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

Year Number of Results
2003 1
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2008 1
2009 3
2010 4
2011 5
2013 3
2014 5
2015 4
2016 3
2017 7
2018 11
2019 16
2020 18
2021 22
2022 21
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2026 0

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164 results

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Page 1
Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review.
Ghasemi MR, Tehrani Fateh S, Moeinafshar A, Sadeghi H, Karimzadeh P, Mirfakhraie R, Rezaei M, Hashemi-Gorji F, Rezvani Kashani M, Fazeli Bavandpour F, Bagheri S, Moghimi P, Rostami M, Madannejad R, Roudgari H, Miryounesi M. Ghasemi MR, et al. Among authors: sadeghi h. BMC Med Genomics. 2024 Feb 13;17(1):51. doi: 10.1186/s12920-024-01810-0. BMC Med Genomics. 2024. PMID: 38347586 Free PMC article.
Cardiovascular Organ-on-a-Chip Platforms for Drug Discovery and Development.
Ribas J, Sadeghi H, Manbachi A, Leijten J, Brinegar K, Zhang YS, Ferreira L, Khademhosseini A. Ribas J, et al. Among authors: sadeghi h. Appl In Vitro Toxicol. 2016 Jun 1;2(2):82-96. doi: 10.1089/aivt.2016.0002. Appl In Vitro Toxicol. 2016. PMID: 28971113 Free PMC article. Review.
Clinical Features and Genetic Characteristics of XLID Patients With KDM5C Gene Mutations: Insights on Phenotype-Genotype Correlations From 175 Previous Cases and Identification of a Novel Variant.
Ghasemi MR, Esmaeilizadeh Z, Tehrani Fateh S, Sadeghi H, Bagheri S, Hashemi-Gorji F, Sheikhi Nooshabadi M, Madannezhad R, Tavabe Ghavami TS, Mirfakhraie R, Miryounesi M. Ghasemi MR, et al. Among authors: sadeghi h. Mol Genet Genomic Med. 2025 Jan;13(1):e70057. doi: 10.1002/mgg3.70057. Mol Genet Genomic Med. 2025. PMID: 39835750 Free PMC article. Review.
Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).
Ghasemi MR, Fateh ST, Ben-Mahmoud A, Gupta V, Stühn LG, Lesca G, Chatron N, Platzer K, Edery P, Sadeghi H, Isidor B, Cogné B, Schulz HL, Krauspe-Stübecke I, Periyasamy R, Nampoothiri S, Mirfakhraie R, Alijanpour S, Syrbe S, Pfeifer U, Spranger S, Grundmann-Hauser K, Haack TB, Papadopoulou MT, da Silva Gonçalves T, Panagiotakaki E, Arzimanoglou A, Tonekaboni SH, Rossi M, Korenke GC, Lacassie Y, Jang MH, Layman LC, Miryounesi M, Kim HG. Ghasemi MR, et al. Among authors: sadeghi h. Am J Med Genet A. 2025 May;197(5):e63963. doi: 10.1002/ajmg.a.63963. Epub 2024 Dec 20. Am J Med Genet A. 2025. PMID: 39707601
CF Bridge of Hope program, a global medical home practice.
Raissi G, Messier R, Sadeghi D, Sadeghi H. Raissi G, et al. Among authors: sadeghi h. Pediatr Pulmonol. 2023 Jun;58(6):1802-1804. doi: 10.1002/ppul.26383. Epub 2023 Mar 21. Pediatr Pulmonol. 2023. PMID: 36945187 No abstract available.
164 results