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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 22
2021 13
2022 11
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Publication date

Search Results

277 results
Results by year
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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.
Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease.
Traschütz A, Cortese A, Reich S, Dominik N, Faber J, Jacobi H, Hartmann AM, Rujescu D, Montaut S, Echaniz-Laguna A, Erer S, Schütz VC, Tarnutzer AA, Sturm M, Haack TB, Vaucamps-Diedhiou N, Puccio H, Schöls L, Klockgether T, van de Warrenburg BP, Paucar M, Timmann D, Hilgers RD, Gazulla J, Strupp M, Moris G, Filla A, Houlden H, Anheim M, Infante J, Basak AN, Synofzik M; RFC1 Study Group. Traschütz A, et al. Among authors: sturm m. Neurology. 2021 Mar 2;96(9):e1369-e1382. doi: 10.1212/WNL.0000000000011528. Epub 2021 Jan 25. Neurology. 2021. PMID: 33495376 Free PMC article.
OptiType: precision HLA typing from next-generation sequencing data.
Szolek A, Schubert B, Mohr C, Sturm M, Feldhahn M, Kohlbacher O. Szolek A, et al. Among authors: sturm m. Bioinformatics. 2014 Dec 1;30(23):3310-6. doi: 10.1093/bioinformatics/btu548. Epub 2014 Aug 20. Bioinformatics. 2014. PMID: 25143287 Free PMC article.
[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.
Multi-omics discovery of exome-derived neoantigens in hepatocellular carcinoma.
Löffler MW, Mohr C, Bichmann L, Freudenmann LK, Walzer M, Schroeder CM, Trautwein N, Hilke FJ, Zinser RS, Mühlenbruch L, Kowalewski DJ, Schuster H, Sturm M, Matthes J, Riess O, Czemmel S, Nahnsen S, Königsrainer I, Thiel K, Nadalin S, Beckert S, Bösmüller H, Fend F, Velic A, Maček B, Haen SP, Buonaguro L, Kohlbacher O, Stevanović S, Königsrainer A; HEPAVAC Consortium, Rammensee HG. Löffler MW, et al. Among authors: sturm m. Genome Med. 2019 Apr 30;11(1):28. doi: 10.1186/s13073-019-0636-8. Genome Med. 2019. PMID: 31039795 Free PMC article.
[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.
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.
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, Sturm M, Vorgerd M, Balousha G, Balousha O, Falna M, Kirschke JS, Kornblum C, Jordan B, Kraya T, Strom TM, Weis J, Schöls L, Schara U, Zierz S, Riess O, Meitinger T, Haack TB. Deschauer M, et al. Among authors: sturm m. Brain. 2021 Mar 3;144(2):574-583. doi: 10.1093/brain/awaa418. Brain. 2021. PMID: 33459760
[Sclero-dermatomyositis].
Hadida E, Payet M, Sayag J, Sturm M. Hadida E, et al. Among authors: sturm m. Bull Soc Fr Dermatol Syphiligr. 1967;74(1):96-7. Bull Soc Fr Dermatol Syphiligr. 1967. PMID: 5582200 French. No abstract available.
277 results