Manfred Schürmann

1.9k total citations
17 papers, 759 citations indexed

About

Manfred Schürmann is a scholar working on Physiology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Manfred Schürmann has authored 17 papers receiving a total of 759 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 7 papers in Pulmonary and Respiratory Medicine and 5 papers in Molecular Biology. Recurrent topics in Manfred Schürmann's work include Sarcoidosis and Beryllium Toxicity Research (8 papers), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (6 papers) and Genomics and Rare Diseases (2 papers). Manfred Schürmann is often cited by papers focused on Sarcoidosis and Beryllium Toxicity Research (8 papers), Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis (6 papers) and Genomics and Rare Diseases (2 papers). Manfred Schürmann collaborates with scholars based in Germany, United Kingdom and Iran. Manfred Schürmann's co-authors include Joachim Müller‐Quernheim, E. Schwinger, Bertram Müller‐Myhsok, Max Schlaak, Stefan Schreiber, Karoline I. Gaede, Annegret Fischer, Sylvia Hofmann, Michael Nothnagel and Achim Nolte and has published in prestigious journals such as Nature Genetics, American Journal of Respiratory and Critical Care Medicine and CHEST Journal.

In The Last Decade

Manfred Schürmann

17 papers receiving 736 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manfred Schürmann Germany 11 486 423 206 96 91 17 759
Rachael Cohen United States 14 79 0.2× 59 0.1× 122 0.6× 25 0.3× 39 0.4× 54 624
Fabrício Souza Neves Brazil 16 45 0.1× 112 0.3× 113 0.5× 23 0.2× 32 0.4× 46 539
Yoichi Mashimo Japan 12 109 0.2× 201 0.5× 127 0.6× 16 0.2× 57 0.6× 24 835
Hsing-Won Wang Taiwan 15 246 0.5× 150 0.4× 103 0.5× 11 0.1× 36 0.4× 48 611
J. P. M. Evans United Kingdom 11 94 0.2× 72 0.2× 82 0.4× 41 0.4× 32 0.4× 15 536
Michel Melanson Canada 11 105 0.2× 36 0.1× 215 1.0× 14 0.1× 97 1.1× 21 580
Marko Vukovic United States 6 249 0.5× 129 0.3× 108 0.5× 33 0.3× 31 0.3× 6 650
N P Cavanagh United Kingdom 14 179 0.4× 120 0.3× 212 1.0× 3 0.0× 98 1.1× 29 737
M. Abel Canada 12 124 0.3× 87 0.2× 92 0.4× 11 0.1× 34 0.4× 22 562
Shigeruko Iijima Japan 12 106 0.2× 26 0.1× 59 0.3× 18 0.2× 73 0.8× 56 461

Countries citing papers authored by Manfred Schürmann

Since Specialization
Citations

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

Fields of papers citing papers by Manfred Schürmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manfred Schürmann

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

All Works

17 of 17 papers shown
1.
Schwerd, Tobias, Manfred Schürmann, Hannah Chen, et al.. (2015). A recessive form of extreme macrocephaly and mild intellectual disability complements the spectrum of PTEN hamartoma tumour syndrome. European Journal of Human Genetics. 24(6). 889–894. 6 indexed citations
2.
Bergmann, Carsten, Saeed Reza Ghaffari, Manfred Schürmann, et al.. (2012). Next-generation Sequencing Of All Known Genes For RP And Allied Diseases Identifies The Causative Mutations In The Majority Of Patients. Investigative Ophthalmology & Visual Science. 53(14). 4525–4525. 1 indexed citations
3.
Fischer, Annegret, Michael Nothnagel, Manfred Schürmann, et al.. (2010). A Genome-Wide Linkage Analysis in 181 German Sarcoidosis Families Using Clustered Biallelic Markers. CHEST Journal. 138(1). 151–157. 13 indexed citations
4.
Hofmann, Sylvia, André Franke, Annegret Fischer, et al.. (2008). Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. Nature Genetics. 40(9). 1103–1106. 179 indexed citations
5.
Fischer, Annegret, Ruta Valentonyte, Almut Nebel, et al.. (2008). Female-specific association of C-C chemokine receptor 5 gene polymorphisms with Löfgren’s syndrome. Journal of Molecular Medicine. 86(5). 553–561. 12 indexed citations
6.
Müller‐Quernheim, Joachim, Manfred Schürmann, Sylvia Hofmann, et al.. (2008). Genetics of Sarcoidosis. Clinics in Chest Medicine. 29(3). 391–414. 52 indexed citations
7.
Valentonyte, Ruta, Jochen Hampe, Peter J.P. Croucher, et al.. (2005). Study of C-C Chemokine Receptor 2 Alleles in Sarcoidosis, with Emphasis on Family-based Analysis. American Journal of Respiratory and Critical Care Medicine. 171(10). 1136–1141. 37 indexed citations
8.
Gaede, Karoline I., et al.. (2005). Function associated transforming growth factor-β gene polymorphism in chronic beryllium disease. Journal of Molecular Medicine. 83(5). 397–405. 17 indexed citations
9.
Schürmann, Manfred. (2003). Genetics of Sarcoidosis. Seminars in Respiratory and Critical Care Medicine. 24(2). 213–222. 4 indexed citations
10.
Schürmann, Manfred, Melanie Albrecht, E. Schwinger, & Manfred Stuhrmann. (2002). CFTR gene mutations in sarcoidosis. European Journal of Human Genetics. 10(11). 729–732. 10 indexed citations
11.
Schürmann, Manfred, et al.. (2001). Results from a Genome-wide Search for Predisposing Genes in Sarcoidosis. American Journal of Respiratory and Critical Care Medicine. 164(5). 840–846. 141 indexed citations
12.
Muraközy, G., Karoline I. Gaede, Ola Gutzeit, et al.. (2001). Gene polymorphisms of immunoregulatory cytokines and angiotensin-converting enzyme in Wegener's granulomatosis. Journal of Molecular Medicine. 79(11). 665–670. 40 indexed citations
13.
Schürmann, Manfred, Penny Lympany, Bertram Müller‐Myhsok, et al.. (2000). Familial Sarcoidosis is Linked to the Major Histocompatibility Complex Region. American Journal of Respiratory and Critical Care Medicine. 162(3). 861–864. 85 indexed citations
14.
Arolt, Volker, Rebekka Lencer, Sabine Purmann, et al.. (1999). Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia. American Journal of Medical Genetics. 88(6). 603–606. 3 indexed citations
15.
Finckh, Ulrich, Suying Xu, Govindasamy Kumaramanickavel, et al.. (1998). Homozygosity Mapping of Autosomal Recessive Retinitis Pigmentosa Locus (RP22) on Chromosome 16p12.1–p12.3. Genomics. 48(3). 341–345. 15 indexed citations
16.
Arolt, Volker, Rebekka Lencer, Achim Nolte, et al.. (1996). Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease. American Journal of Medical Genetics. 67(6). 564–579. 143 indexed citations
17.
Xu, Suying, Manfred Schürmann, & Andreas Gal. (1996). Dinucleotide repeat polymorphisms at D9S171 and D9S741 are identical. Clinical Genetics. 50(6). 531–532. 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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