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

Year Number of Results
1988 1
1989 2
1990 3
1991 3
1992 5
1993 1
1994 8
1996 4
1997 2
1998 1
1999 1
2000 2
2001 2
2002 1
2003 2
2004 3
2005 10
2006 10
2007 11
2008 9
2009 11
2010 6
2011 12
2012 13
2013 11
2014 6
2015 10
2016 14
2017 10
2018 16
2019 14
2020 12
2021 7
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196 results
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Page 1
REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, Musolf A, Li Q, Holzinger E, Karyadi D, Cannon-Albright LA, Teerlink CC, Stanford JL, Isaacs WB, Xu J, Cooney KA, Lange EM, Schleutker J, Carpten JD, Powell IJ, Cussenot O, Cancel-Tassin G, Giles GG, MacInnis RJ, Maier C, Hsieh CL, Wiklund F, Catalona WJ, Foulkes WD, Mandal D, Eeles RA, Kote-Jarai Z, Bustamante CD, Schaid DJ, Hastie T, Ostrander EA, Bailey-Wilson JE, Radivojac P, Thibodeau SN, Whittemore AS, Sieh W. Ioannidis NM, et al. Among authors: cannon albright la. Am J Hum Genet. 2016 Oct 6;99(4):877-885. doi: 10.1016/j.ajhg.2016.08.016. Epub 2016 Sep 22. Am J Hum Genet. 2016. PMID: 27666373 Free PMC article.
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study.
Zhen DB, Rabe KG, Gallinger S, Syngal S, Schwartz AG, Goggins MG, Hruban RH, Cote ML, McWilliams RR, Roberts NJ, Cannon-Albright LA, Li D, Moyes K, Wenstrup RJ, Hartman AR, Seminara D, Klein AP, Petersen GM. Zhen DB, et al. Among authors: cannon albright la. Genet Med. 2015 Jul;17(7):569-77. doi: 10.1038/gim.2014.153. Epub 2014 Nov 20. Genet Med. 2015. PMID: 25356972 Free PMC article.
Pancreatic cancer as a sentinel for hereditary cancer predisposition.
Young EL, Thompson BA, Neklason DW, Firpo MA, Werner T, Bell R, Berger J, Fraser A, Gammon A, Koptiuch C, Kohlmann WK, Neumayer L, Goldgar DE, Mulvihill SJ, Cannon-Albright LA, Tavtigian SV. Young EL, et al. Among authors: cannon albright la. BMC Cancer. 2018 Jun 27;18(1):697. doi: 10.1186/s12885-018-4573-5. BMC Cancer. 2018. PMID: 29945567 Free PMC article.
Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.
Patel D, Mez J, Vardarajan BN, Staley L, Chung J, Zhang X, Farrell JJ, Rynkiewicz MJ, Cannon-Albright LA, Teerlink CC, Stevens J, Corcoran C, Gonzalez Murcia JD, Lopez OL, Mayeux R, Haines JL, Pericak-Vance MA, Schellenberg G, Kauwe JSK, Lunetta KL, Farrer LA; Alzheimer’s Disease Sequencing Project. Patel D, et al. Among authors: cannon albright la. JAMA Netw Open. 2019 Mar 1;2(3):e191350. doi: 10.1001/jamanetworkopen.2019.1350. JAMA Netw Open. 2019. PMID: 30924900 Free PMC article.
A role for the MEGF6 gene in predisposition to osteoporosis.
Teerlink CC, Jurynec MJ, Hernandez R, Stevens J, Hughes DC, Brunker CP, Rowe K, Grunwald DJ, Facelli JC, Cannon-Albright LA. Teerlink CC, et al. Among authors: cannon albright la. Ann Hum Genet. 2021 Mar;85(2):58-72. doi: 10.1111/ahg.12408. Epub 2020 Oct 7. Ann Hum Genet. 2021. PMID: 33026655
Identification and genomic analysis of pedigrees with exceptional longevity identifies candidate rare variants.
Miller JB, Ward E, Staley LA, Stevens J, Teerlink CC, Tavana JP, Cloward M, Page M, Dayton L; Alzheimer's Disease Genetics Consortium, Cannon-Albright LA, Kauwe JSK. Miller JB, et al. Among authors: cannon albright la. Neurobiol Dis. 2020 Sep;143:104972. doi: 10.1016/j.nbd.2020.104972. Epub 2020 Jun 21. Neurobiol Dis. 2020. PMID: 32574725 Free article. Review.
Relative risk for Alzheimer disease based on complete family history.
Cannon-Albright LA, Foster NL, Schliep K, Farnham JM, Teerlink CC, Kaddas H, Tschanz J, Corcoran C, Kauwe JSK. Cannon-Albright LA, et al. Neurology. 2019 Apr 9;92(15):e1745-e1753. doi: 10.1212/WNL.0000000000007231. Epub 2019 Mar 13. Neurology. 2019. PMID: 30867271 Free PMC article.
196 results
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