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

Year Number of Results
1993 1
1997 1
1998 4
1999 1
2000 3
2001 2
2002 3
2003 3
2005 1
2006 2
2007 1
2009 1
2010 1
2011 1
2012 2
2014 3
2015 2
2016 4
2017 3
2018 6
2019 4
2020 1
2021 1
2023 1
2024 0

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46 results

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Page 1
Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Trujillano D, Bertoli-Avella AM, Kumar Kandaswamy K, Weiss ME, Köster J, Marais A, Paknia O, Schröder R, Garcia-Aznar JM, Werber M, Brandau O, Calvo Del Castillo M, Baldi C, Wessel K, Kishore S, Nahavandi N, Eyaid W, Al Rifai MT, Al-Rumayyan A, Al-Twaijri W, Alothaim A, Alhashem A, Al-Sannaa N, Al-Balwi M, Alfadhel M, Rolfs A, Abou Jamra R. Trujillano D, et al. Among authors: brandau o. Eur J Hum Genet. 2017 Feb;25(2):176-182. doi: 10.1038/ejhg.2016.146. Epub 2016 Nov 16. Eur J Hum Genet. 2017. PMID: 27848944 Free PMC article.
Schmerzhafte Knoten.
Valero T, Brandau O, Laccone F, Radakovic S. Valero T, et al. Among authors: brandau o. J Dtsch Dermatol Ges. 2016 Jun;14(6):627-629. doi: 10.1111/ddg.12923_g. J Dtsch Dermatol Ges. 2016. PMID: 27240080 No abstract available.
Painful nodules.
Valero T, Brandau O, Laccone F, Radakovic S. Valero T, et al. Among authors: brandau o. J Dtsch Dermatol Ges. 2016 Jun;14(6):627-629. doi: 10.1111/ddg.12923. J Dtsch Dermatol Ges. 2016. PMID: 27240081 No abstract available.
Amniotic fluid stem cells to study mTOR signaling in differentiation.
Rosner M, Schipany K, Shanmugasundaram B, Lubec G, Brandau O, Hengstschläger M. Rosner M, et al. Among authors: brandau o. Organogenesis. 2012 Jul-Sep;8(3):96-100. doi: 10.4161/org.22038. Epub 2012 Jul 1. Organogenesis. 2012. PMID: 22960547 Free PMC article. Review.
Novel causative variants in patients with achromatopsia.
Abdelkader E, Brandau O, Bergmann C, AlSalamah N, Nowilaty S, Schatz P. Abdelkader E, et al. Among authors: brandau o. Ophthalmic Genet. 2018 Dec;39(6):678-683. doi: 10.1080/13816810.2018.1522653. Epub 2018 Oct 5. Ophthalmic Genet. 2018. PMID: 30289319
Expanding the clinical and genetic spectra of NKX6-2-related disorder.
Baldi C, Bertoli-Avella AM, Al-Sannaa N, Alfadhel M, Al-Thihli K, Alameer S, Elmonairy AA, Al Shamsi AM, Abdelrahman HA, Al-Gazali L, Shawli A, Al-Hakami F, Yavuz H, Kandaswamy KK, Rolfs A, Brandau O, Bauer P. Baldi C, et al. Among authors: brandau o. Clin Genet. 2018 May;93(5):1087-1092. doi: 10.1111/cge.13221. Clin Genet. 2018. PMID: 29388673
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder.
Szot JO, Slavotinek A, Chong K, Brandau O, Nezarati M, Cueto-González AM, Patel MS, Devine WP, Rego S, Acyinena AP, Shannon P, Myles-Reid D, Blaser S, Mieghem TV, Yavuz-Kienle H, Skladny H, Miller K, Riera MDT, Martínez SA, Tizzano EF, Dupuis L, James Stavropoulos D, McNiven V, Mendoza-Londono R, Elliott AM; CAUSES Study; Phillips RS, Chapman G, Dunwoodie SL. Szot JO, et al. Among authors: brandau o. Hum Mutat. 2021 Jul;42(7):862-876. doi: 10.1002/humu.24211. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33942433 Free PMC article.
46 results