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

Year Number of Results
1967 1
2008 1
2011 1
2013 1
2014 1
2016 1
2017 3
2018 1
2019 7
2020 6
2021 3
2022 7
2023 4
2024 0

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31 results

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Page 1
Evidence for 28 genetic disorders discovered by combining healthcare and research data.
Kaplanis J, Samocha KE, Wiel L, Zhang Z, Arvai KJ, Eberhardt RY, Gallone G, Lelieveld SH, Martin HC, McRae JF, Short PJ, Torene RI, de Boer E, Danecek P, Gardner EJ, Huang N, Lord J, Martincorena I, Pfundt R, Reijnders MRF, Yeung A, Yntema HG; Deciphering Developmental Disorders Study; Vissers LELM, Juusola J, Wright CF, Brunner HG, Firth HV, FitzPatrick DR, Barrett JC, Hurles ME, Gilissen C, Retterer K. Kaplanis J, et al. Among authors: wiel l. Nature. 2020 Oct;586(7831):757-762. doi: 10.1038/s41586-020-2832-5. Epub 2020 Oct 14. Nature. 2020. PMID: 33057194 Free PMC article.
The functional impact of rare variation across the regulatory cascade.
Li T, Ferraro N, Strober BJ, Aguet F, Kasela S, Arvanitis M, Ni B, Wiel L, Hershberg E, Ardlie K, Arking DE, Beer RL, Brody J, Blackwell TW, Clish C, Gabriel S, Gerszten R, Guo X, Gupta N, Johnson WC, Lappalainen T, Lin HJ, Liu Y, Nickerson DA, Papanicolaou G, Pritchard JK, Qasba P, Shojaie A, Smith J, Sotoodehnia N, Taylor KD, Tracy RP, Van Den Berg D, Wheeler MT, Rich SS, Rotter JI, Battle A, Montgomery SB. Li T, et al. Among authors: wiel l. Cell Genom. 2023 Sep 6;3(10):100401. doi: 10.1016/j.xgen.2023.100401. eCollection 2023 Oct 11. Cell Genom. 2023. PMID: 37868038 Free PMC article.
Neuropsychological assessment in the multicultural memory clinic: Development and feasibility of the TULIPA battery.
Franzen S, van den Berg E, Bossenbroek W, Kranenburg J, Scheffers EA, van Hout M, van de Wiel L, Goudsmit M, van Bruchem-Visser RL, van Hemmen J, Jiskoot LC, Papma JM. Franzen S, et al. Among authors: van de wiel l. Clin Neuropsychol. 2023 Jan;37(1):60-80. doi: 10.1080/13854046.2022.2043447. Epub 2022 Feb 27. Clin Neuropsychol. 2023. PMID: 35225154 Review.
De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy.
Nabais Sá MJ, Venselaar H, Wiel L, Trimouille A, Lasseaux E, Naudion S, Lacombe D, Piton A, Vincent-Delorme C, Zweier C, Reis A, Trollmann R, Ruiz A, Gabau E, Vetro A, Guerrini R, Bakhtiari S, Kruer MC, Amor DJ, Cooper MS, Bijlsma EK, Barakat TS, van Dooren MF, van Slegtenhorst M, Pfundt R, Gilissen C, Willemsen MA, de Vries BBA, de Brouwer APM, Koolen DA. Nabais Sá MJ, et al. Among authors: wiel l. Genet Med. 2020 Apr;22(4):797-802. doi: 10.1038/s41436-019-0703-y. Epub 2019 Nov 28. Genet Med. 2020. PMID: 31776469 Free article.
Cycles and circulation: a theme in the history of biology and medicine.
Hopwood N, Müller-Wille S, Browne J, Groeben C, Kuriyama S, van der Lugt M, Giglioni G, Nyhart LK, Rheinberger HJ, Dröscher A, Anderson W, Anker P, Grote M, van de Wiel L; Fifteenth Ischia Summer School on the History of the Life Sciences. Hopwood N, et al. Among authors: van de wiel l. Hist Philos Life Sci. 2021 Jul 12;43(3):89. doi: 10.1007/s40656-021-00425-3. Hist Philos Life Sci. 2021. PMID: 34251537 Free PMC article.
Prevalence of children witnessed violence in a pediatric emergency department.
Anastasia F, Wiel LC, Giangreco M, Morabito G, Romito P, Amaddeo A, Barbi E, Germani C. Anastasia F, et al. Among authors: wiel lc. Eur J Pediatr. 2022 Jul;181(7):2695-2703. doi: 10.1007/s00431-022-04474-z. Epub 2022 Apr 19. Eur J Pediatr. 2022. PMID: 35441247 Free PMC article.
31 results