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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1986 1
1988 1
1990 2
1991 1
1992 1
1993 1
1994 1
1995 1
1996 1
1998 1
2001 2
2002 1
2004 1
2006 5
2007 1
2008 3
2009 3
2010 8
2011 5
2012 15
2013 11
2014 11
2015 8
2016 7
2017 7
2018 4
2019 10
2020 5
2021 5
2022 5
2023 7
2024 3

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129 results

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Page 1
Mechanisms of structural chromosomal rearrangement formation.
Burssed B, Zamariolli M, Bellucco FT, Melaragno MI. Burssed B, et al. Among authors: melaragno mi. Mol Cytogenet. 2022 Jun 14;15(1):23. doi: 10.1186/s13039-022-00600-6. Mol Cytogenet. 2022. PMID: 35701783 Free PMC article. Review.
Response to Bassett et al.
Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Among authors: melaragno mi. Am J Hum Genet. 2023 Jul 6;110(7):1219-1220. doi: 10.1016/j.ajhg.2023.05.017. Am J Hum Genet. 2023. PMID: 37419093 Free PMC article. No abstract available.
The impact of 22q11.2 copy-number variants on human traits in the general population.
Zamariolli M, Auwerx C, Sadler MC, van der Graaf A, Lepik K, Schoeler T, Moysés-Oliveira M, Dantas AG, Melaragno MI, Kutalik Z. Zamariolli M, et al. Among authors: melaragno mi. Am J Hum Genet. 2023 Feb 2;110(2):300-313. doi: 10.1016/j.ajhg.2023.01.005. Epub 2023 Jan 26. Am J Hum Genet. 2023. PMID: 36706759 Free PMC article.
Premature ovarian insufficiency is associated with global alterations in the regulatory landscape and gene expression in balanced X-autosome translocations.
Di-Battista A, Favilla BP, Zamariolli M, Nunes N, Defelicibus A, Armelin-Correa L, da Silva IT, Reymond A, Moyses-Oliveira M, Melaragno MI. Di-Battista A, et al. Among authors: melaragno mi. Epigenetics Chromatin. 2023 May 19;16(1):19. doi: 10.1186/s13072-023-00493-8. Epigenetics Chromatin. 2023. PMID: 37202802 Free PMC article.
Rare single-nucleotide variants in oculo-auriculo-vertebral spectrum (OAVS).
Zamariolli M, Colovati M, Moysés-Oliveira M, Nunes N, Caires Dos Santos L, Alvarez Perez AB, Bragagnolo S, Melaragno MI. Zamariolli M, et al. Among authors: melaragno mi. Mol Genet Genomic Med. 2019 Oct;7(10):e00959. doi: 10.1002/mgg3.959. Epub 2019 Aug 30. Mol Genet Genomic Med. 2019. PMID: 31469246 Free PMC article.
Clinical and cytogenomic findings in OAV spectrum.
Bragagnolo S, Colovati MES, Souza MZ, Dantas AG, F de Soares MF, Melaragno MI, Perez AB. Bragagnolo S, et al. Among authors: melaragno mi. Am J Med Genet A. 2018 Mar;176(3):638-648. doi: 10.1002/ajmg.a.38576. Epub 2018 Jan 25. Am J Med Genet A. 2018. PMID: 29368383
GestaltMatcher Database - A global reference for the facial phenotypic variability of rare human diseases.
Lesmann H, Hustinx A, Moosa S, Marchi E, Caro P, Abdelrazek IM, Pantel JT, Klinkhammer H, Hagen MT, Kamphans T, Meiswinkel W, Li JM, Javanmardi B, Knaus A, Uwineza A, Knopp C, Tkemaladze T, Elbracht M, Mattern L, Jamra RA, Velmans C, Strehlow V, Goel H, Nunes BC, Vilella T, Pinheiro IF, Kim CA, Melaragno MI, Barakat TS, Nabil A, Suh J, Averdunk L, Ekure E, Graziano C, Phowthongkum P, Güzel N, Haack TB, Brunet T, Rudnik-Schöneborn S, Platzer K, Borovikov A, Schnabel F, Heuft L, Herrmann V, Martinez-Monseny AF, Höller M, Alaaeldin K, Jezela-Stanek A, Mohamed A, Lasa-Aranzasti A, Sayer JA, Hu P, Ledgister Hanchard SE, Elmakkawy G, Safwat S, Ebstein F, Krüger E, Küry S, Arlt A, Marbach F, Netzer C, Kaptain S, Weiland H, Li D, Dupuis L, Mendoza-Londono R, Houge SD, Weis D, Chung BH, Mak CCY, Devriendt K, Gripp KW, Mücke M, Verloes A, Schaaf CP, Nellåker C, Solomon BD, Waikel RL, Nöthen MM, Abdalla E, Lyon GJ, Krawitz PM, Hsieh TC. Lesmann H, et al. Among authors: melaragno mi. medRxiv [Preprint]. 2024 Mar 8:2023.06.06.23290887. doi: 10.1101/2023.06.06.23290887. medRxiv. 2024. PMID: 37503210 Free PMC article. Preprint.
129 results