Leopold Curfs

8.0k total citations
210 papers, 5.3k citations indexed

About

Leopold Curfs is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Leopold Curfs has authored 210 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Genetics, 48 papers in Cognitive Neuroscience and 45 papers in Molecular Biology. Recurrent topics in Leopold Curfs's work include Genetics and Neurodevelopmental Disorders (74 papers), Genetic Syndromes and Imprinting (55 papers) and Autism Spectrum Disorder Research (39 papers). Leopold Curfs is often cited by papers focused on Genetics and Neurodevelopmental Disorders (74 papers), Genetic Syndromes and Imprinting (55 papers) and Autism Spectrum Disorder Research (39 papers). Leopold Curfs collaborates with scholars based in Netherlands, United Kingdom and United States. Leopold Curfs's co-authors include Robert Didden, Marcel G. Smits, Gerjo Kok, C. T. R. M. Schrander‐Stumpel, Irene Tuffrey‐Wijne, Wiebe Braam, Marian A. Maaskant, Sheila Hollins, Hubert Korzilius and Wil H. E. Buntinx and has published in prestigious journals such as American Journal of Clinical Nutrition, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Leopold Curfs

203 papers receiving 5.1k citations

Peers

Countries citing papers authored by Leopold Curfs

Since Specialization

Citations

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

Fields of papers citing papers by Leopold Curfs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leopold Curfs

This figure shows the co-authorship network connecting the top 25 collaborators of Leopold Curfs. A scholar is included among the top collaborators of Leopold Curfs 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 Leopold Curfs. Leopold Curfs 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	A resource to explore the discovery of rare diseases and their causative genes 2021 ·Scientific Data ·Friederike Ehrhart, Egon Willighagen, Martina Kutmon, (unknown), Leopold Curfs, Chris T. Evelo	15
2	A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration 2021 ·Scientific Data ·Friederike Ehrhart, Annika Jacobsen, Maria Rigau, Mattia Bosio, Rajaram Kaliyaperumal, Jeroen F. J. Laros, Egon Willighagen, Alfonso Valencia, Marco Roos, Salvador Capella-Gutiérrez, Leopold Curfs, Chris T. Evelo	21
3	Food-Related Brain Activation Measured by fMRI in Adults with Prader–Willi Syndrome 2021 ·Journal of Clinical Medicine ·I. Caroline van Nieuwpoort, (unknown), S. Jakobsdóttir, J.B. Deijen, Dick J. Veltman, Leopold Curfs, Madeleine L. Drent	9
4	Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study 2020 ·Research Publications (Maastricht University) ·(unknown), Neerja Gupta, Kees E. P. van Roozendaal, Savita Sapra, Manju Ghosh, Sheffali Gulati, Eric Smeets, Leopold Curfs, Madhulika Kabra	3
5	Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes 2019 ·The World Journal of Biological Psychiatry ·Friederike Ehrhart, Susan L. Coort, Lars Eijssen, Elisa Cirillo, Eric Smeets, (unknown), Chris T. Evelo, Leopold Curfs	20
6	Women Who Love: An Explorative Study on Experiences of Lesbian and Bisexual Women with a Mild Intellectual Disability in The Netherlands 2018 ·Sexuality and Disability ·Joke Stoffelen, Dilana Schaafsma, Gerjo Kok, Leopold Curfs	18
7	Views on Sex Using the Nominal Group Technique to Explore Sexuality and Physical Intimacy in Individuals with Intellectual Disabilities 2018 ·Sexuality and Disability ·Joke Stoffelen, Dilana Schaafsma, Gerjo Kok, Leopold Curfs	11
8	MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases 2018 ·Human Mutation ·(unknown), Friederike Ehrhart, Henk J. van Kranen, Mark D. Wilkinson, Annika Jacobsen, Marco Roos, Egon Willighagen, David van Enckevort, Chris T. Evelo, Leopold Curfs	13
9	Review and gap analysis: molecular pathways leading to fetal alcohol spectrum disorders 2018 ·Molecular Psychiatry ·Friederike Ehrhart, Sylvia Roozen, Jef Verbeek, Ger H. Koek, Gerjo Kok, Henk van Kranen, Chris T. Evelo, Leopold Curfs	54
10	Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders 2018 ·The World Journal of Biological Psychiatry ·Friederike Ehrhart, (unknown), Susan L. Coort, Chris T. Evelo, Leopold Curfs	14
11	Systematic literature review on which maternal alcohol behaviours are related to fetal alcohol spectrum disorders (FASD) 2018 ·BMJ Open ·Sylvia Roozen, Gjalt-Jorn Peters, Gerjo Kok, David Townend, Jan G. Nijhuis, Ger H. Koek, Leopold Curfs	34
12	New insights in Rett syndrome using pathway analysis for transcriptomics data 2016 ·Wiener Medizinische Wochenschrift ·Friederike Ehrhart, Susan L. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, Leopold Curfs	8
13	Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes 2016 ·Orphanet Journal of Rare Diseases ·Friederike Ehrhart, Susan L. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, Leopold Curfs	53
14	Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study 2016 ·American Journal of Medical Genetics Part A ·(unknown), Eric Smeets, Peter O.O. Julu, Ingegerd Witt‐Engerström, Giorgio Pini, Stefania Bigoni, Stig Hansen, Flora Apartopoulos, R. Shane Delamont, Kees van Roozendaal, Maria Flora Scusa, Paolo Borelli, (unknown), Leopold Curfs	13
15	Developing research priorities for palliative care of people with intellectual disabilities in Europe: a consultation process using nominal group technique 2016 ·BMC Palliative Care ·Irene Tuffrey‐Wijne, (unknown), Pauline Heslop, Mary McCarron, Stuart Todd, David Oliver, (unknown), Gerd Ahlström, (unknown), Geralyn Hynes, (unknown), (unknown), Florian Riese, Leopold Curfs	31
16	Psychometric properties of a sleep questionnaire for use in individuals with intellectual disabilities 2011 ·Research in Developmental Disabilities ·(unknown), Robert Didden, Hubert Korzilius, Wiebe Braam, Philippe Collin, Marcel G. Smits, Leopold Curfs	26
17	Psychometric properties of the supports intensity scale (SIS): an international review 2010 ·Journal of Applied Research in Intellectual Disabilities ·(unknown), Bea Maes, Claudia Claes, Leopold Curfs	1
18	End‐of‐life decisions: an important theme in the care for people with intellectual disabilities 2010 ·Journal of Intellectual Disability Research ·(unknown), (unknown), Irene Tuffrey‐Wijne, Guy Widdershoven, Leopold Curfs	45
19	Psychose bij kinderen met het Prader-Willi syndroom 2005 ·Tijdschrift voor psychiatrie ·Philippe Collin, Hans de Boer, Annick Vogels, Leopold Curfs	1
20	Prader-Willi syndrome in a boy with duplication 15q12 karyotype 1997 ·C. T. R. M. Schrander‐Stumpel, (unknown), Leopold Curfs, Jean‐Pierre Fryns	1

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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