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

Year Number of Results
1952 3
1953 3
1954 1
1959 1
1960 1
1963 1
1964 2
1965 1
1966 1
1968 2
1969 2
1970 6
1971 2
1972 2
1973 3
1975 2
1976 6
1977 4
1979 1
1980 1
1982 3
1986 1
1987 1
1990 1
1991 4
1992 1
1993 2
1994 1
1995 2
1996 4
1997 2
1998 1
1999 3
2000 5
2001 2
2002 7
2003 12
2004 2
2005 5
2006 6
2007 4
2008 5
2009 5
2010 1
2011 1
2012 3
2013 3
2014 3
2015 2
2016 2
2018 1
2019 2
2020 1
2021 4
2022 1
2023 1
2024 9
2025 4

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157 results

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Page 1
Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement.
LaFlamme CW, Rastin C, Sengupta S, Pennington HE, Russ-Hall SJ, Schneider AL, Bonkowski ES, Almanza Fuerte EP, Allan TJ, Zalusky MP, Goffena J, Gibson SB, Nyaga DM, Lieffering N, Hebbar M, Walker EV, Darnell D, Olsen SR, Kolekar P, Djekidel MN, Rosikiewicz W, McConkey H, Kerkhof J, Levy MA, Relator R, Lev D, Lerman-Sagie T, Park KL, Alders M, Cappuccio G, Chatron N, Demain L, Genevieve D, Lesca G, Roscioli T, Sanlaville D, Tedder ML, Gupta S, Jones EA, Weisz-Hubshman M, Ketkar S, Dai H, Worley KC, Rosenfeld JA, Chao HT; Undiagnosed Diseases Network; Neale G, Carvill GL; University of Washington Center for Rare Disease Research; Wang Z, Berkovic SF, Sadleir LG, Miller DE, Scheffer IE, Sadikovic B, Mefford HC. LaFlamme CW, et al. Among authors: allan tj. Nat Commun. 2024 Aug 6;15(1):6524. doi: 10.1038/s41467-024-50159-6. Nat Commun. 2024. PMID: 39107278 Free PMC article.
Early mortality in STXBP1-related disorders.
Furia F, Rigby CS, Scheffer IE, Allen N, Baker K, Hengsbach C, Kegele J, Goss J, Gorman K, Mala MI, Nicita F, Allan T, Spalice A, Weber Y; European STXBP1 consortium (ESCO); STXBP1 foundation; Rubboli G, Møller RS, Gardella E. Furia F, et al. Among authors: allan t. Neurol Sci. 2025 Mar;46(3):1339-1347. doi: 10.1007/s10072-024-07783-3. Epub 2024 Oct 11. Neurol Sci. 2025. PMID: 39392525 Free PMC article.
Rhesus nomenclature.
ALLAN TM. ALLAN TM. Lancet. 1952 Mar 22;1(6708):615. doi: 10.1016/s0140-6736(52)90139-6. Lancet. 1952. PMID: 14909496 No abstract available.
Karl Popper.
Allan TM. Allan TM. Lancet. 1973 Sep 15;2(7829):622-4. doi: 10.1016/s0140-6736(73)92459-8. Lancet. 1973. PMID: 4125420 No abstract available.
SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature.
LaFlamme CW, Karimi K, Rastin C, Almanza Fuerte EP, Allan T, Russ-Hall SJ, Schneider AL, Stobo D, Lesca G, Symonds JD, Brunklaus A, Sadleir LG, Scheffer IE, Sadikovic B, Mefford HC. LaFlamme CW, et al. Among authors: allan t. Epilepsia. 2025 Apr;66(4):e66-e72. doi: 10.1111/epi.18315. Epub 2025 Feb 11. Epilepsia. 2025. PMID: 39932319 Free PMC article.
Neuroanatomical abnormalities in chronic tinnitus in the human brain.
Adjamian P, Hall DA, Palmer AR, Allan TW, Langers DR. Adjamian P, et al. Among authors: allan tw. Neurosci Biobehav Rev. 2014 Sep;45:119-33. doi: 10.1016/j.neubiorev.2014.05.013. Epub 2014 Jun 2. Neurosci Biobehav Rev. 2014. PMID: 24892904 Free PMC article. Review.
Blood-groups and reproduction.
ALLAN TM. ALLAN TM. Lancet. 1952 Jan 12;1(6698):102-3. doi: 10.1016/s0140-6736(52)91823-0. Lancet. 1952. PMID: 14889772 No abstract available.
157 results