Karen Bindels‐de Heus

939 total citations
23 papers, 570 citations indexed

About

Karen Bindels‐de Heus is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Karen Bindels‐de Heus has authored 23 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Physiology. Recurrent topics in Karen Bindels‐de Heus's work include Genetic Syndromes and Imprinting (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Tuberous Sclerosis Complex Research (4 papers). Karen Bindels‐de Heus is often cited by papers focused on Genetic Syndromes and Imprinting (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Tuberous Sclerosis Complex Research (4 papers). Karen Bindels‐de Heus collaborates with scholars based in Netherlands, United States and Australia. Karen Bindels‐de Heus's co-authors include Marie‐Claire Y. de Wit, Henriëtte A. Moll, André B. Rietman, Leontine W. ten Hoopen, Iris E. Overwater, Ype Elgersma, Sabine E. Mous, Dimitris Rizopoulos, Floor E. Jansen and Heleen M. Evenhuis and has published in prestigious journals such as Neurology, Epilepsia and Developmental Medicine & Child Neurology.

In The Last Decade

Karen Bindels‐de Heus

21 papers receiving 560 citations

Peers

Countries citing papers authored by Karen Bindels‐de Heus

Since Specialization

Citations

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

Fields of papers citing papers by Karen Bindels‐de Heus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen Bindels‐de Heus. 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 Karen Bindels‐de Heus. The network helps show where Karen Bindels‐de Heus may publish in the future.

Co-authorship network of co-authors of Karen Bindels‐de Heus

This figure shows the co-authorship network connecting the top 25 collaborators of Karen Bindels‐de Heus. A scholar is included among the top collaborators of Karen Bindels‐de Heus 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 Karen Bindels‐de Heus. Karen Bindels‐de Heus 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

#	Work	Indexed citations
1	Age‐Related Trajectories of Autistic Traits in Children With Angelman Syndrome 2025 ·Autism Research ·(unknown), Sabine E. Mous, Leontine W. ten Hoopen, André B. Rietman, (unknown), Karen Bindels‐de Heus, Pieter F. A. de Nijs, (unknown), (unknown), Manon H. J. Hillegers, Henriëtte A. Moll, Marie‐Claire Y. de Wit, Gwen Dieleman	2
2	Language comprehension assessment using the computer-based instrument for low motor language testing (C-BiLLT) in children with Angelman syndrome 2025 ·Augmentative and Alternative Communication ·(unknown), (unknown), Karen Bindels‐de Heus, (unknown), Marc P. van der Schroeff, Johanna Geytenbeek, Marie‐Claire Y. de Wit	1
3	A Dutch paediatric palliative care guideline: a systematic review and recommendations on advance care planning and shared decision-making 2024 ·BMC Palliative Care ·(unknown), Renée L. Mulder, (unknown), Jurrianne C. Fahner, (unknown), Johannes Verheijden, (unknown), (unknown), Leontien C.M. Kremer, Marijke C. Kars, Erna Michiels, Eduard Verhagen, (unknown), Mattijs W. Alsem, (unknown), Karen Bindels‐de Heus, (unknown), Rosa Geurtzen, (unknown), (unknown)	0
4	Outcome measures in Angelman syndrome 2024 ·Journal of Neurodevelopmental Disorders ·(unknown), Karen Bindels‐de Heus, (unknown), (unknown), Leontine W. ten Hoopen, (unknown), Johan J. M. Pel, Koen F. M. Joosten, Manon H. J. Hillegers, Henriëtte A. Moll, Marie‐Claire Y. de Wit, Gwen Dieleman, Sabine E. Mous	2
5	Developmental and epileptic encephalopathy 56 due to YWHAG variants: 12 new cases and review of the literature 2024 ·European Journal of Paediatric Neurology ·(unknown), (unknown), Loreto Martorell, (unknown), (unknown), Malene Landbo Børresen, H. R. M. Johnson, Christian Korff, (unknown), Jérémie Lefranc, Anne‐Sophie Denommé‐Pichon, Elisabeth Sarrazin, (unknown), Jorge Saraiva, (unknown), Anne Goverde, Karen Bindels‐de Heus, Tahsin Stefan Barakat, Juan Darío Ortigoza‐Escobar	2
6	Challenges in body composition assessment using air-displacement plethysmography by BOD POD in pediatric and young adult patients 2023 ·Clinical Nutrition ·(unknown), (unknown), M. Vermeulen, (unknown), (unknown), (unknown), Erica L T van den Akker, (unknown), Barbara A. E. de Koning, (unknown), Gwen Dieleman, (unknown), (unknown), (unknown), Karen Bindels‐de Heus, Anita Hokken-Koelega, Koen F. M. Joosten	2
7	Bone health in children with Angelman syndrome at the ENCORE Expertise Center 2023 ·European Journal of Pediatrics ·Karen Bindels‐de Heus, (unknown), Sabine E. Mous, (unknown), Daniëlle C M van der Kaay, Gerthe F. Kerkhof, Ype Elgersma, Henriëtte A. Moll, Marie‐Claire Y. de Wit	0
8	Child characteristics associated with child quality of life and parenting stress in Angelman syndrome 2023 ·Journal of Intellectual Disability Research ·(unknown), Karen Bindels‐de Heus, (unknown), Leontine W. ten Hoopen, André B. Rietman, Pieter F. A. de Nijs, Manon H. J. Hillegers, Henriëtte A. Moll, Marie‐Claire Y. de Wit, Gwendolyn C. Dieleman, Sabine E. Mous	7
9	Hyperphagia, Growth, and Puberty in Children with Angelman Syndrome 2023 ·Journal of Clinical Medicine ·Karen Bindels‐de Heus, (unknown), (unknown), Daniëlle C M van der Kaay, Gerthe F. Kerkhof, Ype Elgersma, Marie‐Claire Y. de Wit, Sabine E. Mous, Henriëtte A. Moll	2
10	Sleep problems in children with Angelman Syndrome: The effect of a behavioral intervention program 2023 ·Research in Developmental Disabilities ·Karen Bindels‐de Heus, (unknown), Jeroen S. Legerstee, Leontine W. ten Hoopen, Gwen Dieleman, Henriëtte A. Moll, Sabine E. Mous, Marie‐Claire Y. de Wit	8
11	De novo TRPV4 Leu619Pro variant causes a new channelopathy characterised by giant cell lesions of the jaws and skull, skeletal abnormalities and polyneuropathy 2021 ·Journal of Medical Genetics ·(unknown), Carolina Cavaliéri Gomes, Karen Bindels‐de Heus, Renata Lazari Sandoval, Angelia V. Bassenden, Luciano Lauria Dib, Fernando Kok, (unknown), Irene M.J. Mathijssen, (unknown), Robert Eveleigh, Tenzin Gayden, Bas Pullens, Albert M. Berghuis, Marjon van Slegtenhorst, Martina Wilke, Nada Jabado, Grazia M.S. Mancini, Ricardo Santiago Gomez	9
12	An overview of health issues and development in a large clinical cohort of children with Angelman syndrome 2019 ·American Journal of Medical Genetics Part A ·Karen Bindels‐de Heus, Sabine E. Mous, (unknown), (unknown), (unknown), André B. Rietman, Leontine W. ten Hoopen, Alice S. Brooks, Ype Elgersma, Henriëtte A. Moll, Marie‐Claire Y. de Wit	53
13	A randomized controlled trial with everolimus for IQ and autism in tuberous sclerosis complex 2019 ·Neurology ·Iris E. Overwater, André B. Rietman, Sabine E. Mous, Karen Bindels‐de Heus, Dimitris Rizopoulos, Leontine W. ten Hoopen, Thijs van der Vaart, Floor E. Jansen, Ype Elgersma, Henriëtte A. Moll, Marie‐Claire Y. de Wit	82
14	Tuberous sclerosis complex: Concerns and needs of patients and parents from the transitional period to adulthood 2018 ·Epilepsy & Behavior ·(unknown), (unknown), Sabine E. Mous, (unknown), André B. Rietman, Gwen Dieleman, Leontine W. ten Hoopen, (unknown), Marie‐Claire Y. de Wit, Karen Bindels‐de Heus, Henriëtte A. Moll, Agnies M. van Eeghen	30
15	Automated radiogrammetry is a feasible method for measuring bone quality and bone maturation in severely disabled children 2016 ·Pediatric Radiology ·(unknown), de Man, Annemieke M. Boot, Karen Bindels‐de Heus, (unknown), Rick R. van Rijn, Corine Penning, Heleen M. Evenhuis	12
16	CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia 2016 ·Neurology ·Grazia M.S. Mancini, Rachel Schot, Marie‐Claire Y. de Wit, I.F.M. de Coo, Rianne Oostenbrink, Karen Bindels‐de Heus, (unknown), Maarten H. Lequin, Femke A.T. de Vries, Martina Wilke, Marjon A. van Slegtenhorst	15
17	Germline activating AKT3 mutation associated with megalencephaly, polymicrogyria, epilepsy and hypoglycemia 2014 ·Molecular Genetics and Metabolism ·Mark Nellist, Rachel Schot, Marianne Hoogeveen‐Westerveld, Rinze F. Neuteboom, Elles van der Louw, Maarten H. Lequin, Karen Bindels‐de Heus, Barbara Sibbles, I.F.M. de Coo, Alice S. Brooks, Grazia M.S. Mancini	36
18	Transferring Young People With Profound Intellectual and Multiple Disabilities From Pediatric to Adult Medical Care: Parents' Experiences and Recommendations 2013 ·Intellectual and developmental disabilities ·Karen Bindels‐de Heus, AnneLoes van Staa, (unknown), (unknown), Sander R. Hilberink	55
19	ACTA2 mutation with childhood cardiovascular, autonomic and brain anomalies and severe outcome 2013 ·American Journal of Medical Genetics Part A ·Marije Meuwissen, Maarten H. Lequin, Karen Bindels‐de Heus, Hennie T. Brüggenwirth, Maarten F. C. M. Knapen, Michiel Dalinghaus, I.F.M. de Coo, Yolande van Bever, Beerend H. J. Winkelman, Grazia M.S. Mancini	27
20	Epidemiology of low bone mineral density and fractures in children with severe cerebral palsy: a systematic review 2009 ·Developmental Medicine & Child Neurology ·(unknown), Heleen M. Evenhuis, Annemieke M. Boot, de Man, Karen Bindels‐de Heus, (unknown), Corine Penning	75

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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