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
2003 2
2004 4
2005 3
2006 7
2007 7
2008 2
2009 2
2010 1
2011 2
2012 1
2013 2
2015 4
2016 3
2017 4
2018 5
2019 8
2020 9
2021 4
Text availability
Article attribute
Article type
Publication date

Search Results

59 results
Results by year
Filters applied: . Clear all
Page 1
The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis.
Weiss K, Lazar HP, Kurolap A, Martinez AF, Paperna T, Cohen L, Smeland MF, Whalen S, Heide S, Keren B, Terhal P, Irving M, Takaku M, Roberts JD, Petrovich RM, Schrier Vergano SA, Kenney A, Hove H, DeChene E, Quinonez SC, Colin E, Ziegler A, Rumple M, Jain M, Monteil D, Roeder ER, Nugent K, van Haeringen A, Gambello M, Santani A, Medne L, Krock B, Skraban CM, Zackai EH, Dubbs HA, Smol T, Ghoumid J, Parker MJ, Wright M, Turnpenny P, Clayton-Smith J, Metcalfe K, Kurumizaka H, Gelb BD, Baris Feldman H, Campeau PM, Muenke M, Wade PA, Lachlan K. Weiss K, et al. Among authors: cohen l. Genet Med. 2020 Feb;22(2):389-397. doi: 10.1038/s41436-019-0612-0. Epub 2019 Aug 7. Genet Med. 2020. PMID: 31388190
Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures.
Tan TY, Sedmík J, Fitzgerald MP, Halevy RS, Keegan LP, Helbig I, Basel-Salmon L, Cohen L, Straussberg R, Chung WK, Helal M, Maroofian R, Houlden H, Juusola J, Sadedin S, Pais L, Howell KB, White SM, Christodoulou J, O'Connell MA. Tan TY, et al. Among authors: cohen l. Am J Hum Genet. 2020 Apr 2;106(4):467-483. doi: 10.1016/j.ajhg.2020.02.015. Epub 2020 Mar 26. Am J Hum Genet. 2020. PMID: 32220291 Free PMC article.
SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome.
Crippa M, Bestetti I, Maitz S, Weiss K, Spano A, Masciadri M, Smithson S, Larizza L, Low K, Cohen L, Finelli P. Crippa M, et al. Among authors: cohen l. Front Neurol. 2020 Jul 24;11:631. doi: 10.3389/fneur.2020.00631. eCollection 2020. Front Neurol. 2020. PMID: 32793091 Free PMC article.
Behavior: Oxytocin Promotes Fearless Motherhood.
Cohen L, Maroun M, Wagner S. Cohen L, et al. Curr Biol. 2018 Apr 23;28(8):R359-R361. doi: 10.1016/j.cub.2018.02.063. Curr Biol. 2018. PMID: 29689212 Free article.
The insecticidal potential of scorpion beta-toxins.
Gurevitz M, Karbat I, Cohen L, Ilan N, Kahn R, Turkov M, Stankiewicz M, Stühmer W, Dong K, Gordon D. Gurevitz M, et al. Among authors: cohen l. Toxicon. 2007 Mar 15;49(4):473-89. doi: 10.1016/j.toxicon.2006.11.015. Epub 2006 Nov 28. Toxicon. 2007. PMID: 17197009 Review.
Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities.
Bend R, Cohen L, Carter MT, Lyons MJ, Niyazov D, Mikati MA, Rojas SK, Person RE, Si Y, Wentzensen IM; Regeneron Genetics Center, Torti E, Lee JA, Boycott KM, Basel-Salmon L, Ferreira CR, Gonzaga-Jauregui C. Bend R, et al. Among authors: cohen l. Eur J Hum Genet. 2020 Jan;28(1):76-87. doi: 10.1038/s41431-019-0487-1. Epub 2019 Aug 8. Eur J Hum Genet. 2020. PMID: 31395947 Free PMC article.
Quantum-Limited Squeezed Light Detection with a Camera.
Matekole ES, Cuozzo SL, Prajapati N, Bhusal N, Lee H, Novikova I, Mikhailov EE, Dowling JP, Cohen L. Matekole ES, et al. Among authors: cohen l. Phys Rev Lett. 2020 Sep 11;125(11):113602. doi: 10.1103/PhysRevLett.125.113602. Phys Rev Lett. 2020. PMID: 32975994
Late diagnosis of Alstrom syndrome in a Yemenite-Jewish child.
Weiss S, Cohen L, Ben-Yosef T, Ehrenberg M, Goldenberg-Cohen N. Weiss S, et al. Among authors: cohen l. Ophthalmic Genet. 2019 Feb;40(1):7-11. doi: 10.1080/13816810.2018.1561900. Epub 2019 Jan 2. Ophthalmic Genet. 2019. PMID: 30600744
59 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page