Daniele Cusi
Università degli Studi di Milano
H-index: 75
Europe-Italy
Top articles of Daniele Cusi
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer” | EBioMedicine | Timo Hess Carlo Maj Jan Gehlen Oleg Borisov Stephan L Haas | 2023/8/1 |
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy | Nature genetics | Krzysztof Kiryluk Elena Sanchez-Rodriguez Xu-Jie Zhou Francesca Zanoni Lili Liu | 2023/7 |
Dissecting the genetic heterogeneity of gastric cancer | EBioMedicine | Timo Hess Carlo Maj Jan Gehlen Oleg Borisov Stephan L Haas | 2023/6/1 |
Genetic insights into resting heart rate and its role in cardiovascular disease | Nature communications | Yordi J van de Vegte Ruben N Eppinga M Yldau van der Ende Yanick P Hagemeijer Yuvaraj Mahendran | 2023/8/2 |
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals | Nature genetics | Aysu Okbay Yeda Wu Nancy Wang Hariharan Jayashankar Michael Bennett | 2022/4 |
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies | Kidney international | Mathias Gorski Humaira Rasheed Alexander Teumer Laurent F Thomas Sarah E Graham | 2022/9/1 |
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility | Nature genetics | Julien Barc Rafik Tadros Charlotte Glinge David Y Chiang Mariam Jouni | 2022/3 |
Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility | Journal of Neurology | Melissa Sorosina Nadia Barizzone Ferdinando Clarelli Santosh Anand Sara Lupoli | 2022/8 |
Dissecting the polygenic basis of primary hypertension: identification of key pathway-specific components | Frontiers in Cardiovascular Medicine | Carlo Maj Erika Salvi Lorena Citterio Oleg Borisov Marco Simonini | 2022/2/16 |
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility | Journal of neurology | Melissa Sorosina Nadia Barizzone Ferdinando Clarelli Santosh Anand Sara Lupoli | 2022/8 |
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals | Communications biology | Thomas W Winkler Humaira Rasheed Alexander Teumer Mathias Gorski Bryce X Rowan | 2022/6/13 |
Modulation of gut microbiota: The effects of a fruits and vegetables supplement | Frontiers in Nutrition | Arun Prasath Lakshmanan Alessandra Mingione Francesca Pivari Elena Dogliotti Caterina Brasacchio | 2022/9/23 |
Association of colorectal cancer with genetic and epigenetic variation in PEAR1—A population-based cohort study | Plos one | Wen-Yi Yang Benedetta Izzi Adam P Bress Lutgarde Thijs Lorena Citterio | 2022/4/7 |
Identification of risk loci for primary aldosteronism in genome-wide association studies | Nature Communications | Edith Le Floch Teresa Cosentino Casper K Larsen Felix Beuschlein Martin Reincke | 2022/9/3 |
Antihypertensive treatment guided by genetics: PEARL-HT, the randomized proof-of-concept trial comparing rostafuroxin with losartan | The pharmacogenomics journal | Lorena Citterio Giuseppe Bianchi Giuseppe A Scioli Nicola Glorioso Roberto Bigazzi | 2021/6 |
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture | Biorxiv | Ruth Chia Marya S Sabir Sara Bandres-Ciga Sara Saez-Atienzar Regina H Reynolds | 2020/7/6 |
GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy | medRxiv | Krzysztof Kiryluk Elena Sanchez-Rodriguez Xu-jie Zhou Francesca Zanoni Lili Liu | 2021/11/20 |
Genome-wide association study identifies new locus associated with OCD | Medrxiv | Nora I Strom Dongmei Yu Zachary F Gerring Matthew W Halvorsen Abdel Abdellaoui | 2021/10/23 |
Klotho gene in human salt-sensitive hypertension | Clinical Journal of the American Society of Nephrology | Lorena Citterio Simona Delli Carpini Sara Lupoli Elena Brioni Marco Simonini | 2020/3/1 |
Erratum: Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk (Cell (2019) 178 (1)(262),(S0092867419306798),(10.1016/j. cell. 2019.06. 016)) | Cell | M Mitrovic Nikolaos A Patsopoulos Ashley H Beecham Theresa Dankowski An Goris | 2020/1/1 |
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