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

Year Number of Results
1953 1
1958 1
1959 4
1960 6
1961 1
1963 3
1964 3
1966 1
1967 1
1970 1
1971 1
1973 4
1974 3
1975 1
1977 1
1978 4
1979 3
1980 4
1981 5
1982 6
1983 7
1984 3
1985 5
1986 1
1987 5
1988 4
1989 3
1990 6
1991 12
1992 3
1993 5
1994 8
1995 5
1996 2
1997 6
1998 11
1999 6
2000 7
2001 11
2002 9
2003 12
2004 10
2005 10
2006 23
2007 18
2008 20
2009 14
2010 19
2011 38
2012 24
2013 18
2014 29
2015 24
2016 31
2017 25
2018 17
2019 36
2020 30
Text availability
Article attribute
Article type
Publication date

Search Results

528 results
Results by year
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Page 1
The respiratory microbiome and respiratory infections.
Unger SA, Bogaert D. Unger SA, et al. J Infect. 2017 Jun;74 Suppl 1:S84-S88. doi: 10.1016/S0163-4453(17)30196-2. J Infect. 2017. PMID: 28646967 Review.
The Human Immune Response to Respiratory Syncytial Virus Infection.
Russell CD, Unger SA, Walton M, Schwarze J. Russell CD, et al. Among authors: unger sa. Clin Microbiol Rev. 2017 Apr;30(2):481-502. doi: 10.1128/CMR.00090-16. Clin Microbiol Rev. 2017. PMID: 28179378 Free PMC article. Review.
Nosology and classification of genetic skeletal disorders: 2015 revision.
Bonafe L, Cormier-Daire V, Hall C, Lachman R, Mortier G, Mundlos S, Nishimura G, Sangiorgi L, Savarirayan R, Sillence D, Spranger J, Superti-Furga A, Warman M, Unger S. Bonafe L, et al. Among authors: unger s. Am J Med Genet A. 2015 Dec;167A(12):2869-92. doi: 10.1002/ajmg.a.37365. Epub 2015 Sep 23. Am J Med Genet A. 2015. PMID: 26394607
Nosology and classification of genetic skeletal disorders: 2019 revision.
Mortier GR, Cohn DH, Cormier-Daire V, Hall C, Krakow D, Mundlos S, Nishimura G, Robertson S, Sangiorgi L, Savarirayan R, Sillence D, Superti-Furga A, Unger S, Warman ML. Mortier GR, et al. Among authors: unger s. Am J Med Genet A. 2019 Dec;179(12):2393-2419. doi: 10.1002/ajmg.a.61366. Epub 2019 Oct 21. Am J Med Genet A. 2019. PMID: 31633310
[Alagille Syndrome].
Wakim El-Khoury J, Venetz JP, Rutz T, Sciarra A, Unger S, Sempoux C, Moradpour D, Fraga M. Wakim El-Khoury J, et al. Among authors: unger s. Rev Med Suisse. 2019 Aug 28;15(660):1506-1510. Rev Med Suisse. 2019. PMID: 31496175 Review. French.
Current Care and Investigational Therapies in Achondroplasia.
Unger S, Bonafé L, Gouze E. Unger S, et al. Curr Osteoporos Rep. 2017 Apr;15(2):53-60. doi: 10.1007/s11914-017-0347-2. Curr Osteoporos Rep. 2017. PMID: 28224446 Free PMC article. Review.
[Abecedary of colonic polyps].
Archanioti P, Bornand A, Sempoux C, Unger S, Schoepfer A, Robert M, David G. Archanioti P, et al. Among authors: unger s. Rev Med Suisse. 2019 Aug 28;15(660):1483-1487. Rev Med Suisse. 2019. PMID: 31496171 Review. French.
Further delineation of the KAT6B molecular and phenotypic spectrum.
Gannon T, Perveen R, Schlecht H, Ramsden S, Anderson B, Kerr B, Day R, Banka S, Suri M, Berland S, Gabbett M, Ma A, Lyonnet S, Cormier-Daire V, Yilmaz R, Borck G, Wieczorek D, Anderlid BM, Smithson S, Vogt J, Moore-Barton H, Simsek-Kiper PO, Maystadt I, Destrée A, Bucher J, Angle B, Mohammed S, Wakeling E, Price S, Singer A, Sznajer Y, Toutain A, Haye D, Newbury-Ecob R, Fradin M, McGaughran J, Tuysuz B, Tein M, Bouman K, Dabir T, Van den Ende J, Luk HM, Pilz DT, Eason J, Davies S, Reardon W, Garavelli L, Zuffardi O, Devriendt K, Armstrong R, Johnson D, Doco-Fenzy M, Bijlsma E, Unger S, Veenstra-Knol HE, Kohlhase J, Lo IF; DDD study, Smith J, Clayton-Smith J. Gannon T, et al. Among authors: unger s. Eur J Hum Genet. 2015 Sep;23(9):1165-70. doi: 10.1038/ejhg.2014.248. Epub 2014 Nov 26. Eur J Hum Genet. 2015. PMID: 25424711 Free PMC article.
NANS-mediated synthesis of sialic acid is required for brain and skeletal development.
van Karnebeek CD, Bonafé L, Wen XY, Tarailo-Graovac M, Balzano S, Royer-Bertrand B, Ashikov A, Garavelli L, Mammi I, Turolla L, Breen C, Donnai D, Cormier-Daire V, Heron D, Nishimura G, Uchikawa S, Campos-Xavier B, Rossi A, Hennet T, Brand-Arzamendi K, Rozmus J, Harshman K, Stevenson BJ, Girardi E, Superti-Furga G, Dewan T, Collingridge A, Halparin J, Ross CJ, Van Allen MI, Rossi A, Engelke UF, Kluijtmans LA, van der Heeft E, Renkema H, de Brouwer A, Huijben K, Zijlstra F, Heise T, Boltje T, Wasserman WW, Rivolta C, Unger S, Lefeber DJ, Wevers RA, Superti-Furga A. van Karnebeek CD, et al. Among authors: unger s. Nat Genet. 2016 Jul;48(7):777-84. doi: 10.1038/ng.3578. Epub 2016 May 23. Nat Genet. 2016. PMID: 27213289 Free article.
Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.
Wehrle A, Witkos TM, Unger S, Schneider J, Follit JA, Hermann J, Welting T, Fano V, Hietala M, Vatanavicharn N, Schoner K, Spranger J, Schmidts M, Zabel B, Pazour GJ, Bloch-Zupan A, Nishimura G, Superti-Furga A, Lowe M, Lausch E. Wehrle A, et al. Among authors: unger s. JCI Insight. 2019 Feb 7;4(3):e124701. doi: 10.1172/jci.insight.124701. Online ahead of print. JCI Insight. 2019. PMID: 30728324 Free PMC article.
528 results
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