Table 1.

Top 10 most cited publications on PFBC-related researches

SCR	Title	FA	Year	Journal	TC	LC	TCY	NTC	NLC
1	Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis	Wang C.	2012	Nat Genet	323	148	26.92	2.26	2.98
2	Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice	Keller A.	2013	Nat Genet	256	127	23.27	2.64	2.43
3	Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export	Legati A.	2015	Nat Genet	231	111	25.67	3.69	3.81
4	Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification	Nicolas G.	2013	Neurology	226	124	20.55	2.33	2.37
5	Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification	Nicolas G.	2013	Brain	173	95	15.73	1.79	1.82
6	Biallelic mutations in MYORG cause autosomal recessive primary familial brain calcification	Yao X.P.	2018	Neuron	122	75	20.33	3.73	5.93
7	Role of phosphate sensing in bone and mineral metabolism	Chande S.	2018	Nat Rev Endocrinol	122	5	20.33	3.73	0.40
8	Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification	Hsu S.C.	2013	Neurogenetics	117	74	10.64	1.21	1.42
9	Novel overgrowth syndrome phenotype due to recurrent de novo PDGFRB mutation	Takenouchi T.	2015	J Pediatr	85	12	9.44	1.36	0.41
10	Loss of function of SLC20A2 associated with familial idiopathic Basal Ganglia calcification in humans causes brain calcifications in mice	Jensen N.	2013	J Mol Neurosci	83	48	7.55	0.86	0.92

SCR, standard competition ranking; FA, first author; LC, local citation; TC, total citation; TCY, total citation per year; NLC, normalized local citations; NTC, normalized total citation.