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Pancreas|November 13, 2008
Establishment and characterization of 4 new human pancreatic cancer cell lines: evidences of different tumor phenotypesBarbara Chifenti, Mariangela Morelli, Michele Zavaglia, et al.
International Journal of Molecular Medicine|September 8, 2016
Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathyMassimiliano Cecconi, Maria I Parodi, Francesco Formisano, et al.
Human Mutation|July 12, 2002
Identification of fifteen novel mutations in the SLC12A3 gene encoding the Na-Cl Co-transporter in Italian patients with Gitelman syndromeMarie-Louise Syrén, Silvana Tedeschi, Laila Cesareo, et al.
British Journal of Cancer|January 16, 2014
Mutation frequencies of GNAQ, GNA11, BAP1, SF3B1, EIF1AX and TERT in uveal melanoma: detection of an activating mutation in the TERT gene promoter in a single case of uveal melanomaM Dono, G Angelini, M Cecconi, et al.
European Journal of Human Genetics : EJHG|April 26, 2006
The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issuesSirpa Soini, Dolores Ibarreta, Violetta Anastasiadou, et al.
Genes, Chromosomes & Cancer|April 25, 2018
Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanomaSerena Patrone, Irena Maric, Mariangela Rutigliani, et al.
Scientific Reports|November 26, 2024
Clonal hematopoiesis impacts frailty in newly diagnosed multiple myeloma patients: a retrospective multicenter analysisElisa Gelli, Claudia Martinuzzi, Debora Soncini, et al.
Parkinsonism & Related Disorders|June 4, 2008
Parkin analysis in early onset Parkinson's diseaseFrancesca Sironi, Paola Primignani, Michela Zini, et al.
Scientific Data|May 8, 2024
Common conditions of use elements. Atomic concepts for consistent and effective information governanceMaria Del Carmen Sanchez Gonzalez, Pim Kamerling, Mariapia Iermito, et al.
European Journal of Medical Genetics|July 5, 2023
Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe - A multi-professional survey studyKati Koido, Charlotta Ingvoldstad Malmgren, Lejla Pojskic, et al.
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