Esther de Graaff

9.7k total citations
61 papers, 4.4k citations indexed

About

Esther de Graaff is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Esther de Graaff has authored 61 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 33 papers in Molecular Biology and 14 papers in Neurology. Recurrent topics in Esther de Graaff's work include Genetics and Neurodevelopmental Disorders (25 papers), Autoimmune Neurological Disorders and Treatments (12 papers) and Genomic variations and chromosomal abnormalities (12 papers). Esther de Graaff is often cited by papers focused on Genetics and Neurodevelopmental Disorders (25 papers), Autoimmune Neurological Disorders and Treatments (12 papers) and Genomic variations and chromosomal abnormalities (12 papers). Esther de Graaff collaborates with scholars based in Netherlands, United States and Belgium. Esther de Graaff's co-authors include Vassilis Pachnis, Ben A. Oostra, Annemieke J.M.H. Verkerk, Edwin Reyniers, Kristel De Boulle, Rob Willemsen, Casper C. Hoogenraad, Amanda Barlow, Bernadette Van Roy and Lieve Vits and has published in prestigious journals such as Nature, Nature Communications and Neuron.

In The Last Decade

Esther de Graaff

61 papers receiving 4.3k citations

Peers

Countries citing papers authored by Esther de Graaff

Since Specialization

Citations

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

Fields of papers citing papers by Esther de Graaff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Esther de Graaff. 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 Esther de Graaff. The network helps show where Esther de Graaff may publish in the future.

Co-authorship network of co-authors of Esther de Graaff

This figure shows the co-authorship network connecting the top 25 collaborators of Esther de Graaff. A scholar is included among the top collaborators of Esther de Graaff 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 Esther de Graaff. Esther de Graaff 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	Antibodies Associated With Autoimmune Encephalitis in Patients With Presumed Neurodegenerative Dementia 2023 ·Neurology Neuroimmunology & Neuroinflammation ·Anna E.M. Bastiaansen, (unknown), (unknown), Wiesje M. van der Flier, Charlotte E. Teunissen, Esther de Graaff, Mariska M.P. Nagtzaam, Manuela Paunovic, (unknown), Marco W.J. Schreurs, Frank Leypoldt, Peter A.E. Sillevis Smitt, Juna M. de Vries, Harro Seelaar, John C. van Swieten, Frank Jan de Jong, Yolande A.L. Pijnenburg, Maarten J. Titulaer	17
2	Organization and dynamics of the cortical complexes controlling insulin secretion in β-cells 2022 ·Journal of Cell Science ·Ivar Noordstra, (unknown), (unknown), Eugene A. Katrukha, Ka Lou Yu, Roderick P. Tas, Sybren Portegies, (unknown), Esther de Graaff, Casper C. Hoogenraad, Eelco J.P. de Koning, Françoise Carlotti, Lukas C. Kapitein, Anna Akhmanova	16
3	Kinesin-Binding Protein Controls Microtubule Dynamics and Cargo Trafficking by Regulating Kinesin Motor Activity 2016 ·Current Biology ·Josta T. Kevenaar, Sarah Bianchi, (unknown), Natacha Olieric, Joanna Lipka, Cátia P. Frias, Marina Mikhaylova, Martin Harterink, Nanda Keijzer, Phebe S. Wulf, Manuel Hilbert, Lukas C. Kapitein, Esther de Graaff, (unknown), Michel O. Steinmetz, Casper C. Hoogenraad	77
4	Detection and Characterization of Autoantibodies to Neuronal Cell-Surface Antigens in the Central Nervous System 2016 ·Frontiers in Molecular Neuroscience ·Marleen H. van Coevorden‐Hameete, Maarten J. Titulaer, Marco W.J. Schreurs, Esther de Graaff, Peter A.E. Sillevis Smitt, Casper C. Hoogenraad	25
5	A role for Bicaudal-D2 in radial cerebellar granule cell migration 2014 ·Nature Communications ·Dick Jaarsma, Robert van den Berg, Phebe S. Wulf, Susan van Erp, Nanda Keijzer, Max A. Schlager, Esther de Graaff, Chris I. De Zeeuw, R. Jeroen Pasterkamp, Anna Akhmanova, Casper C. Hoogenraad	37
6	Identification of delta/notch‐like epidermal growth factor‐related receptor as the Tr antigen in paraneoplastic cerebellar degeneration 2012 ·Annals of Neurology ·Esther de Graaff, (unknown), Esther Hulsenboom, Robert van den Berg, Martin J. van den Bent, Jeroen Demmers, Pieternella J. Lugtenburg, Casper C. Hoogenraad, Peter Sillevis Smitt	105
7	Pericentrosomal targeting of Rab6 secretory vesicles by Bicaudal-D-related protein 1 (BICDR-1) regulates neuritogenesis 2010 ·The EMBO Journal ·Max A. Schlager, Lukas C. Kapitein, Ilya Grigoriev, Grzegorz Burzynski, Phebe S. Wulf, Nanda Keijzer, Esther de Graaff, Mitsunori Fukuda, Iain T. Shepherd, Anna Akhmanova, Casper C. Hoogenraad	124
8	Deletion of 1 amino acid in Indian hedgehog leads to brachydactylyA1 2008 ·American Journal of Medical Genetics Part A ·Elisabeth M. Lodder, A. Jeannette M. Hoogeboom, J. Henk Coert, Esther de Graaff	16
9	Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems 2005 ·The American Journal of Human Genetics ·Alice S. Brooks, Aida M. Bertoli‐Avella, Grzegorz Burzynski, Guido J. Breedveld, Jan Osinga, Ludolf G. Boven, Jane A. Hurst, Grazia M.S. Mancini, Maarten H. Lequin, I.F.M. de Coo, Ivana Matera, Esther de Graaff, Carel Meijers, Patrick J. Willems, Dick Tibboel, Ben A. Oostra, Robert M.W. Hofstra	106
10	A new locus for postaxial polydactyly type A/B on chromosome 7q21–q34 2003 ·European Journal of Human Genetics ·Robert‐Jan H. Galjaard, Arie P.T. Smits, J.H.A.M. Tuerlings, Aagje G. Bais, (unknown), Guido J. Breedveld, Esther de Graaff, Ben A. Oostra, Peter Heutink	30
11	Enteric Nervous System Progenitors Are Coordinately Controlled by the G Protein-Coupled Receptor EDNRB and the Receptor Tyrosine Kinase RET 2003 ·Neuron ·Amanda Barlow, Esther de Graaff, Vassilis Pachnis	206
12	FMR1 Premutation Allele (CGG)(81) Is Stable in Mice 1997 ·European Journal of Human Genetics ·Carola Bontekoe, Esther de Graaff, Ingeborg M. Nieuwenhuizen, Rob Willemsen, Ben A. Oostra	35
13	The fragile X phenotype in a mosaic male with a deletion showing expression of theFMR1 protein in 28% of the cells 1996 ·American Journal of Medical Genetics ·Esther de Graaff, Bert de Vries, (unknown), J. O. Van Hemel, Serieta Mohkamsing, Ben A. Oostra, (unknown)	34
14	Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor. 1995 ·PubMed ·Esther de Graaff, Rob Willemsen, Nanbert Zhong, C E de Die-Smulders, W. Ted Brown, (unknown), B. A. Oostra	49
15	A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome 1994 ·Human Molecular Genetics ·(unknown), Esther de Graaff, (unknown), R. J. E. Jongbloed, Christine de Die‐Smulders, J.J.M. Engelen, Jean‐Pierre Fryns, (unknown), Ben A. Oostra	97
16	DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR‐1 gene 1994 ·American Journal of Medical Genetics ·Ans M.W. van den Ouweland, Bert B.A. de Vries, (unknown), Wout H. Deelen, Esther de Graaff, J. O. Van Hemel, Ben A. Oostra, Martinus F. Niermeijer, Dicky Halley	43
17	Alternative splicing in the fragile X gene FMR1 1993 ·Human Molecular Genetics ·Annemieke J.M.H. Verkerk, Esther de Graaff, Kristel De Boulle, Evan E. Eichler, David Konecki, Edwin Reyniers, Antonella Manca, Annemarie Poustka, Patrick J. Willems, David L. Nelson, B. A. Oostra	114
18	Characterization and localization of the FMR-1 gene product associated with fragile X syndrome 1993 ·Nature ·(unknown), Cathy Bakker, Esther de Graaff, J. L. M. Keulemans, Rob Willemsen, Annemieke J.M.H. Verkerk, H. Galjaard, Arnold Reuser, A. T. Hoogeveen, Ben A. Oostra	276
19	Alternative splicing in the fragile X gene FMR1 1993 ·Human Molecular Genetics ·Annemieke J.M.H. Verkerk, Esther de Graaff, Kristel De Boulle, Evan E. Eichler, David Konecki, Edwin Reyniers, Antonella Manca, Annemarie Poustka, Patrick J. Willems, David L. Nelson, Ben A. Oostra	86
20	A point mutation in the FMR-1 gene associated with fragile X mental retardation 1993 ·Nature Genetics ·Kristel De Boulle, Annemieke J.M.H. Verkerk, Edwin Reyniers, Lieve Vits, Jan Hendrickx, Bernadette Van Roy, (unknown), Esther de Graaff, Ben A. Oostra, (unknown)	484

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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