BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Knapp KM, Fellows B, Aggarwal S, Dalal A, Bicknell LS. A synonymous variant in a non-canonical exon of CDC45 disrupts splicing in two affected sibs with Meier-Gorlin syndrome with craniosynostosis. Eur J Med Genet 2021;64:104182. [PMID: 33639314 DOI: 10.1016/j.ejmg.2021.104182] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Putri IL, Stephanie A, Pramanasari R, Kon M, Wungu CDK. The role of genetic factors in microtia: A systematic review. F1000Res 2022;11:537. [DOI: 10.12688/f1000research.111995.2] [Reference Citation Analysis]
2 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]
3 Huang S, Wu H, Qi Y, Wei L, Lv X, He Y. Case Report: Balanced Reciprocal Translocation t (17; 22) (p11.2; q11.2) and 10q23.31 Microduplication in an Infertile Male Patient Suffering From Teratozoospermia. Front Genet 2022;13:797813. [PMID: 35719406 DOI: 10.3389/fgene.2022.797813] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [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 Nelakurti DD, Rossetti T, Husbands AY, Petreaca RC. Arginine Depletion in Human Cancers. Cancers (Basel) 2021;13:6274. [PMID: 34944895 DOI: 10.3390/cancers13246274] [Reference Citation Analysis]
6 Jin P, Yan K, Ye S, Qian Y, Wu Z, Wang M, Xu Y, Xu Y, Dong M. Case Report: A Synonymous Mutation in NF1 Located at the Non-canonical Splicing Site Leading to Exon 45 Skipping. Front Genet 2021;12:772958. [PMID: 34868260 DOI: 10.3389/fgene.2021.772958] [Cited by in F6Publishing: 1] [Reference Citation Analysis]