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

Year Number of Results
1998 1
1999 3
2000 1
2001 2
2002 2
2003 1
2004 5
2005 6
2006 4
2007 13
2008 22
2009 15
2010 15
2011 8
2012 1
2013 7
2014 4
2015 6
2016 3
2017 2
2018 2
2019 5
2020 5
2021 3
2022 3
2023 1
2024 0

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122 results

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Page 1
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.
Medina-Gomez C, Mullin BH, Chesi A, Prijatelj V, Kemp JP, Shochat-Carvalho C, Trajanoska K, Wang C, Joro R, Evans TE, Schraut KE, Li-Gao R, Ahluwalia TS, Zillikens MC, Zhu K, Mook-Kanamori DO, Evans DS, Nethander M, Knol MJ, Thorleifsson G, Prokic I, Zemel B, Broer L, McGuigan FE, van Schoor NM, Reppe S, Pawlak MA, Ralston SH, van der Velde N, Lorentzon M, Stefansson K, Adams HHH, Wilson SG, Ikram MA, Walsh JP, Lakka TA, Gautvik KM, Wilson JF, Orwoll ES, van Duijn CM, Bønnelykke K, Uitterlinden AG, Styrkársdóttir U, Akesson KE, Spector TD, Tobias JH, Ohlsson C, Felix JF, Bisgaard H, Grant SFA, Richards JB, Evans DM, van der Eerden B, van de Peppel J, Ackert-Bicknell C, Karasik D, Kague E, Rivadeneira F. Medina-Gomez C, et al. Commun Biol. 2023 Jul 4;6(1):691. doi: 10.1038/s42003-023-04869-0. Commun Biol. 2023. PMID: 37402774 Free PMC article.
Revised reference curves for bone mineral content and areal bone mineral density according to age and sex for black and non-black children: results of the bone mineral density in childhood study.
Zemel BS, Kalkwarf HJ, Gilsanz V, Lappe JM, Oberfield S, Shepherd JA, Frederick MM, Huang X, Lu M, Mahboubi S, Hangartner T, Winer KK. Zemel BS, et al. J Clin Endocrinol Metab. 2011 Oct;96(10):3160-9. doi: 10.1210/jc.2011-1111. Epub 2011 Sep 14. J Clin Endocrinol Metab. 2011. PMID: 21917867 Free PMC article.
Sleep in children with Williams Syndrome.
Mason TB, Arens R, Sharman J, Bintliff-Janisak B, Schultz B, Walters AS, Cater JR, Kaplan P, Pack AI. Mason TB, et al. Sleep Med. 2011 Oct;12(9):892-7. doi: 10.1016/j.sleep.2011.05.003. Epub 2011 Sep 21. Sleep Med. 2011. PMID: 21940205 Free PMC article.
X-chromosome association studies of congenital heart defects.
Agopian AJ, Hoang TT, Goldmuntz E, Hakonarson H, Musfee FI, Mitchell LE; Pediatric Cardiac Genomics Consortium. Agopian AJ, et al. Am J Med Genet A. 2020 Jan;182(1):250-254. doi: 10.1002/ajmg.a.61411. Epub 2019 Nov 15. Am J Med Genet A. 2020. PMID: 31729158 Free PMC article. No abstract available.
Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia.
Lim SH, St Germain E, Tran-Viet KN, Staffieri S, Marino M, Dollfus PH, Nading EB, Crowe S, Gole G, Perdomo-Trujillo Y, Haybittel M, Elder J, Pelletier V, Traboulsi E, Mackey D, Young TL. Lim SH, et al. Ophthalmic Genet. 2014 Mar;35(1):1-6. doi: 10.3109/13816810.2012.752017. Epub 2013 Jun 26. Ophthalmic Genet. 2014. PMID: 23802135 Free PMC article.
122 results