Morris A. Swertz

63.2k citations

118 papers · 4.5k indexed · 1 hit paper · h-index 39

Aging top 2%
Genetics top 1%
- Genomics and Rare Diseases 18
- Genomic variations and chromosomal abnormalities 11
- Genetic Associations and Epidemiology 11
Molecular Biology top 5%
- Biomedical Text Mining and Ontologies 20
- Bioinformatics and Genomic Networks 20
- Gene expression and cancer classification 15
- Genomics and Phylogenetic Studies 13
Cancer Research top 5%
Information Systems and Management top 2%
- Scientific Computing and Data Management 16

Co-authors: Cisca Wijmenga Ritsert C. Jansen Patrick Deelen Lude Franke Freerk van Dijk Rainer Breitling Ronald P. Stolk Salome Scholtens
Cited by: Aging Genetics Molecular Biology
Journals: Nucleic Acids Research (2 papers)Nature Medicine (1 paper)Nature Genetics (2 papers)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Morris A. Swertz

114 papers receiving 4.5k citations

Hit Papers

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Peers

Countries citing papers authored by Morris A. Swertz

Since Specialization

Citations

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

Fields of papers citing papers by Morris A. Swertz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Morris A. Swertz. 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 Morris A. Swertz. The network helps show where Morris A. Swertz may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Morris A. Swertz, 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 Morris A. Swertz Line = papers co-authored together Morris A. Swertz links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	FAIR Data Cube, a FAIR data infrastructure for integrated multi-omics data analysis Journal of Biomedical Semantics ·Xiaofeng Liao,Thomas H. A. Ederveen,Anna Niehues,Casper de Visser,Junda Huang,Firdaws Badmus,Cenna Doornbos,Yuliia Orlova,Purva Kulkarni,K. Joeri van der Velde,Morris A. Swertz,Martin J. Brandt,Alain J. van Gool,Peter A.C. ’t Hoen	2024	2
2	Visualization and exploration of linked data using virtual reality Database ·Alexander Kellmann,Max Postema,Joris de Keijser,Pjotr Svetachov,Rebecca Wilson,David van Enckevort,Morris A. Swertz	2024	1
3	The Impact of Mode of Birth, and Episiotomy, on Postpartum Sexual Function in the Medium- and Longer-Term: An Integrative Systematic Review International Journal of Environmental Research and Public Health ·Anne-Marie Fanshawe,Ank de Jonge,Nicole Ginter,L Takács,Hannah Dahlen,Morris A. Swertz,Lilian L. Peters	2023	8
4	A Resource for Guiding Data Stewards to Make European Rare Disease Patient Registries FAIR Data Science Journal ·Philip van Damme,Pablo Alarcón Moreno,César H. Bernabé,Alberto Cámara Ballesteros,Clémence M. A. Le Cornec,Bruna dos Santos Vieira,K. Joeri van der Velde,Shuxin Zhang,Claudio Carta,Ronald Cornet,Peter A.C. ’t Hoen,Annika Jacobsen,Morris A. Swertz,Marco Roos,Nirupama Benis	2023	2
5	Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry data Journal of Biomedical Semantics ·Rajaram Kaliyaperumal,Mark D. Wilkinson,Pablo Alarcón Moreno,Nirupama Benis,Ronald Cornet,Bruna dos Santos Vieira,Michel Dumontier,César H. Bernabé,Annika Jacobsen,Clémence M. A. Le Cornec,Mario Prieto Godoy,Núria Queralt-Rosiñach,Leo J. Schultze Kool,Morris A. Swertz,Philip van Damme,K. Joeri van der Velde,Nawel Lalout,Shuxin Zhang,Marco Roos	2022	16
6	Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registries Orphanet Journal of Rare Diseases ·Bruna dos Santos Vieira,César H. Bernabé,Shuxin Zhang,Haitham Abaza,Nirupama Benis,Alberto Cámara,Ronald Cornet,Clémence M. A. Le Cornec,Peter A.C. ’t Hoen,Franz Schaefer,K. Joeri van der Velde,Morris A. Swertz,Mark D. Wilkinson,Annika Jacobsen,Marco Roos	2022	15
7	Therapeutic Prospects of Exon Skipping for Epidermolysis Bullosa International Journal of Molecular Sciences ·Franciscus C. Vermeer,Jeroen Bremer,Robert Sietsma,Aileen Sandilands,Robyn P. Hickerson,Maria C. Bolling,Anna M.G. Pasmooij,Henny H. Lemmink,Morris A. Swertz,Nine V.A.M. Knoers,K. van der Velde,Peter C. van den Akker	2021	10
8	Habitual dietary intake of IBD patients differs from population controls: a case–control study European Journal of Nutrition ·Vera Peters,Ettje F. Tigchelaar-Feenstra,Floris Imhann,Jackie Dekens,Morris A. Swertz,Lude Franke,Cisca Wijmenga,Rinse K. Weersma,Behrooz Z. Alizadeh,Gerard Dijkstra,Marjo Campmans‐Kuijpers	2020	38
9	BBMRI-ERIC’s contributions to research and knowledge exchange on COVID-19 European Journal of Human Genetics ·(unknown),Petr Holub,Łukasz Kozera,Francesco Florindi,David van Enckevort,Morris A. Swertz,Robert Reihs,Andrea Wutte,Dalibor Valík,Michaela Th. Mayrhofer	2020	16
10	The 1000IBD project: multi-omics data of 1000 inflammatory bowel disease patients; data release 1 BMC Gastroenterology ·Floris Imhann,K. Joeri van der Velde,Ruggero Barbieri,Rudi Alberts,Michiel Voskuil,Arnau Vich Vila,Valerie Collij,Lieke M. Spekhorst,Kimberley W. J. van der Sloot,Vera Peters,Hendrik M. van Dullemen,Marijn C. Visschedijk,Eleonora A. Festen,Morris A. Swertz,Gerard Dijkstra,Rinse K. Weersma	2019	62
11	reGenotyper: Detecting mislabeled samples in genetic data PLoS ONE ·Konrad Zych,Basten L. Snoek,Mark Elvin,Míriam Antón‐Rodríguez,K. Joeri van der Velde,Danny Arends,Harm-Jan Westra,Morris A. Swertz,Gino Poulin,Jan E. Kammenga,Rainer Breitling,Ritsert C. Jansen,Yang Li	2017	11
12	Population-specific genotype imputations using minimac or IMPUTE2 Nature Protocols ·(unknown),Alexandros Kanterakis,Patrick Deelen,Mathijs Kattenberg,P. Eline Slagboom,Paul I. W. de Bakker,Cisca Wijmenga,Morris A. Swertz,Dorret I. Boomsma,Cornelia M. van Duijn,Lennart C. Karssen,Jouke‐Jan Hottenga	2015	66
13	Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics BMJ Open ·Ettje F. Tigchelaar,Alexandra Zhernakova,Jackie Dekens,Gerben D. A. Hermes,Agnieszka Barańska,Zlatan Mujagic,Morris A. Swertz,Angélica María Muñoz Contreras,Patrick Deelen,María Carmen Cénit,Lude Franke,Salome Scholtens,Ronald P. Stolk,Cisca Wijmenga,Edith J. M. Feskens	2015	129
14	Genome-wide patterns and properties of de novo mutations in humans Nature Genetics ·Laurent C. Francioli,Paz Polak,Amnon Koren,Androniki Menelaou,Sung Chun,Ivo Renkens,Cornelia M. van Duijn,Morris A. Swertz,Cisca Wijmenga,Gert‐Jan B. van Ommen,P. Eline Slagboom,Dorret I. Boomsma,Kai Ye,Victor Guryev,Peter F. Arndt,Wigard P. Kloosterman,Paul I. W. de Bakker,Shamil Sunyaev	2015	238
15	The Hybrid Synthetic Microdata Platform: A Method for Statistical Disclosure Control Biopreservation and Biobanking ·Joël Kuiper,Edwin R. van den Heuvel,Morris A. Swertz	2015	1
16	Consensus and conflict cards for metabolic pathway databases BMC Systems Biology ·Miranda D. Stobbe,Morris A. Swertz,Ines Thiele,Trebor Rengaw,Antoine H. C. van Kampen,Perry D. Moerland	2013	7
17	Observ-OM and Observ-TAB: Universal syntax solutions for the integration, search, and exchange of phenotype and genotype information Human Mutation ·Tomasz Adamusiak,Helen Parkinson,Juha Muilu,Erik T Roos,Kasper Joeri van der Velde,Guðmundur Á. Þórisson,Myles Byrne,Chao Pang,Sirisha Gollapudi,Vincent Ferretti,Hans L. Hillege,Anthony J. Brookes,Morris A. Swertz	2012	16
18	How to kickstart a national biobanking infrastructure – experiences and prospects of BBMRI-NL Nordic Psychology ·Margreet Brandsma,Fredric Baas,Paul I. W. de Bakker,E.P. Beem,D.I. Boomsma,Jasper Bovenberg,Beatriz Mesquita,Cornelia M. van Duijn,Lambertus A. Kiemeney,Olaf H. Klungel,Peter W. de Leeuw,F. van Leeuwen,J. Ridder-Numan,Ronald P. Stolk,P. Eline Slagboom,Morris A. Swertz,Cisca Wijmenga,G.J.B. van Ommen	2012	0
19	Exome sequencing in a family segregating for celiac disease Clinical Genetics ·AM Szperl,Isis Ricaño-Ponce,JK Li,Patrick Deelen,Alexandros Kanterakis,Vincent Plagnol,Freerk van Dijk,H.‐J. Westra,Gosia Trynka,CJ Mulder,Morris A. Swertz,Cisca Wijmenga,Hancheng Zheng	2011	14
20	XGAP: a uniform and extensible data model and software platform for genotype and phenotype experiments Genome Biology ·Morris A. Swertz,K. Joeri van der Velde,Bruno Tesson,Richard A. Scheltema,Danny Arends,Gonzalo Vera,Rudi Alberts,Martijn Dijkstra,Paul N. Schofield,Klaus Schughart,John M. Hancock,Damian Smedley,Katherine Wolstencroft,Carole Goble,E.O. de Brock,Andrew R. Jones,Helen Parkinson,Ritsert C. Jansen,(unknown)	2010	23

About Morris A. Swertz

Morris A. Swertz is a scholar working on Information Systems and Management, Aging and Genetics, having authored 118 papers that have together received 4.5k indexed citations. Recurring topics across this work include Biomedical Text Mining and Ontologies (20 papers), Bioinformatics and Genomic Networks (20 papers), Genomics and Rare Diseases (18 papers), Scientific Computing and Data Management (16 papers), Gene expression and cancer classification (15 papers), Genomics and Phylogenetic Studies (13 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetic Associations and Epidemiology (11 papers). The work is most often cited by research in Aging (134 citations), Genetics (1.3k citations) and Molecular Biology (2.1k citations). Morris A. Swertz has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Cisca Wijmenga, Ritsert C. Jansen, Patrick Deelen, Lude Franke, Freerk van Dijk, Rainer Breitling, Ronald P. Stolk, Salome Scholtens, K. Joeri van der Velde and Bruce H. R. Wolffenbuttel. Their work appears in journals such as Nucleic Acids Research, Nature Medicine and Nature 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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