Annique Claringbould

12.3k total citations
20 papers, 454 citations indexed

About

Annique Claringbould is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Annique Claringbould has authored 20 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in Annique Claringbould's work include Genetic Associations and Epidemiology (11 papers), Epigenetics and DNA Methylation (4 papers) and Genomics and Rare Diseases (3 papers). Annique Claringbould is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Epigenetics and DNA Methylation (4 papers) and Genomics and Rare Diseases (3 papers). Annique Claringbould collaborates with scholars based in Netherlands, Germany and Estonia. Annique Claringbould's co-authors include Judith B. Zaugg, Lude Franke, Peter A.C. ’t Hoen, Patrick Deelen, Cisca Wijmenga, Serena Sanna, Urmo Võsa, Joyce B. J. van Meurs, Daria V. Zhernakova and Rick Jansen and has published in prestigious journals such as Nature Communications, Nature Genetics and Nature Methods.

In The Last Decade

Annique Claringbould

19 papers receiving 450 citations

Peers

Countries citing papers authored by Annique Claringbould

Since Specialization

Citations

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

Fields of papers citing papers by Annique Claringbould

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annique Claringbould

This figure shows the co-authorship network connecting the top 25 collaborators of Annique Claringbould. A scholar is included among the top collaborators of Annique Claringbould 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 Annique Claringbould. Annique Claringbould 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	Single-cell ultra-high-throughput multiplexed chromatin and RNA profiling reveals gene regulatory dynamics 2025 ·Nature Methods ·(unknown), Umut Yildiz, Annique Claringbould, Nila H. Servaas, (unknown), Christian Arnold, (unknown), (unknown), (unknown), Ivan Berest, Karin D. Prummel, Kyung‐Min Noh, Mikael Marttinen, Judith B. Zaugg	4
2	High-sensitivity C-reactive protein mediates age-related vascular dysfunction: the Rotterdam study 2025 ·European Journal of Preventive Cardiology ·(unknown), Annique Claringbould, A.H. Jan Danser, Bruno H. Stricker, Maryam Kavousi, Anton J.M. Roks, Fariba Ahmadizar	0
3	Identification of rare disease genes as drivers of common diseases through tissue-specific gene regulatory networks 2024 ·Scientific Reports ·Olivier B. Bakker, Annique Claringbould, Harm-Jan Westra, (unknown), (unknown), Urmo Võsa, (unknown), Sophie Mulcahy Symmons, (unknown), Marie C. Sadler, Zoltán Kutalik, Iris H. Jonkers, Lude Franke, Patrick Deelen	1
4	Co-expression in tissue-specific gene networks links genes in cancer-susceptibility loci to known somatic driver genes 2024 ·BMC Medical Genomics ·(unknown), (unknown), (unknown), (unknown), (unknown), Olivier B. Bakker, Annique Claringbould, Jeroen de Ridder, Wilbert Zwart, Harm-Jan Westra, Patrick Deelen, Lude Franke	1
5	Using parent‐offspring pairs and trios to estimate indirect genetic effects in education 2024 ·Genetic Epidemiology ·(unknown), Annique Claringbould, (unknown), Albertine J. Oldehinkel, Hanna M. van Loo	3
6	GRaNIE and GRaNPA : inference and evaluation of enhancer‐mediated gene regulatory networks 2023 ·Molecular Systems Biology ·(unknown), Christian Arnold, Annique Claringbould, (unknown), Nila H. Servaas, Maksim Kholmatov, (unknown), (unknown), Sophia Müller‐Dott, Armando Reyes‐Palomares, Giovanni Palla, (unknown), (unknown), Caroline Pabst, Judith B. Zaugg	31
7	Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations 2022 ·Human Genetics and Genomics Advances ·Maarja Lepamets, Chiara Auwerx, Margit Nõukas, Annique Claringbould, Eleonora Porcu, Mart Kals, Tuuli Jürgenson, Andrew P. Morris, Urmo Võsa, Murielle Bochud, Silvia Stringhini, Cisca Wijmenga, Lude Franke, Hedi Peterson, Jaak Vilo, Kaido Lepik, Reedik Mägi, Zoltán Kutalik	5
8	Limited evidence for blood eQTLs in human sexual dimorphism 2022 ·Genome Medicine ·Eleonora Porcu, Annique Claringbould, Antoine Weihs, Kaido Lepik, Tom G. Richardson, Uwe Völker, Federico Santoni, Alexander Teumer, Lude Franke, Alexandre Reymond, Zoltán Kutalik	7
9	Gender differences in the mental health impact of the COVID-19 lockdown: Longitudinal evidence from the Netherlands 2021 ·SSM - Population Health ·(unknown), Rob Alessie, Jochen O. Mierau, Marike Boezen, (unknown), (unknown), Lude Franke, Jackie Dekens, Patrick Deelen, Pauline Lanting, Judith M. Vonk, Ilja M. Nolte, Anil P. S. Ori, Annique Claringbould, (unknown), (unknown), (unknown), Robert Warmerdam, Soesma A. Jankipersadsing	65
10	Sex and Gender-Related Differences in COVID-19 Diagnoses and SARS-CoV-2 Testing Practices During the First Wave of the Pandemic: The Dutch Lifelines COVID-19 Cohort Study 2021 ·Journal of Women s Health ·Aranka Ballering, Sabine Oertelt‐Prigione, Tim olde Hartman, Judith G.M. Rosmalen, Marike Boezen, Jochen O. Mierau, Lude Franke, Jackie Dekens, Patrick Deelen, Pauline Lanting, Judith M. Vonk, Ilja M. Nolte, Anil P. S. Ori, Annique Claringbould, (unknown), (unknown), (unknown), Robert Warmerdam, Soesma A. Jankipersadsing	18
11	Correction for both common and rare cell types in blood is important to identify genes that correlate with age 2021 ·BMC Genomics ·(unknown), Annique Claringbould, (unknown), Dorret I. Boomsma, M. Arfan Ikram, P. Eline Slagboom, Harm-Jan Westra, Lude Franke	3
12	Systematic Prioritization of Candidate Genes in Disease Loci Identifies TRAFD1 as a Master Regulator of IFNγ Signaling in Celiac Disease 2021 ·Frontiers in Genetics ·Adriaan van der Graaf, Maria M. Zorro, Annique Claringbould, Urmo Võsa, Raúl Aguirre‐Gamboa, Chan Li, (unknown), Isis Ricaño-Ponce, Z Borek, Frits Koning, Yvonne Kooy–Winkelaar, Ludvig M. Sollid, Shuo‐Wang Qiao, Vinod Kumar, Yang Li, Lude Franke, Sebo Withoff, Cisca Wijmenga, Serena Sanna, Iris H. Jonkers	23
13	Enhancers in disease: molecular basis and emerging treatment strategies 2021 ·Trends in Molecular Medicine ·Annique Claringbould, Judith B. Zaugg	98
14	Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids 2020 ·Nature Communications ·Adriaan van der Graaf, Annique Claringbould, Antoine Rimbert, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Rick Jansen, Lude Franke, Harm-Jan Westra, Yang Li, Cisca Wijmenga, Serena Sanna	27
15	Evaluation of commonly used analysis strategies for epigenome- and transcriptome-wide association studies through replication of large-scale population studies 2019 ·Genome biology ·Jeroen van Rooij, Pooja R. Mandaviya, Annique Claringbould, Janine F. Felix, Jenny van Dongen, Rick Jansen, Lude Franke, Peter A.C. ’t Hoen, B.T. Heijmans, Joyce B. J. van Meurs	28
16	A characterization of cis- and trans-heritability of RNA-Seq-based gene expression 2019 ·European Journal of Human Genetics ·Klaasjan G. Ouwens, Rick Jansen, Michel G. Nivard, Jenny van Dongen, (unknown), (unknown), Wibowo Arindrarto, Annique Claringbould, Maarten van Iterson, Hailiang Mei, Lude Franke, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Andrew I. Brooks, Brenda W.J.H. Penninx, Dorret I. Boomsma	21
17	Comprehensive Multiple eQTL Detection and Its Application to GWAS Interpretation 2019 ·Genetics ·Biao Zeng, Luke R. Lloyd‐Jones, Grant W. Montgomery, Andres Metspalu, Tōnu Esko, Lude Franke, Urmo Võsa, Annique Claringbould, Kenneth L. Brigham, Arshed A. Quyyumi, Youssef Idaghdour, Jian Yang, Peter M. Visscher, Joseph E. Powell, Greg Gibson	17
18	A SNP panel for identification of DNA and RNA specimens 2018 ·BMC Genomics ·Soheil Yousefi, Tooba Abbassi‐Daloii, Thirsa Kraaijenbrink, Martijn Vermaat, Hailiang Mei, Peter van ‘t Hof, Maarten van Iterson, Daria V. Zhernakova, Annique Claringbould, Lude Franke, Leen M. ‘t Hart, Roderick C. Slieker, Amber van der Heijden, Peter de Knijff, Peter A.C. ’t Hoen	36
19	Individual variations in cardiovascular-disease-related protein levels are driven by genetics and gut microbiome 2018 ·Nature Genetics ·(unknown), Daria V. Zhernakova, Trang Le, Alexander Kurilshikov, Biljana Atanasovska, Marc Jan Bonder, Serena Sanna, Annique Claringbould, Urmo Võsa, Patrick Deelen, Lude Franke, Rudolf A. de Boer, Folkert Kuipers, Mihai G. Netea, Marten H. Hofker, Cisca Wijmenga, Alexandra Zhernakova, Jingyuan Fu	62
20	The genetic architecture of molecular traits 2017 ·Current Opinion in Systems Biology ·Annique Claringbould, Niek de Klein, Lude Franke	4

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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