Manfred Stuhrmann

751 total citations
7 papers, 401 citations indexed

About

Manfred Stuhrmann is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Neurology. According to data from OpenAlex, Manfred Stuhrmann has authored 7 papers receiving a total of 401 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pulmonary and Respiratory Medicine, 2 papers in Molecular Biology and 1 paper in Neurology. Recurrent topics in Manfred Stuhrmann's work include Cystic Fibrosis Research Advances (4 papers), Neonatal Respiratory Health Research (3 papers) and Tracheal and airway disorders (2 papers). Manfred Stuhrmann is often cited by papers focused on Cystic Fibrosis Research Advances (4 papers), Neonatal Respiratory Health Research (3 papers) and Tracheal and airway disorders (2 papers). Manfred Stuhrmann collaborates with scholars based in Germany, Czechia and Poland. Manfred Stuhrmann's co-authors include Thilo Dörk, Dieter Meschede, A Mayerová, Hans-Jürgen Pander, H. H. Seydewitz, Eberhard Passarge, C. Aulehla‐Scholz, H. Sperling, Eberhard Nieschlag and Félix Ratjen and has published in prestigious journals such as Gynecologic Oncology, Human Mutation and Human Genetics.

In The Last Decade

Manfred Stuhrmann

7 papers receiving 388 citations

Peers

Countries citing papers authored by Manfred Stuhrmann

Since Specialization

Citations

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

Fields of papers citing papers by Manfred Stuhrmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manfred Stuhrmann

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1 2009 ·Haematologica ·Doris Steinemann, Larissa Arning, (unknown), Manfred Stuhrmann, Henrik Hasle, (unknown), (unknown), Charlotte M. Niemeyer, Christian Flotho	48
2	Frequency of BRCA1 Mutation 5382insC in German Breast Cancer Patients 1999 ·Gynecologic Oncology ·(unknown), (unknown), Britta Skawran, Thilo Dörk, Manfred Stuhrmann, (unknown), Michael Untch, Alfons Meindl, Renate Burgemeister, Jenny C. Chang, Bernhard H. F. Weber	63
3	Polymorphisms of the humanβ-defensin-1gene 1998 ·Molecular and Cellular Probes ·Thilo Dörk, Manfred Stuhrmann	49
4	Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens 1997 ·Human Genetics ·Thilo Dörk, Bernd Dworniczak, C. Aulehla‐Scholz, Dagmar Wieczorek, (unknown), A Mayerová, H. H. Seydewitz, Eberhard Nieschlag, Dieter Meschede, Jürgen Horst, Hans-Jürgen Pander, H. Sperling, Félix Ratjen, Eberhard Passarge, (unknown), Manfred Stuhrmann	190
5	Transcript analysis of CFTR nonsense mutations in lymphocytes and nasal epithelial cells from cystic fibrosis patients 1995 ·Human Mutation ·Katrin Will, Thilo Dörk, Manfred Stuhrmann, H. von der Hardt, Helmut Ellemunter, Burkhard Tümmler, (unknown)	35
6	The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy 1991 ·Clinical Genetics ·Milan Maçek, Manfred Stuhrmann, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), André Reis, (unknown), Jörg Schmidtke	6
7	Distribution patterns of the ΔF508 mutation in the CFTR gene on CF-linked marker haplotypes in the German population 1990 ·Human Genetics ·André Reis, (unknown), Manfred Schlösser, (unknown), (unknown), J. Hundrieser, Milan Maçek, Manfred Stuhrmann, (unknown), Thilo Dörk, Frank Schnieders, Hans‐Georg Posselt, Ulrich Wahn, (unknown), Friedrich K. Trefz, Burkhard Tümmler, Michael Krawczak, Jörg Schmidtke	10

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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