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2020 | 1 |
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Page 1
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
Hered Cancer Clin Pract. 2022 Oct 1;20(1):36. doi: 10.1186/s13053-022-00241-1.
Hered Cancer Clin Pract. 2022.
PMID: 36182917
Free PMC article.
Editorial: Advances in genetics and molecular diagnosis in colorectal, stomach, and pancreatic cancer.
Vaccaro CA, Soarez J, Dominguez-Valentin M, Pavicic WH.
Vaccaro CA, et al. Among authors: pavicic wh.
Front Oncol. 2022 Dec 19;12:1104671. doi: 10.3389/fonc.2022.1104671. eCollection 2022.
Front Oncol. 2022.
PMID: 36601476
Free PMC article.
No abstract available.
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Maternal ancestry and hematological cancer risk: case-control study in an Argentinean population.
Cerliani MB, Mayordomo AC, Sanchez Dova A, Soarez JN, Fuhr Etcheverry J, Piñero TA, Cajal AR, Jauk F, García-Rivello H, Vaccaro CA, Richard SM, Bravi CM, Pavicic WH.
Cerliani MB, et al. Among authors: pavicic wh.
Per Med. 2021 May;18(3):269-281. doi: 10.2217/pme-2020-0062. Epub 2021 Mar 17.
Per Med. 2021.
PMID: 33728969
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Mono- and biallelic germline variants of DNA glycosylase genes in colon adenomatous polyposis families from two continents.
Olkinuora AP, Mayordomo AC, Kauppinen AK, Cerliani MB, Coraglio M, Collia ÁK, Gutiérrez A, Alvarez K, Cassana A, Lopéz-Köstner F, Jauk F, García-Rivello H, Ristimäki A, Koskenvuo L, Lepistö A, Nieminen TT, Vaccaro CA, Pavicic WH, Peltomäki P.
Olkinuora AP, et al. Among authors: pavicic wh.
Front Oncol. 2022 Oct 28;12:870863. doi: 10.3389/fonc.2022.870863. eCollection 2022.
Front Oncol. 2022.
PMID: 36387175
Free PMC article.
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MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing.
Piñero TA, Soukarieh O, Rolain M, Alvarez K, López-Köstner F, Torrezan GT, Carraro DM, De Oliveira Nascimento IL, Bomfim TF, Machado-Lopes TMB, Freitas JC, Toralles MB, Sandes KA, Rossi BM, Junior SA, Meira J, Dominguez-Valentin M, Møller P, Vaccaro CA, Martins A, Pavicic WH.
Piñero TA, et al. Among authors: pavicic wh.
Fam Cancer. 2020 Oct;19(4):323-336. doi: 10.1007/s10689-020-00182-5.
Fam Cancer. 2020.
PMID: 32363481
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No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in MLH1 and MSH2: A Prospective Lynch Syndrome Database Study.
Dominguez-Valentin M, Plazzer JP, Sampson JR, Engel C, Aretz S, Jenkins MA, Sunde L, Bernstein I, Capella G, Balaguer F, Macrae F, Winship IM, Thomas H, Evans DG, Burn J, Greenblatt M, de Vos Tot Nederveen Cappel WH, Sijmons RH, Nielsen M, Bertario L, Bonanni B, Tibiletti MG, Cavestro GM, Lindblom A, Valle AD, Lopez-Kostner F, Alvarez K, Gluck N, Katz L, Heinimann K, Vaccaro CA, Nakken S, Hovig E, Green K, Lalloo F, Hill J, Vasen HFA, Perne C, Büttner R, Görgens H, Holinski-Feder E, Morak M, Holzapfel S, Hüneburg R, von Knebel Doeberitz M, Loeffler M, Rahner N, Weitz J, Steinke-Lange V, Schmiegel W, Vangala D, Crosbie EJ, Pineda M, Navarro M, Brunet J, Moreira L, Sánchez A, Serra-Burriel M, Mints M, Kariv R, Rosner G, Piñero TA, Pavicic WH, Kalfayan P, Broeke SWT, Mecklin JP, Pylvänäinen K, Renkonen-Sinisalo L, Lepistö A, Peltomäki P, Hopper JL, Win AK, Buchanan DD, Lindor NM, Gallinger S, Marchand LL, Newcomb PA, Figueiredo JC, Thibodeau SN, Therkildsen C, Hansen TVO, Lindberg L, Rødland EA, Neffa F, Esperon P, Tjandra D, Möslein G, Seppälä TT, Møller P.
Dominguez-Valentin M, et al. Among authors: pavicic wh.
J Clin Med. 2021 Jun 28;10(13):2856. doi: 10.3390/jcm10132856.
J Clin Med. 2021.
PMID: 34203177
Free PMC article.
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