Hannie Douben

1.1k citations

25 papers · 644 indexed · h-index 16

Developmental Biology top 10%
Genetics top 10%
- Genomic variations and chromosomal abnormalities 9
- Mesenchymal stem cell research 2
Transplantation top 10%
Genetics top 10%
- Genomic variations and chromosomal abnormalities 9
- Mesenchymal stem cell research 2
Surgery
- Congenital Diaphragmatic Hernia Studies 5
- Tissue Engineering and Regenerative Medicine 2
- Esophageal and GI Pathology 2
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 5
Molecular Biology
- Congenital heart defects research 5
Pulmonary and Respiratory Medicine
- Tracheal and airway disorders 5

Co-authors: Annelies de Klein Dick Tibboel Ronald R. de Krijger Pino J. Poddighe Carla C. Baan Willem Weimar Natascha Goemaere Patricia K. Donahoe
Cited by: Developmental Biology Genetics Transplantation
Journals: PLoS ONE (2 papers)Kidney International (1 paper)The American Journal of Human Genetics (1 paper)
Partner nations: Netherlands United States Italy

In The Last Decade

Hannie Douben

25 papers receiving 626 citations

Peers

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

The 25 scholars most cited alongside Hannie Douben, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hannie Douben Line = papers co-authored together Hannie Douben links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Functional Assays Combined with Pre-mRNA-Splicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome Human Mutation ·Hannie Douben,Marianne Hoogeveen‐Westerveld,Mark Nellist,Jesse Louwen,Marian Kroos-de Haan,Mattijs Punt,Babeth van Ommeren,Leontine van Unen,Peter Elfferich,Esmee Kasteleijn,Yolande van Bever,Margreethe van Vliet,Rianne Oostenbrink,Jasper J. Saris,Anja Wagner,Yvette van Ierland,Tjakko J. van Ham,Rick van Minkelen	2023	2
2	Novel GAA Variants and Mosaicism in Pompe Disease Identified by Extended Analyses of Patients with an Incomplete DNA Diagnosis Molecular Therapy — Methods & Clinical Development ·Stijn L.M. in ‘t Groen,Douglas Oliveira Soares de Faria,Alessandro Iuliano,Johanna M. P. van den Hout,Hannie Douben,Trijnie Dijkhuizen,David Cassiman,Peter Witters,Miguel‐Ángel Barba Romero,Annelies de Klein,Galhana M. Somers‐Bolman,Jasper J. Saris,Lies H. Hoefsloot,Ans T. van der Ploeg,Atze J. Bergsma,W.W.M. Pim Pijnappel	2020	13
3	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 ·Jacob W. P. Potuijt,Martijn Baas,Rivka Sukenik‐Halevy,Hannie Douben,Picard Nguyen,Deon J. Venter,Renée Gallagher,Sigrid Swagemakers,Steven E.R. Hovius,Christianne A. van Nieuwenhoven,Robert‐Jan H. Galjaard,Peter J. van der Spek,Nadav Ahituv,Annelies de Klein	2018	22
4	Stable X Chromosome Reactivation in Female Human Induced Pluripotent Stem Cells Stem Cell Reports ·Tahsin Stefan Barakat,Mehrnaz Ghazvini,Bas de Hoon,Tracy Li,Bert Eussen,Hannie Douben,Reinier van der Linden,Nathalie van der Stap,Marjan Boter,Joop S.E. Laven,Robert‐Jan Galjaard,J. Anton Grootegoed,Annelies de Klein,Joost Gribnau	2015	35
5	An Acute Cellular Rejection With Detrimental Outcome Occurring Under Belatacept-Based Immunosuppressive Therapy Transplantation ·Gretchen N. de Graav,Dennis A. Hesselink,M. Dieterich,Rens Kraaijeveld,Hannie Douben,Annelies de Klein,Dave L. Roelen,Willem Weimar,Joke I. Roodnat,Marian C. Clahsen‐van Groningen,Carla C. Baan	2015	25
6	Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation Stem Cell Reports ·Celine de Esch,Mehrnaz Ghazvini,Friedemann Loos,Nune Schelling-Kazaryan,W. Widagdo,Shashini T. Munshi,Erik van der Wal,Hannie Douben,Nilhan Gunhanlar,Steven A. Kushner,W.W.M. Pim Pijnappel,Femke M.S. de Vrij,Niels Geijsen,Joost Gribnau,Rob Willemsen	2014	44
7	Structural genome variations in individuals with childhood cancer and tumour predisposition syndromes European Journal of Cancer ·Saskia Hopman,Johannes H. M. Merks,Hubertus Eussen,Hannie Douben,Simone Snijder,Raoul C. M. Hennekam,Annelies de Klein,Huib N. Caron	2013	5
8	Culture expansion induces non-tumorigenic aneuploidy in adipose tissue-derived mesenchymal stromal cells Cytotherapy ·M. Roemeling-van Rhijn,Annelies de Klein,Hannie Douben,Qiuwei Pan,Luc J. W. van der Laan,Jan N.M. IJzermans,Michiel G.H. Betjes,Carla C. Baan,Willem Weimar,Martin J. Hoogduijn	2013	35
9	Mesenchymal stem cells derived from adipose tissue are not affected by renal disease Kidney International ·M. Roemeling-van Rhijn,Marlies E. J. Reinders,Annelies de Klein,Hannie Douben,Sander S. Korevaar,F. Mensah,Frank J. M. F. Dor,Jan N.M. IJzermans,Michiel G.H. Betjes,Carla C. Baan,Willem Weimar,Martin J. Hoogduijn	2012	45
10	Overexpression of Full-Length ETV1 Transcripts in Clinical Prostate Cancer Due to Gene Translocation PLoS ONE ·Delila Gasi Tandefelt,Hetty A. van der Korput,Hannie Douben,Annelies de Klein,Corrina M. de Ridder,Wytske M. van Weerden,Jan Trapman	2011	25
11	Comparable levels of folate-induced aneusomy in B-lymphoblasts from oral-cleft patients and controls Mutation Research/Genetic Toxicology and Environmental Mutagenesis ·Bart J. B. Bliek,Régine P.M. Steegers‐Theunissen,Hannie Douben,Jan Lindemans,Eric A.P. Steegers,Annelies de Klein	2011	1
12	Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts European Journal of Human Genetics ·Danielle Veenma,Erwin Brosens,Elisabeth de Jong,Cornelis P. van de Ven,Connie Meeussen,Titia E. Cohen‐Overbeek,Marjan Boter,Hubertus Eussen,Hannie Douben,Dick Tibboel,Annelies de Klein	2011	22
13	Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies Molecular Cytogenetics ·Lars T. van der Veken,Marianne MJ Dieleman,Hannie Douben,Judith C van de Brug,Raoul van de Graaf,A. Jeannette M. Hoogeboom,Pino J. Poddighe,Annelies de Klein	2010	33
14	Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A Molecular Syndromology ·Renske Oegema,Annelies de Klein,Annemieke J.M.H. Verkerk,Rachel Schot,Belinda Dumee,Hannie Douben,Bert Eussen,L. Dubbel,Pino J. Poddighe,I. van der Laar,William B. Dobyns,Peter J. van der Spek,Maarten H. Lequin,I.F.M. de Coo,Marie‐Claire Y. de Wit,M.W. Wessels,Grazia M.S. Mancini	2010	39
15	Comparable Low-Level Mosaicism in Affected and Non Affected Tissue of a Complex CDH Patient PLoS ONE ·Danielle Veenma,Niels Beurskens,Hannie Douben,Bert Eussen,Petra Noomen,Lutgarde Govaerts,E. W. M. Grijseels,Maarten H. Lequin,Ronald R. de Krijger,Dick Tibboel,Annelies de Klein,Diane Van Opstal	2010	10
16	5q11.2 deletion in a patient with tracheal agenesis European Journal of Human Genetics ·Elisabeth M. de Jong,Hannie Douben,Bert Eussen,Janine F. Felix,Marja W. Wessels,Pino J. Poddighe,Peter G. J. Nikkels,Ronald R. de Krijger,Dick Tibboel,Annelies de Klein	2010	27
17	Molecular cytogenetic analysis of archival uveal melanoma with known clinical outcome Cancer Genetics and Cytogenetics ·Hanneke W. Mensink,Emine Kılıç,Jolanda Vaarwater,Hannie Douben,Dion Paridaens,Annelies de Klein	2008	26
18	MN1 affects expression of genes involved in hematopoiesis and can enhance as well as inhibit RAR/RXR-induced gene expression Carcinogenesis ·Magda A. Meester‐Smoor,Marjolein J. F. W. Janssen,Gerard C. Grosveld,Annelies de Klein,Wilfred F. J. van IJcken,Hannie Douben,Ellen C. Zwarthoff	2008	24
19	A familial inverted duplication 2q33–q34 identified and delineated by multiple cytogenetic techniques European Journal of Medical Genetics ·Bert H.J. Eussen,Ingrid M.B.H. van de Laar,Hannie Douben,Leo van Kempen,Ron Hochstenbach,de Man,Diane Van Opstal,Annelies de Klein,Pino J. Poddighe	2006	8
20	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 ·Merel Klaassens,Marieke van Dooren,H. J. Eussen,Hannie Douben,Alexander T. den Dekker,Cliff Lee,Patricia K. Donahoe,R. J. H. Galjaard,Natascha Goemaere,Ronald R. de Krijger,Carine Wouters,J. Wauters,Ben A. Oostra,Dick Tibboel,Annelies de Klein	2005	113

About Hannie Douben

Hannie Douben is a scholar working on Developmental Biology, Genetics and Transplantation, having authored 25 papers that have together received 644 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Congenital Diaphragmatic Hernia Studies (5 papers), Prenatal Screening and Diagnostics (5 papers), Congenital heart defects research (5 papers), Tracheal and airway disorders (5 papers), Mesenchymal stem cell research (2 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Esophageal and GI Pathology (2 papers). The work is most often cited by research in Developmental Biology (21 citations), Genetics (96 citations) and Transplantation (23 citations). Hannie Douben has collaborated with scholars based in Netherlands, United States and Italy. Frequent 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. Their work appears in journals such as PLoS ONE, Kidney International and The American Journal of Human Genetics.

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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