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Table representation of search results timeline featuring number of search results per year.

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
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73 results
Results by year
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Page 1
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
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.
Ferroelectricity in Si-Doped Hafnia: Probing Challenges in Absence of Screening Charges.
Celano U, Gomez A, Piedimonte P, Neumayer S, Collins L, Popovici M, Florent K, McMitchell SRC, Favia P, Drijbooms C, Bender H, Paredis K, Di Piazza L, Jesse S, Van Houdt J, van der Heide P. Celano U, et al. Among authors: van houdt j. Nanomaterials (Basel). 2020 Aug 11;10(8):1576. doi: 10.3390/nano10081576. Nanomaterials (Basel). 2020. PMID: 32796703 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
73 results