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Rosanna Asselta

Full Professor in Medical Genetics

Humanitas University

Italy

Research Interests

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Professors in Italy Professors in Biostatistics Biostatistics professors in Italy

About

Rosanna Asselta is a Full Professor in Medical Genetics at Humanitas University, Italy. Her research primarily focuses on the genetic factors associated with coagulation, neurodegenerative diseases such as Parkinson's, and the genetic influences on COVID-19 severity. She has published extensively on topics including pathogenic variants in genes related to fibrinogen and ceruloplasmin, as well as the implications of genetic variants on cancer screening and coronary artery disease.

Articles (30)

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Collaborators (78)

cristiana bolchini

Full Professor

Politecnico di Milano

ITALY

Rosanna Asselta

Research Interests

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About

Articles (30)

Integrating Host Genetics and Clinical Setting in Machine Learning Models: Predicting COVID-19 Prognosis for Healthcare Decision-Making (The FeMiNa Study)

Multi-omics identifies oxidative stress, prothrombotic pathways, and lactoperoxidase variants as key factors in COVID-19 severity

Lewy pathology formation in patient-derived GBA1 Parkinson’s disease midbrain organoids

Functional characterisation of missense ceruloplasmin variants and real-world prevalence assessment of Aceruloplasminemia using population data.

Applying artificial intelligence to uncover the genetic landscape of coagulation factors.

Impact of prostate cancer screening in European ancestry un-affected men with germline DNA repair pathogenic variants.

The RAB32 p.Ser71Arg Variant in Parkinsonisms: Insights from a Large Italian Cohort

A novel pathogenic variant in the fibrinogen gamma chain gene p.Glu275Lys causes congenital hypofibrinogenemia

Factor XI Deficiency in apoE/FXI Double-Knockout Mice Decreases Atherosclerosis by Lowering MSR1 mRNA Expression Within the Plaque

Neutrophils restricted contribution of CCRL2 genetic variants to COVID-19 severity

A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death

Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database

Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis-like syndrome

Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease

Population Heterogeneity and Selection of Coronary Artery Disease Polygenic Scores

A second update on mapping the human genetic architecture of COVID-19.

Male awareness of prostate cancer risk remains poor in relatives of women with germline variants in DNA‐repair genes

Evaluation of Semen Self-Sampling Yield Predictors and CTC Isolation by Multi-Color Flow Cytometry for Liquid Biopsy of Localized Prostate Cancer

Mechanisms by which the cystic fibrosis transmembrane conductance regulator may influence SARS-CoV-2 infection and COVID-19 disease severity.

Genome-wide epistasis study highlights genetic interactions influencing severity of COVID-19.

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

LLM-PBC: Logic Learning Machine-Based Explainable Rules Accurately Stratify the Genetic Risk of Primary Biliary Cholangitis

The Role of Epigenetics in Primary Biliary Cholangitis

β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration

Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss

X marks the spot in autoimmunity

Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer

MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity

Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management

Collaborators (78)

cristiana bolchini

Veronica Tisato

Xavier Farré Ramon

Pär Ingemar Johansson

Agustin Albillos

Jens C. Schwamborn

Andrea Ganna

Ilaria Meloni

Mario Caceres

Francesca Cogliati

Angelina Passaro

Massimo Lazzeri

Rafael Bayarri‐Olmos

Steven Jones

Mattia Loppini

Francesca Mari

Yohei Mikami

André G Uitterlinden

Emanuele Frattini

Antonio Julià Cano

Sonia Caccia

Donato Gemmati

Mattia Cordioli

Louise MacGillivray

Markus Nöthen

MITSUHIRO YAMADA

Stuart Turvey

James Furniss

David Ellinghaus

Mari Kaunisto

Vincenzo Forgetta

Anthony Rostron

Alessio Gerussi

Eamon Raith

José Manuel Soria Fernández

Philip Jansen

Yasser El-Sherbiny

Minttu Marttila

Caroline Cusick

Shea Andrews

Letizia Straniero

Paul Dark

Khoa Manh Dinh