Gerard W. Dougherty

4.5k total citations
25 papers, 1.0k citations indexed

About

Gerard W. Dougherty is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gerard W. Dougherty has authored 25 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 11 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gerard W. Dougherty's work include Genetic and Kidney Cyst Diseases (14 papers), Cystic Fibrosis Research Advances (10 papers) and Neonatal Respiratory Health Research (4 papers). Gerard W. Dougherty is often cited by papers focused on Genetic and Kidney Cyst Diseases (14 papers), Cystic Fibrosis Research Advances (10 papers) and Neonatal Respiratory Health Research (4 papers). Gerard W. Dougherty collaborates with scholars based in Germany, United States and Italy. Gerard W. Dougherty's co-authors include Heymut Omran, Heike Olbrich, Niki T. Loges, Mary Lou Cutler, Petra Pennekamp, Claudius Werner, Johanna Raidt, Julia Wallmeier, Mario Gimona and Tabea Menchen and has published in prestigious journals such as Developmental Cell, The American Journal of Human Genetics and European Respiratory Journal.

In The Last Decade

Gerard W. Dougherty

24 papers receiving 999 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gerard W. Dougherty Germany	17	437	419	384	187	95	25	1.0k
Ross Kettleborough United Kingdom	10	225 0.5×	659 1.6×	165 0.4×	329 1.8×	30 0.3×	11	1.2k
Gregory B. Vanden Heuvel United States	20	470 1.1×	1.1k 2.6×	124 0.3×	65 0.3×	69 0.7×	35	1.6k
Petra Pennekamp Germany	22	1.1k 2.6×	1.1k 2.7×	500 1.3×	218 1.2×	192 2.0×	51	2.1k
Miriam Schmidts Germany	19	931 2.1×	990 2.4×	367 1.0×	251 1.3×	164 1.7×	49	1.8k
Debora Bogani United Kingdom	22	615 1.4×	1.2k 2.9×	109 0.3×	324 1.7×	52 0.5×	29	1.6k
Bénédicte Duriez France	17	724 1.7×	698 1.7×	291 0.8×	69 0.4×	111 1.2×	25	1.5k
B. Lowell Langille Canada	8	189 0.4×	1.3k 3.0×	104 0.3×	113 0.6×	47 0.5×	8	1.6k
Brian P. Hackett United States	18	359 0.8×	726 1.7×	504 1.3×	77 0.4×	89 0.9×	24	1.2k
Elena Prigmore United Kingdom	18	758 1.7×	742 1.8×	46 0.1×	93 0.5×	164 1.7×	27	1.4k
Bishwanath Chatterjee United States	20	290 0.7×	781 1.9×	225 0.6×	97 0.5×	36 0.4×	50	1.1k

Countries citing papers authored by Gerard W. Dougherty

Since Specialization

Citations

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

Fields of papers citing papers by Gerard W. Dougherty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerard W. Dougherty. 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 Gerard W. Dougherty. The network helps show where Gerard W. Dougherty may publish in the future.

Co-authorship network of co-authors of Gerard W. Dougherty

This figure shows the co-authorship network connecting the top 25 collaborators of Gerard W. Dougherty. A scholar is included among the top collaborators of Gerard W. Dougherty 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 Gerard W. Dougherty. Gerard W. Dougherty 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

Wohlgemuth, Kai, Niki T. Loges, Johanna Raidt, et al.. (2024). Pathogenic variants inCFAP46,CFAP54,CFAP74andCFAP221cause primary ciliary dyskinesia with a defective C1d projection of the central apparatus. European Respiratory Journal. 64(6). 2400790–2400790. 1 indexed citations

Hjeij, Rim, Isabella Aprea, Marco Poeta, et al.. (2023). Pathogenic variants in CLXN encoding the outer dynein arm docking–associated calcium-binding protein calaxin cause primary ciliary dyskinesia. Genetics in Medicine. 25(5). 100798–100798. 6 indexed citations

Aprea, Isabella, Claudia Krallmann, Tabea Nöthe-Menchen, et al.. (2023). Pathogenic gene variants in CCDC39, CCDC40, RSPH1, RSPH9, HYDIN, and SPEF2 cause defects of sperm flagella composition and male infertility. Frontiers in Genetics. 14. 1117821–1117821. 18 indexed citations

Wallmeier, Julia, Hessa S. Alsaif, Gerard W. Dougherty, et al.. (2021). Mutations in TP73 cause impaired mucociliary clearance and lissencephaly. The American Journal of Human Genetics. 108(7). 1318–1329. 21 indexed citations

Hjeij, Rim, Isabella Aprea, Heike Olbrich, Gerard W. Dougherty, & Heymut Omran. (2021). Defects in outer dynein arm docking machinery cause primary ciliary dyskinesia. OA1612–OA1612.

Alfieri, Mariaevelina, Daniela Iaconis, Roberta Tammaro, et al.. (2020). The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progression. Tissue and Cell. 64. 101369–101369. 13 indexed citations

Cindrić, Sandra, Gerard W. Dougherty, Heike Olbrich, et al.. (2019). SPEF2- and HYDIN -Mutant Cilia Lack the Central Pair–associated Protein SPEF2, Aiding Primary Ciliary Dyskinesia Diagnostics. American Journal of Respiratory Cell and Molecular Biology. 62(3). 382–396. 49 indexed citations

Werner, Claudius, et al.. (2018). Comparison of Nocturnal Cough Analysis in Healthy Subjects and in Patients with Cystic Fibrosis and Primary Ciliary Dyskinesia: A Prospective Observational Study. Respiration. 97(1). 60–69. 12 indexed citations

Edelbusch, Christine, Sandra Cindrić, Gerard W. Dougherty, et al.. (2017). Mutation of serine/threonine protein kinase 36 ( STK36 ) causes primary ciliary dyskinesia with a central pair defect. Human Mutation. 38(8). 964–969. 49 indexed citations

10.

Sigg, Monika Abedin, Tabea Menchen, Chanjae Lee, et al.. (2017). Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling Pathways. Developmental Cell. 43(6). 744–762.e11. 70 indexed citations

11.

Amirav, Israel, Julia Wallmeier, Niki T. Loges, et al.. (2016). Systematic Analysis ofCCNOVariants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis. Human Mutation. 37(4). 396–405. 62 indexed citations

12.

Olbrich, Heike, Niki T. Loges, Claudius Werner, et al.. (2015). Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex. The American Journal of Human Genetics. 97(4). 546–554. 84 indexed citations

13.

Raidt, Johanna, Claudius Werner, Tabea Menchen, et al.. (2015). Ciliary function and motor protein composition of human fallopian tubes. Human Reproduction. 30(12). 2871–2880. 71 indexed citations

14.

Raidt, Johanna, Julia Wallmeier, Rim Hjeij, et al.. (2014). Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. European Respiratory Journal. 44(6). 1579–1588. 123 indexed citations

15.

Dougherty, Gerard W., Cynthia C. Jose, Mario Gimona, & Mary Lou Cutler. (2008). The Rsu-1-PINCH1-ILK complex is regulated by Ras activation in tumor cells. European Journal of Cell Biology. 87(8-9). 721–734. 67 indexed citations

16.

Dougherty, Gerard W., et al.. (2005). The Ras suppressor Rsu-1 binds to the LIM 5 domain of the adaptor protein PINCH1 and participates in adhesion-related functions. Experimental Cell Research. 306(1). 168–179. 68 indexed citations

17.

Dougherty, Gerard W., Henry J. Adler, Agnieszka Rzadzinska, et al.. (2005). CLAMP, a novel microtubule-associated protein with EB-type calponin homology. Cell Motility and the Cytoskeleton. 62(3). 141–156. 31 indexed citations

18.

Adler, Henry J., et al.. (2003). Expression of prestin, a membrane motor protein, in the mammalian auditory and vestibular periphery. Hearing Research. 184(1-2). 27–40. 51 indexed citations

19.

Dougherty, Gerard W., et al.. (2002). Identification of an Alternatively Spliced RNA for the Ras Suppressor RSU-1 in Human Gliomas. Journal of Neuro-Oncology. 60(3). 201–211. 20 indexed citations

20.

Vasaturo, Fortunata, Gerard W. Dougherty, & Mary Lou Cutler. (2000). Ectopic expression of Rsu-1 results in elevation of p21CIP and inhibits anchorage-independent growth of MCF7 breast cancer cells. Breast Cancer Research and Treatment. 61(1). 69–78. 31 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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