5× 454 0.9× 70 1.7k
Kimiyo Raymond United States 27 553 0.4× 946 1.0× 280 0.4× 202 0.4× 164 0.3× 71 1.9k
Daniel Leclerc Canada 30 343 0.2× 1.5k 1.6× 530 0.7× 127 0.2× 320 0.7× 65 3.2k
L. Michael Snyder United States 23 923 0.6× 495 0.5× 307 0.4× 24 0.0× 238 0.5× 65 1.8k
Claude F. Reed United States 14 836 0.6× 622 0.6× 227 0.3× 27 0.1× 262 0.5× 18 1.6k
Yoshiro Wada Japan 25 171 0.1× 1.0k 1.1× 288 0.4× 67 0.1× 112 0.2× 109 2.0k

Countries citing papers authored by W Kühl

Since Specialization
Citations

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

Fields of papers citing papers by W Kühl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W Kühl

This figure shows the co-authorship network connecting the top 25 collaborators of W Kühl. A scholar is included among the top collaborators of W Kühl 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 Kühl. W Kühl 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.
Zimran, Ari, et al.. (1995). Prenatal molecular diagnosis of gaucher disease. Prenatal Diagnosis. 15(12). 1185–1188. 14 indexed citations
2.
Lee, Pauline, et al.. (1994). Homology between a Human Protein and a Protein of the Green Garden Pea. Genomics. 21(2). 371–378. 44 indexed citations
3.
Beutler, Ernest, et al.. (1992). Prenatal Diagnosis of Glucose-6-Phosphate-Dehydrogenase Deficiency. Acta Haematologica. 87(1-2). 103–104. 12 indexed citations
4.
Beutler, Ernest, Beryl Westwood, W Kühl, & Y. Edward Hsia. (1992). Glucose-6-Phosphate Dehydrogenase Variants in Hawaii. Human Heredity. 42(5). 327–329. 26 indexed citations
5.
Beutler, Elliot K., Terri Gelbart, W Kühl, Ari Zimran, & Carol West. (1992). Mutations in Jewish patients with Gaucher disease. Blood. 79(7). 1662–1666. 100 indexed citations
6.
Beutler, Ernest, et al.. (1991). Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica. Human Genetics. 87(4). 462–4. 50 indexed citations
7.
Beutler, Ernest, Beryl Westwood, & W Kühl. (1991). Definition of the Mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD ‘Lejeune’. Acta Haematologica. 86(4). 179–182. 47 indexed citations
8.
Beutler, Ernest, Terri Gelbart, W Kühl, Joseph A. Sorge, & Carol West. (1991). Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state.. Proceedings of the National Academy of Sciences. 88(23). 10544–10547. 121 indexed citations
9.
Beutler, Ernest, W Kühl, Eva María Aguaded Ramírez, & R Lisker. (1991). Some Mexican glucose-6-phosphate dehydrogenase variants revisited. Human Genetics. 86(4). 371–4. 23 indexed citations
10.
Beutler, Ernest, Terri Gelbart, & W Kühl. (1990). Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X chromosome-encoded cDNA. Cell. 62(1). 7–9. 9 indexed citations
11.
12.
Corrons, Joan‐Lluís Vives, et al.. (1990). Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A.. PubMed. 47(3). 575–9. 46 indexed citations
13.
Beutler, Ernest & W Kühl. (1988). Volume control of erythrocytes during storage. Transfusion. 28(4). 353–357. 30 indexed citations
14.
Sorge, Joseph A., W Kühl, Carol West, & Ernest Beutler. (1987). Complete correction of the enzymatic defect of type I Gaucher disease fibroblasts by retroviral-mediated gene transfer.. Proceedings of the National Academy of Sciences. 84(4). 906–909. 62 indexed citations
15.
Beutler, Ernest, W Kühl, & Terri Gelbart. (1985). 6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.. Proceedings of the National Academy of Sciences. 82(11). 3876–3878. 18 indexed citations
16.
Beutler, Ernest, et al.. (1983). Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.. Journal of Clinical Investigation. 72(2). 648–655. 31 indexed citations
17.
Beutler, Ernest, GL Dale, & W Kühl. (1980). Repacement therapy in Gaucher disease.. PubMed. 16(1). 369–81. 2 indexed citations
18.
Beutler, Ernest, W Kühl, Flávia E. Matsumoto, & Gerassimos A. Pangalis. (1976). Acid hydrolases in leukocytes and platelets of normal subjects and in patients with Gaucher's and Fabry's disease.. The Journal of Experimental Medicine. 143(4). 975–980. 75 indexed citations
19.
Beutler, Ernst, Enriqueta R. Guinto, & W Kühl. (1975). Placental acid hydrolase purification on concanavalin A-sepharose.. PubMed. 85(4). 672–7. 16 indexed citations
20.
Beutler, Ernest & W Kühl. (1970). The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of beta-glucosidase activity in peripheral blood leukocytes.. PubMed. 76(5). 747–55. 128 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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