BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Carraro M, Monzon AM, Chiricosta L, Reggiani F, Aspromonte MC, Bellini M, Pagel K, Jiang Y, Radivojac P, Kundu K, Pal LR, Yin Y, Limongelli I, Andreoletti G, Moult J, Wilson SJ, Katsonis P, Lichtarge O, Chen J, Wang Y, Hu Z, Brenner SE, Ferrari C, Murgia A, Tosatto SCE, Leonardi E. Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI-5 intellectual disability challenge. Hum Mutat 2019;40:1330-45. [PMID: 31144778 DOI: 10.1002/humu.23823] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Katsonis P, Wilhelm K, Williams A, Lichtarge O. Genome interpretation using in silico predictors of variant impact. Hum Genet 2022. [PMID: 35488922 DOI: 10.1007/s00439-022-02457-6] [Reference Citation Analysis]
2 Martinez-esteve Melnikova A, Pijuan J, Aparicio J, Ramírez A, Altisent-huguet A, Vilanova-adell A, Arzimanoglou A, Armstrong J, Palau F, Hoenicka J, San Antonio-arce V. The p.Glu787Lys variant in the GRIA3 gene causes developmental and epileptic encephalopathy mimicking structural epilepsy in a female patient. European Journal of Medical Genetics 2022. [DOI: 10.1016/j.ejmg.2022.104442] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Liu H, Liu DT, Lan S, Yang Y, Huang J, Huang J, Fang L. ASH1L mutation caused seizures and intellectual disability in twin sisters. J Clin Neurosci 2021;91:69-74. [PMID: 34373061 DOI: 10.1016/j.jocn.2021.06.038] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Schultz-Rogers L, Muthusamy K, Pinto E Vairo F, Klee EW, Lanpher B. Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report. BMC Med Genet 2020;21:219. [PMID: 33167890 DOI: 10.1186/s12881-020-01159-y] [Reference Citation Analysis]
5 Andreoletti G, Pal LR, Moult J, Brenner SE. Reports from the fifth edition of CAGI: The Critical Assessment of Genome Interpretation. Hum Mutat 2019;40:1197-201. [PMID: 31334884 DOI: 10.1002/humu.23876] [Cited by in Crossref: 24] [Cited by in F6Publishing: 18] [Article Influence: 8.0] [Reference Citation Analysis]