statistiche ricercatore

Nome	#
Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer	179
A de novo PUF60 mutation in a child with a syndromic form of coloboma and persistent fetal vasculature	151
Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy	151
Genomic profiles of primary and metastatic esophageal adenocarcinoma identified via digital sorting of pure cell populations: Results from a case report	142
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder.	126
HDAC8 Loss of Function and SHOX Haploinsufficiency: Two Independent Genetic Defects Responsible for a Complex Phenotype	116
Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role	115
Rasal1 and ros1 gene variants in hereditary breast cancer	101
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction	76
Targeted Sequencing of Sorted Esophageal Adenocarcinoma Cells Unveils Known and Novel Mutations in the Separated Subpopulations	74
Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma	51
miRNA–221 and miRNA–483–3p Dysregulation in Esophageal Adenocarcinoma	39
Glutamine Supplementation as a Novel Metabolic Therapeutic Strategy for LIG3-Dependent Chronic Intestinal Pseudo-obstruction	33
Totale	1.354

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	111	0	0	0	0	0	0	24	24	22	26	11	4
2020/2021	174	20	4	9	35	31	6	5	11	16	15	6	16
2021/2022	227	9	12	5	11	19	8	5	26	7	18	74	33
2022/2023	275	23	37	22	28	13	21	6	23	46	18	23	15
2023/2024	154	16	17	9	11	10	36	3	9	6	10	15	12
2024/2025	299	33	42	91	52	51	24	6	0	0	0	0	0
Totale													1.354

CRIS Current Research Information System