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

Year Number of Results
1986 1
1989 1
1992 1
1993 2
1995 1
1996 2
1997 4
1998 6
1999 5
2000 6
2001 2
2002 1
2003 2
2004 2
2005 1
2006 1
2007 3
2008 2
2009 4
2010 1
2011 1
2012 2
2013 2
2014 1
2015 3
2016 2
2017 4
2018 4
2019 1
2020 3
2021 4
2022 4
2023 4
2024 2

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77 results

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Page 1
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study.
Swen JJ, van der Wouden CH, Manson LE, Abdullah-Koolmees H, Blagec K, Blagus T, Böhringer S, Cambon-Thomsen A, Cecchin E, Cheung KC, Deneer VH, Dupui M, Ingelman-Sundberg M, Jonsson S, Joefield-Roka C, Just KS, Karlsson MO, Konta L, Koopmann R, Kriek M, Lehr T, Mitropoulou C, Rial-Sebbag E, Rollinson V, Roncato R, Samwald M, Schaeffeler E, Skokou M, Schwab M, Steinberger D, Stingl JC, Tremmel R, Turner RM, van Rhenen MH, Dávila Fajardo CL, Dolžan V, Patrinos GP, Pirmohamed M, Sunder-Plassmann G, Toffoli G, Guchelaar HJ; Ubiquitous Pharmacogenomics Consortium. Swen JJ, et al. Among authors: steinberger d. Lancet. 2023 Feb 4;401(10374):347-356. doi: 10.1016/S0140-6736(22)01841-4. Lancet. 2023. PMID: 36739136 Clinical Trial.
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, de Brouwer AP, Weinert S, Froyen G, Frints SG, Laumonnier F, Zemojtel T, Love MI, Richard H, Emde AK, Bienek M, Jensen C, Hambrock M, Fischer U, Langnick C, Feldkamp M, Wissink-Lindhout W, Lebrun N, Castelnau L, Rucci J, Montjean R, Dorseuil O, Billuart P, Stuhlmann T, Shaw M, Corbett MA, Gardner A, Willis-Owen S, Tan C, Friend KL, Belet S, van Roozendaal KE, Jimenez-Pocquet M, Moizard MP, Ronce N, Sun R, O'Keeffe S, Chenna R, van Bömmel A, Göke J, Hackett A, Field M, Christie L, Boyle J, Haan E, Nelson J, Turner G, Baynam G, Gillessen-Kaesbach G, Müller U, Steinberger D, Budny B, Badura-Stronka M, Latos-Bieleńska A, Ousager LB, Wieacker P, Rodríguez Criado G, Bondeson ML, Annerén G, Dufke A, Cohen M, Van Maldergem L, Vincent-Delorme C, Echenne B, Simon-Bouy B, Kleefstra T, Willemsen M, Fryns JP, Devriendt K, Ullmann R, Vingron M, Wrogemann K, Wienker TF, Tzschach A, van Bokhoven H, Gecz J, Jentsch TJ, Chen W, Ropers HH, Kalscheuer VM. Hu H, et al. Among authors: steinberger d. Mol Psychiatry. 2016 Jan;21(1):133-48. doi: 10.1038/mp.2014.193. Epub 2015 Feb 3. Mol Psychiatry. 2016. PMID: 25644381 Free PMC article.
Molecular genetics of craniosynostotic syndromes.
Müller U, Steinberger D, Kunze S. Müller U, et al. Among authors: steinberger d. Graefes Arch Clin Exp Ophthalmol. 1997 Sep;235(9):545-50. doi: 10.1007/BF00947081. Graefes Arch Clin Exp Ophthalmol. 1997. PMID: 9342602 Review.
Lymphadenopathy after the third Covid-19 vaccine.
Özütemiz C, Potter DA, Özütemiz AÖ, Steinberger D. Özütemiz C, et al. Among authors: steinberger d. Curr Probl Cancer Case Rep. 2021 Dec;4:100127. doi: 10.1016/j.cpccr.2021.100127. Epub 2021 Oct 30. Curr Probl Cancer Case Rep. 2021. PMID: 34746900 Free PMC article.
Molecular diagnosis of bilateral coronal synostosis.
Mulliken JB, Steinberger D, Kunze S, Müller U. Mulliken JB, et al. Among authors: steinberger d. Plast Reconstr Surg. 1999 Nov;104(6):1603-15. doi: 10.1097/00006534-199911000-00001. Plast Reconstr Surg. 1999. PMID: 10541159 Review.
Clinical and molecular genetics of primary dystonias.
Müller U, Steinberger D, Németh AH. Müller U, et al. Among authors: steinberger d. Neurogenetics. 1998 Mar;1(3):165-77. doi: 10.1007/s100480050025. Neurogenetics. 1998. PMID: 10737119 Review.
Mutations of GCH1 in Dopa-responsive dystonia.
Müller U, Steinberger D, Topka H. Müller U, et al. Among authors: steinberger d. J Neural Transm (Vienna). 2002 Mar;109(3):321-8. doi: 10.1007/s007020200026. J Neural Transm (Vienna). 2002. PMID: 11956954 Review.
77 results