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

Year Number of Results
1981 4
1982 1
1983 3
1985 1
1986 1
1987 1
1988 5
1990 2
1991 2
1992 6
1993 2
1994 3
1995 7
1996 4
1997 10
1998 11
1999 8
2000 10
2001 14
2002 16
2003 11
2004 14
2005 22
2006 31
2007 27
2008 18
2009 25
2010 44
2011 35
2012 39
2013 31
2014 34
2015 24
2016 38
2017 36
2018 42
2019 38
2020 30
2021 44
2022 43
2023 43
2024 19

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Page 1
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants.
Zanetti A, D'Avanzo F, AlSayed M, Brusius-Facchin AC, Chien YH, Giugliani R, Izzo E, Kasper DC, Lin HY, Lin SP, Pollard L, Singh A, Tonin R, Wood T, Morrone A, Tomanin R. Zanetti A, et al. Among authors: lin sp. Hum Mutat. 2021 Nov;42(11):1384-1398. doi: 10.1002/humu.24270. Epub 2021 Aug 23. Hum Mutat. 2021. PMID: 34387910 Free PMC article. Review.
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.
Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F. Braun DA, et al. Among authors: lin sp. Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14. Nat Genet. 2017. PMID: 28805828 Free PMC article.
Editorial: Legacies of epigenetic perturbations.
da Rocha ST, Lin SP, Youngson NA. da Rocha ST, et al. Among authors: lin sp. Front Cell Dev Biol. 2023 Jun 13;11:1228115. doi: 10.3389/fcell.2023.1228115. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37384254 Free PMC article. No abstract available.
Cri-du-chat syndrome.
Chang CY, Lin SP, Lin HY, Chen YJ, Kao HA, Yeung CY, Hsu CH, Chi H. Chang CY, et al. Among authors: lin sp. Acta Paediatr Taiwan. 2007 Nov-Dec;48(6):328-31. Acta Paediatr Taiwan. 2007. PMID: 18437967
Training in clinical genetics and genetic counseling in Asia.
Cutiongco-de la Paz EM, Chung BH, Faradz SMH, Thong MK, David-Padilla C, Lai PS, Lin SP, Chen YH, Sura T, Laurino M. Cutiongco-de la Paz EM, et al. Among authors: lin sp. Am J Med Genet C Semin Med Genet. 2019 Jun;181(2):177-186. doi: 10.1002/ajmg.c.31703. Epub 2019 Apr 29. Am J Med Genet C Semin Med Genet. 2019. PMID: 31037827 Review.
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