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

Year Number of Results
1972 1
1973 3
1974 2
1975 3
1976 2
1978 3
1979 3
1980 3
1981 7
1982 9
1983 2
1984 4
1985 6
1986 6
1987 5
1988 9
1989 10
1990 10
1991 5
1992 12
1993 16
1994 7
1995 9
1996 8
1997 5
1998 2
1999 7
2000 6
2001 6
2002 7
2003 2
2004 5
2005 1
2006 5
2007 4
2008 6
2009 4
2010 3
2011 6
2012 8
2013 5
2014 8
2015 7
2016 5
2017 6
2018 8
2019 10
2020 8
2021 10
2022 3
Text availability
Article attribute
Article type
Publication date

Search Results

272 results
Results by year
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Page 1
Osteogenesis imperfecta.
Marini JC, Forlino A, Bächinger HP, Bishop NJ, Byers PH, Paepe A, Fassier F, Fratzl-Zelman N, Kozloff KM, Krakow D, Montpetit K, Semler O. Marini JC, et al. Among authors: byers ph. Nat Rev Dis Primers. 2017 Aug 18;3:17052. doi: 10.1038/nrdp.2017.52. Nat Rev Dis Primers. 2017. PMID: 28820180 Review.
The Ehlers-Danlos syndromes.
Malfait F, Castori M, Francomano CA, Giunta C, Kosho T, Byers PH. Malfait F, et al. Among authors: byers ph. Nat Rev Dis Primers. 2020 Jul 30;6(1):64. doi: 10.1038/s41572-020-0194-9. Nat Rev Dis Primers. 2020. PMID: 32732924 Review.
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.
Byers PH, Belmont J, Black J, De Backer J, Frank M, Jeunemaitre X, Johnson D, Pepin M, Robert L, Sanders L, Wheeldon N. Byers PH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):40-47. doi: 10.1002/ajmg.c.31553. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306228 Review.
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
Marini JC, Forlino A, Cabral WA, Barnes AM, San Antonio JD, Milgrom S, Hyland JC, Körkkö J, Prockop DJ, De Paepe A, Coucke P, Symoens S, Glorieux FH, Roughley PJ, Lund AM, Kuurila-Svahn K, Hartikka H, Cohn DH, Krakow D, Mottes M, Schwarze U, Chen D, Yang K, Kuslich C, Troendle J, Dalgleish R, Byers PH. Marini JC, et al. Among authors: byers ph. Hum Mutat. 2007 Mar;28(3):209-21. doi: 10.1002/humu.20429. Hum Mutat. 2007. PMID: 17078022 Free PMC article. Review.
Aneurysm syndromes caused by mutations in the TGF-beta receptor.
Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ, Cameron DE, Braverman AC, Byers PH, De Paepe AM, Dietz HC. Loeys BL, et al. Among authors: byers ph. N Engl J Med. 2006 Aug 24;355(8):788-98. doi: 10.1056/NEJMoa055695. N Engl J Med. 2006. PMID: 16928994 Free article.
Vascular Ehlers-Danlos Syndrome.
Byers PH. Byers PH. 1999 Sep 2 [updated 2019 Feb 21]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 1999 Sep 2 [updated 2019 Feb 21]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301667 Free Books & Documents. Review.
Procollagen.
Martin GR, Byers PH, Piez KA. Martin GR, et al. Among authors: byers ph. Adv Enzymol Relat Areas Mol Biol. 1975;42:167-91. doi: 10.1002/9780470122877.ch3. Adv Enzymol Relat Areas Mol Biol. 1975. PMID: 1093363 Review. No abstract available.
2020 McKusick Award address.
Byers PH. Byers PH. Am J Hum Genet. 2021 May 6;108(5):761-763. doi: 10.1016/j.ajhg.2021.03.021. Am J Hum Genet. 2021. PMID: 33961778 Free PMC article.
272 results