Machteld M. Oud

2.0k total citations
19 papers, 360 citations indexed

About

Machteld M. Oud is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Machteld M. Oud has authored 19 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Machteld M. Oud's work include Genetic and Kidney Cyst Diseases (11 papers), Immunotherapy and Immune Responses (4 papers) and Protist diversity and phylogeny (4 papers). Machteld M. Oud is often cited by papers focused on Genetic and Kidney Cyst Diseases (11 papers), Immunotherapy and Immune Responses (4 papers) and Protist diversity and phylogeny (4 papers). Machteld M. Oud collaborates with scholars based in Netherlands, Germany and Canada. Machteld M. Oud's co-authors include Carl G. Figdor, Suzanne F. G. van Helden, Frank N. van Leeuwen, Heleen H. Arts, Ideke J.C. Lamers, Ben Joosten, Koen van den Dries, Ronald Roepman, Joost te Riet and Carlo Manzo and has published in prestigious journals such as The Journal of Immunology, Journal of Cell Science and Cellular and Molecular Life Sciences.

In The Last Decade

Machteld M. Oud

19 papers receiving 346 citations

Peers

Countries citing papers authored by Machteld M. Oud

Since Specialization

Citations

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

Fields of papers citing papers by Machteld M. Oud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Machteld M. Oud. 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 Machteld M. Oud. The network helps show where Machteld M. Oud may publish in the future.

Co-authorship network of co-authors of Machteld M. Oud

This figure shows the co-authorship network connecting the top 25 collaborators of Machteld M. Oud. A scholar is included among the top collaborators of Machteld M. Oud 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 Machteld M. Oud. Machteld M. Oud is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Genome and RNA sequencing were essential to reveal cryptic intronic variants associated to defective ATP6AP1 mRNA processing 2024 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Rafael Artuch, Àngels García‐Cazorla, Mar O’Callaghan, Jolanta Sykut‐Cegielska, Jaume Campistol, Pedro Moreno, Machteld M. Oud, Ron A. Wevers, Dirk J. Lefeber, Anna Esteve‐Codina, Vicente A. Yépez, Julien Gagneur, Saskia B. Wortmann, Holger Prokisch, Antònia Ribes, Judit García‐Villoria, Frederic Tort	2
2	Utilization of automated cilia analysis to characterize novel INPP5E variants in patients with non-syndromic retinitis pigmentosa 2024 ·European Journal of Human Genetics ·(unknown), Lonneke Haer‐Wigman, Ralph J. Florijn, Ronald van Beek, Machteld M. Oud, Astrid S. Plomp, Camiel J. F. Boon, Hester Y. Kroes, Ronald Roepman	1
3	Ciliary phenotyping in renal epithelial cells in a cranioectodermal dysplasia patient with WDR35 variants 2023 ·Frontiers in Molecular Biosciences ·Joanna Walczak‐Sztulpa, Anna Wawrocka, (unknown), (unknown), (unknown), Mirosław Andrusiewicz, M Krawczyński, Anna Latos‐Bieleńska, (unknown), Ryszard Grenda, Anna Materna‐Kiryluk, Machteld M. Oud, Witold Szaflarski	1
4	Inherited metabolic disorders in adults: systematic review on patient characteristics and diagnostic yield of broad sequencing techniques (exome and genome sequencing) 2023 ·Frontiers in Neurology ·(unknown), Mark J. Buijs, (unknown), Joost G. Daams, Mareen R. Datema, Marc Engelen, Clara D.M. van Karnebeek, Machteld M. Oud, Frédéric M. Vaz, Mirjam M. C. Wamelink, Saskia N. van der Crabben, Mirjam Langeveld	3
5	Identical IFT140 Variants Cause Variable Skeletal Ciliopathy Phenotypes—Challenges for the Accurate Diagnosis 2022 ·Frontiers in Genetics ·Joanna Walczak‐Sztulpa, Anna Wawrocka, (unknown), Ronald van Beek, Anna Sowińska‐Seidler, Aleksander Jamsheer, Ewelina Bukowska‐Olech, Anna Latos‐Bieleńska, Ryszard Grenda, Ernie M.H.F. Bongers, Miriam Schmidts, Ewa Obersztyn, M Krawczyński, Machteld M. Oud	5
6	Cell-based assay for ciliopathy patients to improve accurate diagnosis using ALPACA 2021 ·European Journal of Human Genetics ·(unknown), Ronald van Beek, Ernie M.H.F. Bongers, Dorien Lugtenberg, Peter H.M. Klaren, Lisenka E.L.M. Vissers, Ronald Roepman, Machteld M. Oud	11
7	Interfamilial clinical variability in four Polish families with cranioectodermal dysplasia and identical compound heterozygous variants in WDR35 2021 ·American Journal of Medical Genetics Part A ·Joanna Walczak‐Sztulpa, Anna Wawrocka, Małgorzata Stańczyk, Karolina Pesz, (unknown), (unknown), Ewelina Bukowska‐Olech, (unknown), Heleen H. Arts, Machteld M. Oud, Robert Śmigiel, Ryszard Grenda, Ewa Obersztyn, Krystyńa Chrzańowska, Anna Latos‐Bieleńska	6
8	Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease 2020 ·Orphanet Journal of Rare Diseases ·Joanna Walczak‐Sztulpa, Renata Posmyk, Ewelina Bukowska‐Olech, Anna Wawrocka, Aleksander Jamsheer, Machteld M. Oud, Miriam Schmidts, Heleen H. Arts, Anna Latos‐Bieleńska, Anna Wasilewska	12
9	Cellular ciliary phenotyping indicates pathogenicity of novel variants in IFT140 and confirms a Mainzer–Saldino syndrome diagnosis 2018 ·PubMed ·Machteld M. Oud, Brooke Latour, Zeineb Bakey, Stef J.F. Letteboer, Dorien Lugtenberg, Ka Man Wu, Elisabeth A. M. Cornelissen, Helger G. Yntema, Miriam Schmidts, Ronald Roepman, Ernie M.H.F. Bongers	25
10	The KOUNCIL Consortium: From Genetic Defects to Therapeutic Development for Nephronophthisis 2018 ·Frontiers in Pediatrics ·Kirsten Y. Renkema, Rachel H. Giles, Marc R. Liliën, Philip L. Beales, Ronald Roepman, Machteld M. Oud, Heleen H. Arts, Nine V.A.M. Knoers	3
11	Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa 2017 ·Journal of Medical Genetics ·Thanh-Minh T. Nguyen, Sarah Hull, Ronald Roepman, L. Ingeborgh van den Born, Machteld M. Oud, Erik de Vrieze, Lisette Hetterschijt, Stef J.F. Letteboer, Sylvia E. C. van Beersum, Ellen A.W. Blokland, Helger G. Yntema, Frans P.M. Cremers, Paul A. van der Zwaag, Gavin Arno, Erwin van Wijk, Andrew R. Webster, Lonneke Haer‐Wigman	18
12	Ciliopathies: Genetics in Pediatric Medicine 2016 ·Journal of Pediatric Genetics ·Machteld M. Oud, Ideke J.C. Lamers, Heleen H. Arts	46
13	De novo 14q24.2q24.3 microdeletion including IFT43 is associated with intellectual disability, skeletal anomalies, cardiac anomalies, and myopia 2016 ·American Journal of Medical Genetics Part A ·Marijn F. Stokman, Machteld M. Oud, Ellen van Binsbergen, Gisela G. Slaats, Nayia Nicolaou, Kirsten Y. Renkema, Isaäc J. Nijman, Ronald Roepman, Rachel H. Giles, Heleen H. Arts, Nine Knoers, Mieke M. van Haelst	15
14	Early presentation of cystic kidneys in a family with a homozygous INVS mutation 2014 ·American Journal of Medical Genetics Part A ·Machteld M. Oud, Bregje W.M. van Bon, Ernie M.H.F. Bongers, Alexander Hoischen, Carlo Marcelis, Nicole de Leeuw, (unknown), Geert Mortier, Nine Knoers, Han G. Brunner, Ronald Roepman, Heleen H. Arts	6
15	Unraveling the human dendritic cell phagosome proteome by organellar enrichment ranking 2011 ·Journal of Proteomics ·Sonja I. Buschow, Edwin Lasonder, Radek Szklarczyk, Machteld M. Oud, I. Jolanda M. de Vries, Carl G. Figdor	23
16	Geometry sensing by dendritic cells dictates spatial organization and PGE2-induced dissolution of podosomes 2011 ·Cellular and Molecular Life Sciences ·Koen van den Dries, Suzanne F. G. van Helden, Joost te Riet, (unknown), Carlo Manzo, Machteld M. Oud, Frank N. van Leeuwen, Roland Brock, M.F. Garcia Parajo, Alessandra Cambi, Carl G. Figdor	64
17	Dominant Processes during Human Dendritic Cell Maturation Revealed by Integration of Proteome and Transcriptome at the Pathway Level 2010 ·Journal of Proteome Research ·Sonja I. Buschow, Edwin Lasonder, Hanneke W. M. van Deutekom, Machteld M. Oud, Luca Beltrame, Martijn A. Huynen, I. Jolanda M. de Vries, Carl G. Figdor, Duccio Cavalieri	21
18	TLR4-Mediated Podosome Loss Discriminates Gram-Negative from Gram-Positive Bacteria in Their Capacity to Induce Dendritic Cell Migration and Maturation 2009 ·The Journal of Immunology ·Suzanne F. G. van Helden, Koen van den Dries, Machteld M. Oud, Reinier Raymakers, Mihai G. Netea, Frank N. van Leeuwen, Carl G. Figdor	25
19	PGE2-mediated podosome loss in dendritic cells is dependent on actomyosin contraction downstream of the RhoA–Rho-kinase axis 2008 ·Journal of Cell Science ·Suzanne F. G. van Helden, Machteld M. Oud, Ben Joosten, (unknown), Carl G. Figdor, Frank N. van Leeuwen	73

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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