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Year Number of Results
2001 1
2002 1
2005 1
2007 1
2010 1
2013 3
2014 1
2015 2
2017 5
2018 2
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2022 5
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Page 1
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Wilcox N, Dumont M, González-Neira A, Carvalho S, Joly Beauparlant C, Crotti M, Luccarini C, Soucy P, Dubois S, Nuñez-Torres R, Pita G, Gardner EJ, Dennis J, Alonso MR, Álvarez N, Baynes C, Collin-Deschesnes AC, Desjardins S, Becher H, Behrens S, Bolla MK, Castelao JE, Chang-Claude J, Cornelissen S, Dörk T, Engel C, Gago-Dominguez M, Guénel P, Hadjisavvas A, Hahnen E, Hartman M, Herráez B; SGBCC Investigators; Jung A, Keeman R, Kiechle M, Li J, Loizidou MA, Lush M, Michailidou K, Panayiotidis MI, Sim X, Teo SH, Tyrer JP, van der Kolk LE, Wahlström C, Wang Q, Perry JRB, Benitez J, Schmidt MK, Schmutzler RK, Pharoah PDP, Droit A, Dunning AM, Kvist A, Devilee P, Easton DF, Simard J. Wilcox N, et al. Among authors: crotti m. Nat Genet. 2023 Sep;55(9):1435-1439. doi: 10.1038/s41588-023-01466-z. Epub 2023 Aug 17. Nat Genet. 2023. PMID: 37592023 Free PMC article.
Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk.
Wilcox N, Dumont M, González-Neira A, Carvalho S, Joly Beauparlant C, Crotti M, Luccarini C, Soucy P, Dubois S, Nuñez-Torres R, Pita G, Gardner EJ, Dennis J, Alonso MR, Álvarez N, Baynes C, Collin-Deschesnes AC, Desjardins S, Becher H, Behrens S, Bolla MK, Castelao JE, Chang-Claude J, Cornelissen S, Dörk T, Engel C, Gago-Dominguez M, Guénel P, Hadjisavvas A, Hahnen E, Hartman M, Herráez B; SGBCC Investigators; Jung A, Keeman R, Kiechle M, Li J, Loizidou MA, Lush M, Michailidou K, Panayiotidis MI, Sim X, Teo SH, Tyrer JP, van der Kolk LE, Wahlström C, Wang Q, Perry JRB, Benitez J, Schmidt MK, Schmutzler RK, Pharoah PDP, Droit A, Dunning AM, Kvist A, Devilee P, Easton DF, Simard J. Wilcox N, et al. Among authors: crotti m. Nat Genet. 2023 Nov;55(11):2009. doi: 10.1038/s41588-023-01549-x. Nat Genet. 2023. PMID: 37752376 Free PMC article. No abstract available.
The Lombardy Rare Donor Programme.
Revelli N, Villa MA, Paccapelo C, Manera MC, Rebulla P, Migliaccio AR, Marconi M; Members of the Lombardy Rare Donor Programme. Revelli N, et al. Blood Transfus. 2014 Jan;12 Suppl 1(Suppl 1):s249-55. doi: 10.2450/2013.0182-12. Epub 2013 Feb 21. Blood Transfus. 2014. PMID: 23522888 Free PMC article.
Genetic identification of medullary neurons underlying congenital hypoventilation.
Cui K, Xia Y, Patnaik A, Salivara A, Lowenstein ED, Isik EG, Knorz AL, Airaghi L, Crotti M, Garratt AN, Meng F, Schmitz D, Studer M, Rijli FM, Nothwang HG, Rost BR, Strauß U, Hernandez-Miranda LR. Cui K, et al. Among authors: crotti m. Sci Adv. 2024 Jun 21;10(25):eadj0720. doi: 10.1126/sciadv.adj0720. Epub 2024 Jun 19. Sci Adv. 2024. PMID: 38896627 Free PMC article.
[Evaluation and treatment of hyperemesis gravidarum].
Crotti M, Aguzzoli L, Carossino E, Accorsi P, Gargano G, Masellis G. Crotti M, et al. Minerva Ginecol. 2001 Dec;53(6):413-9. Minerva Ginecol. 2001. PMID: 11723426 Review. Italian.
50 results