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Cited by in F6Publishing
For: Pode-Shakked B, Barel O, Singer A, Regev M, Poran H, Eliyahu A, Finezilber Y, Segev M, Berkenstadt M, Yonath H, Reznik-Wolf H, Gazit Y, Chorin O, Heimer G, Gabis LV, Tzadok M, Nissenkorn A, Bar-Yosef O, Zohar-Dayan E, Ben-Zeev B, Mor N, Kol N, Nayshool O, Shimshoviz N, Bar-Joseph I, Marek-Yagel D, Javasky E, Einy R, Gal M, Grinshpun-Cohen J, Shohat M, Dominissini D, Raas-Rothschild A, Rechavi G, Pras E, Greenbaum L. A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies. Sci Rep 2021;11:19099. [PMID: 34580403 DOI: 10.1038/s41598-021-98646-w] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 O'reilly D, Dempsey S, O'grady MJ, Yousif TI. Whole exome sequencing based identification of a case of cardiofaciocutaneous syndrome type 3: the benefits of new sequencing technology in children with neurodevelopmental delay. BMJ Case Rep 2022;15:e251871. [DOI: 10.1136/bcr-2022-251871] [Reference Citation Analysis]
2 Chorin O, Hirsch Y, Rock R, Salzer Sheelo L, Goldberg Y, Mandel H, Hershkovitz T, Fleischer N, Greenbaum L, Katz U, Barel O, Hamed N, Ben-zeev B, Greenberger S, Nasser Samra N, Stern Zimmer M, Raas-rothschild A, Pode-shakked B. Vici syndrome in Israel: Clinical and molecular insights. Front Genet 2022;13:991721. [DOI: 10.3389/fgene.2022.991721] [Reference Citation Analysis]
3 Williams HJ, Odhams C, Genomics England Research Consortium. Improved diagnosis of rare disease patients through application of constrained coding region annotation and de novo status.. [DOI: 10.1101/2022.08.19.22278944] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Eliyahu A, Barel O, Greenbaum L, Zaks Hoffer G, Goldberg Y, Raas-rothschild A, Singer A, Bar-joseph I, Kunik V, Javasky E, Staretz-chacham O, Pode-shakked N, Bazak L, Ruhrman-shahar N, Pras E, Frydman M, Shohat M, Pode-shakked B. Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay. Front Pediatr 2022;10:844845. [DOI: 10.3389/fped.2022.844845] [Reference Citation Analysis]
5 Kiraz A, Tubaş F, Seber T. A truncating variant in the THOC6 gene with new findings in a patient with Beaulieu‐Boycott‐Innes syndrome. American J of Med Genetics Pt A. [DOI: 10.1002/ajmg.a.62667] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]