Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

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

Year Number of Results
1974 1
1978 1
1980 1
1984 2
1985 1
1986 1
1987 3
1988 2
1989 1
1991 2
1992 2
1993 1
1996 2
1997 1
1998 6
1999 2
2001 4
2002 1
2003 6
2004 6
2005 1
2006 3
2007 2
2008 2
2009 1
2012 1
2013 2
2014 1
2015 3
2016 1
2017 2
2018 1
2020 2
2022 1
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

65 results

Results by year

Filters applied: . Clear all
Page 1
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, Sheppard B, Xu X, Bhaduri A, Norman U, Brand H, Schwartz G, Nguyen R, Guerrero EE, Dias C; Autism Sequencing Consortium; iPSYCH-Broad Consortium; Betancur C, Cook EH, Gallagher L, Gill M, Sutcliffe JS, Thurm A, Zwick ME, Børglum AD, State MW, Cicek AE, Talkowski ME, Cutler DJ, Devlin B, Sanders SJ, Roeder K, Daly MJ, Buxbaum JD. Satterstrom FK, et al. Cell. 2020 Feb 6;180(3):568-584.e23. doi: 10.1016/j.cell.2019.12.036. Epub 2020 Jan 23. Cell. 2020. PMID: 31981491 Free PMC article.
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. Fu JM, et al. Among authors: gargus jj. Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982160 Free PMC article.
Why migraines strike.
Dodick DW, Gargus JJ. Dodick DW, et al. Among authors: gargus jj. Sci Am. 2008 Aug;299(2):56-63. doi: 10.1038/scientificamerican0808-56. Sci Am. 2008. PMID: 18666680 No abstract available.
Chromosome deletion 1q42-43.
Watson MS, Gargus JJ, Blakemore KJ, Katz SN, Breg WR. Watson MS, et al. Among authors: gargus jj. Am J Med Genet. 1986 May;24(1):1-6. doi: 10.1002/ajmg.1320240102. Am J Med Genet. 1986. PMID: 3706398
Relative carnitine deficiency in autism.
Filipek PA, Juranek J, Nguyen MT, Cummings C, Gargus JJ. Filipek PA, et al. Among authors: gargus jj. J Autism Dev Disord. 2004 Dec;34(6):615-23. doi: 10.1007/s10803-004-5283-1. J Autism Dev Disord. 2004. PMID: 15679182
Diffuse large B-cell non-Hodgkin's lymphoma in Gaucher disease.
Bonesteele G, Gargus JJ, Curtin E, Tang M, Rosenbloom B, Kimonis V. Bonesteele G, et al. Among authors: gargus jj. Mol Genet Metab Rep. 2020 Oct 21;25:100663. doi: 10.1016/j.ymgmr.2020.100663. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33101982 Free PMC article.
65 results