Brigitte Wulf

458 total citations
9 papers, 353 citations indexed

About

Brigitte Wulf is a scholar working on Pulmonary and Respiratory Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Brigitte Wulf has authored 9 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pulmonary and Respiratory Medicine, 1 paper in Molecular Biology and 1 paper in Genetics. Recurrent topics in Brigitte Wulf's work include Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (7 papers) and Tracheal and airway disorders (3 papers). Brigitte Wulf is often cited by papers focused on Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (7 papers) and Tracheal and airway disorders (3 papers). Brigitte Wulf collaborates with scholars based in Germany, Israel and Canada. Brigitte Wulf's co-authors include Thomas Neumann, Ulrich Wulbrand, Nanette Kälin, Thilo Dörk, Rainer Fislage, H. von der Hardt, Thomas Richter, Heiner Wolfes, H. Weißbrodt and Heinz Geerlings and has published in prestigious journals such as The Lancet, Clinica Chimica Acta and Advances in experimental medicine and biology.

In The Last Decade

Brigitte Wulf

9 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brigitte Wulf Germany	6	311	64	45	40	17	9	353
K.W. Southern United Kingdom	7	209 0.7×	31 0.5×	119 2.6×	75 1.9×	20 1.2×	20	348
Marie des Georges France	15	463 1.5×	102 1.6×	104 2.3×	108 2.7×	37 2.2×	23	573
Federico Cresta Italy	13	268 0.9×	21 0.3×	50 1.1×	10 0.3×	22 1.3×	27	343
David Waltz United States	7	603 1.9×	31 0.5×	105 2.3×	32 0.8×	22 1.3×	11	648
Whitney Wolf United States	5	172 0.6×	15 0.2×	61 1.4×	82 2.0×	31 1.8×	12	243
Juliet Scully United Kingdom	5	117 0.4×	9 0.1×	30 0.7×	50 1.3×	7 0.4×	6	274
Marc A. Sala United States	7	111 0.4×	10 0.2×	33 0.7×	8 0.2×	7 0.4×	14	173
Sofìa Kitsiou Greece	10	38 0.1×	14 0.2×	71 1.6×	155 3.9×	33 1.9×	25	260
Erica Sanford Kobayashi United States	10	47 0.2×	13 0.2×	95 2.1×	183 4.6×	30 1.8×	22	293
Adrianne K. Crooke United States	5	112 0.4×	6 0.1×	55 1.2×	18 0.5×	40 2.4×	5	170

Countries citing papers authored by Brigitte Wulf

Since Specialization

Citations

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

Fields of papers citing papers by Brigitte Wulf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brigitte Wulf

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

Dörk, Thilo, Frauke Mekus, Karen Schmidt, et al.. (1994). Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients. Human Genetics. 94(5). 533–542. 71 indexed citations

2.

Fislage, Rainer, et al.. (1994). Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations. Human Genetics. 93(1). 67–73. 41 indexed citations

3.

Tümmler, Burkhard, Thilo Dörk, Rainer Fislage, et al.. (1993). Cystic fibrosis: the impact of analytical technology for genotype-phenotype studies. Clinica Chimica Acta. 217(1). 23–28. 3 indexed citations

4.

Dörk, Thilo, Ulrich Wulbrand, Nanette Kälin, et al.. (1993). Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis. The Lancet. 341(8839). 189–193. 79 indexed citations

5.

Dörk, Thilo, Thomas Neumann, Ulrich Wulbrand, et al.. (1992). Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families. Human Genetics. 88(4). 417–425. 58 indexed citations

6.

Stuhrmann, Manfred, Thilo Dörk, Michael Krawczak, et al.. (1991). Genotype-Phenotype Correlations in Cystic Fibrosis Patients. Advances in experimental medicine and biology. 290. 97–103. 3 indexed citations

7.

Dörk, Thilo, Ulrich Wulbrand, Thomas Richter, et al.. (1991). Cystic fibrosis with three mutations in the cystic fibrosis transmembrane regulator gene. 1 indexed citations

8.

Wulbrand, Ulrich, et al.. (1991). Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene. Human Genetics. 87(4). 441–6. 87 indexed citations

9.

Hundrieser, J., Frank Peinemann, Manfred Stuhrmann, et al.. (1990). Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patients. Human Genetics. 85(4). 409–410. 10 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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