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

Year Number of Results
1960 1
1966 1
1967 1
1969 1
1970 1
1975 1
1976 3
1978 1
1979 1
1984 1
1985 3
1986 1
1987 5
1988 4
1989 1
1990 2
1991 4
1992 3
1993 1
1995 1
1996 7
1997 2
1998 2
2001 2
2002 5
2003 2
2004 5
2005 4
2006 2
2007 3
2008 2
2009 3
2010 3
2011 4
2012 5
2013 6
2014 6
2015 4
2016 3
2017 4
2018 4
2019 11
2020 7
2021 3
2022 5
2023 2
2024 2

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136 results

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Page 1
Final efficacy, immunogenicity, and safety analyses of a nine-valent human papillomavirus vaccine in women aged 16-26 years: a randomised, double-blind trial.
Huh WK, Joura EA, Giuliano AR, Iversen OE, de Andrade RP, Ault KA, Bartholomew D, Cestero RM, Fedrizzi EN, Hirschberg AL, Mayrand MH, Ruiz-Sternberg AM, Stapleton JT, Wiley DJ, Ferenczy A, Kurman R, Ronnett BM, Stoler MH, Cuzick J, Garland SM, Kjaer SK, Bautista OM, Haupt R, Moeller E, Ritter M, Roberts CC, Shields C, Luxembourg A. Huh WK, et al. Among authors: bartholomew d. Lancet. 2017 Nov 11;390(10108):2143-2159. doi: 10.1016/S0140-6736(17)31821-4. Epub 2017 Sep 5. Lancet. 2017. PMID: 28886907 Clinical Trial.
Craniofacial-deafness-hand syndrome revisited.
Sommer A, Bartholomew DW. Sommer A, et al. Among authors: bartholomew dw. Am J Med Genet A. 2003 Nov 15;123A(1):91-4. doi: 10.1002/ajmg.a.20501. Am J Med Genet A. 2003. PMID: 14556253
De novo variants in ATP2B1 lead to neurodevelopmental delay.
Rahimi MJ, Urban N, Wegler M, Sticht H, Schaefer M, Popp B, Gaunitz F, Morleo M, Nigro V, Maitz S, Mancini GMS, Ruivenkamp C, Suk EK, Bartolomaeus T, Merkenschlager A, Koboldt D, Bartholomew D, Stegmann APA, Sinnema M, Duynisveld I, Salvarinova R, Race S, de Vries BBA, Trimouille A, Naudion S, Marom D, Hamiel U, Henig N, Demurger F, Rahner N, Bartels E, Hamm JA, Putnam AM, Person R, Abou Jamra R, Oppermann H. Rahimi MJ, et al. Among authors: bartholomew d. Am J Hum Genet. 2022 May 5;109(5):944-952. doi: 10.1016/j.ajhg.2022.03.009. Epub 2022 Mar 30. Am J Hum Genet. 2022. PMID: 35358416 Free PMC article.
Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant.
Arredondo K, Myers C, Hansen-Kiss E, Mathew MT, Jayaraman V, Siemon A, Bartholomew D, Herman GE, Mori M. Arredondo K, et al. Among authors: bartholomew d. J Child Neurol. 2022 May;37(6):517-523. doi: 10.1177/08830738221089741. Epub 2022 Apr 6. J Child Neurol. 2022. PMID: 35384780
The Influence of the Scheduling Horizon on New Patient Arrivals.
Woodcock E, Nokes D, Bolton H, Bartholomew D, Johnson E, Shakarchi AF. Woodcock E, et al. Among authors: bartholomew d. J Ambul Care Manage. 2020 Jul/Sep;43(3):221-229. doi: 10.1097/JAC.0000000000000334. J Ambul Care Manage. 2020. PMID: 32467435 Free PMC article.
Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder.
Hunter JM, Massingham LJ, Manickam K, Bartholomew D, Williamson RK, Schwab JL, Marhabaie M, Siemon A, de Los Reyes E, Reshmi SC, Cottrell CE, Wilson RK, Koboldt DC. Hunter JM, et al. Among authors: bartholomew d. Cold Spring Harb Mol Case Stud. 2022 Mar 24;8(2):a006180. doi: 10.1101/mcs.a006180. Print 2022 Feb. Cold Spring Harb Mol Case Stud. 2022. PMID: 35091509 Free PMC article.
Telemedicine in an Academic Movement Disorders Center during COVID-19.
Esper CD, Scorr L, Papazian S, Bartholomew D, Esper GJ, Factor SA. Esper CD, et al. Among authors: bartholomew d. J Mov Disord. 2021 May;14(2):119-125. doi: 10.14802/jmd.20099. Epub 2021 Mar 18. J Mov Disord. 2021. PMID: 33725762 Free PMC article.
136 results