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
1977 3
1978 1
1981 5
1982 4
1983 1
1984 1
1985 1
1989 3
1990 1
1992 3
1993 4
1994 7
1995 6
1996 9
1997 11
1998 6
1999 16
2000 5
2001 10
2002 6
2003 12
2004 7
2005 10
2006 11
2007 13
2008 11
2009 8
2010 1
2011 5
2012 5
2013 7
2014 1
2015 7
2016 9
2017 7
2018 8
2019 5
2020 3
Text availability
Article attribute
Article type
Publication date

Search Results

225 results
Results by year
Filters applied: . Clear all
Page 1
Genomic diagnosis for children with intellectual disability and/or developmental delay.
Bowling KM, Thompson ML, Amaral MD, Finnila CR, Hiatt SM, Engel KL, Cochran JN, Brothers KB, East KM, Gray DE, Kelley WV, Lamb NE, Lose EJ, Rich CA, Simmons S, Whittle JS, Weaver BT, Nesmith AS, Myers RM, Barsh GS, Bebin EM, Cooper GM. Bowling KM, et al. Among authors: barsh gs. Genome Med. 2017 May 30;9(1):43. doi: 10.1186/s13073-017-0433-1. Genome Med. 2017. PMID: 28554332 Free PMC article.
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies.
Carvill GL, Engel KL, Ramamurthy A, Cochran JN, Roovers J, Stamberger H, Lim N, Schneider AL, Hollingsworth G, Holder DH, Regan BM, Lawlor J, Lagae L, Ceulemans B, Bebin EM, Nguyen J; EuroEPINOMICS Rare Epilepsy Syndrome, Myoclonic-Astatic Epilepsy, and Dravet Working Group, Barsh GS, Weckhuysen S, Meisler M, Berkovic SF, De Jonghe P, Scheffer IE, Myers RM, Cooper GM, Mefford HC. Carvill GL, et al. Among authors: barsh gs. Am J Hum Genet. 2018 Dec 6;103(6):1022-1029. doi: 10.1016/j.ajhg.2018.10.023. Am J Hum Genet. 2018. PMID: 30526861 Free PMC article.
Molecular and evolutionary history of melanism in North American gray wolves.
Anderson TM, vonHoldt BM, Candille SI, Musiani M, Greco C, Stahler DR, Smith DW, Padhukasahasram B, Randi E, Leonard JA, Bustamante CD, Ostrander EA, Tang H, Wayne RK, Barsh GS. Anderson TM, et al. Among authors: barsh gs. Science. 2009 Mar 6;323(5919):1339-43. doi: 10.1126/science.1165448. Epub 2009 Feb 5. Science. 2009. PMID: 19197024 Free PMC article.
Central nervous system control of food intake and body weight.
Morton GJ, Cummings DE, Baskin DG, Barsh GS, Schwartz MW. Morton GJ, et al. Among authors: barsh gs. Nature. 2006 Sep 21;443(7109):289-95. doi: 10.1038/nature05026. Nature. 2006. PMID: 16988703 Review.
Developmental mechanisms of stripe patterns in rodents.
Mallarino R, Henegar C, Mirasierra M, Manceau M, Schradin C, Vallejo M, Beronja S, Barsh GS, Hoekstra HE. Mallarino R, et al. Among authors: barsh gs. Nature. 2016 Nov 24;539(7630):518-523. doi: 10.1038/nature20109. Epub 2016 Nov 2. Nature. 2016. PMID: 27806375 Free PMC article.
Doubling down on forensic twin studies.
Copenhaver GP, Weir B, Rothstein M, Tang H, Williams SM, Barsh GS. Copenhaver GP, et al. Among authors: barsh gs. PLoS Genet. 2018 Dec 20;14(12):e1007831. doi: 10.1371/journal.pgen.1007831. eCollection 2018 Dec. PLoS Genet. 2018. PMID: 30571773 Free PMC article. No abstract available.
The Plight of Muntaser Ibrahim.
Sirugo G, Williams SM, Tishkoff SA, Cordell HJ, Marchini J, Barsh GS, Copenhaver GP. Sirugo G, et al. Among authors: barsh gs. PLoS Genet. 2019 Mar 25;15(3):e1008100. doi: 10.1371/journal.pgen.1008100. eCollection 2019 Mar. PLoS Genet. 2019. PMID: 30908486 Free PMC article. No abstract available.
Making room for opinions.
Copenhaver GP, Barsh GS. Copenhaver GP, et al. Among authors: barsh gs. PLoS Genet. 2019 Feb 28;15(2):e1008015. doi: 10.1371/journal.pgen.1008015. eCollection 2019 Feb. PLoS Genet. 2019. PMID: 30817769 Free PMC article. No abstract available.
[Attractin].
Shen SL, Barsh GS, Wu ZB. Shen SL, et al. Among authors: barsh gs. Zhonghua Bing Li Xue Za Zhi. 2005 Jul;34(7):429-31. Zhonghua Bing Li Xue Za Zhi. 2005. PMID: 16251053 Review. Chinese. No abstract available.
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay.
Hiatt SM, Neu MB, Ramaker RC, Hardigan AA, Prokop JW, Hancarova M, Prchalova D, Havlovicova M, Prchal J, Stranecky V, Yim DKC, Powis Z, Keren B, Nava C, Mignot C, Rio M, Revah-Politi A, Hemati P, Stong N, Iglesias AD, Suchy SF, Willaert R, Wentzensen IM, Wheeler PG, Brick L, Kozenko M, Hurst ACE, Wheless JW, Lacassie Y, Myers RM, Barsh GS, Sedlacek Z, Cooper GM. Hiatt SM, et al. Among authors: barsh gs. PLoS Genet. 2018 Nov 30;14(11):e1007671. doi: 10.1371/journal.pgen.1007671. eCollection 2018 Nov. PLoS Genet. 2018. PMID: 30500825 Free PMC article.
225 results
Jump to page
Feedback