Martin Elferink

1.3k total citations
24 papers, 589 citations indexed

About

Martin Elferink is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Martin Elferink has authored 24 papers receiving a total of 589 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Martin Elferink's work include Genetic and phenotypic traits in livestock (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Martin Elferink is often cited by papers focused on Genetic and phenotypic traits in livestock (6 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Martin Elferink collaborates with scholars based in Netherlands, United States and Belgium. Martin Elferink's co-authors include Martien A. M. Groenen, R.P.M.A. Crooijmans, A. Jungerius, Hendrik‐Jan Megens, Addie Vereijken, Tineke Veenendaal, Pieter Van As, Xiaoxiang Hu, Koen L.I. van Gassen and Bert van der Zwaag and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and SHILAP Revista de lepidopterología.

In The Last Decade

Martin Elferink

22 papers receiving 579 citations

Peers

Countries citing papers authored by Martin Elferink

Since Specialization

Citations

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

Fields of papers citing papers by Martin Elferink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Elferink

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Elferink. A scholar is included among the top collaborators of Martin Elferink 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 Martin Elferink. Martin Elferink 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	Comprehensive analysis across SMN2 excludes DNA methylation as an epigenetic biomarker for spinal muscular atrophy 2025 ·iScience ·(unknown), (unknown), (unknown), Martin Elferink, (unknown), (unknown), Paul J. Hop, Ramona A. J. Zwamborn, (unknown), (unknown), Hanneke W. M. van Deutekom, Wouter van Rheenen, (unknown), (unknown), Renske I. Wadman, W. Ludo van der Pol, (unknown), Ewout J. N. Groen	0
2	Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophy 2025 ·Genome Medicine ·(unknown), Martin Elferink, (unknown), (unknown), Laura Campello Blasco, (unknown), (unknown), Ivo Renkens, (unknown), (unknown), Carlo Vermeulen, Roy Straver, Hanneke W. M. van Deutekom, Jan H. Veldink, Fay‐Lynn Asselman, Eduardo F. Tizzano, Renske I. Wadman, W. Ludo van der Pol, (unknown), Ewout J. N. Groen	1
3	The Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Disease 2024 ·Kidney International Reports ·(unknown), Robert F. Ernst, Martin Elferink, Hanneke W. M. van Deutekom, Bert van der Zwaag, Albertien M. van Eerde	0
4	The patient with 41 reports: Analysis of laboratory exome sequencing reporting of a “virtual patient” 2022 ·Genetics in Medicine ·Danya F. Vears, Martin Elferink, Marjolein Kriek, Pascal Borry, Koen L.I. van Gassen	2
5	Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndrome 2022 ·Journal of Clinical Investigation ·Andres Ramirez-Martinez, Yichi Zhang, Marie-José van den Boogaard, John McAnally, (unknown), Andreas C. Chai, Francesco Chemello, (unknown), Inge Cuppen, Martin Elferink, Robert J.J. van Es, Nard G. Janssen, (unknown), Ning Liu, Rhonda Bassel‐Duby, Richard H. van Jaarsveld, Eric N. Olson	17
6	Accurate detection of circulating tumor DNA using nanopore consensus sequencing 2021 ·npj Genomic Medicine ·Alessio Marcozzi, Myrthe Jager, Martin Elferink, Roy Straver, (unknown), (unknown), Li‐Ting Chen, Ivo Renkens, Joyce van Kuik, Chris H.J. Terhaard, Remco de Bree, Lot A. Devriese, Stefan M. Willems, Wigard P. Kloosterman, Jeroen de Ridder	31
7	Analysis of laboratory reporting practices using a quality assessment of a virtual patient 2020 ·Genetics in Medicine ·Danya F. Vears, Martin Elferink, Marjolein Kriek, Pascal Borry, Koen L.I. van Gassen	9
8	Genetics-first approach improves diagnostics of ESKD patients <50 years old 2020 ·Nephrology Dialysis Transplantation ·Rozemarijn Snoek, Richard H. van Jaarsveld, Tri Q. Nguyen, Edith Peters, Martin Elferink, Robert F. Ernst, Maarten B. Rookmaaker, Marc R. Liliën, Eric Spierings, Roel Goldschmeding, Nine Knoers, Bert van der Zwaag, Arjan D. van Zuilen, Albertien M. van Eerde	28
9	Discordant NIPT result in a viable trisomy‐21 pregnancy due to prolonged contribution to cf DNA by a demised trisomy‐14 cotwin 2018 ·Clinical Case Reports ·Ron Hochstenbach, Martin Elferink, (unknown), Klaske D. Lichtenbelt, (unknown), Heleen Schuring‐Blom, Godelieve C.M.L. Page‐Christiaens	8
10	Mutations in N-acetylglucosamine (O-GlcNAc) transferase in patients with X-linked intellectual disability 2017 ·Journal of Biological Chemistry ·(unknown), Mehmet Gundogdu, Marlies Kempers, Jacques C. Giltay, Rolph Pfundt, Martin Elferink, (unknown), Joris Fuijkschot, Andrew T. Ferenbach, Koen L.I. van Gassen, Daan M. F. van Aalten, Dirk J. Lefeber	66
11	Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing 2017 ·Scientific Reports ·Lennart Johansson, Eddy N. de Boer, (unknown), Freerk van Dijk, Martin Elferink, G. Heleen Schuring‐Blom, Ron F. Suijkerbuijk, Richard J. Sinke, Gerard J. te Meerman, Rolf H. Sijmons, Morris A. Swertz, Birgit Sikkema‐Raddatz	10
12	Maternal vitamin B12 deficiency and abnormal cell-free DNA results in pregnancy 2016 ·Prenatal Diagnosis ·Heleen Schuring‐Blom, Klaske D. Lichtenbelt, Karin P. M. van Galen, Martin Elferink, Marjan M. Weiss, Joris Vermeesch, (unknown)	12
13	Targeted next-generation sequencing: A novel diagnostic tool for primary immunodeficiencies 2013 ·Journal of Allergy and Clinical Immunology ·Isaäc J. Nijman, Joris M. van Montfrans, Marlous Hoogstraat, Marianne Boes, Lisette van de Corput, Ellen D. Renner, (unknown), Stef van Lieshout, Martin Elferink, Mirjam van der Burg, Clementien L. Vermont, Bert van der Zwaag, Esther Janson, Edwin Cuppen, Johannes Kristian Ploos van Amstel, Mariëlle van Gijn	95
14	Signatures of Selection in the Genomes of Commercial and Non-Commercial Chicken Breeds 2012 ·PLoS ONE ·Martin Elferink, Hendrik‐Jan Megens, Addie Vereijken, Xiaoxiang Hu, R.P.M.A. Crooijmans, Martien A. M. Groenen	58
15	Whole genome SNP discovery and analysis of genetic diversity in Turkey (Meleagris gallopavo) 2012 ·BMC Genomics ·Muhammad Luqman Aslam, J.W.M. Bastiaansen, Martin Elferink, Hendrik‐Jan Megens, R.P.M.A. Crooijmans, Le Ann Blomberg, Robert C. Fleischer, Curtis P. Van Tassell, Tad S. Sonstegard, Steven Schroeder, Martien A. M. Groenen, Julie A. Long	62
16	Genetic correlation between heart ratio and body weight as a function of ascites frequency in broilers split up into sex and health status 2012 ·Poultry Science ·(unknown), P. Van As, Martin Elferink, (unknown), Martien A. M. Groenen, Addie Vereijken, J.A.M. van Arendonk, H. Bovenhuis	14
17	Signatures of selection in Holstein Friesian dairy cattle 2012 ·Socio-Environmental Systems Modeling ·Martin Elferink, H. Bovenhuis, R.F. Veerkamp, M.P. Coffey, E. Wall, S. McParland, (unknown), J.W.M. Bastiaansen	1
18	Regional differences in recombination hotspots between two chicken populations 2010 ·BMC Genetics ·Martin Elferink, Pieter Van As, Tineke Veenendaal, R.P.M.A. Crooijmans, Martien A. M. Groenen	48
19	The use of blood gas parameters to predict ascites susceptibility in juvenile broilers 2010 ·Poultry Science ·P. Van As, Martin Elferink, (unknown), Addie Vereijken, H. Bovenhuis, R.P.M.A. Crooijmans, Eddy Decuypere, Martien A. M. Groenen	13
20	Partial duplication of the PRLR and SPEF2 genes at the late feathering locus in chicken 2008 ·BMC Genomics ·Martin Elferink, (unknown), A. Jungerius, R.P.M.A. Crooijmans, Martien A. M. Groenen	90

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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