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
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 5
2022 8
2023 3
2024 1
2025 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

71 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 Free PMC article.
De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder.
Sleyp Y, Valenzuela I, Accogli A, Ballon K, Ben-Zeev B, Berkovic SF, Broly M, Callaerts P, Caylor RC, Charles P, Chatron N, Cohen L, Coppola A, Cordeiro D, Cuccurullo C, Cuscó I, Janette diMonda, Duran-Romaña R, Ekhilevitch N, Fernández-Alvarez P, Gordon CT, Isidor B, Keren B, Lesca G, Maljaars J, Mercimek-Andrews S, Morrow MM, Muir AM; University of Washington Center for Mendelian Genomics; Rousseau F, Salpietro V, Scheffer IE, Schnur RE, Schymkowitz J, Souche E, Steyaert J, Stolerman ES, Vengoechea J, Ville D, Washington C, Weiss K, Zaid R, Sadleir LG, Mefford HC, Peeters H. Sleyp Y, et al. Among authors: cohen l. Genet Med. 2022 Dec;24(12):2464-2474. doi: 10.1016/j.gim.2022.08.020. Epub 2022 Oct 11. Genet Med. 2022. PMID: 36214804 Free article.
National Rapid Genome Sequencing in Neonatal Intensive Care.
Marom D, Mory A, Reytan-Miron S, Amir Y, Kurolap A, Cohen JG, Morhi Y, Smolkin T, Cohen L, Zangen S, Shalata A, Riskin A, Peleg A, Lavie-Nevo K, Mandel D, Chervinsky E, Fisch CF, Fleisher Sheffer V, Falik-Zaccai TC, Rips J, Shlomai NO, Friedman SE, Shporen CH, Ben-Yehoshua SJ, Simmonds A, Yaacobi RG, Bauer-Rusek S, Omari H, Weiss K, Hochwald O, Koifman A, Globus O, Batzir NA, Yaron N, Segel R, Morag I, Reish O, Eliyahu A, Leibovitch L, Schwartz ME, Abramsky R, Hochberg A, Oron A, Banne E, Portnov I, Samra NN, Singer A, Baris Feldman H. Marom D, et al. Among authors: cohen l. JAMA Netw Open. 2024 Feb 5;7(2):e240146. doi: 10.1001/jamanetworkopen.2024.0146. JAMA Netw Open. 2024. PMID: 38386321 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.
Wave-front reconstruction via single-pixel homodyne imaging.
Cuozzo SL, Gabaldon C, Barge PJ, Niu Z, Lee H, Cohen L, Novikova I, Mikhailov EE. Cuozzo SL, et al. Among authors: cohen l. Opt Express. 2022 Oct 10;30(21):37938-37945. doi: 10.1364/OE.472253. Opt Express. 2022. PMID: 36258372 Free 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.
Weak thermal state quadrature-noise shadow imaging.
Barge PJ, Niu Z, Cuozzo SL, Mikhailov EE, Novikova I, Lee H, Cohen L. Barge PJ, et al. Among authors: cohen l. Opt Express. 2022 Aug 1;30(16):29401-29408. doi: 10.1364/OE.455646. Opt Express. 2022. PMID: 36299115 Free article.
The Solubility Limit of Carbon in Alumina at 1,600°C.
Cohen LO, Ghosh P, Berner A, Marder R, Kaplan WD. Cohen LO, et al. Microsc Microanal. 2022 Sep 8:1-11. doi: 10.1017/S1431927622012491. Online ahead of print. Microsc Microanal. 2022. PMID: 36073062
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.
71 results