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Year Number of Results
1983 1
1984 1
1986 2
1987 1
1988 5
1989 1
1990 2
1992 1
1995 1
2000 1
2003 1
2005 2
2007 1
2008 3
2009 9
2010 7
2011 2
2012 10
2014 4
2015 3
2016 3
2017 2
2018 9
2019 3
2020 1
2021 1
2022 1
2023 2
2024 0

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75 results

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Page 1
Diversity and Clonality of T Cell Receptor Repertoire and Antigen Specificities in Small Joints of Early Rheumatoid Arthritis.
Turcinov S, Af Klint E, Van Schoubroeck B, Kouwenhoven A, Mia S, Chemin K, Wils H, Van Hove C, De Bondt A, Keustermans K, Van Houdt J, Reumers J, Felix N, Rao NL, Peeters P, Stevenaert F, Klareskog L, McKinnon M, Baker D, Suri A, Malmström V. Turcinov S, et al. Among authors: van houdt j. Arthritis Rheumatol. 2023 May;75(5):673-684. doi: 10.1002/art.42407. Epub 2023 Feb 26. Arthritis Rheumatol. 2023. PMID: 36409582
The flexoelectric effect in Al-doped hafnium oxide.
Celano U , Popovici M , Florent K , Lavizzari S , Favia P , Paulussen K , Bender H , di Piazza L , Van Houdt J , Vandervorst W . Celano U , et al. Among authors: van houdt j. Nanoscale. 2018 May 10;10(18):8471-8476. doi: 10.1039/c8nr00618k. Nanoscale. 2018. PMID: 29691544
Comparative analysis of antibody- and lipid-based multiplexing methods for single-cell RNA-seq.
Mylka V, Matetovici I, Poovathingal S, Aerts J, Vandamme N, Seurinck R, Verstaen K, Hulselmans G, Van den Hoecke S, Scheyltjens I, Movahedi K, Wils H, Reumers J, Van Houdt J, Aerts S, Saeys Y. Mylka V, et al. Among authors: van houdt j. Genome Biol. 2022 Feb 16;23(1):55. doi: 10.1186/s13059-022-02628-8. Genome Biol. 2022. PMID: 35172874 Free PMC article.
Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome.
Van Houdt JK, Nowakowska BA, Sousa SB, van Schaik BD, Seuntjens E, Avonce N, Sifrim A, Abdul-Rahman OA, van den Boogaard MJ, Bottani A, Castori M, Cormier-Daire V, Deardorff MA, Filges I, Fryer A, Fryns JP, Gana S, Garavelli L, Gillessen-Kaesbach G, Hall BD, Horn D, Huylebroeck D, Klapecki J, Krajewska-Walasek M, Kuechler A, Lines MA, Maas S, Macdermot KD, McKee S, Magee A, de Man SA, Moreau Y, Morice-Picard F, Obersztyn E, Pilch J, Rosser E, Shannon N, Stolte-Dijkstra I, Van Dijck P, Vilain C, Vogels A, Wakeling E, Wieczorek D, Wilson L, Zuffardi O, van Kampen AH, Devriendt K, Hennekam R, Vermeesch JR. Van Houdt JK, et al. Nat Genet. 2012 Feb 26;44(4):445-9, S1. doi: 10.1038/ng.1105. Nat Genet. 2012. PMID: 22366787
A catalog of hemizygous variation in 127 22q11 deletion patients.
Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, Vermeesch JR. Hestand MS, et al. Among authors: van houdt j. Hum Genome Var. 2016 Jan 14;3:15065. doi: 10.1038/hgv.2015.65. eCollection 2016. Hum Genome Var. 2016. PMID: 27274857 Free PMC article.
Comprehensive Investigation of Constant Voltage Stress Time-Dependent Breakdown and Cycle-to-Breakdown Reliability in Y-Doped and Si-Doped HfO2 Metal-Ferroelectric-Metal Memory.
Chang TY, Wang KC, Liu HY, Hseun JH, Peng WC, Ronchi N, Celano U, Banerjee K, Van Houdt J, Wu TL. Chang TY, et al. Among authors: van houdt j. Nanomaterials (Basel). 2023 Jul 19;13(14):2104. doi: 10.3390/nano13142104. Nanomaterials (Basel). 2023. PMID: 37513115 Free PMC article.
Pseudoautosomal region 1 length polymorphism in the human population.
Mensah MA, Hestand MS, Larmuseau MH, Isrie M, Vanderheyden N, Declercq M, Souche EL, Van Houdt J, Stoeva R, Van Esch H, Devriendt K, Voet T, Decorte R, Robinson PN, Vermeesch JR. Mensah MA, et al. Among authors: van houdt j. PLoS Genet. 2014 Nov 6;10(11):e1004578. doi: 10.1371/journal.pgen.1004578. eCollection 2014 Nov. PLoS Genet. 2014. PMID: 25375121 Free PMC article.
75 results