Daphne Heijsman

943 total citations
11 papers, 221 citations indexed

About

Daphne Heijsman is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Daphne Heijsman has authored 11 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Daphne Heijsman's work include Aortic Disease and Treatment Approaches (3 papers), Aortic aneurysm repair treatments (3 papers) and Connective tissue disorders research (2 papers). Daphne Heijsman is often cited by papers focused on Aortic Disease and Treatment Approaches (3 papers), Aortic aneurysm repair treatments (3 papers) and Connective tissue disorders research (2 papers). Daphne Heijsman collaborates with scholars based in Netherlands, Belgium and United States. Daphne Heijsman's co-authors include Daniëlle Majoor‐Krakauer, Jaap I. van Waning, Eric Boersma, Andreas Kremer, Peter J. van der Spek, Arne IJpma, Hans Stroink, Cathryn Poulton, Rachel Schot and Jeannette Hoogeboom and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cardiovascular Research and Journal of Vascular Surgery.

In The Last Decade

Daphne Heijsman

10 papers receiving 220 citations

Peers

Countries citing papers authored by Daphne Heijsman

Since Specialization

Citations

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

Fields of papers citing papers by Daphne Heijsman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daphne Heijsman

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Increased risk for thoracic aneurysms in female and familial abdominal aortic aneurysm patients 2025 ·Journal of Vascular Surgery ·(unknown), Jorg L. de Bruin, Arne IJpma, (unknown), Daphne Heijsman, (unknown), (unknown), Hennie T. Brüggenwirth, Jolien W. Roos‐Hesselink, Sander Ten Raa, (unknown), (unknown), Heleen M.M. van Beusekom, Daniëlle Majoor‐Krakauer	0
2	The proprotein convertase FURIN is a novel aneurysm predisposition gene impairing TGF-β signalling 2024 ·Cardiovascular Research ·Zongsheng He, Arne IJpma, Dianne Vreeken, Daphne Heijsman, (unknown), Hence J.M. Verhagen, Jorg L. de Bruin, Hennie T. Brüggenwirth, Jolien W. Roos‐Hesselink, Jos A. Bekkers, Danny Huylebroeck, Heleen M.M. van Beusekom, John W.M. Creemers, Daniëlle Majoor‐Krakauer	2
3	Systematic Review of Genotype‐Phenotype Correlations in Noncompaction Cardiomyopathy 2019 ·Journal of the American Heart Association ·Jaap I. van Waning, (unknown), Daphne Heijsman, Eric Boersma, Daniëlle Majoor‐Krakauer	62
4	FLNC Missense Variants in Familial Noncompaction Cardiomyopathy 2019 ·SHILAP Revista de lepidopterología ·Jaap I. van Waning, Yvonne M. Hoedemaekers, (unknown), (unknown), Daphne Heijsman, Kadir Çalişkan, Elke S. Hoendermis, Tineke P. Willems, Arthur van den Wijngaard, Albert J.H. Suurmeijer, Marjon van Slegtenhorst, Jan D.H. Jongbloed, Daniëlle Majoor‐Krakauer, (unknown)	3
5	First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm 2015 ·Human Genetics ·Koen M. van de Luijtgaarden, Daphne Heijsman, Alessandra Maugeri, Marjan M. Weiss, Hence J.M. Verhagen, Arne IJpma, Hennie T. Brüggenwirth, Daniëlle Majoor‐Krakauer	27
6	Tumor-specific mutations in low-frequency genes affect their functional properties 2015 ·Journal of Neuro-Oncology ·Lale Erdem‐Eraslan, Daphne Heijsman, Maurice de Wit, Andreas Kremer, Andrea Sacchetti, Peter J. van der Spek, Peter A.E. Sillevis Smitt, Pim J. French	10
7	Differential Gene Expression of the Intermediate and Outer Interzone Layers of Developing Articular Cartilage in Murine Embryos 2014 ·Stem Cells and Development ·Florien Jenner, Arne IJpma, (unknown), Daphne Heijsman, Roberto Narcisi, Peter J. van der Spek, Andreas Kremer, René van Weeren, Pieter A.J. Brama, Gerjo J.V.M. van Osch	22
8	Pollitt syndrome patients carry mutation in TTDN1 2014 ·Meta Gene ·Sigrid Swagemakers, Nicolaas G.J. Jaspers, Anja Raams, Daphne Heijsman, Wim Vermeulen, Christine Troelstra, Andreas Kremer, Stephen E. Lincoln, Rick Tearle, Jan H.J. Hoeijmakers, Peter J. van der Spek	4
9	Boston type craniosynostosis: Report of a second mutation in MSX2 2013 ·American Journal of Medical Genetics Part A ·(unknown), Annemieke J.M.H. Verkerk, (unknown), A. Jeannette M. Hoogeboom, Sigrid M. A. Swagemakers, Andreas Kremer, Daphne Heijsman, Maarten H. Lequin, Irene M.J. Mathijssen, Peter J. van der Spek	21
10	Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations 2012 ·Neurogenetics ·Cathryn Poulton, Renske Oegema, Daphne Heijsman, Jeannette Hoogeboom, Rachel Schot, Hans Stroink, Michèl A.A.P. Willemsen, Frans W. Verheijen, Peter J. van der Spek, Andreas Kremer, Grazia M.S. Mancini	55
11	Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection 2012 ·PubMed ·Andrew Stubbs, Elizabeth McClellan, (unknown), Saskia Hiltemann, (unknown), (unknown), Anton H. J. Koning, (unknown), Joke Reumers, Daphne Heijsman, Sigrid M. A. Swagemakers, Andreas Kremer, Jules P.P. Meijerink, Diether Lambrechts, Peter J. van der Spek	15

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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