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

Year Number of Results
1962 1
1985 1
1986 1
1990 1
1992 1
1994 4
1995 2
2001 1
2002 1
2003 1
2004 1
2008 2
2009 2
2010 1
2011 2
2012 3
2013 5
2015 7
2016 10
2017 3
2018 4
2019 4
2020 6
2021 3
2022 4
2024 0

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62 results

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Page 1
Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients.
Bryant L, Li D, Cox SG, Marchione D, Joiner EF, Wilson K, Janssen K, Lee P, March ME, Nair D, Sherr E, Fregeau B, Wierenga KJ, Wadley A, Mancini GMS, Powell-Hamilton N, van de Kamp J, Grebe T, Dean J, Ross A, Crawford HP, Powis Z, Cho MT, Willing MC, Manwaring L, Schot R, Nava C, Afenjar A, Lessel D, Wagner M, Klopstock T, Winkelmann J, Catarino CB, Retterer K, Schuette JL, Innis JW, Pizzino A, Lüttgen S, Denecke J, Strom TM, Monaghan KG; DDD Study; Yuan ZF, Dubbs H, Bend R, Lee JA, Lyons MJ, Hoefele J, Günthner R, Reutter H, Keren B, Radtke K, Sherbini O, Mrokse C, Helbig KL, Odent S, Cogne B, Mercier S, Bezieau S, Besnard T, Kury S, Redon R, Reinson K, Wojcik MH, Õunap K, Ilves P, Innes AM, Kernohan KD; Care4Rare Canada Consortium; Costain G, Meyn MS, Chitayat D, Zackai E, Lehman A, Kitson H; CAUSES Study; Martin MG, Martinez-Agosto JA; Undiagnosed Diseases Network; Nelson SF, Palmer CGS, Papp JC, Parker NH, Sinsheimer JS, Vilain E, Wan J, Yoon AJ, Zheng A, Brimble E, Ferrero GB, Radio FC, Carli D, Barresi S, Brusco A, Tartaglia M, Thomas JM, Umana L, Weiss MM, Gotway G, Stuurman KE, Thompson ML, McWalter K, Stumpel CTRM, Stevens SJC, Stegmann APA, Tveten K, Vøllo A, Pres… See abstract for full author list ➔ Bryant L, et al. Among authors: schuette jl. Sci Adv. 2020 Dec 2;6(49):eabc9207. doi: 10.1126/sciadv.abc9207. Print 2020 Dec. Sci Adv. 2020. PMID: 33268356 Free PMC article.
New Trainee Intubations: The Good, the Bad, and the Not So Ugly.
Wadia RS, Schuette JJ, Shaffner DH. Wadia RS, et al. Among authors: schuette jj. Pediatr Crit Care Med. 2020 Dec;21(12):1083-1084. doi: 10.1097/PCC.0000000000002535. Pediatr Crit Care Med. 2020. PMID: 33278213 No abstract available.
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Waggoner D, Wain KE, Dubuc AM, Conlin L, Hickey SE, Lamb AN, Martin CL, Morton CC, Rasmussen K, Schuette JL, Schwartz S, Miller DT; ACMG Professional Practice and Guidelines Committee. Waggoner D, et al. Among authors: schuette jl. Genet Med. 2018 Oct;20(10):1105-1113. doi: 10.1038/s41436-018-0040-6. Epub 2018 Jun 18. Genet Med. 2018. PMID: 29915380 Free PMC article. Review.
Standardized Training for Physicians Practicing Pediatric Cardiac Critical Care.
Tabbutt S, Krawczeski C, McBride M, Amirnovin R, Owens G, Smith A, Wolf M, Rhodes L, Hehir D, Asija R, Teele SA, Ghanayem N, Zyblewski S, Thiagarajan R, Yeh J, Shin AY, Schwartz SM, Schuette J, Scahill C, Roth SJ, Hoffman TM, Cooper DS, Byrnes J, Bergstrom C, Vesel T, Scott JP, Rossi A, Kwiatkowski D, DiPietro LM, Connor C, Chen J, Charpie J, Bochkoris M, Affolter J, Bronicki RA. Tabbutt S, et al. Among authors: schuette j. Pediatr Crit Care Med. 2022 Jan 1;23(1):60-64. doi: 10.1097/PCC.0000000000002815. Pediatr Crit Care Med. 2022. PMID: 34554132
Transport Medical Control Education for Pediatric Critical Care Fellows: A National Needs Assessment Study.
Good RJ, Zurca AD, Turner DA, Bjorklund AR, Boyer DL, Krennerich EC, Petrillo T, Rozenfeld RA, Sasser WC, Schuette J, Tcharmtchi MH, Watson CM, Czaja AS; Education in Pediatric Intensive Care (EPIC) Investigators. Good RJ, et al. Among authors: schuette j. Pediatr Crit Care Med. 2022 Jan 1;23(1):e55-e59. doi: 10.1097/PCC.0000000000002803. Pediatr Crit Care Med. 2022. PMID: 34261945
62 results