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Institution

University of Milan

EducationMilan, Italy
About: University of Milan is a education organization based out in Milan, Italy. It is known for research contribution in the topics: Population & Transplantation. The organization has 58413 authors who have published 139784 publications receiving 4636354 citations. The organization is also known as: Università degli Studi di Milano & Statale.


Papers
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Posted ContentDOI
Arang Rhie1, Shane A. McCarthy2, Olivier Fedrigo3, Joana Damas4, Giulio Formenti3, Sergey Koren1, Marcela Uliano-Silva2, William Chow2, Arkarachai Fungtammasan, Gregory Gedman3, Lindsey J. Cantin3, Françoise Thibaud-Nissen1, Leanne Haggerty5, Chul Hee Lee6, Byung June Ko6, J. H. Kim6, Iliana Bista2, Michelle Smith2, Bettina Haase3, Jacquelyn Mountcastle3, Sylke Winkler7, Sadye Paez3, Jason T. Howard8, Sonja C. Vernes7, Tanya M. Lama9, Frank Grützner10, Wesley C. Warren11, Christopher N. Balakrishnan12, Dave W Burt13, Jimin George14, Matthew T. Biegler3, David Iorns15, Andrew Digby, Daryl Eason, Taylor Edwards16, Mark Wilkinson17, George F. Turner18, Axel Meyer19, Andreas F. Kautt19, Paolo Franchini19, H. William Detrich20, Hannes Svardal21, Maximilian Wagner22, Gavin J. P. Naylor23, Martin Pippel7, Milan Malinsky2, Mark Mooney, Maria Simbirsky, Brett T. Hannigan, Trevor Pesout24, Marlys L. Houck, Ann C Misuraca, Sarah B. Kingan25, Richard Hall25, Zev N. Kronenberg25, Jonas Korlach25, Ivan Sović25, Christopher Dunn25, Zemin Ning2, Alex Hastie, Joyce V. Lee, Siddarth Selvaraj, Richard E. Green24, Nicholas H. Putnam, Jay Ghurye26, Erik Garrison24, Ying Sims2, Joanna Collins2, Sarah Pelan2, James Torrance2, Alan Tracey2, Jonathan Wood2, Dengfeng Guan27, Sarah E. London28, David F. Clayton14, Claudio V. Mello29, Samantha R. Friedrich29, Peter V. Lovell29, Ekaterina Osipova7, Farooq O. Al-Ajli30, Simona Secomandi31, Heebal Kim6, Constantina Theofanopoulou3, Yang Zhou32, Robert S. Harris33, Kateryna D. Makova33, Paul Medvedev33, Jinna Hoffman1, Patrick Masterson1, Karen Clark1, Fergal J. Martin5, Kevin L. Howe5, Paul Flicek5, Brian P. Walenz1, Woori Kwak, Hiram Clawson24, Mark Diekhans24, Luis R Nassar24, Benedict Paten24, Robert H. S. Kraus19, Harris A. Lewin4, Andrew J. Crawford34, M. Thomas P. Gilbert32, Guojie Zhang32, Byrappa Venkatesh35, Robert W. Murphy36, Klaus-Peter Koepfli37, Beth Shapiro24, Warren E. Johnson37, Federica Di Palma38, Tomas Marques-Bonet39, Emma C. Teeling40, Tandy Warnow41, Jennifer A. Marshall Graves42, Oliver A. Ryder43, David Haussler24, Stephen J. O'Brien44, Kerstin Howe2, Eugene W. Myers45, Richard Durbin2, Adam M. Phillippy1, Erich D. Jarvis3 
23 May 2020-bioRxiv
TL;DR: The Vertebrate Genomes Project is embarked on, an effort to generate high-quality, complete reference genomes for all ~70,000 extant vertebrate species and help enable a new era of discovery across the life sciences.
Abstract: High-quality and complete reference genome assemblies are fundamental for the application of genomics to biology, disease, and biodiversity conservation. However, such assemblies are only available for a few non-microbial species. To address this issue, the international Genome 10K (G10K) consortium has worked over a five-year period to evaluate and develop cost-effective methods for assembling the most accurate and complete reference genomes to date. Here we summarize these developments, introduce a set of quality standards, and present lessons learned from sequencing and assembling 16 species representing major vertebrate lineages (mammals, birds, reptiles, amphibians, teleost fishes and cartilaginous fishes). We confirm that long-read sequencing technologies are essential for maximizing genome quality and that unresolved complex repeats and haplotype heterozygosity are major sources of error in assemblies. Our new assemblies identify and correct substantial errors in some of the best historical reference genomes. Adopting these lessons, we have embarked on the Vertebrate Genomes Project (VGP), an effort to generate high-quality, complete reference genomes for all ~70,000 extant vertebrate species and help enable a new era of discovery across the life sciences.

567 citations

Journal ArticleDOI
Sagi Abelson1, Grace Collord2, Grace Collord3, Stanley W.K. Ng4, Omer Weissbrod5, Netta Mendelson Cohen5, Elisabeth Niemeyer5, Noam Barda, Philip C. Zuzarte6, Lawrence E. Heisler6, Yogi Sundaravadanam6, Robert Luben3, Shabina Hayat3, Ting Ting Wang4, Ting Ting Wang1, Zhen Zhao1, Iulia Cirlan1, Trevor J. Pugh1, Trevor J. Pugh6, Trevor J. Pugh4, David Soave6, Karen Ng6, Calli Latimer2, Claire Hardy2, Keiran Raine2, David T. Jones2, Diana Hoult3, Abigail Britten3, John Douglas Mcpherson6, Mattias Johansson7, Faridah Mbabaali6, Jenna Eagles6, Jessica Miller6, Danielle Pasternack6, Lee Timms6, Paul M. Krzyzanowski6, Philip Awadalla6, Rui Costa8, Eran Segal5, Scott V. Bratman6, Scott V. Bratman4, Scott V. Bratman1, Philip A. Beer2, Sam Behjati3, Sam Behjati2, Inigo Martincorena2, Jean C.Y. Wang1, Jean C.Y. Wang4, Jean C.Y. Wang9, Kristian M. Bowles10, Kristian M. Bowles11, J. Ramón Quirós, Anna Karakatsani12, Carlo La Vecchia13, Antonia Trichopoulou, Elena Salamanca-Fernández14, José María Huerta, Aurelio Barricarte, Ruth C. Travis15, Rosario Tumino, Giovanna Masala16, Heiner Boeing, Salvatore Panico17, Rudolf Kaaks18, Alwin Krämer18, Sabina Sieri, Elio Riboli19, Paolo Vineis19, Matthieu Foll7, James McKay7, Silvia Polidoro, Núria Sala, Kay-Tee Khaw3, Roel Vermeulen20, Peter J. Campbell3, Peter J. Campbell2, Elli Papaemmanuil2, Elli Papaemmanuil21, Mark D. Minden, Amos Tanay5, Ran D. Balicer, Nicholas J. Wareham3, Moritz Gerstung2, Moritz Gerstung8, John E. Dick4, John E. Dick1, Paul Brennan7, George S. Vassiliou2, George S. Vassiliou3, Liran I. Shlush5, Liran I. Shlush1 
09 Jul 2018-Nature
TL;DR: Deep sequencing is used to analyse genes that are recurrently mutated in AML to distinguish between individuals who have a high risk of developing AML and those with benign ARCH, providing proof-of-concept that it is possible to discriminate ARCH from pre-AML many years before malignant transformation.
Abstract: The incidence of acute myeloid leukaemia (AML) increases with age and mortality exceeds 90% when diagnosed after age 65. Most cases arise without any detectable early symptoms and patients usually present with the acute complications of bone marrow failure1. The onset of such de novo AML cases is typically preceded by the accumulation of somatic mutations in preleukaemic haematopoietic stem and progenitor cells (HSPCs) that undergo clonal expansion2,3. However, recurrent AML mutations also accumulate in HSPCs during ageing of healthy individuals who do not develop AML, a phenomenon referred to as age-related clonal haematopoiesis (ARCH)4–8. Here we use deep sequencing to analyse genes that are recurrently mutated in AML to distinguish between individuals who have a high risk of developing AML and those with benign ARCH. We analysed peripheral blood cells from 95 individuals that were obtained on average 6.3 years before AML diagnosis (pre-AML group), together with 414 unselected age- and gender-matched individuals (control group). Pre-AML cases were distinct from controls and had more mutations per sample, higher variant allele frequencies, indicating greater clonal expansion, and showed enrichment of mutations in specific genes. Genetic parameters were used to derive a model that accurately predicted AML-free survival; this model was validated in an independent cohort of 29 pre-AML cases and 262 controls. Because AML is rare, we also developed an AML predictive model using a large electronic health record database that identified individuals at greater risk. Collectively our findings provide proof-of-concept that it is possible to discriminate ARCH from pre-AML many years before malignant transformation. This could in future enable earlier detection and monitoring, and may help to inform intervention.

567 citations

Journal ArticleDOI
TL;DR: Prophylactic treatment with levofloxacin is an effective and well-tolerated way of preventing febrile episodes and other relevant infection-related outcomes in patients with cancer and profound and protracted neutropenia.
Abstract: Background The prophylactic use of fluoroquinolones in patients with cancer and neutropenia is controversial and is not a recommended intervention. Methods We randomly assigned 760 consecutive adult patients with cancer in whom chemotherapy-induced neutropenia (<1000 neutrophils per cubic millimeter) was expected to occur for more than seven days to receive either oral levofloxacin (500 mg daily) or placebo from the start of chemotherapy until the resolution of neutropenia. Patients were stratified according to their underlying disease (acute leukemia vs. solid tumor or lymphoma). Results An intention-to-treat analysis showed that fever was present for the duration of neutropenia in 65 percent of patients who received levofloxacin prophylaxis, as compared with 85 percent of those receiving placebo (243 of 375 vs. 308 of 363; relative risk, 0.76; absolute difference in risk, –20 percent; 95 percent confidence interval, –26 to –14 percent; P=0.001). The levofloxacin group had a lower rate of microbiological...

566 citations

Journal ArticleDOI
TL;DR: Cardiovascular variability is altered in patients with OSA, evident even in the absence of hypertension, heart failure, or other disease states and may be linked to the severity of OSA.
Abstract: Background—Altered cardiovascular variability is a prognostic indicator for cardiovascular events. Patients with obstructive sleep apnea (OSA) are at an increased risk for cardiovascular disease. We tested the hypothesis that OSA is accompanied by alterations in cardiovascular variability, even in the absence of overt cardiovascular disease. Methods and Results—Spectral analysis of variability of muscle sympathetic nerve activity, RR interval, and blood pressure were obtained during undisturbed supine rest in 15 patients with moderate-to-severe OSA, 18 patients with mild OSA, and 16 healthy control subjects in whom sleep disordered breathing was excluded by complete overnight polysomnography. Patients with OSA were newly diagnosed, never treated for OSA, and free of any other known diseases. Patients with moderate-to-severe OSA had shorter RR intervals (793±27 ms) and increased sympathetic burst frequency (49±4 bursts/min) compared with control subjects (947±42 ms; 24±3 bursts/min; P=0.008 and P<0.001, re...

563 citations

Journal ArticleDOI
TL;DR: It is suggested that a significant proportion of patients with angiographically documented coronary artery disease have erectile dysfunction and that this latter condition may become evident prior to angina symptoms in almost 70% of cases.

562 citations


Authors

Showing all 58902 results

NameH-indexPapersCitations
Yi Cui2201015199725
Peter J. Barnes1941530166618
Thomas C. Südhof191653118007
Charles A. Dinarello1901058139668
Alberto Mantovani1831397163826
John J.V. McMurray1781389184502
Giuseppe Remuzzi1721226160440
Russel J. Reiter1691646121010
Jean Louis Vincent1611667163721
Tobin J. Marks1591621111604
Tomas Hökfelt158103395979
José Baselga156707122498
Naveed Sattar1551326116368
Silvia Franceschi1551340112504
Frederik Barkhof1541449104982
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023240
2022777
20219,390
20209,000
20197,475
20186,804