Danielle Veenma

843 total citations
18 papers, 450 citations indexed

About

Danielle Veenma is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Danielle Veenma has authored 18 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Surgery, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Danielle Veenma's work include Congenital Diaphragmatic Hernia Studies (11 papers), Tracheal and airway disorders (5 papers) and Congenital heart defects research (4 papers). Danielle Veenma is often cited by papers focused on Congenital Diaphragmatic Hernia Studies (11 papers), Tracheal and airway disorders (5 papers) and Congenital heart defects research (4 papers). Danielle Veenma collaborates with scholars based in Netherlands, United States and Canada. Danielle Veenma's co-authors include Annelies de Klein, Dick Tibboel, Titia E. Cohen‐Overbeek, Daryl A. Scott, Johannes J. Duvekot, John J. Greer, Régine P.M. Steegers‐Theunissen, Jan Lindemans, Kevin P. Lally and Anita C. S. Hokken‐Koelega and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

Danielle Veenma

18 papers receiving 444 citations

Peers

Danielle Veenma

SURGE

PRM

GENET

EDM

Man‐Ting So Hong Kong

Laurence Perrin France

Roberta Villa Italy

Michael Muchow United States

Ye Jee Shim South Korea

Elodie Tron France

Maria‐Mercè Garcia‐Barceló Hong Kong

Judith M.A. Verhagen Netherlands

Melanie Jäger Germany

Naoaki Hori Japan

Man‐Ting So Hong Kong

Danielle Veenma

439 ×1.6

SURGE

85 ×0.4

PRM

163 ×1.0

225 ×2.0

GENET

11 ×0.3

EDM

Citations per year, relative to Danielle Veenma Danielle Veenma (= 1×) peers Man‐Ting So

Countries citing papers authored by Danielle Veenma

Since Specialization

Citations

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

Fields of papers citing papers by Danielle Veenma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle Veenma

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

All Works

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18 of 18 papers shown

Cheung, J., Geeske M. van Woerden, & Danielle Veenma. (2024). CAMK2; four genes, one syndrome? Delineation of genotype–phenotype correlations. Current Opinion in Neurobiology. 90. 102935–102935. 1 indexed citations

Brosens, Erwin, N. Peters, Rutger W. W. Brouwer, et al.. (2022). Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge. Frontiers in Pediatrics. 9. 800915–800915. 11 indexed citations

Dwyer, Bonnie K., Danielle Veenma, Kiki Chang, Howard Schulman, & Geeske M. van Woerden. (2022). Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys). Frontiers in Pharmacology. 13. 794008–794008. 6 indexed citations

Weerts, Marjolein J.A., Danielle Veenma, Carsten R. Lincke, et al.. (2022). 5q35 duplication syndrome: Narrowing the critical region on the distal side and further evidence of intrafamilial variability and expression. American Journal of Medical Genetics Part A. 191(3). 835–841. 3 indexed citations

Luca, Stephanie, Gregory Costain, Maria Marano, et al.. (2021). Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective?. Journal of Genetic Counseling. 31(2). 523–533. 9 indexed citations

Goverde, Anne, Fernanda Sarquis Jehee, Erwin Brosens, et al.. (2021). Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?. Frontiers in Pediatrics. 9. 8 indexed citations

Veenma, Danielle, Dawn Cordeiro, Neal Sondheimer, & Saadet Mercimek‐Andrews. (2018). DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis. European Journal of Human Genetics. 26(12). 1867–1870. 21 indexed citations

Wat, Margaret, T. Beck, Andrés Hernández, et al.. (2012). Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1. Human Molecular Genetics. 21(18). 4115–4125. 64 indexed citations

Beck, T., Danielle Veenma, Oleg A. Shchelochkov, et al.. (2012). Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Human Molecular Genetics. 22(5). 1026–1038. 31 indexed citations

10.

Veenma, Danielle, Annelies de Klein, & Dick Tibboel. (2012). Developmental and genetic aspects of congenital diaphragmatic hernia. Pediatric Pulmonology. 47(6). 534–545. 54 indexed citations

11.

Veenma, Danielle, Robbert J. Rottier, Annelies de Klein, et al.. (2012). Etiological and Pathogenic Factors in Congenital Diaphragmatic Hernia. European Journal of Pediatric Surgery. 22(5). 345–354. 12 indexed citations

12.

Wat, Margaret, Danielle Veenma, Jacob S. Hogue, et al.. (2011). Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia. Journal of Medical Genetics. 48(5). 299–307. 65 indexed citations

13.

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

14.

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

15.

Veenma, Danielle, Linda Joosen, Pino J. Poddighe, et al.. (2010). Congenital diaphragmatic hernia and a complex heart defect in association with Wolf–Hirschhorn syndrome. American Journal of Medical Genetics Part A. 152A(11). 2891–2894. 13 indexed citations

16.

Argente, Jesús, et al.. (2010). PROP1, HESX1, POU1F1, LHX3 and LHX4 Mutation and Deletion Screening and GH1 P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency. Hormone Research in Paediatrics. 73(5). 363–371. 27 indexed citations

17.

Tibboel, Dick, Jan Lindemans, Johannes J. Duvekot, et al.. (2010). Retinol Status of Newborn Infants Is Associated With Congenital Diaphragmatic Hernia. PEDIATRICS. 126(4). 712–720. 74 indexed citations

18.

Argente, Jesús, Danielle Veenma, Edith C. H. Friesema, et al.. (2008). Genetic screening of a Dutch population with isolated GH deficiency (IGHD). Clinical Endocrinology. 70(5). 742–750. 19 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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