statistiche ricercatore

Nome	#
The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool	69
Mitochondrial DNA haplogroup K is associated with a lower risk of parkinson's disease in Italians	55
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycosides	51
Rare primary mitochondrial DNA mutations and probable synergistic variants in leber's hereditary optic neuropathy	44
Clinical expression of leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background	43
Author Correction: Uncovering the sources of DNA found on the Turin Shroud	36
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484	33
Totale	331

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2020/2021	105	0	0	0	73	4	2	0	2	12	1	11	0
2021/2022	65	0	4	7	3	7	0	0	9	12	0	6	17
2022/2023	53	13	2	0	3	7	7	0	4	13	0	3	1
2023/2024	26	1	4	3	4	1	3	2	1	0	0	1	6
2024/2025	82	6	33	5	10	28	0	0	0	0	0	0	0
Totale													331