Morris Swertz

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Cisca Wijmenga, PhDERC advanced investigator; Professor of Human Genetics, Dept Genetics (MGE), UMCG, Groningen, theVerified email at umcg.nl
K. Joeri van der VeldeUniversity Medical Center Groningen, Dept. of Genetics, Genomics Coordination CenterVerified email at umcg.nl
Lude FrankeProfessor of Functional Genomics, University Medical Centre GroningenVerified email at cleverfranke.com
Patrick DeelenPost-doc researcher at University Medical Center GroningenVerified email at umcg.nl
ritsert jansenProfessor of Bioinformatics, Dean of Talent DevelopmentVerified email at rug.nl
Freerk van DijkProgrammer at University Medical Center GroningenVerified email at umcg.nl
richard sinkeProfessor of Genome Analysis, dept. Genetics (MGE), University Medical Center GroningenVerified email at ziggo.nl
Alexandra (Sasha) ZhernakovaProfessor of Human Genome and Exposome, University Medical Centre Groningen, The NetherlandsVerified email at umcg.nl
Yang Li, PhDProfessor of Computational Biology, Director of CiiM, Helmholtz Centre for Infection Research (HZI)Verified email at helmholtz-hzi.de
Paul I W de BakkerVertex PharmaceuticalsVerified email at vrtx.com
Alexandros KanterakisInstitute of Computer Science, FORTH, GreeceVerified email at ics.forth.gr
Lennart JohanssonUniversity Medical Centre GroningenVerified email at umcg.nl
Martijn DijkstraPostdoc bioinformatics, University of GroningenVerified email at rug.nl
P. Eline SlagboomProfessor Molecular Epidemiology, Leiden University Medical CenterVerified email at lumc.nl
Ettje F TigchelaarResearcher at University Medical Center GroningenVerified email at umcg.nl
Rainer BreitlingProfessor of Systems Biology, Manchester Institute of Biotechnology, University of ManchesterVerified email at manchester.ac.uk
Tomasz Adamusiak MD PhDChief Scientist, Clinical Quality and Data ScienceVerified email at mitre.org
Jingyuan Fu, PhDProfessor, University Medical Center Groningen, NetherlandsVerified email at umcg.nl
Rolf SijmonsProfessor of Medical Translational Genetics, dept Genetics, University Medical Center GroningenVerified email at umcg.nl
Conny van Ravenswaaij-ArtsProfessor in Dysmorphology, Department of Genetics, UMC Groningen, University of GroningenVerified email at umcg.nl

Morris Swertz

Full Professor / Head of Genomics Coordination Center, Dept of Genetics, University Medical

Verified email at rug.nl - Homepage

bioinformatics


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1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function M Gorski, PJ Van der Most, A Teumer, AY Chu, M Li, V Mijatovic, IM Nolte, ... Scientific reports 7 (1), 45040, 2017	139	2017
14· Rachel Foong 15, 16· Veit Grote 17· Sido Haakma 18· Mark Hanson 19, 20· Jennifer R. Harris 21, 22· Barbara Heude 4· Rae-Chi Huang 15· Hazel Inskip 20 AMN Andersen, A Elhakeem, R Foong, V Grote, S Haakma, M Hanson, ...		2020
265 An International Patient Registry and Database for Microvillus Inclusion Disease and Associated MYO5B Mutations HS Dhekne, R Wagner, EH Rings, MA Swertz, SC van IJzendoorn Gastroenterology 5 (144), S-59, 2013		2013
A framework for the detection of de novo mutations in family-based sequencing data LC Francioli, M Cretu-Stancu, KV Garimella, M Fromer, WP Kloosterman, ... European Journal of Human Genetics 25 (2), 227-233, 2017	29	2017
A functional genomics approach to understand variation in cytokine production in humans Y Li, M Oosting, SP Smeekens, M Jaeger, R Aguirre-Gamboa, KTT Le, ... Cell 167 (4), 1099-1110. e14, 2016	322	2016
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ... Nature communications 7 (1), 12989, 2016	105	2016
A high-quality reference panel reveals the complexity and distribution of structural genome changes in a human population JY Hehir-Kwa, T Marschall, WP Kloosterman, LC Francioli, JA Baaijens, ... Biorxiv, 036897, 2016	4	2016
A high-throughput processing service for retention time alignment of complex proteomics and metabolomics LC-MS data I Ahmad, F Suits, B Hoekman, MA Swertz, H Byelas, M Dijkstra, R Hooft, ... Bioinformatics 27 (8), 1176-1178, 2011	18	2011
A meta-analysis of genome-wide association studies for serum hepcidin TE Galesloot, N Verweij, M Traglia, F van Dijk, AJ Geurts-Moespot, ... Hepcidin: population-based studies into genetic determinants and effects on …, 0
A Molecular Genetics Information System (MOLGENIS) for Genetical Genomics experiments MA Swertz, BM Tesson, RA Scheltema, G Vera, RC Jansen
A new workflow for classification of genetic variants pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic AutoInflammatory … M van Gijn, I Ceccherini, Y Shinar, E Carbo, M Slofstra, J Arostgui, ...		2019
A novel biomarker panel for irritable bowel syndrome and the application in the general population Z Mujagic, EF Tigchelaar, A Zhernakova, T Ludwig, J Ramiro-Garcia, ... Scientific reports 6 (1), 26420, 2016	54	2016
A novel faecal and plasma biomarker panel for IBS Z Mujagic, EF Tigchelaar, A Zhernakova, T Ludwig, J Ramiro-Garcia, ... Irritable bowel syndrome: pathophysiology, symptoms and biomarkers, 209, 2015		2015
A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature KJ van der Velde, S van den Hoek, F van Dijk, D Hendriksen, ... Advanced Genetics 1 (1), e10023, 2020	4	2020
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape JS Ried, J Jeff M, AY Chu, JL Bragg-Gresham, J Van Dongen, JE Huffman, ... Nature communications 7 (1), 1-11, 2016	89	2016
A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016	2968	2016
A resource for guiding data stewards to make European rare disease patient registries FAIR P Van Damme, PA Moreno, CH Bernabé, AC Ballesteros, CMA Le Cornec, ... Data Science Journal 22, 12, 2023	3	2023
A review of tools to automatically infer chromosomal positions from dbSNP and HGVS genetic variants A Kanterakis, T Katsila, G Potamias, GP Patrinos, MA Swertz Human Genome Informatics, 133-156, 2018	2	2018
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing AS Denommé-Pichon, L Matalonga, E de Boer, A Jackson, E Benetti, ... Genetics in Medicine 25 (4), 100018, 2023	7	2023
A unified data infrastructure to support large-scale rare disease research LF Johansson, S Laurie, D Spalding, S Gibson, D Ruvolo, C Thomas, ... medRxiv, 2023.12. 20.23299950, 2023		2023

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