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

Year Number of Results
1926 1
1948 1
1959 1
1964 1
1966 2
1970 1
1971 1
1975 3
1978 1
1979 1
1980 2
1982 5
1983 2
1984 1
1985 5
1986 4
1987 4
1988 5
1989 2
1990 3
1991 5
1992 8
1993 3
1994 5
1995 2
1996 2
1997 1
1998 2
1999 1
2000 1
2001 1
2002 2
2003 1
2004 1
2005 3
2006 1
2007 1
2012 1
2013 2
2014 3
2015 2
2016 5
2017 2
2018 3
2020 4
2021 5
2022 4
2023 4
2024 3

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116 results

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Page 1
Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations.
Tatton-Brown K, Douglas J, Coleman K, Baujat G, Cole TR, Das S, Horn D, Hughes HE, Temple IK, Faravelli F, Waggoner D, Turkmen S, Cormier-Daire V, Irrthum A, Rahman N; Childhood Overgrowth Collaboration. Tatton-Brown K, et al. Among authors: hughes he. Am J Hum Genet. 2005 Aug;77(2):193-204. doi: 10.1086/432082. Epub 2005 Jun 7. Am J Hum Genet. 2005. PMID: 15942875 Free PMC article.
Epidemiology of respiratory syncytial virus in children younger than 5 years in England during the COVID-19 pandemic, measured by laboratory, clinical, and syndromic surveillance: a retrospective observational study.
Bardsley M, Morbey RA, Hughes HE, Beck CR, Watson CH, Zhao H, Ellis J, Smith GE, Elliot AJ. Bardsley M, et al. Among authors: hughes he. Lancet Infect Dis. 2023 Jan;23(1):56-66. doi: 10.1016/S1473-3099(22)00525-4. Epub 2022 Sep 2. Lancet Infect Dis. 2023. PMID: 36063828 Free PMC article.
Sotos syndrome.
Cole TR, Hughes HE. Cole TR, et al. Among authors: hughes he. J Med Genet. 1990 Sep;27(9):571-6. doi: 10.1136/jmg.27.9.571. J Med Genet. 1990. PMID: 2231650 Free PMC article. No abstract available.
Weaver syndrome.
Cole TR, Dennis NR, Hughes HE. Cole TR, et al. Among authors: hughes he. J Med Genet. 1992 May;29(5):332-7. doi: 10.1136/jmg.29.5.332. J Med Genet. 1992. PMID: 1583661 Free PMC article. No abstract available.
Imprinting in Albright's hereditary osteodystrophy.
Davies SJ, Hughes HE. Davies SJ, et al. Among authors: hughes he. J Med Genet. 1993 Feb;30(2):101-3. doi: 10.1136/jmg.30.2.101. J Med Genet. 1993. PMID: 8383205 Free PMC article. Review.
Risk of malignancy in Sotos syndrome.
Hersh JH, Cole TR, Bloom AS, Bertolone SJ, Hughes HE. Hersh JH, et al. Among authors: hughes he. J Pediatr. 1992 Apr;120(4 Pt 1):572-4. doi: 10.1016/s0022-3476(10)80004-6. J Pediatr. 1992. PMID: 1552397 Review.
Lateral meningocele syndrome: three new patients and review of the literature.
Gripp KW, Scott CI Jr, Hughes HE, Wallerstein R, Nicholson L, States L, Bason LD, Kaplan P, Zderic SA, Duhaime AC, Miller F, Magnusson MR, Zackai EH. Gripp KW, et al. Among authors: hughes he. Am J Med Genet. 1997 Jun 13;70(3):229-39. Am J Med Genet. 1997. PMID: 9188658 Review.
Persistent elevation in incidence of pneumonia in children in England, 2023/24.
Todkill D, Lamagni T, Pebody R, Ramsay M, Woolham D, Demirjian A, Salzmann A, Chand M, Hughes HE, Bennett C, Hope R, Watson CH, Brown CS, Elliot AJ. Todkill D, et al. Among authors: hughes he. Euro Surveill. 2024 Aug;29(32):2400485. doi: 10.2807/1560-7917.ES.2024.29.32.2400485. Euro Surveill. 2024. PMID: 39119723 Free PMC article.
Maxillonasal dysplasia (Binder's syndrome).
Quarrell OW, Koch M, Hughes HE. Quarrell OW, et al. Among authors: hughes he. J Med Genet. 1990 Jun;27(6):384-7. doi: 10.1136/jmg.27.6.384. J Med Genet. 1990. PMID: 2359101 Free PMC article. No abstract available.
116 results