Kaman Wu

477 total citations
2 papers, 112 citations indexed

About

Kaman Wu is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Kaman Wu has authored 2 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Pulmonary and Respiratory Medicine, 2 papers in Genetics and 1 paper in Molecular Biology. Recurrent topics in Kaman Wu's work include Cystic Fibrosis Research Advances (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Genetic Syndromes and Imprinting (1 paper). Kaman Wu is often cited by papers focused on Cystic Fibrosis Research Advances (2 papers), Genetic and Kidney Cyst Diseases (2 papers) and Genetic Syndromes and Imprinting (1 paper). Kaman Wu collaborates with scholars based in Netherlands, Germany and Kuwait. Kaman Wu's co-authors include Miriam Schmidts, Claudius Werner, Heymut Omran, Zeineb Bakey, Inga M. Höben, Dimitra Micha, Eric G. Haarman, Isabella Aprea, Gerard Pals and Gerard W. Dougherty and has published in prestigious journals such as The American Journal of Human Genetics and European Journal of Medical Genetics.

In The Last Decade

Kaman Wu

2 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kaman Wu Netherlands	2	74	55	51	18	10	2	112
Sandra Cindrić Germany	5	77 1.0×	75 1.4×	62 1.2×	17 0.9×	14 1.4×	9	142
Anita Becker-Heck Germany	2	102 1.4×	75 1.4×	78 1.5×	17 0.9×	15 1.5×	3	148
Katarzyna Voelkel Poland	6	110 1.5×	117 2.1×	74 1.5×	12 0.7×	21 2.1×	8	180
Inga M. Höben Germany	3	104 1.4×	74 1.3×	69 1.4×	23 1.3×	19 1.9×	5	163
Mellisa Dixon United Kingdom	7	133 1.8×	167 3.0×	71 1.4×	15 0.8×	17 1.7×	9	233
Tabea Nöthe-Menchen Germany	4	78 1.1×	44 0.8×	44 0.9×	13 0.7×	28 2.8×	5	127
Jörg Müsebeck Germany	5	48 0.6×	16 0.3×	72 1.4×	51 2.8×	14 1.4×	5	165
Michelle Steinraths Canada	8	104 1.4×	23 0.4×	60 1.2×	6 0.3×	60 6.0×	12	168
Isabella Aprea Germany	5	143 1.9×	99 1.8×	89 1.7×	30 1.7×	36 3.6×	7	231
Pauline Marzin France	7	79 1.1×	8 0.1×	62 1.2×	8 0.4×	15 1.5×	14	120

Countries citing papers authored by Kaman Wu

Since Specialization

Citations

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

Fields of papers citing papers by Kaman Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaman Wu

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

All Works

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2 of 2 papers shown

1.

Antony, Dinu, Narayanan Nampoory, Chiara Bacchelli, et al.. (2017). Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature. European Journal of Medical Genetics. 60(12). 658–666. 10 indexed citations

2.

Paff, Tamara, Niki T. Loges, Isabella Aprea, et al.. (2016). Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects. The American Journal of Human Genetics. 100(1). 160–168. 102 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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