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Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.
Blood Cells, Molecules & Diseases|March 5, 2013
Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type IIRoberta Russo, Concetta Langella, Maria Rosaria Esposito, et al.
American Journal of Hematology|November 19, 2019
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathwayImmacolata Andolfo, Barbara Eleni Rosato, Francesco Manna, et al.
American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
Light, Science & Applications|September 1, 2018
Tomographic flow cytometry by digital holographyFrancesco Merola, Pasquale Memmolo, Lisa Miccio, et al.
Analytical Chemistry|May 25, 2018
Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited AnemiasMartina Mugnano, Pasquale Memmolo, Lisa Miccio, et al.
Frontiers in Physiology|June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Frontiers in Physiology|August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 ProteinRoberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
American Journal of Hematology|July 17, 2015
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis)Immacolata Andolfo, Roberta Russo, Francesco Manna, et al.
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