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For: Knapp KM, Jenkins DE, Sullivan R, Harms FL, von Elsner L, Ockeloen CW, de Munnik S, Bongers EMHF, Murray J, Pachter N, Denecke J, Kutsche K, Bicknell LS. MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency. Eur J Hum Genet 2021;29:1110-20. [PMID: 33654309 DOI: 10.1038/s41431-021-00839-4] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
Number Citing Articles
1 Nazarenko MS, Viakhireva IV, Skoblov MY, Soloveva EV, Sleptcov AA, Nazarenko LP. Meier–Gorlin Syndrome: Clinical Misdiagnosis, Genetic Testing and Functional Analysis of ORC6 Mutations and the Development of a Prenatal Test. IJMS 2022;23:9234. [DOI: 10.3390/ijms23169234] [Reference Citation Analysis]
2 Mansour F, Hinze C, Telugu NS, Kresoja J, Shaheed IB, Mosimann C, Diecke S, Schmidt-ott KM. The centrosomal protein 83 (CEP83) regulates human pluripotent stem cell differentiation towards the kidney lineage.. [DOI: 10.1101/2022.06.20.496810] [Reference Citation Analysis]
3 Sanders J, Castiglione M, Shun T, Vollmer LL, Schurdak ME, Vogt A, Schwacha A. Validation of a high throughput screening assay to identify small molecules that target the eukaryotic replicative helicase. SLAS Discovery 2022;27:229-241. [DOI: 10.1016/j.slasd.2021.12.006] [Reference Citation Analysis]
4 Mcquaid ME, Ahmed K, Tran S, Rousseau J, Shaheen R, Kernohan KD, Yuki KE, Grover P, Dreseris ES, Ahmed S, Dupuis L, Stimec J, Shago M, Al-hassnan ZN, Tremblay R, Maass PG, Wilson MD, Grunebaum E, Boycott KM, Boisvert F, Maddirevula S, Faqeih EA, Almanjomi F, Khan ZU, Alkuraya FS, Campeau PM, Kannu P, Campos EI, Wurtele H. Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome. JCI Insight 2022;7:e155648. [DOI: 10.1172/jci.insight.155648] [Reference Citation Analysis]
5 Gauss C, Rowland D, Ergun-longmire B. An Update on Genetics of Adrenal Gland and Associated Disorders. Endocrines 2022;3:187-97. [DOI: 10.3390/endocrines3020017] [Reference Citation Analysis]
6 Zammouri J, Vatier C, Capel E, Auclair M, Storey-London C, Bismuth E, Mosbah H, Donadille B, Janmaat S, Fève B, Jéru I, Vigouroux C. Molecular and Cellular Bases of Lipodystrophy Syndromes. Front Endocrinol (Lausanne) 2021;12:803189. [PMID: 35046902 DOI: 10.3389/fendo.2021.803189] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
7 Zabnenkova V, Shchagina O, Makienko O, Matyushchenko G, Ryzhkova O. Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome. Appl Clin Genet 2022;15:1-10. [PMID: 35023948 DOI: 10.2147/TACG.S342804] [Reference Citation Analysis]
8 Mei L, Cook JG. Efficiency and equity in origin licensing to ensure complete DNA replication. Biochem Soc Trans 2021;49:2133-41. [PMID: 34545932 DOI: 10.1042/BST20210161] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 McNeill A. Clinical genetics-it's polygenic. Eur J Hum Genet 2021;29:1037. [PMID: 34267340 DOI: 10.1038/s41431-021-00931-9] [Reference Citation Analysis]