Lutz-Peter Berg

480 total citations
15 papers, 281 citations indexed

About

Lutz-Peter Berg is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Lutz-Peter Berg has authored 15 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Hematology, 8 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Lutz-Peter Berg's work include Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (4 papers) and Cancer-related gene regulation (3 papers). Lutz-Peter Berg is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (4 papers) and Cancer-related gene regulation (3 papers). Lutz-Peter Berg collaborates with scholars based in United Kingdom, Germany and Spain. Lutz-Peter Berg's co-authors include D.N. Cooper, Jochen Reiss, Vijay V. Kakkar, Ryszard Słomski, V V Kakkar, Kerstin Wieland, Anwar Alhaq, Monee K. Shamsher, Michael J. Wagner and Michael Wagner and has published in prestigious journals such as The Journal of Immunology, Biochemical Journal and FEBS Letters.

In The Last Decade

Lutz-Peter Berg

14 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lutz-Peter Berg United Kingdom	11	148	85	44	40	36	15	281
Amy J. Lambert United States	10	87 0.6×	42 0.5×	28 0.6×	52 1.3×	44 1.2×	15	219
Michael L. Bloom United States	11	228 1.5×	126 1.5×	37 0.8×	95 2.4×	69 1.9×	18	472
Yupo Ma United States	9	147 1.0×	55 0.6×	26 0.6×	61 1.5×	46 1.3×	15	359
Sarah Middleton United States	7	133 0.9×	87 1.0×	35 0.8×	12 0.3×	10 0.3×	9	292
Maria Konstantoulaki United States	5	299 2.0×	36 0.4×	26 0.6×	7 0.2×	9 0.3×	7	432
Parisa Imanirad United States	7	248 1.7×	88 1.0×	56 1.3×	12 0.3×	71 2.0×	8	453
C. Mignon France	11	327 2.2×	18 0.2×	31 0.7×	176 4.4×	11 0.3×	14	434
Shinsuke Ninomiya Japan	14	268 1.8×	24 0.3×	43 1.0×	210 5.3×	16 0.4×	31	444
Raffaella Spina United States	10	230 1.6×	26 0.3×	32 0.7×	25 0.6×	47 1.3×	15	325
Vik Van Duppen Belgium	4	180 1.2×	30 0.4×	20 0.5×	28 0.7×	65 1.8×	6	355

Countries citing papers authored by Lutz-Peter Berg

Since Specialization

Citations

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

Fields of papers citing papers by Lutz-Peter Berg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lutz-Peter Berg. 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 Lutz-Peter Berg. The network helps show where Lutz-Peter Berg may publish in the future.

Co-authorship network of co-authors of Lutz-Peter Berg

This figure shows the co-authorship network connecting the top 25 collaborators of Lutz-Peter Berg. A scholar is included among the top collaborators of Lutz-Peter Berg 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 Lutz-Peter Berg. Lutz-Peter Berg 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

Berg, Lutz-Peter, et al.. (2002). Functional Consequences of Noncognate Interactions Between CD4+ Memory T Lymphocytes and the Endothelium. The Journal of Immunology. 168(7). 3227–3234. 20 indexed citations

Siegert, Gabriele, et al.. (2001). Follow-up von Patienten mit persistierender APC-Resistenz ohne Faktor V Leiden. VASA. 30(1). 24–27.

Schwarz, T., Gabriele Siegert, S. Gehrisch, et al.. (2001). Patients with persistent APC-resistance without factor V Leiden mutation.. PubMed. 30(1). 24–7. 1 indexed citations

Chuzhanova, Nadia, Brad A. Friedman, Anwar Alhaq, et al.. (2000). Identification of an intronic regulatory element in the human protein C ( PROC) gene. Human Genetics. 107(5). 458–465. 19 indexed citations

Berg, Lutz-Peter, et al.. (1997). Expression of human TRPC genes in the megakaryocytic cell lines MEG01, DAMI and HEL. FEBS Letters. 403(1). 83–86. 26 indexed citations

Soria, José Manuel, Lutz-Peter Berg, J. Fontcuberta, et al.. (1996). Ectopic Transcript Analysis Indicates that Allelic Exclusion is an Important Cause of Type I Protein C Deficiency in Patients with Nonsense and Frameshift Mutations in the PROC Gene. Thrombosis and Haemostasis. 75(6). 870–876. 7 indexed citations

Benzakour, Omar, Chryso Kanthou, Ulla Dennehy, et al.. (1995). Evaluation of the use of the luciferase-reporter-gene system for gene-regulation studies involving cyclic AMP-elevating agents. Biochemical Journal. 309(2). 385–387. 13 indexed citations

Berg, Lutz-Peter, et al.. (1994). Combined factor VIII/factor XI deficiency may cause intra-familial clinical variability in haemophilia A among Ashkenazi Jews. Blood Coagulation & Fibrinolysis. 5(1). 59–62. 18 indexed citations

Cooper, D.N., Lutz-Peter Berg, Vijay V. Kakkar, & Jochen Reiss. (1994). Ectopic (Illegitimate) Transcription: New Possibilities for the Analysis and Diagnosis of Human Genetic Disease. Annals of Medicine. 26(1). 9–14. 32 indexed citations

10.

Berg, Lutz-Peter, et al.. (1994). Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia. Human Molecular Genetics. 3(12). 2147–2152. 21 indexed citations

11.

Berg, Lutz-Peter, C Grundy, Frank J. Thomas, et al.. (1992). De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysis. Genomics. 13(4). 1359–1361. 27 indexed citations

12.

Słomski, Ryszard, et al.. (1992). Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts. Human Genetics. 89(6). 615–9. 32 indexed citations

13.

Wieland, Kerstin, Lutz-Peter Berg, V V Kakkar, D.N. Cooper, & U. Martinowitz. (1990). Molecular genetic analysis of a novel form of haemophilia a characterized by the variable expression of factor VIII. Thrombosis Research. 59(5). 871–877. 6 indexed citations

14.

Berg, Lutz-Peter, et al.. (1990). Detection of a novel point mutation causing haemophilia A by PCR/direct sequencing of ectopically-transcribed factor VIII mRNA. Human Genetics. 85(6). 655–8. 36 indexed citations

15.

Słomski, Ryszard, M. Wagner, Jochen Reiss, et al.. (1990). Characterization of pathological dystrophin transcripts from the lymphocytes of a muscular dystrophy carrier.. PubMed. 7(6). 519–23. 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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