J. Seidel

479 total citations
9 papers, 217 citations indexed

About

J. Seidel is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, J. Seidel has authored 9 papers receiving a total of 217 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Oncology and 3 papers in Genetics. Recurrent topics in J. Seidel's work include Bone health and treatments (2 papers), Alkaline Phosphatase Research Studies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). J. Seidel is often cited by papers focused on Bone health and treatments (2 papers), Alkaline Phosphatase Research Studies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). J. Seidel collaborates with scholars based in Germany, United States and United Kingdom. J. Seidel's co-authors include Beyhan Tüysüz, Mahmut Çöker, Belinda Chong, Donald R. Love, John А. Kanis, Cristina Tau, Madhuri Hegde, Hamilton Cassinelli, Bilgin Yüksel and Tim Cundy and has published in prestigious journals such as Journal of Bone and Mineral Research, Human Genetics and European Journal of Human Genetics.

In The Last Decade

J. Seidel

9 papers receiving 211 citations

Peers

J. Seidel

MB

ONCOL

GENET

RHEUM

IMMUN

Kikuchi Japan

Gina M. Kavanagh United Kingdom

Anna Laura Putignano Italy

Masutaka Tokuda Japan

Mara Epstein United States

Yeo‐Kyeoung Kim South Korea

W. Sanger United States

Emanuel Bs United States

Hayato Maruoka Japan

Ya‐Zhen Qin China

Kikuchi Japan

J. Seidel

122 ×1.1

MB

69 ×0.7

ONCOL

21 ×0.4

GENET

42 ×0.9

RHEUM

45 ×1.5

IMMUN

Citations per year, relative to J. Seidel J. Seidel (= 1×) peers Kikuchi

Countries citing papers authored by J. Seidel

Since Specialization

Citations

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

Fields of papers citing papers by J. Seidel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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9 of 9 papers shown

1.

Gijsbers, Antoinet C.J., Barbara D′haene, Yvonne Hilhorst‐Hofstee, et al.. (2008). Identification of copy number variants associated with BPES-like phenotypes. Human Genetics. 124(5). 489–498. 12 indexed citations

2.

Gruhn, Bernd, J. Seidel, F Zintl, et al.. (2007). Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure. Orphanet Journal of Rare Diseases. 2(1). 5–5. 47 indexed citations

3.

Oexle, Konrad, Denise Horn, Annegret Buske, et al.. (2005). Childhood overgrowth in patients with common NF1 microdeletions. European Journal of Human Genetics. 13(7). 883–888. 30 indexed citations

4.

Liehr, Thomas, Heike Starke, Anja Weise, et al.. (2003). Evidence for a new microdeletion syndrome in 15q21. International Journal of Molecular Medicine. 11(5). 575–7. 15 indexed citations

5.

Chong, Belinda, Madhuri Hegde, Hamilton Cassinelli, et al.. (2003). Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype. Journal of Bone and Mineral Research. 18(12). 2095–2104. 92 indexed citations

6.

Röth, Andreas, Κ. Abendroth, J. Seidel, Hendrik Neubert, & R. Venbrocks. (1996). Management of primary idiopathic hyperphosphatasemia with calcitonin. International Orthopaedics. 20(1). 58–60. 3 indexed citations

7.

Link, H., J. Seidel, Monika Stoll, et al.. (1990). Regeneration of Granulopoiesis with Recombinant Human Granulocyte-Macrophage Colony-Stimulating Factor After Bone Marrow Transplantation. Hämatologie und Bluttransfusion. 33. 741–746. 4 indexed citations

8.

Link, H., Mathias Freund, H. Lester Kirchner, et al.. (1988). Recombinant human granulocyte-macrophage colony stimulating factor (rh GM-CSF) after bone marrow transplantation.. PubMed. 313–9. 13 indexed citations

9.

Stangel, W, et al.. (1986). [Granulocyte functions in stored blood].. PubMed. 15. 231–52. 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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