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For: Imbert-Bouteille M, Mau Them FT, Thevenon J, Guignard T, Gatinois V, Riviere JB, Boland A, Meyer V, Deleuze JF, Sanchez E, Apparailly F, Geneviève D, Willems M. LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. Eur J Med Genet 2019;62:161-6. [PMID: 30006060 DOI: 10.1016/j.ejmg.2018.07.003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Al-Hinai A, Al-Hashmi S, Ganesh A, Al-Hashmi N, Al-Saegh A, Al-Mamari W, Al-Murshedi F, Al-Thihli K, Al-Kindi A, Al-Maawali A. Further phenotypic delineation of Alazami syndrome. Am J Med Genet A 2022. [PMID: 35567578 DOI: 10.1002/ajmg.a.62778] [Reference Citation Analysis]
2 Palumbo P, Palumbo O, Leone MP, di Muro E, Castellana S, Bisceglia L, Mazza T, Carella M, Castori M. Compound Phenotype Due to Recessive Variants in LARP7 and OTOG Genes Disclosed by an Integrated Approach of SNP-Array and Whole Exome Sequencing. Genes (Basel) 2020;11:E379. [PMID: 32244554 DOI: 10.3390/genes11040379] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Gana S, Plumari M, Rossi E, Saracino A, Iorio M, Zanaboni MP, Orcesi S, Valente EM. Alazami syndrome: Phenotypic expansion and clinical resemblance to Smith-Lemli-Opitz syndrome. Am J Med Genet A 2020;182:2722-6. [PMID: 32888391 DOI: 10.1002/ajmg.a.61832] [Reference Citation Analysis]
4 Schneeberger PE, Bierhals T, Neu A, Hempel M, Kutsche K. de novo MEPCE nonsense variant associated with a neurodevelopmental disorder causes disintegration of 7SK snRNP and enhanced RNA polymerase II activation. Sci Rep 2019;9:12516. [PMID: 31467394 DOI: 10.1038/s41598-019-49032-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
5 Wojcik MH, Linnea K, Stoler JM, Rappaport L. Updating the neurodevelopmental profile of Alazami syndrome: Illustrating the role of developmental assessment in rare genetic disorders. Am J Med Genet A 2019;179:1565-9. [PMID: 31074943 DOI: 10.1002/ajmg.a.61189] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
6 Hasler D, Meister G, Fischer U. Stabilize and connect: the role of LARP7 in nuclear non-coding RNA metabolism. RNA Biol 2021;18:290-303. [PMID: 32401147 DOI: 10.1080/15476286.2020.1767952] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
7 Liu Y, Olajide T, Sun M, Ji M, Yoong J, Weng X. Physicochemical properties of red palm oil extruded potato and sweet potato snacks. grasasaceites 2021;72:e412. [DOI: 10.3989/gya.0214201] [Reference Citation Analysis]
8 Patalan M, Leśniak A, Bernatowicz K, Romanowska H, Krzywińska-Zdeb E, Walczak M, Giżewska M. Patient with Phenylketonuria and Intellectual Disability-Problem Not Always Caused Exclusively by Insufficient Metabolic Control (Coexistence of PKU and Alazami Syndrome). Int J Environ Res Public Health 2022;19:2574. [PMID: 35270292 DOI: 10.3390/ijerph19052574] [Reference Citation Analysis]