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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 25
2009 14
2010 21
2011 27
2012 16
2013 13
2014 15
2015 15
2016 17
2017 16
2018 15
2019 12
2020 14
2021 12
2022 18
2023 8
2024 15

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368 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.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, Joset P, Röpke A, Moog U, Riess A, Thiel CT, Tzschach A, Wiesener A, Wohlleber E, Zweier C, Ekici AB, Zink AM, Rump A, Meisinger C, Grallert H, Sticht H, Schenck A, Engels H, Rappold G, Schröck E, Wieacker P, Riess O, Meitinger T, Reis A, Strom TM. Rauch A, et al. Among authors: albrecht b. Lancet. 2012 Nov 10;380(9854):1674-82. doi: 10.1016/S0140-6736(12)61480-9. Epub 2012 Sep 27. Lancet. 2012. PMID: 23020937
Efficacy and safety of once daily oral administration of sodium-glucose cotransporter-2 inhibitor velagliflozin compared with twice daily insulin injection in diabetic cats.
Niessen SJM, Kooistra HS, Forcada Y, Bjørnvad CR, Albrecht B, Roessner F, Herberich E, Kroh C. Niessen SJM, et al. Among authors: albrecht b. J Vet Intern Med. 2024 Jul-Aug;38(4):2099-2119. doi: 10.1111/jvim.17124. Epub 2024 Jun 17. J Vet Intern Med. 2024. PMID: 38884190 Free PMC article.
Generation and characterization of antagonistic anti-human CD39 nanobodies.
Menzel S, Duan Y, Hambach J, Albrecht B, Wendt-Cousin D, Winzer R, Tolosa E, Rissiek A, Guse AH, Haag F, Magnus T, Koch-Nolte F, Rissiek B. Menzel S, et al. Among authors: albrecht b. Front Immunol. 2024 Mar 25;15:1328306. doi: 10.3389/fimmu.2024.1328306. eCollection 2024. Front Immunol. 2024. PMID: 38590528 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.
Epidemiology and treatment of invasive Bartonella spp. infections in the United States.
Pizzuti M, Bailey P, Derrick C, Albrecht B, Carr AL, Covington EW, Deri CR, Green SB, Hayes J, Hobbs ALV, Hornback KM, Keil E, Lukas JG, Seddon M, Taylor AD, Torrisi J, Bookstaver PB. Pizzuti M, et al. Among authors: albrecht b. Infection. 2024 Aug;52(4):1307-1314. doi: 10.1007/s15010-024-02177-1. Epub 2024 Feb 1. Infection. 2024. PMID: 38300353
A Baker's Dozen of Top Antimicrobial Stewardship Intervention Publications in 2022.
Barfield RK, Brown ML, Albrecht B, Barber KE, Bouchard J, Carr AL, Chahine EB, Cluck D, Covington EW, Deri CR, Durham SH, Faulkner-Fennell C, Freeman LK, Gauthier TP, Gibson GM, Green SB, Hobbs ALV, Jones BM, Jozefczyk CC, Marx AH, McGee EU, McKamey LJ, Musgrove R, Perez E, Slain D, Stover KR, Turner MS, White C, Bookstaver PB, Bland CM. Barfield RK, et al. Among authors: albrecht b. Open Forum Infect Dis. 2024 Jan 4;11(3):ofad687. doi: 10.1093/ofid/ofad687. eCollection 2024 Mar. Open Forum Infect Dis. 2024. PMID: 38434614 Free PMC article. Review.
368 results