Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 2 |
2022 | 4 |
2023 | 1 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Rare ATG7 genetic variants predispose patients to severe fatty liver disease.
J Hepatol. 2022 Sep;77(3):596-606. doi: 10.1016/j.jhep.2022.03.031. Epub 2022 Apr 9.
J Hepatol. 2022.
PMID: 35405176
Free article.
Extensive Placental Methylation Profiling in Normal Pregnancies.
Rondinone O, Murgia A, Costanza J, Tabano S, Camanni M, Corsaro L, Fontana L, Colapietro P, Calzari L, Motta S, Santaniello C, Radaelli T, Ferrazzi E, Bosari S, Gentilini D, Sirchia SM, Miozzo M.
Rondinone O, et al. Among authors: santaniello c.
Int J Mol Sci. 2021 Feb 21;22(4):2136. doi: 10.3390/ijms22042136.
Int J Mol Sci. 2021.
PMID: 33669975
Free PMC article.
Item in Clipboard
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Elli FM, Mattinzoli D, Lucca C, Piu M, Maffini MA, Costanza J, Fontana L, Santaniello C, Forino C, Milani D, Bonati MT, Secco A, Gastaldi R, Alfieri C, Messa P, Miozzo M, Arosio M, Mantovani G.
Elli FM, et al. Among authors: santaniello c.
J Bone Miner Res. 2022 Mar;37(3):465-474. doi: 10.1002/jbmr.4490. Epub 2022 Jan 17.
J Bone Miner Res. 2022.
PMID: 34897794
Free PMC article.
Item in Clipboard
Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology.
Moresco G, Rondinone O, Mauri A, Costanza J, Santaniello C, Colapietro P, Micaglio E, Marfia G, Pesenti C, Grilli F, Rinaldi B, Prada E, Scuvera G, Villa R, Bedeschi MF, Miozzo MR, Milani D, Fontana L.
Moresco G, et al. Among authors: santaniello c.
Genes Genomics. 2023 May;45(5):637-655. doi: 10.1007/s13258-022-01341-x. Epub 2022 Dec 1.
Genes Genomics. 2023.
PMID: 36454368
Item in Clipboard
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136.
Rondinone O, Murgia A, Costanza J, Tabano S, Camanni M, Corsaro L, Fontana L, Colapietro P, Calzari L, Motta S, Santaniello C, Radaelli T, Ferrazzi E, Bosari S, Gentilini D, Sirchia SM, Miozzo M.
Rondinone O, et al. Among authors: santaniello c.
Int J Mol Sci. 2022 May 10;23(10):5298. doi: 10.3390/ijms23105298.
Int J Mol Sci. 2022.
PMID: 35628670
Free PMC article.
Item in Clipboard
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith-Wiedemann syndrome.
Fontana L, Bedeschi MF, Cagnoli GA, Costanza J, Persico N, Gangi S, Porro M, Ajmone PF, Colapietro P, Santaniello C, Crippa M, Sirchia SM, Miozzo M, Tabano S.
Fontana L, et al. Among authors: santaniello c.
Mol Genet Genomic Med. 2020 Sep;8(9):e1386. doi: 10.1002/mgg3.1386. Epub 2020 Jul 6.
Mol Genet Genomic Med. 2020.
PMID: 32627967
Free PMC article.
Item in Clipboard
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report.
Moresco G, Costanza J, Santaniello C, Rondinone O, Grilli F, Prada E, Orcesi S, Coro I, Pichiecchio A, Marchisio P, Miozzo M, Fontana L, Milani D.
Moresco G, et al. Among authors: santaniello c.
Ital J Pediatr. 2021 Mar 31;47(1):81. doi: 10.1186/s13052-021-01033-4.
Ital J Pediatr. 2021.
PMID: 33789733
Free PMC article.
Item in Clipboard
Cite
Cite