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

Year Number of Results
1931 1
1932 1
1933 1
1934 1
1945 1
1947 2
1948 4
1949 5
1950 7
1952 1
1953 4
1954 3
1955 14
1956 9
1957 6
1958 6
1959 1
1960 6
1961 2
1962 4
1963 5
1964 6
1965 6
1966 7
1967 6
1968 2
1969 3
1970 5
1971 4
1972 2
1973 8
1974 5
1975 13
1976 2
1977 6
1978 11
1979 6
1980 6
1981 8
1982 7
1983 6
1984 7
1985 14
1986 7
1987 9
1988 11
1989 13
1990 15
1991 16
1992 9
1993 14
1994 14
1995 13
1996 16
1997 21
1998 15
1999 21
2000 19
2001 14
2002 13
2003 11
2004 10
2005 22
2006 21
2007 19
2008 26
2009 37
2010 27
2011 27
2012 37
2013 35
2014 28
2015 27
2016 29
2017 31
2018 36
2019 37
2020 45
2021 40
2022 50
2023 41
2024 48
2025 7

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1,062 results

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Page 1
A comprehensive classification system for lipids.
Fahy E, Subramaniam S, Brown HA, Glass CK, Merrill AH Jr, Murphy RC, Raetz CR, Russell DW, Seyama Y, Shaw W, Shimizu T, Spener F, van Meer G, VanNieuwenhze MS, White SH, Witztum JL, Dennis EA. Fahy E, et al. Among authors: dennis ea. J Lipid Res. 2005 May;46(5):839-61. doi: 10.1194/jlr.E400004-JLR200. Epub 2005 Feb 16. J Lipid Res. 2005. PMID: 15722563 Free article. Review.
Trans-chromosomal methylation.
Greaves I, Groszmann M, Dennis ES, Peacock WJ. Greaves I, et al. Among authors: dennis es. Epigenetics. 2012 Aug;7(8):800-5. doi: 10.4161/epi.20820. Epub 2012 Jun 18. Epigenetics. 2012. PMID: 22705969 Free PMC article. Review.
Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.
Zhao S, Mekbib KY, van der Ent MA, Allington G, Prendergast A, Chau JE, Smith H, Shohfi J, Ocken J, Duran D, Furey CG, Hao LT, Duy PQ, Reeves BC, Zhang J, Nelson-Williams C, Chen D, Li B, Nottoli T, Bai S, Rolle M, Zeng X, Dong W, Fu PY, Wang YC, Mane S, Piwowarczyk P, Fehnel KP, See AP, Iskandar BJ, Aagaard-Kienitz B, Moyer QJ, Dennis E, Kiziltug E, Kundishora AJ, DeSpenza T Jr, Greenberg ABW, Kidanemariam SM, Hale AT, Johnston JM, Jackson EM, Storm PB, Lang SS, Butler WE, Carter BS, Chapman P, Stapleton CJ, Patel AB, Rodesch G, Smajda S, Berenstein A, Barak T, Erson-Omay EZ, Zhao H, Moreno-De-Luca A, Proctor MR, Smith ER, Orbach DB, Alper SL, Nicoli S, Boggon TJ, Lifton RP, Gunel M, King PD, Jin SC, Kahle KT. Zhao S, et al. Among authors: dennis e. Nat Commun. 2023 Nov 17;14(1):7452. doi: 10.1038/s41467-023-43062-z. Nat Commun. 2023. PMID: 37978175 Free PMC article.
Vernalization in cereals.
Dennis ES, Peacock WJ. Dennis ES, et al. J Biol. 2009;8(6):57. doi: 10.1186/jbiol156. Epub 2009 Jun 22. J Biol. 2009. PMID: 19591652 Free PMC article. Review.
Human genetics and molecular genomics of Chiari malformation type 1.
Mekbib KY, Muñoz W, Allington G, McGee S, Mehta NH, Shofi JP, Fortes C, Le HT, Nelson-Williams C, Nanda P, Dennis E, Kundishora AJ, Khanna A, Smith H, Ocken J, Greenberg ABW, Wu R, Moreno-De-Luca A, DeSpenza T Jr, Zhao S, Marlier A, Jin SC, Alper SL, Butler WE, Kahle KT. Mekbib KY, et al. Among authors: dennis e. Trends Mol Med. 2023 Dec;29(12):1059-1075. doi: 10.1016/j.molmed.2023.08.013. Epub 2023 Oct 4. Trends Mol Med. 2023. PMID: 37802664 Review.
Ankle Injuries in Dancers.
Vosseller JT, Dennis ER, Bronner S. Vosseller JT, et al. Among authors: dennis er. J Am Acad Orthop Surg. 2019 Aug 15;27(16):582-589. doi: 10.5435/JAAOS-D-18-00596. J Am Acad Orthop Surg. 2019. PMID: 30789380 Review.
Dysregulation of FLVCR1a-dependent mitochondrial calcium handling in neural progenitors causes congenital hydrocephalus.
Bertino F, Mukherjee D, Bonora M, Bagowski C, Nardelli J, Metani L, Zanin Venturini DI, Chianese D, Santander N, Salaroglio IC, Hentschel A, Quarta E, Genova T, McKinney AA, Allocco AL, Fiorito V, Petrillo S, Ammirata G, De Giorgio F, Dennis E, Allington G, Maier F, Shoukier M, Gloning KP, Munaron L, Mussano F, Salsano E, Pareyson D, di Rocco M, Altruda F, Panagiotakos G, Kahle KT, Gressens P, Riganti C, Pinton PP, Roos A, Arnold T, Tolosano E, Chiabrando D. Bertino F, et al. Among authors: dennis e. Cell Rep Med. 2024 Jul 16;5(7):101647. doi: 10.1016/j.xcrm.2024.101647. Cell Rep Med. 2024. PMID: 39019006 Free PMC article.
TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus.
Duy PQ, Jux B, Zhao S, Mekbib KY, Dennis E, Dong W, Nelson-Williams C, Mehta NH, Shohfi JP, Juusola J, Allington G, Smith H, Marlin S, Belhous K, Monteleone B, Schaefer GB, Pisarska MD, Vásquez J, Estrada-Veras JI, Keren B, Mignot C, Flore LA, Palafoll IV, Alper SL, Lifton RP, Haider S, Moreno-De-Luca A, Jin SC, Kolanus W, Kahle KT. Duy PQ, et al. Among authors: dennis e. Brain. 2024 Dec 3;147(12):4292-4305. doi: 10.1093/brain/awae175. Brain. 2024. PMID: 38833623
1,062 results