Jurg Rohrer

1.9k total citations
25 papers, 1.4k citations indexed

About

Jurg Rohrer is a scholar working on Immunology, Genetics and Genetics. According to data from OpenAlex, Jurg Rohrer has authored 25 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Immunology, 16 papers in Genetics and 10 papers in Genetics. Recurrent topics in Jurg Rohrer's work include Immunodeficiency and Autoimmune Disorders (19 papers), Chronic Lymphocytic Leukemia Research (15 papers) and Platelet Disorders and Treatments (7 papers). Jurg Rohrer is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (19 papers), Chronic Lymphocytic Leukemia Research (15 papers) and Platelet Disorders and Treatments (7 papers). Jurg Rohrer collaborates with scholars based in United States, South Africa and Croatia. Jurg Rohrer's co-authors include Mary Ellen Conley, Yoshiyuki Minegishi, Dario Campana, Elaine Coustan‐Smith, Ornella Parolini, Howard M. Lederman, Andrew C. Chan, Rajita Pappu, Derrick Mathias and Jason Treadaway and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Jurg Rohrer

25 papers receiving 1.4k citations

Peers

Jurg Rohrer

IMMUN

GENET

HEMAT

Shirley G. Quan United States

M. J. Hobart United Kingdom

Yasuo Fukumori Japan

Andrew Getahun United States

M Takahashi Japan

Harry W. Snyder United States

Gaby Brouns Netherlands

Gilda F. Linton United States

Nadia Catalan France

Thomas R. Bauer United States

Shirley G. Quan United States

Jurg Rohrer

1.5k ×1.3

IMMUN

678 ×1.3

GENET

296 ×0.7

GENET

261 ×1.1

HEMAT

320 ×1.4

Citations per year, relative to Jurg Rohrer Jurg Rohrer (= 1×) peers Shirley G. Quan

Countries citing papers authored by Jurg Rohrer

Since Specialization

Citations

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

Fields of papers citing papers by Jurg Rohrer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jurg Rohrer

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

Miyara, Makoto, Édouard Sage, Daisuke Sugiyama, et al.. (2015). Sialyl Lewis x (CD15s) identifies highly differentiated and most suppressive FOXP3 ^high regulatory T cells in humans. Proceedings of the National Academy of Sciences. 112(23). 7225–7230. 119 indexed citations

Rohrer, Jurg, et al.. (2011). Optimization of loading conditions for a violet dye for use in cell proliferation studies (65.9). The Journal of Immunology. 186(1_Supplement). 65.9–65.9. 1 indexed citations

Porpiglia, Andrea S., Jurg Rohrer, & Mary Ellen Conley. (2003). Reconstitution of B cell function in murine models of immunodeficiency. Clinical Immunology. 107(2). 90–97. 8 indexed citations

Richter, Darko, et al.. (2001). A contiguous deletion syndrome of X‐linked agammaglobulinemia and sensorineural deafness. Pediatric Allergy and Immunology. 12(2). 107–111. 23 indexed citations

Conley, Mary Ellen, Jurg Rohrer, & Yoshiyuki Minegishi. (2000). X-Linked Agammaglobulinemia. Clinical Reviews in Allergy & Immunology. 19(2). 183–204. 79 indexed citations

Conley, Mary Ellen, et al.. (2000). Defects in early B‐cell development: comparing the consequences of abnormalities in pre‐BCR signaling in the human and the mouse. Immunological Reviews. 178(1). 75–90. 86 indexed citations

Rohrer, Jurg, et al.. (1999). Unusual Mutations in Btk: An Insertion, a Duplication, an Inversion, and Four Large Deletions. Clinical Immunology. 90(1). 28–37. 57 indexed citations

Conley, Mary Ellen, et al.. (1999). Gene Conversion Events Contribute to the Polymorphic Variation of the Surrogate Light Chain Gene λ5/14.1. Clinical Immunology. 93(2). 162–167. 10 indexed citations

Minegishi, Yoshiyuki, Jurg Rohrer, & Mary Ellen Conley. (1999). Recent progress in the diagnosis and treatment of patients with defects in early B-cell development. Current Opinion in Pediatrics. 11(6). 528–532. 24 indexed citations

10.

Conley, Mary Ellen, Derrick Mathias, Jason Treadaway, Yoshiyuki Minegishi, & Jurg Rohrer. (1998). Mutations in Btk in Patients with Presumed X-Linked Agammaglobulinemia. The American Journal of Human Genetics. 62(5). 1034–1043. 125 indexed citations

11.

Lin, Qun, Jurg Rohrer, R.Cutler Allen, et al.. (1996). A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome.. Journal of Clinical Investigation. 97(1). 196–201. 30 indexed citations

12.

Rohrer, Jurg, et al.. (1996). Wiskott-Aldrich syndrome in a family with Fanconi anemia. The Journal of Pediatrics. 129(1). 50–55. 7 indexed citations

13.

Farrar, Jason E., Jurg Rohrer, & Mary Ellen Conley. (1996). Neutropenia in X-Linked Agammaglobulinemia. Clinical Immunology and Immunopathology. 81(3). 271–276. 62 indexed citations

14.

Yel, Leman, Yoshiyuki Minegishi, Elaine Coustan‐Smith, et al.. (1996). Mutations in the Mu Heavy-Chain Gene in Patients with Agammaglobulinemia. New England Journal of Medicine. 335(20). 1486–1493. 175 indexed citations

15.

Conley, Mary Ellen & Jurg Rohrer. (1995). The spectrum of mutations in Btk that cause X-linked agammaglobulinemia. Clinical Immunology and Immunopathology. 76(3). S192–S197. 21 indexed citations

16.

Parolini, Ornella, et al.. (1995). B-cell-specific demethylation of BTK, the defective gene in X-linked agammaglobulinemia. Immunogenetics. 42(2). 129–35. 7 indexed citations

17.

Rohrer, Jurg, Ornella Parolini, Mary Ellen Conley, & John W. Belmont. (1994). The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia. Immunogenetics. 40(5). 319–324. 45 indexed citations

18.

Conley, Mary Ellen, Ornella Parolini, Jurg Rohrer, & Dario Campana. (1994). X‐Linked Agammaglobulinemia: New Approaches to Old Questions based on the Identification of the Defective Gene. Immunological Reviews. 138(1). 5–21. 71 indexed citations

19.

Conley, Mary Ellen, et al.. (1994). Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase. Human Molecular Genetics. 3(10). 1751–1756. 80 indexed citations

20.

Rohrer, Jurg & Douglas E. Rawlings. (1993). Regulation of mobilization of the broad‐host‐range plasmid pTF‐FC2. Molecular Microbiology. 9(5). 1051–1059. 4 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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