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

Year Number of Results
2003 1
2006 4
2007 4
2008 7
2009 5
2010 1
2011 6
2012 10
2013 8
2014 7
2015 5
2016 7
2017 16
2018 15
2019 21
2020 12
2021 20
2022 16
2023 27
2024 35
2025 2

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191 results

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Page 1
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder.
Schmid CM, Gregor A, Costain G, Morel CF, Massingham L, Schwab J, Quélin C, Faoucher M, Kaplan J, Procopio R, Saunders CJ, Cohen ASA, Lemire G, Sacharow S, O'Donnell-Luria A, Segal RJ, Kianmahd Shamshoni J, Schweitzer D, Ebrahimi-Fakhari D, Monaghan K, Palculict TB, Napier MP, Tao A, Isidor B, Moradkhani K, Reis A, Sticht H; Care4Rare Canada; Chung WK, Zweier C. Schmid CM, et al. Genet Med. 2023 Jul;25(7):100839. doi: 10.1016/j.gim.2023.100839. Epub 2023 Apr 11. Genet Med. 2023. PMID: 37057675 Free article.
3q29 duplications: A cohort of 46 patients and a literature review.
Massier M, Doco-Fenzy M, Egloff M, Le Guillou X, Le Guyader G, Redon S, Benech C, Le Millier K, Uguen K, Ropars J, Sacaze E, Audebert-Bellanger S, Apetrei A, Molin A, Gruchy N, Vincent-Devulder A, Spodenkiewicz M, Jacquin C, Loron G, Thibaud M, Delplancq G, Brisset S, Lesieur-Sebellin M, Malan V, Romana S, Rio M, Marlin S, Amiel J, Marquet V, Dauriat B, Moradkhani K, Mercier S, Isidor B, Arpin S, Pujalte M, Jedraszak G, Pebrel-Richard C, Salaun G, Laffargue F, Boudjarane J, Missirian C, Chelloug N, Toutain A, Chiesa J, Keren B, Mignot C, Gouy E, Jaillard S, Landais E, Poirsier C. Massier M, et al. Am J Med Genet A. 2024 Jul;194(7):e63531. doi: 10.1002/ajmg.a.63531. Epub 2024 Feb 29. Am J Med Genet A. 2024. PMID: 38421086 Review.
Indentation fracture resistance of brittle materials using irregular cracks: A review.
Moradkhani A, Panahizadeh V, Hoseinpour M. Moradkhani A, et al. Heliyon. 2023 Aug 22;9(9):e19361. doi: 10.1016/j.heliyon.2023.e19361. eCollection 2023 Sep. Heliyon. 2023. PMID: 37662782 Free PMC article. Review.
The equation of the Vickers indentation fracture (VIF) proposed by Moradkhani et al. (J. Adv. Ceram. 2, 87-102 (2013)) has been used for the determination of indentation fracture resistance from indented area containing irregular and branch cracks formed around Vickers dia …
The equation of the Vickers indentation fracture (VIF) proposed by Moradkhani et al. (J. Adv. Ceram. 2, 87-102 (2013)) has been used …
Immunoregulatory role of melatonin in cancer.
Moradkhani F, Moloudizargari M, Fallah M, Asghari N, Heidari Khoei H, Asghari MH. Moradkhani F, et al. J Cell Physiol. 2020 Feb;235(2):745-757. doi: 10.1002/jcp.29036. Epub 2019 Jul 4. J Cell Physiol. 2020. PMID: 31270813 Review.
Haploinsufficiency of the Sin3/HDAC corepressor complex member SIN3B causes a syndromic intellectual disability/autism spectrum disorder.
Latypova X, Vincent M, Mollé A, Adebambo OA, Fourgeux C, Khan TN, Caro A, Rosello M, Orellana C, Niyazov D, Lederer D, Deprez M, Capri Y, Kannu P, Tabet AC, Levy J, Aten E, den Hollander N, Splitt M, Walia J, Immken LL, Stankiewicz P, McWalter K, Suchy S, Louie RJ, Bell S, Stevenson RE, Rousseau J, Willem C, Retiere C, Yang XJ, Campeau PM, Martinez F, Rosenfeld JA, Le Caignec C, Küry S, Mercier S, Moradkhani K, Conrad S, Besnard T, Cogné B, Katsanis N, Bézieau S, Poschmann J, Davis EE, Isidor B. Latypova X, et al. Am J Hum Genet. 2021 May 6;108(5):929-941. doi: 10.1016/j.ajhg.2021.03.017. Epub 2021 Apr 2. Am J Hum Genet. 2021. PMID: 33811806 Free PMC article.
Decarboxylative 1,3-dipolar cycloadditions of l-proline.
Doraghi F, Serajian A, Karimian S, Ghanbarlou M, Moradkhani F, Larijani B, Mahdavi M. Doraghi F, et al. RSC Adv. 2024 Mar 13;14(12):8481-8501. doi: 10.1039/d3ra08160e. eCollection 2024 Mar 6. RSC Adv. 2024. PMID: 38482067 Free PMC article. Review.
Nanotechnology application to local anaesthesia (LA).
Moradkhani MR, Karimi A, Negahdari B. Moradkhani MR, et al. Artif Cells Nanomed Biotechnol. 2018 Mar;46(2):355-360. doi: 10.1080/21691401.2017.1313263. Epub 2017 Apr 10. Artif Cells Nanomed Biotechnol. 2018. PMID: 28395522 Free article. Review.
Prenatal findings in 1p36 deletion syndrome: New cases and a literature review.
Guterman S, Beneteau C, Redon S, Dupont C, Missirian C, Jaeger P, Herve B, Jacquin C, Douet-Guilbert N, Till M, Tabet AC, Moradkhani K, Malan V, Doco-Fenzy M, Vialard F. Guterman S, et al. Prenat Diagn. 2019 Sep;39(10):871-882. doi: 10.1002/pd.5498. Epub 2019 Jul 5. Prenat Diagn. 2019. PMID: 31172545 Review.
191 results