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Results by year

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

Year Number of Results
2005 1
2009 1
2010 4
2011 9
2012 4
2013 7
2014 5
2015 5
2016 6
2017 5
2018 5
2019 3
2020 6
2021 4
2022 5
2023 12

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Search Results

77 results

Results by year

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Page 1
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death.
Byrne AB, Arts P, Ha TT, Kassahn KS, Pais LS, O'Donnell-Luria A; Broad Institute Center for Mendelian Genomics; Babic M, Frank MSB, Feng J, Wang P, Lawrence DM, Eshraghi L, Arriola L, Toubia J, Nguyen H; Genomic Autopsy Study Research Network; McGillivray G, Pinner J, McKenzie F, Morrow R, Lipsett J, Manton N, Khong TY, Moore L, Liebelt JE, Schreiber AW, King-Smith SL, Hardy TSE, Jackson MR, Barnett CP, Scott HS. Byrne AB, et al. Nat Med. 2023 Jan;29(1):180-189. doi: 10.1038/s41591-022-02142-1. Epub 2023 Jan 19. Nat Med. 2023. PMID: 36658419 Free PMC article.
A nanonewton-scale biomimetic mechanosensor.
Zhang C, Wu M, Li M, Che L, Tan Z, Guo D, Kang Z, Cao S, Zhang S, Sui Y, Sun J, Wang L, Liu J. Zhang C, et al. Among authors: sui y. Microsyst Nanoeng. 2023 Jul 11;9:87. doi: 10.1038/s41378-023-00560-w. eCollection 2023. Microsyst Nanoeng. 2023. PMID: 37440869 Free PMC article.
Growth factors in the treatment of Achilles tendon injury.
Lin M, Li W, Ni X, Sui Y, Li H, Chen X, Lu Y, Jiang M, Wang C. Lin M, et al. Among authors: sui y. Front Bioeng Biotechnol. 2023 Sep 14;11:1250533. doi: 10.3389/fbioe.2023.1250533. eCollection 2023. Front Bioeng Biotechnol. 2023. PMID: 37781529 Free PMC article. Review.
Genetics of hereditary neurological disorders in children.
Huang Y, Yu S, Wu Z, Tang B. Huang Y, et al. Among authors: yu s. Transl Pediatr. 2014 Apr;3(2):108-19. doi: 10.3978/j.issn.2224-4336.2014.03.04. Transl Pediatr. 2014. PMID: 26835329 Free PMC article. Review.
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.
Gribouval O, Morinière V, Pawtowski A, Arrondel C, Sallinen SL, Saloranta C, Clericuzio C, Viot G, Tantau J, Blesson S, Cloarec S, Machet MC, Chitayat D, Thauvin C, Laurent N, Sampson JR, Bernstein JA, Clemenson A, Prieur F, Daniel L, Levy-Mozziconacci A, Lachlan K, Alessandri JL, Cartault F, Rivière JP, Picard N, Baumann C, Delezoide AL, Belar Ortega M, Chassaing N, Labrune P, Yu S, Firth H, Wellesley D, Bitzan M, Alfares A, Braverman N, Krogh L, Tolmie J, Gaspar H, Doray B, Majore S, Bonneau D, Triau S, Loirat C, David A, Bartholdi D, Peleg A, Brackman D, Stone R, DeBerardinis R, Corvol P, Michaud A, Antignac C, Gubler MC. Gribouval O, et al. Among authors: yu s. Hum Mutat. 2012 Feb;33(2):316-26. doi: 10.1002/humu.21661. Epub 2011 Dec 22. Hum Mutat. 2012. PMID: 22095942 Review.
In vitro enzymatic degradation of the PTMC/cross-linked PEGDA blends.
Li W, Lin M, Wang C, Lu Y, Sui Y, Ni X, Guo J, Jiang M, Yang L, Cui H. Li W, et al. Among authors: sui y. Front Bioeng Biotechnol. 2023 Sep 1;11:1253221. doi: 10.3389/fbioe.2023.1253221. eCollection 2023. Front Bioeng Biotechnol. 2023. PMID: 37736328 Free PMC article.
BAP1 Tumour Predisposition Syndrome Due to Whole BAP1 Gene Deletion.
Pandithan D, Klebe S, McKavanagh G, Rawlings L, Yu S, Nicholl J, Poplawski N. Pandithan D, et al. Among authors: yu s. Case Rep Genet. 2022 Sep 13;2022:5503505. doi: 10.1155/2022/5503505. eCollection 2022. Case Rep Genet. 2022. PMID: 36148247 Free PMC article.
77 results