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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

283 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A large data resource of genomic copy number variation across neurodevelopmental disorders.
Zarrei M, Burton CL, Engchuan W, Young EJ, Higginbotham EJ, MacDonald JR, Trost B, Chan AJS, Walker S, Lamoureux S, Heung T, Mojarad BA, Kellam B, Paton T, Faheem M, Miron K, Lu C, Wang T, Samler K, Wang X, Costain G, Hoang N, Pellecchia G, Wei J, Patel RV, Thiruvahindrapuram B, Roifman M, Merico D, Goodale T, Drmic I, Speevak M, Howe JL, Yuen RKC, Buchanan JA, Vorstman JAS, Marshall CR, Wintle RF, Rosenberg DR, Hanna GL, Woodbury-Smith M, Cytrynbaum C, Zwaigenbaum L, Elsabbagh M, Flanagan J, Fernandez BA, Carter MT, Szatmari P, Roberts W, Lerch J, Liu X, Nicolson R, Georgiades S, Weksberg R, Arnold PD, Bassett AS, Crosbie J, Schachar R, Stavropoulos DJ, Anagnostou E, Scherer SW. Zarrei M, et al. Among authors: bassett as. NPJ Genom Med. 2019 Oct 7;4:26. doi: 10.1038/s41525-019-0098-3. eCollection 2019. NPJ Genom Med. 2019. PMID: 31602316 Free PMC article.
22q11 deletion syndrome in adults with schizophrenia.
Bassett AS, Hodgkinson K, Chow EW, Correia S, Scutt LE, Weksberg R. Bassett AS, et al. Am J Med Genet. 1998 Jul 10;81(4):328-37. Am J Med Genet. 1998. PMID: 9674980 Free PMC article.
Phenotype of adults with the 22q11 deletion syndrome: A review.
Cohen E, Chow EW, Weksberg R, Bassett AS. Cohen E, et al. Among authors: bassett as. Am J Med Genet. 1999 Oct 8;86(4):359-65. doi: 10.1002/(sici)1096-8628(19991008)86:4<359::aid-ajmg10>3.0.co;2-v. Am J Med Genet. 1999. PMID: 10494092 Free PMC article. Review.
Chromosomal abnormalities and schizophrenia.
Bassett AS, Chow EW, Weksberg R. Bassett AS, et al. Am J Med Genet. 2000 Spring;97(1):45-51. doi: 10.1002/(sici)1096-8628(200021)97:1<45::aid-ajmg6>3.0.co;2-9. Am J Med Genet. 2000. PMID: 10813803 Free PMC article. Review.
Patterns of dysmorphic features in schizophrenia.
Scutt LE, Chow EW, Weksberg R, Honer WG, Bassett AS. Scutt LE, et al. Among authors: bassett as. Am J Med Genet. 2001 Dec 8;105(8):713-23. doi: 10.1002/ajmg.1612. Am J Med Genet. 2001. PMID: 11803519 Free PMC article.
Schizophrenia and genetics: new insights.
Bassett AS, Chow EW, Weksberg R, Brzustowicz L. Bassett AS, et al. Curr Psychiatry Rep. 2002 Aug;4(4):307-14. doi: 10.1007/s11920-996-0051-x. Curr Psychiatry Rep. 2002. PMID: 12126600 Free PMC article. Review.
The schizophrenia phenotype in 22q11 deletion syndrome.
Bassett AS, Chow EW, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. Bassett AS, et al. Am J Psychiatry. 2003 Sep;160(9):1580-6. doi: 10.1176/appi.ajp.160.9.1580. Am J Psychiatry. 2003. PMID: 12944331 Free PMC article.
283 results