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

Year Number of Results
2001 1
2002 1
2003 1
2004 4
2005 2
2006 5
2007 4
2008 9
2009 6
2010 6
2011 7
2012 5
2013 3
2014 8
2015 3
2016 6
2017 10
2018 8
2019 9
2020 13
2021 13
2022 15
2023 14
2024 5

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131 results

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Page 1
Long-term culture of genome-stable bipotent stem cells from adult human liver.
Huch M, Gehart H, van Boxtel R, Hamer K, Blokzijl F, Verstegen MM, Ellis E, van Wenum M, Fuchs SA, de Ligt J, van de Wetering M, Sasaki N, Boers SJ, Kemperman H, de Jonge J, Ijzermans JN, Nieuwenhuis EE, Hoekstra R, Strom S, Vries RR, van der Laan LJ, Cuppen E, Clevers H. Huch M, et al. Among authors: fuchs sa. Cell. 2015 Jan 15;160(1-2):299-312. doi: 10.1016/j.cell.2014.11.050. Epub 2014 Dec 18. Cell. 2015. PMID: 25533785 Free PMC article.
Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy.
Parenti I, Lehalle D, Nava C, Torti E, Leitão E, Person R, Mizuguchi T, Matsumoto N, Kato M, Nakamura K, de Man SA, Cope H, Shashi V; Undiagnosed Diseases Network; Friedman J, Joset P, Steindl K, Rauch A, Muffels I, van Hasselt PM, Petit F, Smol T, Le Guyader G, Bilan F, Sorlin A, Vitobello A, Philippe C, van de Laar IMBH, van Slegtenhorst MA, Campeau PM, Au PYB, Nakashima M, Saitsu H, Yamamoto T, Nomura Y, Louie RJ, Lyons MJ, Dobson A, Plomp AS, Motazacker MM, Kaiser FJ, Timberlake AT, Fuchs SA, Depienne C, Mignot C. Parenti I, et al. Among authors: fuchs sa. Hum Genet. 2021 Jul;140(7):1109-1120. doi: 10.1007/s00439-021-02283-2. Epub 2021 May 4. Hum Genet. 2021. PMID: 33944996 Free PMC article.
Macrocephaly and developmental delay caused by missense variants in RAB5C.
Koop K, Yuan W, Tessadori F, Rodriguez-Polanco WR, Grubbs J, Zhang B, Osmond M, Graham G, Sawyer S, Conboy E, Vetrini F, Treat K, Płoski R, Pienkowski VM, Kłosowska A, Fieg E, Krier J, Mallebranche C, Alban Z, Aldinger KA, Ritter D, Macnamara E, Sullivan B, Herriges J, Alaimo JT, Helbig C, Ellis CA, van Eyk C, Gecz J, Farrugia D, Osei-Owusu I, Adès L, van den Boogaard MJ, Fuchs S, Bakker J, Duran K, Dawson ZD, Lindsey A, Huang H, Baldridge D, Silverman GA, Grant BD, Raizen D; Undiagnosed Diseases Network; van Haaften G, Pak SC, Rehmann H, Schedl T, van Hasselt P. Koop K, et al. Among authors: fuchs s. Hum Mol Genet. 2023 Oct 17;32(21):3063-3077. doi: 10.1093/hmg/ddad130. Hum Mol Genet. 2023. PMID: 37552066 Free PMC article.
Ethical challenges for pediatric liver organoid transplantation.
Schneemann SA, Boers SN, van Delden JJM, Nieuwenhuis EES, Fuchs SA, Bredenoord AL. Schneemann SA, et al. Among authors: fuchs sa. Sci Transl Med. 2020 Jul 15;12(552):eaau8471. doi: 10.1126/scitranslmed.aau8471. Sci Transl Med. 2020. PMID: 32669425 Review.
In reply.
Fuchs S. Fuchs S. Dtsch Arztebl Int. 2015 Feb 20;112(8):136. doi: 10.3238/arztebl.2015.0136b. Dtsch Arztebl Int. 2015. PMID: 25759981 Free PMC article. No abstract available.
Response to Shen et al.
Kok G, van Karnebeek CDM, Fuchs SA. Kok G, et al. Among authors: fuchs sa. Genet Med. 2022 Feb;24(2):506-507. doi: 10.1016/j.gim.2021.09.022. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906483 Free article. No abstract available.
Towards incentivising integration: A typology of payments for integrated care.
Stokes J, Struckmann V, Kristensen SR, Fuchs S, van Ginneken E, Tsiachristas A, Rutten van Mölken M, Sutton M. Stokes J, et al. Among authors: fuchs s. Health Policy. 2018 Sep;122(9):963-969. doi: 10.1016/j.healthpol.2018.07.003. Epub 2018 Jul 11. Health Policy. 2018. PMID: 30033204 Free article. Review.
131 results