B. Hellkuhl

428 total citations
15 papers, 356 citations indexed

About

B. Hellkuhl is a scholar working on Molecular Biology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, B. Hellkuhl has authored 15 papers receiving a total of 356 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Nutrition and Dietetics. Recurrent topics in B. Hellkuhl's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Biochemical and Molecular Research (2 papers) and Lysosomal Storage Disorders Research (2 papers). B. Hellkuhl is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Biochemical and Molecular Research (2 papers) and Lysosomal Storage Disorders Research (2 papers). B. Hellkuhl collaborates with scholars based in Germany, Austria and Finland. B. Hellkuhl's co-authors include K.-H. Grzeschik, Karl‐Heinz Grzeschik, T. Mohandas, R S Sparkes, Larry J. Shapiro, Mark Worwood, B. M. Jones, J. David Brook, Susan Roberts and Duncan J. Shaw and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Pediatric Research and Human Genetics.

In The Last Decade

B. Hellkuhl

14 papers receiving 328 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. Hellkuhl Germany	8	216	191	64	50	49	15	356
Isabelle Gicquel France	13	312 1.4×	236 1.2×	62 1.0×	24 0.5×	37 0.8×	21	453
Caroline Stone United Kingdom	10	100 0.5×	35 0.2×	124 1.9×	29 0.6×	47 1.0×	14	301
Lionel Le Gallic France	11	249 1.2×	55 0.3×	10 0.2×	32 0.6×	48 1.0×	16	418
Yasunao Kamikawa Japan	10	452 2.1×	50 0.3×	37 0.6×	22 0.4×	14 0.3×	18	513
Anne Bergmann United States	10	394 1.8×	289 1.5×	12 0.2×	39 0.8×	8 0.2×	15	484
Andrea Harničarová Czechia	10	520 2.4×	65 0.3×	21 0.3×	59 1.2×	5 0.1×	11	601
de Grouchy J France	10	195 0.9×	221 1.2×	17 0.3×	101 2.0×	4 0.1×	37	353
Frank W. Schmitges Canada	7	601 2.8×	70 0.4×	10 0.2×	90 1.8×	15 0.3×	7	671
Junji Tsuchida Japan	12	282 1.3×	167 0.9×	4 0.1×	36 0.7×	25 0.5×	22	507
Isabel Peixeiro Portugal	4	423 2.0×	33 0.2×	14 0.2×	28 0.6×	7 0.1×	5	496

Countries citing papers authored by B. Hellkuhl

Since Specialization

Citations

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

Fields of papers citing papers by B. Hellkuhl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Hellkuhl

This figure shows the co-authorship network connecting the top 25 collaborators of B. Hellkuhl. A scholar is included among the top collaborators of B. Hellkuhl 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 B. Hellkuhl. B. Hellkuhl is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Oberlé, I., Giovanna Camerino, C. Kloepfer, et al.. (1986). Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Human Genetics. 72(1). 43–49. 67 indexed citations

Worwood, Mark, J. David Brook, S. J. Cragg, et al.. (1985). Assignment of human ferritin genes to chromosomes 11 and 19q13.3→19qter. Human Genetics. 69(4). 371–374. 90 indexed citations

Hellkuhl, B., et al.. (1983). Elimination of mycoplasma contamination from mammalian cell cultures by the bibenzimidazole derivative Hoechst 33258. Cytogenetic and Genome Research. 36(3). 584–585. 1 indexed citations

Hellkuhl, B., Albert de la Chapelle, & Karl‐Heinz Grzeschik. (1982). Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X; autosome translocation. Human Genetics. 60(2). 126–129. 27 indexed citations

Hellkuhl, B., et al.. (1981). Regional mapping of human chromosome 3. Assignment of a glutathione peroxidase-1 gene to 3p13→3q12. Human Genetics. 56(3). 361–363. 6 indexed citations

Mohandas, T., R S Sparkes, B. Hellkuhl, K.-H. Grzeschik, & Larry J. Shapiro. (1980). Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.. Proceedings of the National Academy of Sciences. 77(11). 6759–6763. 80 indexed citations

Stranzinger, G., et al.. (1980). X-chromosome gene assignment of swine and cattle. Die Naturwissenschaften. 67(1). 48–49. 16 indexed citations

Hellkuhl, B., et al.. (1980). A New Variant of Galactosemia: Galactose-1-phosphate Uridylytransferase Sensitive to Product Inhibition by Glucose 1-phosphate. Pediatric Research. 14(5). 729–734. 1 indexed citations

Hellkuhl, B., et al.. (1978). Regional assignment of the gene for human β-glucuronidase by the use of human-mouse cell hybrids. Cytogenetic and Genome Research. 22(1-6). 434–436. 5 indexed citations

10.

Hellkuhl, B., Wolfgang R. Mayr, & K.-H. Grzeschik. (1978). Localization of MPI, PKM2, IDHM, and the α subunit of hexosaminidase (HEXA) to the q21→qter region of human chromosome 15. Cytogenetic and Genome Research. 22(1-6). 503–505. 12 indexed citations

11.

Hellkuhl, B. & K.-H. Grzeschik. (1978). Partial reactivation of a human inactive X chromosome in human-mouse somatic cell hybrids. Cytogenetic and Genome Research. 22(1-6). 527–530. 21 indexed citations

12.

Hellkuhl, B. & Karl‐Heinz Grzeschik. (1978). Assignment of a gene for arylsulfatase B to human chromosome 5 using human-mouse somatic cell hybrids. Cytogenetic and Genome Research. 22(1-6). 203–206. 18 indexed citations

13.

Hellkuhl, B. & Karl‐Heinz Grzeschik. (1976). Regional mapping of human chromosome 10: Assignment of the gene for cytoplasmic glutamate-oxaloacetate transaminase to 10q24 � qter. Human Genetics. 33(2). 109–12. 4 indexed citations

14.

Hellkuhl, B. & Karl‐Heinz Grzeschik. (1976). Localization of GOTs to the q24→qter region of human chromosome 10. Cytogenetic and Genome Research. 16(1-5). 157–158. 4 indexed citations

15.

Wild, D. & B. Hellkuhl. (1976). Isolation of mammalian cell mutants deficient in glucose 6-phosphate dehydrogenase by means of a replica-plating technique. Human Genetics. 32(3). 315–322. 4 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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