B. Horsthemke

872 total citations
13 papers, 444 citations indexed

About

B. Horsthemke is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, B. Horsthemke has authored 13 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in B. Horsthemke's work include Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Epigenetics and DNA Methylation (3 papers). B. Horsthemke is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Epigenetics and DNA Methylation (3 papers). B. Horsthemke collaborates with scholars based in Germany, United Kingdom and Norway. B. Horsthemke's co-authors include Karin Buiting, Michael Zeschnigk, Birgit Schmitz, Bärbel Dittrich, Walter Doerfler, Shinji Saitoh, J Arnemann, Peter K. Rogan, Jessica L. Buxton and Robert D. Nicholls and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Human Molecular Genetics.

In The Last Decade

B. Horsthemke

12 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. Horsthemke Germany	9	326	321	135	34	30	13	444
Jaime Garcia‐Heras United States	14	208 0.6×	244 0.8×	93 0.7×	79 2.3×	13 0.4×	25	440
Sonia Nizard France	10	131 0.4×	227 0.7×	87 0.6×	21 0.6×	21 0.7×	12	357
Kiyoshi Kikkawa Japan	12	182 0.6×	211 0.7×	103 0.8×	56 1.6×	13 0.4×	27	378
G. Del Porto Italy	12	154 0.5×	186 0.6×	64 0.5×	54 1.6×	55 1.8×	26	344
Anna Newlin United States	12	147 0.5×	210 0.7×	96 0.7×	16 0.5×	53 1.8×	17	425
Poustka Annemarie Germany	8	431 1.3×	287 0.9×	109 0.8×	14 0.4×	14 0.5×	9	514
Anna Sowińska‐Seidler Poland	13	254 0.8×	237 0.7×	74 0.5×	23 0.7×	31 1.0×	38	409
M. F. Croquette France	11	274 0.8×	293 0.9×	49 0.4×	100 2.9×	45 1.5×	17	444
Jack H. Jung Canada	13	218 0.7×	208 0.6×	83 0.6×	61 1.8×	14 0.5×	19	411
Pietro Sirleto Italy	12	221 0.7×	137 0.4×	33 0.2×	27 0.8×	44 1.5×	25	399

Countries citing papers authored by B. Horsthemke

Since Specialization

Citations

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

Fields of papers citing papers by B. Horsthemke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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13 of 13 papers shown

Weise, Anja, Kristin Mrasek, Hasmik Mkrtchyan, et al.. (2008). Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level. International Journal of Molecular Medicine. 21(2). 189–200. 27 indexed citations

Webb, T., J. Whittington, A J Holland, et al.. (2005). CD36 expression and its relationship with obesity in blood cells from people with and without Prader–Willi syndrome. Clinical Genetics. 69(1). 26–32. 5 indexed citations

Zeschnigk, Michael, B. Horsthemke, & Dietmar Lohmann. (1999). Detection of homozygous deletions in tumors by hybridization of representational difference analysis (RDA) products to chromosome-specific YAC clone arrays. Nucleic Acids Research. 27(21). i–vii. 2 indexed citations

Yılmaz, Sedat, et al.. (1998). Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Human Mutation. 12(6). 434–434. 21 indexed citations

Buiting, Karin, et al.. (1997). The murine <i>Ext1</i> gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15. Cytogenetic and Genome Research. 76(3-4). 164–166. 7 indexed citations

Zeschnigk, Michael, Birgit Schmitz, Bärbel Dittrich, et al.. (1997). Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method. Human Molecular Genetics. 6(3). 387–395. 104 indexed citations

Buiting, Karin, et al.. (1996). A pseudogene for the human ribosomal protein L5 (RPL5P1) maps within an intron of the SNRPN transcription unit on human chromosome 15. Cytogenetic and Genome Research. 75(4). 224–226. 17 indexed citations

Saitoh, Shinji, Karin Buiting, Peter K. Rogan, et al.. (1996). Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.. Proceedings of the National Academy of Sciences. 93(15). 7811–7815. 146 indexed citations

Klink, Albrecht, K. Schiebel, M. Winkelmann, et al.. (1995). The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability. Human Molecular Genetics. 4(5). 869–878. 52 indexed citations

10.

Buiting, Karin, Valerie Greger, Bernard H. Brownstein, et al.. (1992). A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.. Proceedings of the National Academy of Sciences. 89(12). 5457–5461. 39 indexed citations

11.

Humphries, Steve E., et al.. (1989). Gene probes in diagnosis of familial hypercholesterolemia.. PubMed. 9(1 Suppl). I59–65. 11 indexed citations

12.

Davison, John, et al.. (1987). Recombinant DNA technology and low-density lipoprotein receptor defects. Biochemical Society Transactions. 15(2). 202–203. 1 indexed citations

13.

Broeckhoven, Christine Van, H. Backhovens, Peter Raeymaekers, et al.. (1987). LINKAGE STUDY BETWEEN THE AMYLOID GENE AND FAMILIAL ALZHEIMERS-DISEASE. Oxford University Research Archive (ORA) (University of Oxford). 46. 708–708. 12 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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