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Results by year

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

Year Number of Results
1949 1
1966 1
1967 1
1968 1
1971 1
1972 2
1973 4
1974 2
1975 3
1977 1
1981 2
1983 1
1984 1
1986 1
1987 1
1988 2
1989 5
1990 4
1991 3
1992 6
1993 3
1994 5
1995 2
1996 4
1997 6
1998 4
1999 6
2000 5
2001 2
2003 3
2004 5
2005 5
2006 4
2007 5
2008 7
2009 6
2010 9
2011 11
2012 13
2013 13
2014 16
2015 13
2016 13
2017 15
2018 14
2019 22
2020 23
2021 13
2022 13
2023 15
2024 6

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299 results

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Page 1
Guidelines for diagnostic next-generation sequencing.
Matthijs G, Souche E, Alders M, Corveleyn A, Eck S, Feenstra I, Race V, Sistermans E, Sturm M, Weiss M, Yntema H, Bakker E, Scheffer H, Bauer P; EuroGentest; European Society of Human Genetics. Matthijs G, et al. Among authors: sturm m. Eur J Hum Genet. 2016 Jan;24(1):2-5. doi: 10.1038/ejhg.2015.226. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508566 Free PMC article.
Recommendations for whole genome sequencing in diagnostics for rare diseases.
Souche E, Beltran S, Brosens E, Belmont JW, Fossum M, Riess O, Gilissen C, Ardeshirdavani A, Houge G, van Gijn M, Clayton-Smith J, Synofzik M, de Leeuw N, Deans ZC, Dincer Y, Eck SH, van der Crabben S, Balasubramanian M, Graessner H, Sturm M, Firth H, Ferlini A, Nabbout R, De Baere E, Liehr T, Macek M, Matthijs G, Scheffer H, Bauer P, Yntema HG, Weiss MM. Souche E, et al. Among authors: sturm m. Eur J Hum Genet. 2022 Sep;30(9):1017-1021. doi: 10.1038/s41431-022-01113-x. Epub 2022 May 16. Eur J Hum Genet. 2022. PMID: 35577938 Free PMC article.
Genomes in clinical care.
Riess O, Sturm M, Menden B, Liebmann A, Demidov G, Witt D, Casadei N, Admard J, Schütz L, Ossowski S, Taylor S, Schaffer S, Schroeder C, Dufke A, Haack T. Riess O, et al. Among authors: sturm m. NPJ Genom Med. 2024 Mar 14;9(1):20. doi: 10.1038/s41525-024-00402-2. NPJ Genom Med. 2024. PMID: 38485733 Free PMC article. Review.
Approaches in Sustainable, Biobased Multilayer Packaging Solutions.
Eissenberger K, Ballesteros A, De Bisschop R, Bugnicourt E, Cinelli P, Defoin M, Demeyer E, Fürtauer S, Gioia C, Gómez L, Hornberger R, Ißbrücker C, Mennella M, von Pogrell H, Rodriguez-Turienzo L, Romano A, Rosato A, Saile N, Schulz C, Schwede K, Sisti L, Spinelli D, Sturm M, Uyttendaele W, Verstichel S, Schmid M. Eissenberger K, et al. Among authors: sturm m. Polymers (Basel). 2023 Feb 26;15(5):1184. doi: 10.3390/polym15051184. Polymers (Basel). 2023. PMID: 36904425 Free PMC article. Review.
[Intracoronary ultrasound].
Hausmann D, Sturm M, Fischer D, Meyer GP. Hausmann D, et al. Among authors: sturm m. Z Kardiol. 2000;89 Suppl 1:11-4. doi: 10.1007/s003920070117. Z Kardiol. 2000. PMID: 10907294 Review. German.
[Management of Rib Fractures].
Raab S, Grieser T, Sturm M, Beyer M, Reindl S. Raab S, et al. Among authors: sturm m. Zentralbl Chir. 2019 Jun;144(3):305-321. doi: 10.1055/a-0774-3401. Epub 2019 Jun 5. Zentralbl Chir. 2019. PMID: 31167271 German.
Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.
Park J, Tucci A, Cipriani V, Demidov G, Rocca C, Senderek J, Butryn M, Velic A, Lam T, Galanaki E, Cali E, Vestito L, Maroofian R, Deininger N, Rautenberg M, Admard J, Hahn GA, Bartels C, van Os NJH, Horvath R, Chinnery PF, Tiet MY, Hewamadduma C, Hadjivassiliou M, Tofaris GK; Genomics England Research Consortium; Wood NW, Hayer SN, Bender F, Menden B, Cordts I, Klein K, Nguyen HP, Krauss JK, Blahak C, Strom TM, Sturm M, van de Warrenburg B, Lerche H, Maček B, Synofzik M, Ossowski S, Timmann D, Wolf ME, Smedley D, Riess O, Schöls L, Houlden H, Haack TB, Hengel H. Park J, et al. Among authors: sturm m. Genet Med. 2022 Oct;24(10):2079-2090. doi: 10.1016/j.gim.2022.07.006. Epub 2022 Aug 20. Genet Med. 2022. PMID: 35986737 Free article.
Endoscopic imaging techniques: beyond narrow band.
Sturm MB, Wang TD. Sturm MB, et al. Am J Gastroenterol. 2018 Aug;113(8):1103-1107. doi: 10.1038/s41395-018-0054-3. Am J Gastroenterol. 2018. PMID: 29748560 No abstract available.
299 results