Anneke Maat‐Kievit

2.7k citations

36 papers · 1.6k indexed · h-index 21

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 13
Neurology top 5%
- Neurological disorders and treatments 7
Physiology top 5%
- Tuberous Sclerosis Complex Research 9
- Histiocytic Disorders and Treatments 5
Genetics top 5%
Molecular Biology
- DNA Repair Mechanisms 7
- Mitochondrial Function and Pathology 7
Oncology
- Polyomavirus and related diseases 4
Pathology and Forensic Medicine
- Tumors and Oncological Cases 3

Co-authors: Dicky Halley Mark Nellist Ans van den Ouweland Ben A. Oostra Aad Tibben Miriam Goedbloed Bernard A. Zonnenberg Esther Brusse
Cited by: Cellular and Molecular Neuroscience Neurology Physiology
Journals: PLoS ONE (1 paper)Neurology (1 paper)The American Journal of Human Genetics (1 paper)
Partner nations: Netherlands United States Germany

In The Last Decade

Anneke Maat‐Kievit

35 papers receiving 1.6k citations

Peers

Countries citing papers authored by Anneke Maat‐Kievit

Since Specialization

Citations

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

Fields of papers citing papers by Anneke Maat‐Kievit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anneke Maat‐Kievit. 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 Anneke Maat‐Kievit. The network helps show where Anneke Maat‐Kievit may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations BMC Medical Genetics ·Mark Nellist,Rutger W. W. Brouwer,Christel Kockx,Monique van Veghel‐Plandsoen,Caroline Withagen-Hermans,Lida Prins-Bakker,Marianne Hoogeveen‐Westerveld,Alan Mršić,Mike MP van den Berg,Anna E. Koopmans,Marie‐Claire Y. de Wit,Floor E. Jansen,Anneke Maat‐Kievit,Ans van den Ouweland,Dicky Halley,Annelies de Klein,Wilfred F. J. van IJcken	2015	58
2	Clinical utility gene card for: Tuberous sclerosis complex (TSC1, TSC2) European Journal of Human Genetics ·Karin Mayer,Christa Fonatsch,Katharina Wimmer,Ans MW van den Ouweland,Anneke Maat‐Kievit	2013	3
3	Cerebral cavernous malformations: from molecular pathogenesis to genetic counselling and clinical management European Journal of Human Genetics ·Remco Haasdijk,Caroline Cheng,Anneke Maat‐Kievit,Henricus J. Duckers	2011	57
4	Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co‐segregates with tuberous sclerosis complex in mildly affected kindreds Clinical Genetics ·Marjolein Wentink,Mark Nellist,Marianne Hoogeveen‐Westerveld,Bernard A. Zonnenberg,DM van der Kolk,Ton van Essen,S. M. Park,Geoffrey Woods,Petra E. Cohn‐Hokke,Wim Brussel,Eric Smeets,Alice S. Brooks,Dicky Halley,Ans van den Ouweland,Anneke Maat‐Kievit	2011	24
5	Analysis of TSC1 truncations defines regions involved in TSC1 stability, aggregation and interaction Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Marianne Hoogeveen‐Westerveld,Carla Exalto,Anneke Maat‐Kievit,Ans van den Ouweland,Dicky Halley,Mark Nellist	2010	21
6	Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patients European Journal of Human Genetics ·Ans M.W. van den Ouweland,Peter Elfferich,Bernard A. Zonnenberg,Willem F. Arts,Tjitske Kleefstra,M. Nellist,José M. Millán,Caroline Withagen-Hermans,Anneke Maat‐Kievit,Dicky Halley	2010	9
7	Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder European Journal of Human Genetics ·Rinus Vegt,Aida M. Bertoli‐Avella,J.H.M. Tulen,Bianca de Graaf,Annemieke J.M.H. Verkerk,Jeroen Vervoort,Carla M Twigt,Anneke Maat‐Kievit,Ruud van Tuijl,Marieke van der Lijn,Michiel W. Hengeveld,Ben A. Oostra	2009	12
8	Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach–Rott syndrome American Journal of Medical Genetics Part A ·Vered Shkalim,Hagit Baris,Gavriel Gal,Ruth Gleiss,Shlomo Calderon,Marja W. Wessels,Anneke Maat‐Kievit,Björn Menten,Elfride De Baere,Raoul C. M. Hennekam,Anja Schirmacher,Sherri J. Bale,Mordechai Shohat,Patrick J. Willems	2009	4
9	Missense mutations to the TSC1 gene cause tuberous sclerosis complex European Journal of Human Genetics ·Mark Nellist,Diana van den Heuvel,Diane Schluep,Carla Exalto,Miriam Goedbloed,Anneke Maat‐Kievit,Ton van Essen,Karin van Spaendonck‐Zwarts,Floor E. Jansen,Paula Helderman,G. Bartalini,Outi Vierimaa,Maila Penttinen,Jenneke van den Ende,Ans van den Ouweland,Dicky Halley	2008	21
10	A MELAS-Associated ND1 Mutation Causing Leber Hereditary Optic Neuropathy and Spastic Dystonia Archives of Neurology ·Liesbeth Spruijt,Hubert Smeets,Alexandra T.M. Hendrickx,Marijke Wefers Bettink‐Remeijer,Anneke Maat‐Kievit,Kees Schoonderwoerd,Wim J. Sluiter,I.F.M. de Coo,Rogier Q. Hintzen	2007	41
11	Large Deletion at the TSC1 Locus in a Family with Tuberous Sclerosis Complex Genetic Testing ·Mark Nellist,Őzgür Sancak,Miriam Goedbloed,Monique van Veghel‐Plandsoen,Anneke Maat‐Kievit,Dick Lindhout,Bert H.J. Eussen,Annelies de Klein,Dicky Halley,A.M.W. van den Ouweland	2005	8
12	Adverse Effects of Predictive Testing for Huntington Disease Underestimated: Long-Term Effects 7-10 Years After the Test. Health Psychology ·Reinier Timman,Raymund A.C. Roos,Anneke Maat‐Kievit,Aad Tibben	2004	86
13	A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia The American Journal of Human Genetics ·John C. van Swieten,Esther Brusse,Bianca M. de Graaf,Elmar Krieger,Raoul van de Graaf,Inge de Koning,Anneke Maat‐Kievit,Peter A. J. Leegwater,Dennis Dooijes,Ben A. Oostra,Peter Heutink	2003	205
14	Testing the test—why pursue a better test for Huntington disease? American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Reinier Timman,Anneke Maat‐Kievit,Christine Brouwer‐DudokdeWit,Moniek Zoeteweij,Martijn H. Breuning,Aad Tibben	2002	2
15	Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease American Journal of Medical Genetics ·Anneke Maat‐Kievit,Paula Helderman‐van den Enden,Monique Losekoot,Peter de Knijff,René D.M. Belfroid,M Vegter-van der Vlis,Raymund A.C. Roos,Martijn H. Breuning	2001	15
16	Paradox of a better test for Huntington's disease Journal of Neurology Neurosurgery & Psychiatry ·Anneke Maat‐Kievit	2000	50
17	Predictive testing of 25 percent at-risk individuals for Huntington disease (1987-1997) American Journal of Medical Genetics ·Anneke Maat‐Kievit,M Vegter-van der Vlis,Moniek Zoeteweij,Monique Losekoot,Arie van Haeringen,Raymund A.C. Roos	1999	17
18	Early Cognitive and Motor Symptoms in Identified Carriers of the Gene for Huntington Disease Archives of Neurology ·Gerly M. de Boo,Aad Tibben,J.B.K. Lanser,A. Jennekens‐Schinkel,J. Hermans,Anneke Maat‐Kievit,R. A. C. Roos	1997	57
19	The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients European Journal of Pediatrics ·C. T. R. M. Schrander‐Stumpel,Peter Meinecke,Golder N. Wilson,G. Gilleseen-Kaesbach,Sigrid Tinschert,Rainer König,N. Philip,Renata Rizzo,J. J. P. Schrander,L Pfeiffer,Anneke Maat‐Kievit,I. van der Bürgt,T. van Essen,E. Latta,U. Hillig,Alain Verloès,Hubert Journel,J P Fryns	1994	88
20	Two additional cases of the Ohdo blepharophimosis syndrome American Journal of Medical Genetics ·Anneke Maat‐Kievit,Han G. Brunner,P. D. Maaswinkel‐Mooij	1993	19

About Anneke Maat‐Kievit

Anneke Maat‐Kievit is a scholar working on Cellular and Molecular Neuroscience, Neurology and Developmental Biology, having authored 36 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (13 papers), Tuberous Sclerosis Complex Research (9 papers), DNA Repair Mechanisms (7 papers), Mitochondrial Function and Pathology (7 papers), Neurological disorders and treatments (7 papers), Histiocytic Disorders and Treatments (5 papers), Polyomavirus and related diseases (4 papers) and Tumors and Oncological Cases (3 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (453 citations), Neurology (325 citations) and Physiology (525 citations). Anneke Maat‐Kievit has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Dicky Halley, Mark Nellist, Ans van den Ouweland, Ben A. Oostra, Aad Tibben, Miriam Goedbloed, Bernard A. Zonnenberg, Esther Brusse, Raymund A.C. Roos and Őzgür Sancak. Their work appears in journals such as PLoS ONE, Neurology and The American Journal of Human Genetics.

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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