H. Heilbronner

543 total citations
17 papers, 368 citations indexed

About

H. Heilbronner is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, H. Heilbronner has authored 17 papers receiving a total of 368 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Plant Science. Recurrent topics in H. Heilbronner's work include Cancer Research and Treatments (2 papers), Cancer, Hypoxia, and Metabolism (2 papers) and Metabolism and Genetic Disorders (2 papers). H. Heilbronner is often cited by papers focused on Cancer Research and Treatments (2 papers), Cancer, Hypoxia, and Metabolism (2 papers) and Metabolism and Genetic Disorders (2 papers). H. Heilbronner collaborates with scholars based in Germany, France and Netherlands. H. Heilbronner's co-authors include C. Aulehla‐Scholz, W. Schempp, Hjalmar S. Kühl, H. Enders, Hans‐Hilger Ropers, Bellinda van den Helm, Andreas Dufke, Michael H. Walter, Kay Nieselt and Jamel Chelly and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Genomics and Human Mutation.

In The Last Decade

H. Heilbronner

15 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
H. Heilbronner Germany	10	221	171	74	54	40	17	368
Shane C. Quinonez United States	11	221 1.0×	172 1.0×	28 0.4×	56 1.0×	60 1.5×	29	396
Laurel L. Estabrooks United States	10	240 1.1×	280 1.6×	93 1.3×	102 1.9×	5 0.1×	11	429
Imma Rost Germany	9	157 0.7×	212 1.2×	74 1.0×	45 0.8×	7 0.2×	24	322
Miaofei Xu China	10	173 0.8×	140 0.8×	34 0.5×	18 0.3×	10 0.3×	17	318
Ellen K. Brundage United States	11	225 1.0×	141 0.8×	36 0.5×	27 0.5×	133 3.3×	12	327
Farida Mébarki France	15	550 2.5×	269 1.6×	21 0.3×	24 0.4×	30 0.8×	19	800
Richard L. Neu United States	13	214 1.0×	375 2.2×	85 1.1×	267 4.9×	17 0.4×	41	581
Alba Sanchis‐Juan United Kingdom	8	234 1.1×	224 1.3×	16 0.2×	48 0.9×	35 0.9×	15	431
Z Gelman-Kohan Israel	8	264 1.2×	54 0.3×	12 0.2×	48 0.9×	149 3.7×	12	370
Júlia Baptista United Kingdom	12	254 1.1×	291 1.7×	122 1.6×	95 1.8×	12 0.3×	22	496

Countries citing papers authored by H. Heilbronner

Since Specialization

Citations

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

Fields of papers citing papers by H. Heilbronner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Heilbronner

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

All Works

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17 of 17 papers shown

Heilbronner, H., et al.. (2008). Pränatale Diagnose der Gaucher-Krankheit. DMW - Deutsche Medizinische Wochenschrift. 106(20). 652–654.

Gomes, Marina de Nadai Bonin, Michael H. Walter, Ulrike A. Mau‐Holzmann, et al.. (2007). Specific transcriptional changes in human fetuses with autosomal trisomies. Cytogenetic and Genome Research. 119(3-4). 171–184. 63 indexed citations

Tzschach, Andreas, Maria Hoeltzenbein, Kirsten Hoffmann, et al.. (2006). Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3. European Journal of Human Genetics. 14(12). 1317–1320. 14 indexed citations

Hospach, Toni, P Lohse, H. Heilbronner, Guenther E. Dannecker, & Peter Lohse. (2005). Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins. Arthritis & Rheumatism. 52(11). 3606–3610. 9 indexed citations

Aulehla‐Scholz, C. & H. Heilbronner. (2003). Mutational spectrum in German patients with phenylalanine hydroxylase deficiency. Human Mutation. 21(4). 399–400. 38 indexed citations

Kühl, Hjalmar S., et al.. (2001). Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs). Chromosome Research. 9(3). 215–222. 44 indexed citations

Yntema, Helger G., Bellinda van den Helm, J. Kissing, et al.. (1999). A Novel Ribosomal S6-Kinase (RSK4; RPS6KA6) Is Commonly Deleted in Patients with Complex X-Linked Mental Retardation. Genomics. 62(3). 332–343. 93 indexed citations

David, D., Ulrike Orth, H. Heilbronner, & Andreas Gal. (1996). A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome. Human Mutation. 7(2). 181–182. 3 indexed citations

Heilbronner, H., et al.. (1994). [Sex chromosome aberration with the 48 XYYY karyotype. A case report of the phenotype of a rare sex chromosome aneuploidy].. PubMed. 22(2). 130–4. 2 indexed citations

10.

Steinbach, Peter, Gholamali Tariverdian, Ingo Kennerknecht, et al.. (1993). Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families. Human Genetics. 92(5). 491–498. 12 indexed citations

11.

Stuhrmann, Manfred, H. Heilbronner, André Reis, et al.. (1991). Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenita. Human Genetics. 86(4). 414–5. 15 indexed citations

12.

Kömpf, J., H. J. Staab, H. Heilbronner, F. A. Anderer, & H. Ritter. (1984). Cell fusion responsible for horizontal oncogenesis by human tumors in nude mice. Biochemical and Biophysical Research Communications. 124(3). 933–938. 6 indexed citations

13.

Schmid, Michael, et al.. (1984). Satellited Y chromosomes: Structure, origin, and clinical significance. Human Genetics. 67(1). 72–85. 34 indexed citations

14.

Staab, H. J., H. Heilbronner, M. Schrader, & F. A. Anderer. (1983). In vivo induction of neoplastic growth in nude mouse connective tissue adjacent to xenografted human tumors. Journal of Cancer Research and Clinical Oncology. 106(1). 27–35. 9 indexed citations

15.

Ranke, MB, et al.. (1982). Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.. PubMed. 80(2). 142–50. 2 indexed citations

16.

Siebert, G., H. Ritter, H. Heilbronner, et al.. (1980). Data on linkage relations between GLO and 21-hydroxylase. Human Genetics. 54(3). 419–420. 1 indexed citations

17.

Heilbronner, H., et al.. (1978). Cytogenetische Untersuchungen an Trichlor�thylen-Arbeitern. Archives of Toxicology. 40(3). 201–206. 23 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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