Hannie Douben

1.1k total citations
25 papers, 644 citations indexed

About

Hannie Douben is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Hannie Douben has authored 25 papers receiving a total of 644 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 9 papers in Surgery. Recurrent topics in Hannie Douben's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital Diaphragmatic Hernia Studies (5 papers) and Prenatal Screening and Diagnostics (5 papers). Hannie Douben is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital Diaphragmatic Hernia Studies (5 papers) and Prenatal Screening and Diagnostics (5 papers). Hannie Douben collaborates with scholars based in Netherlands, United States and Italy. Hannie Douben's co-authors include Annelies de Klein, Dick Tibboel, Ronald R. de Krijger, Pino J. Poddighe, Carla C. Baan, Willem Weimar, Natascha Goemaere, Patricia K. Donahoe, Alexander T. den Dekker and R. J. H. Galjaard and has published in prestigious journals such as PLoS ONE, Kidney International and The American Journal of Human Genetics.

In The Last Decade

Hannie Douben

25 papers receiving 626 citations

Peers

Hannie Douben

SURGE

GENET

PRM

GENET

Moise Danielpour United States

Yves Lacassie United States

Serena Redaelli Italy

Yolande van Bever Netherlands

Pamela Brock United States

Isabella Torrente Italy

Rodger Palmer United Kingdom

Caroline Astbury United States

Elisa Tassano Italy

Heather J. Stalker United States

Moise Danielpour United States

Hannie Douben

174 ×0.6

182 ×0.8

SURGE

152 ×0.8

GENET

89 ×0.6

PRM

93 ×1.0

GENET

Citations per year, relative to Hannie Douben Hannie Douben (= 1×) peers Moise Danielpour

Countries citing papers authored by Hannie Douben

Since Specialization

Citations

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

Fields of papers citing papers by Hannie Douben

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hannie Douben

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

Douben, Hannie, Marianne Hoogeveen‐Westerveld, Mark Nellist, et al.. (2023). Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome. Human Mutation. 2023. 1–14. 2 indexed citations

Groen, Stijn L.M. in ‘t, Johanna M. P. van den Hout, Hannie Douben, et al.. (2020). Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis. Molecular Therapy — Methods & Clinical Development. 17. 337–348. 13 indexed citations

Sukenik‐Halevy, Rivka, Hannie Douben, Deon J. Venter, et al.. (2018). A point mutation in the pre-ZRS disrupts sonic hedgehog expression in the limb bud and results in triphalangeal thumb–polysyndactyly syndrome. Genetics in Medicine. 20(11). 1405–1413. 22 indexed citations

Barakat, Tahsin Stefan, Mehrnaz Ghazvini, Tracy Li, et al.. (2015). Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells. Stem Cell Reports. 4(2). 199–208. 35 indexed citations

Graav, Gretchen N. de, Dennis A. Hesselink, M. Dieterich, et al.. (2015). An Acute Cellular Rejection With Detrimental Outcome Occurring Under Belatacept-Based Immunosuppressive Therapy. Transplantation. 100(5). 1111–1119. 25 indexed citations

Esch, Celine de, Mehrnaz Ghazvini, Friedemann Loos, et al.. (2014). Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation. Stem Cell Reports. 3(4). 548–555. 44 indexed citations

Hopman, Saskia, Johannes H. M. Merks, Hannie Douben, et al.. (2013). Structural genome variations in individuals with childhood cancer and tumour predisposition syndromes. European Journal of Cancer. 49(9). 2170–2178. 5 indexed citations

Rhijn, M. Roemeling-van, Annelies de Klein, Hannie Douben, et al.. (2013). Culture expansion induces non-tumorigenic aneuploidy in adipose tissue-derived mesenchymal stromal cells. Cytotherapy. 15(11). 1352–1361. 35 indexed citations

Rhijn, M. Roemeling-van, Marlies E. J. Reinders, Annelies de Klein, et al.. (2012). Mesenchymal stem cells derived from adipose tissue are not affected by renal disease. Kidney International. 82(7). 748–758. 45 indexed citations

10.

Tandefelt, Delila Gasi, Hetty A. van der Korput, Hannie Douben, et al.. (2011). Overexpression of Full-Length ETV1 Transcripts in Clinical Prostate Cancer Due to Gene Translocation. PLoS ONE. 6(1). e16332–e16332. 25 indexed citations

11.

Steegers‐Theunissen, Régine P.M., et al.. (2011). Comparable levels of folate-induced aneusomy in B-lymphoblasts from oral-cleft patients and controls. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 741(1-2). 76–80. 1 indexed citations

12.

Veenma, Danielle, Erwin Brosens, Cornelis P. van de Ven, et al.. (2011). Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts. European Journal of Human Genetics. 20(3). 298–304. 22 indexed citations

13.

Veken, Lars T. van der, Hannie Douben, Raoul van de Graaf, et al.. (2010). Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies. Molecular Cytogenetics. 3(1). 13–13. 33 indexed citations

14.

Oegema, Renske, Annelies de Klein, Annemieke J.M.H. Verkerk, et al.. (2010). Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A. Molecular Syndromology. 1(3). 113–120. 39 indexed citations

15.

Veenma, Danielle, Hannie Douben, Bert Eussen, et al.. (2010). Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient. PLoS ONE. 5(12). e15348–e15348. 10 indexed citations

16.

Jong, Elisabeth M. de, Hannie Douben, Janine F. Felix, et al.. (2010). 5q11.2 deletion in a patient with tracheal agenesis. European Journal of Human Genetics. 18(11). 1265–1268. 27 indexed citations

17.

Mensink, Hanneke W., Emine Kılıç, Jolanda Vaarwater, et al.. (2008). Molecular cytogenetic analysis of archival uveal melanoma with known clinical outcome. Cancer Genetics and Cytogenetics. 181(2). 108–111. 26 indexed citations

18.

Meester‐Smoor, Magda A., Marjolein J. F. W. Janssen, Gerard C. Grosveld, et al.. (2008). MN1 affects expression of genes involved in hematopoiesis and can enhance as well as inhibit RAR/RXR-induced gene expression. Carcinogenesis. 29(10). 2025–2034. 24 indexed citations

19.

Eussen, Bert H.J., Ingrid M.B.H. van de Laar, Hannie Douben, et al.. (2006). A familial inverted duplication 2q33–q34 identified and delineated by multiple cytogenetic techniques. European Journal of Medical Genetics. 50(2). 112–119. 8 indexed citations

20.

Klaassens, Merel, Marieke van Dooren, H. J. Eussen, et al.. (2005). Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization. The American Journal of Human Genetics. 76(5). 877–882. 113 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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