U. Burck

498 total citations
28 papers, 367 citations indexed

About

U. Burck is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, U. Burck has authored 28 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Physiology. Recurrent topics in U. Burck's work include Hedgehog Signaling Pathway Studies (5 papers), Lysosomal Storage Disorders Research (4 papers) and Genetic and rare skin diseases. (3 papers). U. Burck is often cited by papers focused on Hedgehog Signaling Pathway Studies (5 papers), Lysosomal Storage Disorders Research (4 papers) and Genetic and rare skin diseases. (3 papers). U. Burck collaborates with scholars based in Germany, Poland and Switzerland. U. Burck's co-authors include Hans H. Goebel, H Kuhlendahl, K. M. Goebel, Karsten R. Held, Alfried Kohlschütter, Kenji Ikeda, K. R. Held, John M. Opitz, J. Siebert and H. Moore Arnold and has published in prestigious journals such as Neurology, Acta Neuropathologica and Human Genetics.

In The Last Decade

U. Burck

27 papers receiving 348 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
U. Burck Germany	11	181	129	59	56	52	28	367
Yasuyuki Fukuhara Japan	9	115 0.6×	66 0.5×	119 2.0×	19 0.3×	14 0.3×	18	351
Julien Marcadier Canada	11	210 1.2×	119 0.9×	15 0.3×	10 0.2×	66 1.3×	15	417
Takanori Tachibe Japan	8	169 0.9×	79 0.6×	22 0.4×	19 0.3×	16 0.3×	11	335
Gösta Holmgren Sweden	9	186 1.0×	50 0.4×	25 0.4×	7 0.1×	26 0.5×	17	272
S. Kumar United States	7	208 1.1×	116 0.9×	17 0.3×	9 0.2×	10 0.2×	14	306
E. Keck Germany	12	153 0.8×	81 0.6×	39 0.7×	2 0.0×	22 0.4×	46	477
Shiro Okuno Japan	14	300 1.7×	141 1.1×	105 1.8×	2 0.0×	40 0.8×	22	551
S. Murano Japan	8	194 1.1×	27 0.2×	150 2.5×	11 0.2×	13 0.3×	15	333
Jean‐Paul Leroy France	9	323 1.8×	49 0.4×	38 0.6×	4 0.1×	77 1.5×	10	454
Elke Botzenhart Germany	7	175 1.0×	50 0.4×	26 0.4×	4 0.1×	10 0.2×	8	331

Countries citing papers authored by U. Burck

Since Specialization

Citations

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

Fields of papers citing papers by U. Burck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of U. Burck

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

Miller, Konstantin, et al.. (1997). Mosaicism in trisomy 8: phenotype differences according to tissular repartition of normal and trisomic clones.. PubMed. 40(3). 181–4. 14 indexed citations

Burck, U., H. Moore Arnold, & J. Siebert. (1984). Unilateral Skin Lesions Associated with Multiple Neoplasms. Dermatology. 168(2). 78–81. 15 indexed citations

Goebel, Hans H., et al.. (1984). “Killer” cells in Duchenne disease. Neurology. 34(3). 295–295. 7 indexed citations

Burck, U.. (1983). Genetic aspects of hemifacial microsomia. Human Genetics. 64(3). 291–296. 42 indexed citations

Burck, U.. (1982). Mesomelic dysplasia with punctate epiphyseal calcifications?a new entity of chondrodysplasia punctata?. European Journal of Pediatrics. 138(1). 67–72. 17 indexed citations

Ikeda, Kenji, Hans H. Goebel, U. Burck, & Alfried Kohlschütter. (1982). Ultrastructural pathology of human lymphocytes in lysosomal disorders: a contribution to their morphological diagnosis. European Journal of Pediatrics. 138(2). 179–185. 24 indexed citations

Goebel, Hans H., et al.. (1982). Fetal congenital lethal hypophosphatasia: Histochemical absence of alkaline phosphatase activity in endothelial cells of intramuscular capillaries. Acta Neuropathologica. 57(2-3). 236–238. 3 indexed citations

Burck, U., et al.. (1982). Optikusatrophie, Typ-I-Diabetes mellitus und Schallempfindungsstörung. Ein familiäres Syndrom. Klinische Monatsblätter für Augenheilkunde. 180(6). 559–562. 1 indexed citations

Burck, U. & Karsten R. Held. (1982). Unilateral Skin Lesions, Cataracts, Optic Glioma and Retardation – a Variant of the Epidermal Nevus Syndrome?. Dermatology. 165(3). 208–214. 10 indexed citations

10.

Burck, U., et al.. (1982). Clinical, radiological, morphological and biochemical data on fetal congenital lethal hypophosphatasia.. PubMed. 104. 149–54. 3 indexed citations

11.

Burck, U., et al.. (1981). NEUROMYOPATHY AND VITAMIN E DEFICIENCY in MAN¹. Neuropediatrics. 12(3). 267–278. 110 indexed citations

12.

Burck, U., et al.. (1981). Congenital malformation syndromes and elevation of amniotic fluid α₁‐fetoprotein. Teratology. 24(2). 125–130. 2 indexed citations

13.

Held, K. R., et al.. (1981). Pränatale Geschlechts bestimmung durch den GBN-Speicheltest. Ein Vergleich mit den Ergebnissen der pränatalen Chromo somendiagnostik. Geburtshilfe und Frauenheilkunde. 41(9). 619–621. 2 indexed citations

14.

Burck, U., et al.. (1981). Holoprosencephaly in monozygotic twins – clinical and computer tomographic findings. American Journal of Medical Genetics. 9(1). 13–17. 15 indexed citations

15.

Ikeda, Kenji, U. Burck, & Hans H. Goebel. (1981). Ultrastructure of lymphocytes and skin in mucopolysaccharidosis IV A (Morquio Syndrome). Brain and Development. 3(3). 329–331. 2 indexed citations

16.

Goebel, Hans H., Kenji Ikeda, Frederik Schulz, U. Burck, & Alfried Kohlschütter. (1981). Fingerprint profiles in lymphocytic vacuoles of mucopolysaccharidoses I-H, II, III-A, and III-B. Acta Neuropathologica. 55(3). 247–249. 13 indexed citations

17.

Burck, U.. (1981). Neuromyopathy and vitamin E deficiency. Medical Entomology and Zoology. 12. 267–278. 1 indexed citations

18.

Burck, U., et al.. (1981). Bilateral femoral dysgenesis with micrognathia, cleft palate, anomalies of the spine and pelvis, and foot deformities. Clinical and radiological findings.. PubMed. 36(5). 473–82. 4 indexed citations

19.

Burck, U. & I Lagenstein. (1980). CAT scan findings in clinically healthy relatives of tuberous sclerosis patients. European Journal of Pediatrics. 135(1). 117–118. 2 indexed citations

20.

Burck, U.. (1974). [De Barsy syndrome, a further case (author's transl)].. PubMed. 186(5). 441–4. 8 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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