Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1991 2
1992 1
1993 3
1994 1
1995 1
1996 1
1997 2
1998 1
2001 3
2002 3
2003 1
2004 4
2005 3
2006 5
2007 3
2008 8
2009 6
2010 2
2011 9
2012 5
2013 11
2014 6
2015 4
2016 8
2017 7
2018 10
2019 8
2020 9
2021 4
Text availability
Article attribute
Article type
Publication date

Search Results

118 results
Results by year
Filters applied: . Clear all
Page 1
15q Duplication Syndrome and Related Disorders.
Finucane BM, Lusk L, Arkilo D, Chamberlain S, Devinsky O, Dindot S, Jeste SS, LaSalle JM, Reiter LT, Schanen NC, Spence SJ, Thibert RL, Calvert G, Luchsinger K, Cook EH. Finucane BM, et al. Among authors: lasalle jm. 2016 Jun 16. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 2016 Jun 16. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 27308687 Free Books & Documents. Review.
Editorial: Secondary vs. Idiopathic Autism.
Casanova MF, Casanova EL, Frye RE, Baeza-Velasco C, LaSalle JM, Hagerman RJ, Scherer SW, Natowicz MR. Casanova MF, et al. Among authors: lasalle jm. Front Psychiatry. 2020 Apr 14;11:297. doi: 10.3389/fpsyt.2020.00297. eCollection 2020. Front Psychiatry. 2020. PMID: 32346372 Free PMC article. No abstract available.
Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genes.
Mordaunt CE, Jianu JM, Laufer BI, Zhu Y, Hwang H, Dunaway KW, Bakulski KM, Feinberg JI, Volk HE, Lyall K, Croen LA, Newschaffer CJ, Ozonoff S, Hertz-Picciotto I, Fallin MD, Schmidt RJ, LaSalle JM. Mordaunt CE, et al. Among authors: lasalle jm. Genome Med. 2020 Oct 14;12(1):88. doi: 10.1186/s13073-020-00785-8. Genome Med. 2020. PMID: 33054850 Free PMC article.
Genetics and epigenetic factors of Wilson disease.
Medici V, LaSalle JM. Medici V, et al. Among authors: lasalle jm. Ann Transl Med. 2019 Apr;7(Suppl 2):S58. doi: 10.21037/atm.2019.01.67. Ann Transl Med. 2019. PMID: 31179295 Free PMC article. Review.
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Justice CM, Cuellar A, Bala K, Sabourin JA, Cunningham ML, Crawford K, Phipps JM, Zhou Y, Cilliers D, Byren JC, Johnson D, Wall SA, Morton JEV, Noons P, Sweeney E, Weber A, Rees KEM, Wilson LC, Simeonov E, Kaneva R, Yaneva N, Georgiev K, Bussarsky A, Senders C, Zwienenberg M, Boggan J, Roscioli T, Tamburrini G, Barba M, Conway K, Sheffield VC, Brody L, Mills JL, Kay D, Sicko RJ, Langlois PH, Tittle RK, Botto LD, Jenkins MM, LaSalle JM, Lattanzi W, Wilkie AOM, Wilson AF, Romitti PA, Boyadjiev SA; National Birth Defects Prevention Study. Justice CM, et al. Among authors: lasalle jm. Hum Genet. 2020 Aug;139(8):1077-1090. doi: 10.1007/s00439-020-02157-z. Epub 2020 Apr 7. Hum Genet. 2020. PMID: 32266521
mtDNA depletion-like syndrome in Wilson disease.
Medici V, Sarode GV, Napoli E, Song GY, Shibata NM, Guimarães AO, Mordaunt CE, Kieffer DA, Mazi TA, Czlonkowska A, Litwin T, LaSalle JM, Giulivi C. Medici V, et al. Among authors: lasalle jm. Liver Int. 2020 Nov;40(11):2776-2787. doi: 10.1111/liv.14646. Epub 2020 Sep 30. Liver Int. 2020. PMID: 32996699
Integrated analysis of a compendium of RNA-Seq datasets for splicing factors.
Yu P, Li J, Deng SP, Zhang F, Grozdanov PN, Chin EWM, Martin SD, Vergnes L, Islam MS, Sun D, LaSalle JM, McGee SL, Goh E, MacDonald CC, Jin P. Yu P, et al. Among authors: lasalle jm. Sci Data. 2020 Jun 16;7(1):178. doi: 10.1038/s41597-020-0514-7. Sci Data. 2020. PMID: 32546682 Free PMC article.
118 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page