J. Horst

459 total citations
23 papers, 329 citations indexed

About

J. Horst is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, J. Horst has authored 23 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Genetics. Recurrent topics in J. Horst's work include Hemoglobinopathies and Related Disorders (7 papers), Iron Metabolism and Disorders (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). J. Horst is often cited by papers focused on Hemoglobinopathies and Related Disorders (7 papers), Iron Metabolism and Disorders (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). J. Horst collaborates with scholars based in Germany, United States and Australia. J. Horst's co-authors include H. Fraenkel‐Conrat, Stanley Mandeles, Robert H. Rice, Ernst‐Ulrich Griese, Konrad Beyreuther, Helena Ayyub, Douglas R. Higgs, F E Cash, W. Gerok and Ingrid M. Weiss and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Biochemistry.

In The Last Decade

J. Horst

22 papers receiving 301 citations

Peers

J. Horst

GENET

ECOLO

Dale Lindsley United States

Fatine Benjelloun France

Marina Bengtström Finland

Kenneth D. McMilin United States

David Newsom United States

Jinduo Yuan China

Barnett B. Rosenblum United States

Chengbo Long China

V. Wunderlich Germany

M. Ehn Sweden

Dale Lindsley United States

J. Horst

527 ×3.2

141 ×1.1

GENET

46 ×0.7

GENET

57 ×1.0

77 ×1.8

ECOLO

Citations per year, relative to J. Horst J. Horst (= 1×) peers Dale Lindsley

Countries citing papers authored by J. Horst

Since Specialization

Citations

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

Fields of papers citing papers by J. Horst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Horst

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

Saad, Eddy, et al.. (2024). 1707P A plasma proteomic based algorithm is associated with prognosis in renal cell carcinoma. Annals of Oncology. 35. S1023–S1024.

Meschede, Dieter, H. M. Behre, Eberhard Nieschlag, & J. Horst. (2008). Kallmann-Syndrom: Pathophysiologie und Klinik. DMW - Deutsche Medizinische Wochenschrift. 119(42). 1436–1442. 1 indexed citations

Kennerknecht, Ingo, Rita Exeler, J. Horst, et al.. (2004). Mild phenotype in two unrelated patients with a partial deletion of 21q22.2‐q22.3 defined by FISH and molecular studies. American Journal of Medical Genetics Part A. 131A(3). 265–372. 27 indexed citations

Hunter, Michael, Janina Hantke, Dora Angelicheva, et al.. (2002). Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families. Human Mutation. 19(3). 240–250. 6 indexed citations

Burke, Valerie, Nadia Bogdanova, Neil Boudville, et al.. (2001). Angiotensin‐converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney disease. Nephrology Dialysis Transplantation. 16(12). 2323–2327. 21 indexed citations

Pennekamp, Petra, Nadja Bogdanova, Monika Wilda, et al.. (1998). Characterization of the murine polycystic kidney disease ( Pkd2 ) gene. Mammalian Genome. 9(9). 749–752. 15 indexed citations

Steger, Heinrich, A. Eigel, G. Flatz, & J. Horst. (1993). Hemoglobin E and codon 17 nonsense: Two β-globin gene mutations common in Southeast Asia detected by the use of ARMS. Annals of Hematology. 67(3). 119–120. 2 indexed citations

Kalaydjieva, Luba, et al.. (1992). Heterogeneity of mutations in Bulgarian phenylketonuria haplotype 1 and 4 alleles. Clinical Genetics. 41(3). 123–128. 7 indexed citations

Schnee, Janet, C. Aulehla‐Scholz, A. Eigel, & J. Horst. (1990). Hb D Los Angeles (D-Punjab) and Hb Presbyterian: analysis of the defect at the DNA level. Human Genetics. 84(4). 365–7. 11 indexed citations

10.

Liebhaber, Stephen A., Ernst‐Ulrich Griese, Ingrid M. Weiss, et al.. (1990). Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene cluster.. Proceedings of the National Academy of Sciences. 87(23). 9431–9435. 46 indexed citations

11.

Spiegelberg, R., et al.. (1989). A ?-thalassemia mutant caused by a 300-bp deletion in the human ?-globin gene. Human Genetics. 81(3). 298–9. 12 indexed citations

12.

Griese, Ernst‐Ulrich, E. Kohne, & J. Horst. (1985). Heterogeneity of the ?-globin gene defects in German ?-thalassemia affected families. Human Genetics. 71(2). 134–7. 2 indexed citations

13.

Horst, J., et al.. (1983). DNA restriction mapping identifies the chromosome carrying the mutant Hb Presbyterian ?-globin gene. Human Genetics. 64(3). 263–266. 5 indexed citations

14.

Horst, J., et al.. (1982). Integration and expression of a truncated simian virus 40 early gene fragment in mammalian cells.. Proceedings of the National Academy of Sciences. 79(15). 4645–4649. 2 indexed citations

15.

Horst, J., et al.. (1981). Heptacarpo-octatarso-dactyly combined with multiple malformations. European Journal of Pediatrics. 136(2). 207–210. 4 indexed citations

16.

Rice, Robert H. & J. Horst. (1972). Isoelectric focusing of viruses in polyacrylamide gels. Virology. 49(2). 602–604. 20 indexed citations

17.

Horst, J., et al.. (1972). The active components of crotoxin. Biochemical and Biophysical Research Communications. 46(3). 1042–1047. 48 indexed citations

18.

Horst, J., H. Fraenkel‐Conrat, & Stanley Mandeles. (1971). Terminal heterogeneity at both ends of the satellite tobacco necrosis virus ribonucleic acid. Biochemistry. 10(25). 4748–4752. 54 indexed citations

19.

Mussgay, M., Peter-Joachim Enzmann, & J. Horst. (1970). Influence of an arbovirus infection (Sindbis virus) on the protein and ribonucleic acid synthesis of cultivated chick embryo cells. Archives of Virology. 31(1-2). 81–92. 8 indexed citations

20.

Glossmann, Hartmut, et al.. (1970). [Hemoglobins. 18. Isoelectric focussing of hemoglobins (erythrocruorins) from insects (Chironomus thummi, thummi, Diptera)].. PubMed. 351(3). 342–8. 1 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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