Dirk S. Paul

23.1k total citations · 1 hit paper
34 papers, 2.0k citations indexed

About

Dirk S. Paul is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Dirk S. Paul has authored 34 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Genetics and 5 papers in Hematology. Recurrent topics in Dirk S. Paul's work include Epigenetics and DNA Methylation (10 papers), Genetic Associations and Epidemiology (7 papers) and RNA modifications and cancer (5 papers). Dirk S. Paul is often cited by papers focused on Epigenetics and DNA Methylation (10 papers), Genetic Associations and Epidemiology (7 papers) and RNA modifications and cancer (5 papers). Dirk S. Paul collaborates with scholars based in United Kingdom, United States and Finland. Dirk S. Paul's co-authors include Adam S. Butterworth, John Danesh, Benjamin B. Sun, Stephen Burgess, Stephan Beck, Praveen Surendran, James R Staley, Robin Young, James Blackshaw and Ian O. Ellis and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Genetics.

In The Last Decade

Dirk S. Paul

34 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

PhenoScanner: a database of human genotype–phenotype associations

2016 883 citations James R Staley, James Blackshaw et al. Bioinformatics profile →

Peers

Countries citing papers authored by Dirk S. Paul

Since Specialization

Citations

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

Fields of papers citing papers by Dirk S. Paul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dirk S. Paul. 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 Dirk S. Paul. The network helps show where Dirk S. Paul may publish in the future.

Co-authorship network of co-authors of Dirk S. Paul

This figure shows the co-authorship network connecting the top 25 collaborators of Dirk S. Paul. A scholar is included among the top collaborators of Dirk S. Paul 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 Dirk S. Paul. Dirk S. Paul 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	Donor whole blood DNA methylation is not a strong predictor of acute graft versus host disease in unrelated donor allogeneic haematopoietic cell transplantation 2024 ·Frontiers in Genetics ·Amy P. Webster, Simone Ecker, Ismail Moghul, Xiaohong Liu, Pawan Dhami, Sarah J. Marzi, Dirk S. Paul, Michelle Kuxhausen, Stephanie J. Lee, Stephen R. Spellman, Tao Wang, Andrew Feber, Vardhman K. Rakyan, Karl S. Peggs, Stephan Beck	1
2	Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank 2023 ·The American Journal of Human Genetics ·Abhishek Nag, Ryan S. Dhindsa, (unknown), Xiao Jiang, Dimitrios Vitsios, Eleanor M. Wigmore, Erik L. Allman, Anna Reznichenko, Keren Carss, Katherine R. Smith, Quanli Wang, Benjamin Challis, Dirk S. Paul, Andrew R. Harper, Slavé Petrovski	8
3	Genetically personalised organ-specific metabolic models in health and disease 2022 ·Nature Communications ·Carles Foguet, Yu Xu, Scott C. Ritchie, Samuel A. Lambert, Elodie Persyn, Artika P. Nath, Emma E. Davenport, David J. Roberts, Dirk S. Paul, Emanuele Di Angelantonio, John Danesh, Adam S. Butterworth, Christopher Yau, Michael Inouye	13
4	Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans 2022 ·eLife ·Susanna Lemmelä, Eleanor M. Wigmore, Christian Benner, Aki S. Havulinna, (unknown), Tibor Kempf, Kai C. Wollert, Stefan Blankenberg, Tanja Zeller, James E. Peters, Veikko Salomaa, (unknown), Ruth March, Aarno Palotie, Mark J. Daly, Adam S. Butterworth, Mervi Alanne-Kinnunen, Dirk S. Paul, Athena Matakidou	14
5	Pharmacogenomic Study of Heart Failure and Candesartan Response from the CHARM Programme 2022 ·ESC Heart Failure ·Marie‐Pierre Dubé, Olympe Chazara, Audrey Lemaçon, Géraldine Asselin, Sylvie Provost, Amina Barhdadi, Louis‐Philippe Lemieux Perreault, Ian Mongrain, Quanli Wang, Keren Carss, Dirk S. Paul, Jonathan W. Cunningham, Jean L. Rouleau, Scott D. Solomon, John J.V. McMurray, Salim Yusuf, C. B. Granger, Carolina Haefliger, Simon de Denus, Jean‐Claude Tardif	5
6	ProGeM: a framework for the prioritization of candidate causal genes at molecular quantitative trait loci 2018 ·Nucleic Acids Research ·David Stacey, Eric B. Fauman, Daniel Ziemek, Benjamin B. Sun, Eric L. Harshfield, Angela Wood, Adam S. Butterworth, Karsten Suhre, Dirk S. Paul	57
7	Increased DNA methylation variability in rheumatoid arthritis-discordant monozygotic twins 2018 ·Genome Medicine ·Amy P. Webster, Darren Plant, Simone Ecker, Flore Zufferey, Jordana T. Bell, Andrew Feber, Dirk S. Paul, Stephan Beck, Anne Barton, Frances M. K. Williams, Jane Worthington	60
8	Correlation of an epigenetic mitotic clock with cancer risk 2016 ·Genome biology ·Zhen Yang, Andrew Wong, Diana Kuh, Dirk S. Paul, Vardhman K. Rakyan, Richard David Leslie, Shijie Zheng, Martin Widschwendter, Stephan Beck, Andrew E. Teschendorff	190
9	PhenoScanner: a database of human genotype–phenotype associations breakdown → 2016 ·Bioinformatics ·James R Staley, James Blackshaw, Mihir Kamat, Ian O. Ellis, Praveen Surendran, Benjamin B. Sun, Dirk S. Paul, (unknown), Stephen Burgess, John Danesh, Robin Young, Adam S. Butterworth	883
10	A donor-specific epigenetic classifier for acute graft-versus-host disease severity in hematopoietic stem cell transplantation 2015 ·Genome Medicine ·Dirk S. Paul, Allison Jones, Rob S. Sellar, Neema P. Mayor, Andrew Feber, Amy P. Webster, (unknown), Ruhena Sergeant, Richard Szydlo, Jane F. Apperley, Martin Widschwendter, Stephen Mackinnon, Steven G. E. Marsh, J. Alejandro Madrigal, Vardhman K. Rakyan, Karl S. Peggs, Stephan Beck	6
11	Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics 2014 ·Genome Medicine ·Paul Guilhamon, Lee M Butcher, Nadège Presneau, Gareth A. Wilson, Andrew Feber, Dirk S. Paul, Moritz Schütte, Johannes Haybaeck, Ulrich Keilholz, (unknown), Mark T. Ross, Adrienne M. Flanagan, Stephan Beck	19
12	Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing 2014 ·Epigenetics ·Dirk S. Paul, Paul Guilhamon, Anna Karpathakis, Lee M Butcher, Christina Thirlwell, Andrew Feber, Stephan Beck	22
13	Advances in epigenome-wide association studies for common diseases 2014 ·Trends in Molecular Medicine ·Dirk S. Paul, Stephan Beck	40
14	Inflammatory response to acute exposure to welding fumes during the working day 2013 ·International Journal of Occupational Medicine and Environmental Health ·(unknown), Dirk S. Paul, Timo Tuomi, Ritva Luukkonen, Harri Lindholm, Riina Nieminen, Eeva Moilanen, Timo Hannu	25
15	Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci 2013 ·Genome Research ·Dirk S. Paul, Cornelis A. Albers, Augusto Rendon, Katrin Voß, Jonathan Stephens, Pim van der Harst, John C. Chambers, Nicole Soranzo, Willem H. Ouwehand, Panos Deloukas	25
16	Functional interpretation of non‐coding sequence variation: Concepts and challenges 2013 ·BioEssays ·Dirk S. Paul, Nicole Soranzo, Stephan Beck	33
17	A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site 2012 ·Blood ·Sylvia Nürnberg, Augusto Rendon, Peter A. Smethurst, Dirk S. Paul, Katrin Voß, Jonathan N. Thon, Heather Lloyd-Jones, Jennifer G. Sambrook, Marloes R. Tijssen, Joseph E. Italiano, Panos Deloukas, Berthold Göttgens, Nicole Soranzo, Willem H. Ouwehand	31
18	Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits 2011 ·PLoS Genetics ·Dirk S. Paul, James Nisbet, Tsun-Po Yang, Stuart Meacham, Augusto Rendon, (unknown), Jonna Tallila, Jacqui White, Marloes R. Tijssen, Suthesh Sivapalaratnam, Hanneke Basart, Mieke D. Trip, (unknown), Nicole Soranzo, Willem H. Ouwehand, Panos Deloukas	2
19	Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits 2011 ·PLoS Genetics ·Dirk S. Paul, James Nisbet, Tsun-Po Yang, Stuart Meacham, Augusto Rendon, (unknown), Jonna Tallila, Jacqui White, Marloes R. Tijssen, Suthesh Sivapalaratnam, Hanneke Basart, Mieke D. Trip, Berthold Göttgens, Nicole Soranzo, Willem H. Ouwehand, Panos Deloukas	29
20	A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population 2001 ·Nature Genetics ·Tarja Laitinen, Mark J. Daly, John D. Rioux, Dirk S. Paul, Catherine Laprise, Tuula Petäys, Todd Green, Michele Cargill, Tari Haahtela, Eric S. Lander, Lauri A. Laitinen, Thomas J. Hudson, Juha Kere	144

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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