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

Year Number of Results
1977 1
1980 1
1982 3
1989 2
1990 3
1991 2
1992 4
1993 1
1994 1
1995 1
1996 2
1997 1
1998 3
1999 1
2000 1
2001 2
2002 2
2003 2
2004 5
2005 2
2006 2
2007 3
2008 5
2009 5
2010 4
2011 10
2012 9
2013 8
2014 3
2015 12
2016 16
2017 18
2018 14
2019 19
2020 23
2021 22
2022 3
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198 results
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Page 1
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns.
Stamberger H, Hammer TB, Gardella E, Vlaskamp DRM, Bertelsen B, Mandelstam S, de Lange I, Zhang J, Myers CT, Fenger C, Afawi Z, Almanza Fuerte EP, Andrade DM, Balcik Y, Ben Zeev B, Bennett MF, Berkovic SF, Isidor B, Bouman A, Brilstra E, Busk ØL, Cairns A, Caumes R, Chatron N, Dale RC, de Geus C, Edery P, Gill D, Granild-Jensen JB, Gunderson L, Gunning B, Heimer G, Helle JR, Hildebrand MS, Hollingsworth G, Kharytonov V, Klee EW, Koeleman BPC, Koolen DA, Korff C, Küry S, Lesca G, Lev D, Leventer RJ, Mackay MT, Macke EL, McEntagart M, Mohammad SS, Monin P, Montomoli M, Morava E, Moutton S, Muir AM, Parrini E, Procopis P, Ranza E, Reed L, Reif PS, Rosenow F, Rossi M, Sadleir LG, Sadoway T, Schelhaas HJ, Schneider AL, Shah K, Shalev R, Sisodiya SM, Smol T, Stumpel CTRM, Stuurman K, Symonds JD, Mau-Them FT, Verbeek N, Verhoeven JS, Wallace G, Yosovich K, Zarate YA, Zerem A, Zuberi SM, Guerrini R, Mefford HC, Patel C, Zhang YH, Møller RS, Scheffer IE. Stamberger H, et al. Among authors: hammer tb. Genet Med. 2021 Feb;23(2):363-373. doi: 10.1038/s41436-020-00988-9. Epub 2020 Nov 4. Genet Med. 2021. PMID: 33144681
Not all animals need a microbiome.
Hammer TJ, Sanders JG, Fierer N. Hammer TJ, et al. FEMS Microbiol Lett. 2019 May 1;366(10):fnz117. doi: 10.1093/femsle/fnz117. FEMS Microbiol Lett. 2019. PMID: 31132110 Review.
DNA methylation episignature in Gabriele-de Vries syndrome.
Cherik F, Reilly J, Kerkhof J, Levy M, McConkey H, Barat-Houari M, Butler KM, Coubes C, Lee JA, Le Guyader G, Louie RJ, Patterson WG, Tedder ML, Bak M, Hammer TB, Craigen W, Démurger F, Dubourg C, Fradin M, Franciskovich R, Frengen E, Friedman J, Palares NR, Iascone M, Misceo D, Monin P, Odent S, Philippe C, Rouxel F, Saletti V, Strømme P, Thulin PC, Sadikovic B, Genevieve D. Cherik F, et al. Among authors: hammer tb. Genet Med. 2022 Jan 10:S1098-3600(21)05422-8. doi: 10.1016/j.gim.2021.12.003. Online ahead of print. Genet Med. 2022. PMID: 35027293
Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene.
Matricardi S, De Liso P, Freri E, Costa P, Castellotti B, Magri S, Gellera C, Granata T, Musante L, Lesca G, Oertel J, Craiu D, Hammer TB, Møller RS, Barisic N, Abou Jamra R, Polster T, Vigevano F, Marini C. Matricardi S, et al. Among authors: hammer tb. Epilepsia. 2020 Nov;61(11):2474-2485. doi: 10.1111/epi.16699. Epub 2020 Oct 16. Epilepsia. 2020. PMID: 33063863 Review.
Determining treatment choices after the cochlear implant evaluation process.
Redmann AJ, Tawfik K, Hammer T, Wenstrup L, Stevens S, Breen JT, Samy RN. Redmann AJ, et al. Among authors: hammer t. Laryngoscope Investig Otolaryngol. 2021 Mar 26;6(2):320-324. doi: 10.1002/lio2.546. eCollection 2021 Apr. Laryngoscope Investig Otolaryngol. 2021. PMID: 33869764 Free PMC article.
198 results