Danielle Veenma

843 citations

18 papers · 450 · h-index 12

Impact in

Surgery
- Congenital Diaphragmatic Hernia Studies
- Congenital Anomalies and Fetal Surgery
Pulmonary and Respiratory Medicine top 10%
- Neonatal Respiratory Health Research
- Tracheal and airway disorders

Papers in

Surgery 11
- Congenital Diaphragmatic Hernia Studies 11
- Congenital Anomalies and Fetal Surgery 3
Genetics 8
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2

Co-authors: Annelies de Klein (11 shared papers)Dick Tibboel (10 shared papers)Titia E. Cohen‐Overbeek (2 shared papers)Daryl A. Scott (3 shared papers)Jan Lindemans (1 shared paper)Johannes J. Duvekot (1 shared paper)Régine P.M. Steegers‐Theunissen (1 shared paper)John J. Greer (1 shared paper)
Journals: Frontiers in Pediatrics (2 papers)European Journal of Human Genetics (2 papers)Human Molecular Genetics (2 papers)Pediatric Pulmonology (1 paper)PEDIATRICS (1 paper)
Partner nations: Netherlands United States Canada

In The Last Decade

Danielle Veenma

18 papers receiving 444 citations

Peers

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-authors

The 25 scholars most cited alongside Danielle Veenma, 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 Danielle Veenma Line = papers co-authored together Danielle Veenma links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Retinol Status of Newborn Infants Is Associated With Congenital Diaphragmatic Hernia PEDIATRICS ·Leonardus W.J.E. Beurskens, Dick Tibboel, Jan Lindemans, Johannes J. Duvekot, Titia E. Cohen‐Overbeek, Danielle Veenma, Annelies de Klein, John J. Greer, Régine P.M. Steegers‐Theunissen	2010	74
2	Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia Journal of Medical Genetics ·Margaret Wat, Danielle Veenma, Jacob S. Hogue, Ashley M. Holder, Z. Yu, Jeanette J. Wat, Neil A. Hanchard, O A Shchelochkov, Caraciolo J. Fernandes, Anthony E. Johnson, Kevin P. Lally, Anne Slavotinek, Olivier Danhaive, T Schaible, S.W. Cheung, Katherine A. Rauen, Vijay S. Tonk, Dick Tibboel, Annelies de Klein, Daryl A. Scott	2011	65
3	Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1 Human Molecular Genetics ·Margaret Wat, T. Beck, Andrés Hernández, Zhiyin Yu, Danielle Veenma, M. Aragonés García, Ashley M. Holder, Jeanette J. Wat, Yuqing Chen, Carrie Mohila, Kevin P. Lally, Mary E. Dickinson, Dick Tibboel, Annelies de Klein, Brendan Lee, Daryl A. Scott	2012	64
4	Developmental and genetic aspects of congenital diaphragmatic hernia Pediatric Pulmonology ·Danielle Veenma, Annelies de Klein, Dick Tibboel	2012	54
5	Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice Human Molecular Genetics ·T. Beck, Danielle Veenma, Oleg A. Shchelochkov, Zhiyin Yu, Bum‐Joon Kim, Hitisha P. Zaveri, Yolande van Bever, Sunju Choi, Hannie Douben, Terry Bertin, Pragna I. Patel, Brendan Lee, Dick Tibboel, Annelies de Klein, David W. Stockton, Monica J. Justice, Daryl A. Scott	2012	31
6	<i>PROP1, HESX1, POU1F1, LHX3 </i>and<i> LHX4</i> Mutation and Deletion Screening and <i>GH1 </i>P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency Hormone Research in Paediatrics ·Laura C. G. de Graaff, Jesús Argente, Danielle Veenma, Madeleine L. Drent, André G. Uitterlinden, Anita C. S. Hokken‐Koelega	2010	27
7	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
8	DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis European Journal of Human Genetics ·Danielle Veenma, Dawn Cordeiro, Neal Sondheimer, Saadet Mercimek‐Andrews	2018	21
9	Genetic screening of a Dutch population with isolated GH deficiency (IGHD) Clinical Endocrinology ·Laura C. G. de Graaff, Jesús Argente, Danielle Veenma, Maaike A. C. Herrebout, Edith C. H. Friesema, André G. Uitterlinden, Madeleine L. Drent, Ángel Campos‐Barros, Anita C. S. Hokken‐Koelega	2008	19
10	Congenital diaphragmatic hernia and a complex heart defect in association with Wolf–Hirschhorn syndrome American Journal of Medical Genetics Part A ·Juliane Tautz, Danielle Veenma, Bert Eussen, Linda Joosen, Pino J. Poddighe, Dick Tibboel, Annelies de Klein, Thomas Schaible	2010	13
11	Etiological and Pathogenic Factors in Congenital Diaphragmatic Hernia European Journal of Pediatric Surgery ·Danielle Veenma, Rhiannon van Loenhout, Robbert J. Rottier, Annelies de Klein, Richard Keijzer, Martin Post, Dick Tibboel, Ilona Sluiter	2012	12
12	Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge Frontiers in Pediatrics ·Erwin Brosens, N. Peters, Kim S. van Weelden, Charlotte Bendixen, Rutger W. W. Brouwer, Frank Sleutels, Hennie T. Brüggenwirth, Wilfred F. J. van IJcken, Danielle Veenma, Suzan C.M. Cochius-den Otter, René Wijnen, Alex J. Eggink, Marieke F. van Dooren, Heiko Reutter, Robbert J. Rottier, J. Marco Schnater, Dick Tibboel, Annelies de Klein	2022	11
13	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
14	Genome sequencing among children with medical complexity: What constitutes value from parents’ perspective? Journal of Genetic Counseling ·Whiwon Lee, Stephanie Luca, Gregory Costain, Meaghan Snell, Maria Marano, Meredith Curtis, Kourtney Dunsmore, Danielle Veenma, Susan Walker, Ronald D. Cohn, Christian R. Marshall, Eyal Cohen, M. Stephen Meyn, Julia Orkin, Robin Z. Hayeems	2021	9
15	Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause? Frontiers in Pediatrics ·Linda Gaillard, Anne Goverde, Quincy C. C. van den Bosch, Fernanda Sarquis Jehee, Erwin Brosens, Danielle Veenma, Frank Magielsen, Annelies de Klein, Irene M. J. Mathijssen, Marieke F. van Dooren	2021	8
16	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 ·Bonnie K. Dwyer, Danielle Veenma, Kiki Chang, Howard Schulman, Geeske M. van Woerden	2022	6
17	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 ·Neeltje Margreth van der Lugt, Marjolein J.A. Weerts, Danielle Veenma, Carsten R. Lincke, Saskia J. Gischler, Mariëlle Alders, Yvette van Ierland	2022	3
18	CAMK2; four genes, one syndrome? Delineation of genotype–phenotype correlations Current Opinion in Neurobiology ·J. Cheung, Geeske M. van Woerden, Danielle Veenma	2024	1

About Danielle Veenma

Danielle Veenma is a scholar working on Surgery, Genetics, Molecular Biology, Pulmonary and Respiratory Medicine and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 450 indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (11 papers), Tracheal and airway disorders (5 papers), Congenital heart defects research (4 papers), Congenital Anomalies and Fetal Surgery (3 papers), Neonatal Respiratory Health Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Pituitary Gland Disorders and Treatments (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Surgery (273 citations), Pulmonary and Respiratory Medicine (201 citations), Genetics (111 citations), Endocrinology, Diabetes and Metabolism (43 citations) and Molecular Biology (156 citations). Danielle Veenma has collaborated with scholars based in Netherlands, United States and Canada. Frequent co-authors include Annelies de Klein, Dick Tibboel, Titia E. Cohen‐Overbeek, Daryl A. Scott, Jan Lindemans, Johannes J. Duvekot, Régine P.M. Steegers‐Theunissen, John J. Greer, Margaret Wat and Madeleine L. Drent. Their work appears in journals such as Frontiers in Pediatrics, European Journal of Human Genetics, Human Molecular Genetics, Pediatric Pulmonology and PEDIATRICS.

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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Danielle Veenma

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