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

Year Number of Results
1977 1
1978 2
1979 4
1981 2
1987 2
1989 1
1991 4
1992 2
1993 3
1995 3
1997 2
2000 1
2001 4
2002 2
2003 1
2004 1
2005 1
2006 3
2007 6
2008 2
2009 3
2010 2
2011 7
2012 5
2013 2
2014 2
2015 3
2016 7
2017 3
2018 2
2019 7
2020 1
2021 3
2022 5
2023 2
2024 1

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90 results

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Page 1
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
Fischer-Zirnsak B, Segebrecht L, Schubach M, Charles P, Alderman E, Brown K, Cadieux-Dion M, Cartwright T, Chen Y, Costin C, Fehr S, Fitzgerald KM, Fleming E, Foss K, Ha T, Hildebrand G, Horn D, Liu S, Marco EJ, McDonald M, McWalter K, Race S, Rush ET, Si Y, Saunders C, Slavotinek A, Stockler-Ipsiroglu S, Telegrafi A, Thiffault I, Torti E, Tsai AC, Wang X, Zafar M, Keren B, Kornak U, Boerkoel CF, Mirzaa G, Ehmke N. Fischer-Zirnsak B, et al. Among authors: fehr s. Am J Hum Genet. 2019 Sep 5;105(3):631-639. doi: 10.1016/j.ajhg.2019.07.002. Epub 2019 Jul 25. Am J Hum Genet. 2019. PMID: 31353024 Free PMC article.
Oxidative Fluorination of Cu/ZnO Methanol Catalysts.
Dybbert V, Fehr SM, Klein F, Schaadt A, Hoffmann A, Frei E, Erdem E, Ludwig T, Hillebrecht H, Krossing I. Dybbert V, et al. Among authors: fehr sm. Angew Chem Int Ed Engl. 2019 Sep 9;58(37):12935-12939. doi: 10.1002/anie.201811267. Epub 2019 Jul 4. Angew Chem Int Ed Engl. 2019. PMID: 31169940
Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss.
Tropitzsch A, Schade-Mann T, Gamerdinger P, Dofek S, Schulte B, Schulze M, Fehr S, Biskup S, Haack TB, Stöbe P, Heyd A, Harre J, Lesinski-Schiedat A, Büchner A, Lenarz T, Warnecke A, Müller M, Vona B, Dahlhoff E, Löwenheim H, Holderried M. Tropitzsch A, et al. Among authors: fehr s. Ear Hear. 2023 Nov-Dec 01;44(6):1464-1484. doi: 10.1097/AUD.0000000000001386. Epub 2023 Jul 13. Ear Hear. 2023. PMID: 37438890 Free PMC article.
Coronary Artery Bypass Grafting in Patients With High Risk of Bleeding.
Demal TJ, Fehr S, Mariscalco G, Reiter B, Bibiza E, Reichenspurner H, Gatti G, Onorati F, Faggian G, Salsano A, Santini F, Perrotti A, Santarpino G, Zanobini M, Saccocci M, Musumeci F, Rubino AS, De Feo M, Bancone C, Nicolini F, Dalén M, Maselli D, Bounader K, Mäkikallio T, Juvonen T, Ruggieri VG, Biancari F. Demal TJ, et al. Among authors: fehr s. Heart Lung Circ. 2022 Feb;31(2):263-271. doi: 10.1016/j.hlc.2021.06.519. Epub 2021 Jul 28. Heart Lung Circ. 2022. PMID: 34330630
Organization and expression of bovine TSPY.
Vogel T, Dechend F, Manz E, Jung C, Jakubiczka S, Fehr S, Schmidtke J, Schnieders F. Vogel T, et al. Among authors: fehr s. Mamm Genome. 1997 Jul;8(7):491-6. doi: 10.1007/s003359900482. Mamm Genome. 1997. PMID: 9195993
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases.
Marcogliese PC, Deal SL, Andrews J, Harnish JM, Bhavana VH, Graves HK, Jangam S, Luo X, Liu N, Bei D, Chao YH, Hull B, Lee PT, Pan H, Bhadane P, Huang MC, Longley CM, Chao HT, Chung HL, Haelterman NA, Kanca O, Manivannan SN, Rossetti LZ, German RJ, Gerard A, Schwaibold EMC, Fehr S, Guerrini R, Vetro A, England E, Murali CN, Barakat TS, van Dooren MF, Wilke M, van Slegtenhorst M, Lesca G, Sabatier I, Chatron N, Brownstein CA, Madden JA, Agrawal PB, Keren B, Courtin T, Perrin L, Brugger M, Roser T, Leiz S, Mau-Them FT, Delanne J, Sukarova-Angelovska E, Trajkova S, Rosenhahn E, Strehlow V, Platzer K, Keller R, Pavinato L, Brusco A, Rosenfeld JA, Marom R, Wangler MF, Yamamoto S. Marcogliese PC, et al. Among authors: fehr s. Cell Rep. 2022 Mar 15;38(11):110517. doi: 10.1016/j.celrep.2022.110517. Cell Rep. 2022. PMID: 35294868 Free PMC article.
90 results