Rosanna Asselta (R Asselta)

Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 43

Top Venues

Nature genetics

Genes

International journal of molecular sciences

Blood advances

Humanitas University

University of Milan (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Humanitas University Oct 13 2014

Italy

Associate Professor in Medical Genetics :: Department of Biomedical Sciences

University of Milan Jan 02 2005 - Oct 12 2014

Italy

Assistant Professor in Molecular Biology :: Deprtment of Medical Biotechnology and Translational Medicine

Education History

University of Milan

Italy

PHD

University of Milan

Italy

MSC

Publications

Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Valentina Granata, Dario Strina, Valentina Possetti, Roberto Leone, Sonia Valentino, Katia Chiappetta, Mattia Loppini, Alberto Mantovani, Barbara Bottazzi, Rosanna Asselta, Cristina Sobacchi, Antonio Inforzato
Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty. Genes 15 (5) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Valentina Granata, Dario Strina, Valentina Possetti, Roberto Leone, Sonia Valentino, Katia Chiappetta, Mattia Loppini, Alberto Mantovani, Barbara Bottazzi, Rosanna Asselta, Cristina Sobacchi, Antonio Inforzato
Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty. Genes 15 (5) (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances 8 (6) (2024)
Francesca Cogliati, Letizia Straniero, Valeria Rimoldi, Maura Masciadri, Sara Perego, Berardo Rinaldi, Donatella Milani, Davide Gentilini, Lidia Larizza, Rosanna Asselta, Silvia Russo, Maria Francesca Bedeschi
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2024)
Valentina Granata, Dario Strina, Valentina Possetti, Roberto Leone, Sonia Valentino, Katia Chiappetta, Mattia Loppini, Alberto Mantovani, Barbara Bottazzi, Rosanna Asselta, Cristina Sobacchi, Antonio Inforzato
Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty. Genes 15 (5) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Francesca Cogliati, Letizia Straniero, Valeria Rimoldi, Maura Masciadri, Sara Perego, Berardo Rinaldi, Donatella Milani, Davide Gentilini, Lidia Larizza, Rosanna Asselta, Silvia Russo, Maria Francesca Bedeschi
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 195 (6) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Samanta Mazzetti, Elena Contaldi, Milo Jarno Basellini, Claudia Novello, Alessandra Maria Calogero, Letizia Straniero, Federica Garrì, Valentina Ferri, Daniela Calandrella, Francesca Del Sorbo, Rosanna Asselta, Emanuele Cereda, Graziella Cappelletti, Ioannis Ugo Isaias, Gianni Pezzoli
Comparing GBA1-Parkinson's disease and idiopathic Parkinson's disease: α-Synuclein oligomers and synaptic density as biomarkers in the skin biopsy. Brain pathology (Zurich, Switzerland) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Siboni Simona Maria, Jan Blatný, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E G Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta A P Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael P Makris, Caryl Lockley, Andrew D Mumford, Andrew Harvey, Steven Kenneth Austin, Amy D Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database. Blood advances (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Valentina Granata, Dario Strina, Valentina Possetti, Roberto Leone, Sonia Valentino, Katia Chiappetta, Mattia Loppini, Alberto Mantovani, Barbara Bottazzi, Rosanna Asselta, Cristina Sobacchi, Antonio Inforzato
Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty. Genes 15 (5) (2024)
Shiqi Lin, Xingjian Gao, Frauke Degenhardt, Yu Qian, Tianzi Liu, Xavier Farre Ramon, Syed Sibte Hadi, Manuel Romero, Javier Fernández, Agustín Albillos Martínez, Maria Buti Ferret, Luis Bujanda, Antonio Julià, Rafael de Cid, Rosanna Asselta, Andre Franke, Fan Liu
Genome-wide epistasis study highlights genetic interactions influencing severity of COVID-19. European journal of epidemiology (2023)
Philip R Tedbury, Candela Manfredi, Frauke Degenhardt, Joseph Conway, Michael C Horwath, Courtney E McCracken, Adam J Sorscher, Sandy Moreau, Christine Wright, Carolina Edwards, Jo Brewer, Jeannette Guarner, Emmie de Wit, Brandi N Williamson, Mehul S Suthar, Yee T Ong, John D Roback, David N Alter, Jan Cato Holter, Tom H Karlsen, Nicoletta Sacchi, Manuel Romero, Invernizzi Pietro, Javier Fernández, Maria Buti Ferret, Agustín Albillos Martínez, Antonio Julià, Luca Vittorio Valenti, Rosanna Asselta, Jesus Maria Banales, Luis Bujanda, Rafael de Cid, Andre Franke, null null, Stefan G Sarafianos, Jeong S Hong, Eric J Sorscher, Annette Ehrhardt
Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection and COVID-19 disease severity. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 37 (11) (2023)
Cesare Saitta, Ilaria De Simone, Vittorio Fasulo, Marinella Corbetta, Stefano Duga, Chiara Chiereghin, Federico Simone Colombo, Alessio Benetti, Roberto Contieri, Pier Paolo Avolio, Alessandro Uleri, Alberto Saita, Giorgio Ferruccio Guazzoni, Rodolfo Hurle, Piergiuseppe Colombo, Nicolò Maria Buffi, Paolo Casale, Giovanni Lughezzani, Rosanna Asselta, Giulia Soldà, Massimo Lazzeri
Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer. Cancers 15 (10) (2023)
Letizia Straniero, Valeria Rimoldi, Edoardo Monfrini, Salvatore Bonvegna, Giada Melistaccio, Julie Lake, Giulia Soldà, Massimo Aureli, null Shankaracharya, Pamela Keagle, Tatiana Foroud, John E Landers, Cornelis Blauwendraat, Anna Zecchinelli, Roberto Cilia, Alessio Di Fonzo, Gianni Pezzoli, Stefano Duga, Rosanna Asselta
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk. Movement disorders : official journal of the Movement Disorder Society 37 (6) (2022)
Giulia Lunghi, Emma Veronica Carsana, Nicoletta Loberto, Laura Cioccarelli, Simona Prioni, Laura Mauri, Rosaria Bassi, Stefano Duga, Letizia Straniero, Rosanna Asselta, Giulia Soldà, Alessio di Fonzo, Emanuele Frattini, Manuela Magni, Nara Liessi, Andrea Armirotti, Elena Ferrari, Maura Samarani, Massimo Aureli
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration. Cells 11 (15) (2022)
Chiara Chiereghin, Michela Robusto, Valentina Massa, Pierangela Castorina, Umberto Ambrosetti, Rosanna Asselta, Giulia Soldà
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss. Cells 11 (11) (2022)
Alessio Gerussi, Chiara Caime, Eleonora Binatti, Claudio Cappadona, Laura Cristoferi, Rosanna Asselta, M Eric Gershwin, Invernizzi Pietro
X marks the spot in autoimmunity. Expert review of clinical immunology 18 (5) (2022)
Alessio Gerussi, Elvezia Maria Paraboschi, Claudio Cappadona, Chiara Caime, Eleonora Binatti, Laura Cristoferi, Rosanna Asselta, Invernizzi Pietro
The Role of Epigenetics in Primary Biliary Cholangitis. International journal of molecular sciences 23 (9) (2022)
Rosanna Asselta, Elvezia Maria Paraboschi, Matteo Stravalaci, Invernizzi Pietro, Paolo Bonfanti, Andrea Biondi, Isabel Pagani, Mattia Pedotti, Andrea Doni, Francesco Scavello, Sarah N Mapelli, Marina Sironi, Chiara Perucchini, Luca Varani, Milos Matkovic, Andrea Cavalli, Daniela Cesana, Pierangela Gallina, Nicoletta Pedemonte, Valeria Capurro, Nicola Clementi, Nicasio Mancini, Rafael Bayarri-Olmos, Peter Garred, Rino Rappuoli, Stefano Duga, Barbara Bottazzi, Mariagrazia Uguccioni, Elisa Vicenzi, Alberto Mantovani, Garlanda Cecilia
Reply to: Hultström et al., Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19. Mannose-binding lectin genetics in COVID-19. Nature immunology 23 (6) (2022)
Alessio Gerussi, Damiano Verda, Claudio Cappadona, Laura Cristoferi, Davide Paolo Bernasconi, Sandro Bottaro, Marco Carbone, Marco Muselli, Invernizzi Pietro, Rosanna Asselta, null On Behalf Of The Italian Pbc Genetics Study Group
LLM-PBC: Logic Learning Machine-Based Explainable Rules Accurately Stratify the Genetic Risk of Primary Biliary Cholangitis. Journal of personalized medicine 12 (10) (2022)
Matteo Stravalaci, Isabel Pagani, Elvezia Maria Paraboschi, Mattia Pedotti, Andrea Doni, Francesco Scavello, Sarah N Mapelli, Marina Sironi, Chiara Perucchini, Luca Varani, Milos Matkovic, Andrea Cavalli, Daniela Cesana, Pierangela Gallina, Nicoletta Pedemonte, Valeria Capurro, Nicola Clementi, Nicasio Mancini, Invernizzi Pietro, Rafael Bayarri-Olmos, Peter Garred, Rino Rappuoli, Stefano Duga, Barbara Bottazzi, Mariagrazia Uguccioni, Rosanna Asselta, Elisa Vicenzi, Alberto Mantovani, Garlanda Cecilia
Recognition and inhibition of SARS-CoV-2 by humoral innate immunity pattern recognition molecules. Nature immunology 23 (2) (2022)
Margarita Kirienko, Martina Sollini, Marinella Corbetta, Emanuele Voulaz, Noemi Gozzi, Matteo Interlenghi, Francesca Gallivanone, Isabella Castiglioni, Rosanna Asselta, Stefano Duga, Giulia Soldà, Arturo Chiti
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer. European journal of nuclear medicine and molecular imaging 48 (11) (2021)
Tomas Simurda, Rosanna Asselta, Jana Zolkova, Monika Brunclikova, Miroslava Dobrotova, Zuzana Kolkova, Dusan Loderer, Ingrid Skornova, Jan Hudecek, Zora Lasabova, Jan Stasko, Peter Kubisz
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management. Diagnostics (Basel, Switzerland) 11 (11) (2021)
Marianna Rossi, Manja Meggendorfer, Matteo Zampini, Mauro Tettamanti, Emma Riva, Erica Travaglino, Matteo Bersanelli, Sara Mandelli, Alessia Antonella Galbussera, Ettore Mosca, Elena Saba, Chiara Chiereghin, Nicla Manes, Chiara Milanesi, Marta Ubezio, Lucio Morabito, Clelia Peano, Giulia Soldà, Rosanna Asselta, Stefano Duga, Carlo Francesco Selmi, Maria De Santis, Karolina Malik, Giulia Maggioni, Maria Elena Bicchieri, Alessia Campagna, Cristina A Tentori, Antonio Russo, Efrem Civilini, Paola Allavena, Rocco Giovanni Piazza, Giovanni Corrao, Claudia Sala, Alberto Termanini, Laura Giordano, Paolo Detoma, Aurelio Malabaila, Luca Sala, Stefano Rosso, Roberto Zanetti, Claudia Saitta, Elena Riva, Gianluigi Condorelli, Francesco Passamonti, Armando Santoro, Francisco Solé, Uwe Platzbecker, Pierre Fenaux, Niccolò Bolli, Gastone Castellani, Wolfgang Kern, George S Vassiliou, Torsten Haferlach, Ugo Lucca, Matteo Giovanni Della Porta
Clinical relevance of clonal hematopoiesis in persons aged ≥80 years. Blood 138 (21) (2021)
Claudio Cappadona, Elvezia Maria Paraboschi, Nicole Ziliotto, Sandro Bottaro, Valeria Rimoldi, Alessio Gerussi, Andrea Azimonti, Daniele Brenna, Andrea Brunati, Charlotte Cameroni, Giovanni Campanaro, Francesca Carloni, Giacomo Cavadini, Martina Ciravegna, Antonio Composto, Giuseppe Converso, Pierluigi Corbella, Davide D'Eugenio, Giovanna Dal Rì, Sofia Maria Di Giorgio, Maria Chiara Grondelli, Lorenza Guerrera, Georges Laffoucriere, Beatrice Lando, Leandro Lopedote, Benedetta Maizza, Elettra Marconi, Carlotta Mariola, Guia Margherita Matronola, Luca Maria Menga, Giulia Montorsi, Antonio Papatolo, Riccardo Patti, Lorenzo Profeta, Vera Rebasti, Alice Smidili, Sofia Maria Tarchi, Francesco Carlo Tartaglia, Gaia Tettamanzi, Elena Tinelli, Riccardo Stuani, Cristiana Bolchini, Linda Pattini, Invernizzi Pietro, Frauke Degenhardt, Andre Franke, Stefano Duga, Rosanna Asselta
MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity. Journal of personalized medicine 11 (11) (2021)
Giovanni Birolo, Serena Aneli, Cornelia Di Gaetano, Giovanni Cugliari, Alessia Russo, Alessandra Allione, Elisabetta Casalone, Elisa Giorgio, Elvezia Maria Paraboschi, Diego Ardissino, Stefano Duga, Rosanna Asselta, Giuseppe Matullo
Functional and clinical implications of genetic structure in 1686 Italian exomes. Human mutation 42 (3) (2021)
Rosanna Asselta, Elvezia Maria Paraboschi, Stefano Duga
Hereditary Hypofibrinogenemia with Hepatic Storage. International journal of molecular sciences 21 (21) (2020)
Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Valeria Rimoldi, Giada Melistaccio, Giulia Soldà, Massimo Aureli, Matteo Giovanni Della Porta, Ugo Lucca, Alessio di Fonzo, Anna Zecchinelli, Gianni Pezzoli, Roberto Cilia, Stefano Duga
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD. Neurology. Genetics 6 (6) (2020)
Elvezia Maria Paraboschi, Marzia Menegatti, Flora Peyvandi, Stefano Duga, Rosanna Asselta
Understanding the Impact of Aberrant Splicing in Coagulation Factor V Deficiency. International journal of molecular sciences 20 (4) (2019)
Veronica Tisato, Giovanni Zuliani, Marco Vigliano, Giovanna Longo, Eugenia Franchini, Paola Secchiero, Giorgio Zauli, Elvezia Maria Paraboschi, Ajay Vikram Singh, Maria Luisa Serino, Beatrice Ortolani, Amedeo Zurlo, Cristina Bosi, Antonio Greco, Davide Seripa, Rosanna Asselta, Donato Gemmati
Gene-gene interactions among coding genes of iron-homeostasis proteins and APOE-alleles in cognitive impairment diseases. PloS one 13 (3) (2018)
Giulia Cardamone, Elvezia Maria Paraboschi, Giulia Soldà, Stefano Duga, Janna Saarela, Rosanna Asselta
Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients. Biomedicines 6 (4) (2018)
Chiara Chiereghin, Michela Robusto, Antonio Mastrangelo, Pierangela Castorina, Giovanni Montini, Marisa Giani, Stefano Duga, Rosanna Asselta, Giulia Soldà
Alport syndrome cold cases: Missing mutations identified by exome sequencing and functional analysis. PloS one 12 (6) (2017)
Rosanna Asselta, Elvezia Maria Paraboschi, Valeria Rimoldi, Marzia Menegatti, Flora Peyvandi, Ophira Salomon, Stefano Duga
Exploring the global landscape of genetic variation in coagulation factor XI deficiency. Blood 130 (4) (2017)
Letizia Straniero, Ilaria Guella, Roberto Cilia, Laura Parkkinen, Valeria Rimoldi, Alexander Young, Rosanna Asselta, Giulia Soldà, Vesna Sossi, A Jon Stoessl, Alberto Priori, Kenya Nishioka, Nobutaka Hattori, Jordan Follett, Alex Rajput, Nenad Blau, Gianni Pezzoli, Matthew J Farrer, Stefano Goldwurm, Ali H Rajput, Stefano Duga
DNAJC12 and dopa-responsive nonprogressive parkinsonism. Annals of neurology 82 (4) (2017)
Elvezia Maria Paraboschi, Stefano Duga, Rosanna Asselta
Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains. International journal of molecular sciences 18 (12) (2017)
V Rimoldi, Elvezia Maria Paraboschi, Marzia Menegatti, Flora Peyvandi, O Salomon, Stefano Duga, Rosanna Asselta
Molecular investigation of 41 patients affected by coagulation factor XI deficiency. Haemophilia : the official journal of the World Federation of Hemophilia 24 (2) (2017)

Rosanna Asselta.css-eqlu8i{font-size:small;padding-left:4px;} (R Asselta)

Publication Activity (10 Years)

Top Topics

Top Venues

Rosanna Asselta (R Asselta)