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

Year Number of Results
1948 1
1966 1
1971 1
1972 3
1974 1
1975 1
1978 1
1981 1
1982 2
1984 2
1985 2
1986 1
1987 4
1989 2
1990 2
1991 1
1992 2
1993 3
1994 3
1995 9
1996 2
1997 7
1998 6
1999 4
2000 10
2001 10
2002 11
2003 9
2004 10
2005 8
2006 3
2007 9
2008 22
2009 12
2010 15
2011 20
2012 16
2013 12
2014 15
2015 15
2016 17
2017 16
2018 15
2019 12
2020 14
2021 12
2022 17
2023 7
2024 4

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338 results

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Page 1
ANKRD11 variants: KBG syndrome and beyond.
Parenti I, Mallozzi MB, Hüning I, Gervasini C, Kuechler A, Agolini E, Albrecht B, Baquero-Montoya C, Bohring A, Bramswig NC, Busche A, Dalski A, Guo Y, Hanker B, Hellenbroich Y, Horn D, Innes AM, Leoni C, Li YR, Lynch SA, Mariani M, Medne L, Mikat B, Milani D, Onesimo R, Ortiz-Gonzalez X, Prott EC, Reutter H, Rossier E, Selicorni A, Wieacker P, Wilkens A, Wieczorek D, Zackai EH, Zampino G, Zirn B, Hakonarson H, Deardorff MA, Gillessen-Kaesbach G, Kaiser FJ. Parenti I, et al. Among authors: albrecht b. Clin Genet. 2021 Aug;100(2):187-200. doi: 10.1111/cge.13977. Epub 2021 May 14. Clin Genet. 2021. PMID: 33955014 Free article.
Genetics of intellectual disability in consanguineous families.
Hu H, Kahrizi K, Musante L, Fattahi Z, Herwig R, Hosseini M, Oppitz C, Abedini SS, Suckow V, Larti F, Beheshtian M, Lipkowitz B, Akhtarkhavari T, Mehvari S, Otto S, Mohseni M, Arzhangi S, Jamali P, Mojahedi F, Taghdiri M, Papari E, Soltani Banavandi MJ, Akbari S, Tonekaboni SH, Dehghani H, Ebrahimpour MR, Bader I, Davarnia B, Cohen M, Khodaei H, Albrecht B, Azimi S, Zirn B, Bastami M, Wieczorek D, Bahrami G, Keleman K, Vahid LN, Tzschach A, Gärtner J, Gillessen-Kaesbach G, Varaghchi JR, Timmermann B, Pourfatemi F, Jankhah A, Chen W, Nikuei P, Kalscheuer VM, Oladnabi M, Wienker TF, Ropers HH, Najmabadi H. Hu H, et al. Among authors: albrecht b. Mol Psychiatry. 2019 Jul;24(7):1027-1039. doi: 10.1038/s41380-017-0012-2. Epub 2018 Jan 4. Mol Psychiatry. 2019. PMID: 29302074
De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.
Rivière JB, Mirzaa GM, O'Roak BJ, Beddaoui M, Alcantara D, Conway RL, St-Onge J, Schwartzentruber JA, Gripp KW, Nikkel SM, Worthylake T, Sullivan CT, Ward TR, Butler HE, Kramer NA, Albrecht B, Armour CM, Armstrong L, Caluseriu O, Cytrynbaum C, Drolet BA, Innes AM, Lauzon JL, Lin AE, Mancini GM, Meschino WS, Reggin JD, Saggar AK, Lerman-Sagie T, Uyanik G, Weksberg R, Zirn B, Beaulieu CL; Finding of Rare Disease Genes (FORGE) Canada Consortium; Majewski J, Bulman DE, O'Driscoll M, Shendure J, Graham JM Jr, Boycott KM, Dobyns WB. Rivière JB, et al. Among authors: albrecht b. Nat Genet. 2012 Jun 24;44(8):934-40. doi: 10.1038/ng.2331. Nat Genet. 2012. PMID: 22729224 Free PMC article.
Charles Bonnet Syndrome With Superimposed Delirium.
Karson C, Kang C, Albrecht B, Levin G. Karson C, et al. Among authors: albrecht b. Cureus. 2022 Aug 1;14(8):e27570. doi: 10.7759/cureus.27570. eCollection 2022 Aug. Cureus. 2022. PMID: 36059364 Free PMC article.
A Baker's Dozen of Top Antimicrobial Stewardship Intervention Publications in Non-Hospital Care Settings in 2021.
Green SB, Marx AH, Chahine EB, Hayes JE, Albrecht B, Barber KE, Brown ML, Childress D, Durham SH, Furgiuele G, McKamey LJ, Sizemore S, Turner MS, Winders HR, Bookstaver PB, Bland CM. Green SB, et al. Among authors: albrecht b. Open Forum Infect Dis. 2022 Nov 3;9(11):ofac599. doi: 10.1093/ofid/ofac599. eCollection 2022 Nov. Open Forum Infect Dis. 2022. PMID: 36467301 Free PMC article. Review.
Benzodiazepine use and aggressive behaviour: a systematic review.
Albrecht B, Staiger PK, Hall K, Miller P, Best D, Lubman DI. Albrecht B, et al. Aust N Z J Psychiatry. 2014 Dec;48(12):1096-114. doi: 10.1177/0004867414548902. Epub 2014 Sep 2. Aust N Z J Psychiatry. 2014. PMID: 25183003 Review.
338 results