Alessandro Bruselles

Author

Also Known As

A Bruselles, A. Bruselles, Alessandro Bruselles, Bruselles Alessandro, Bruselles, Alessandro, M. Mutarelli, Omics Sciences - Bioinformatics and Epigenetics Working Groups of the Italian Society of Human Genetics (SIGU), Trevor Pugh

123

Publications

Citations

H-Index

106

Concepts

All Affiliations

Istituto Superiore di Sanità Bambino Gesù Children's Hospital Istituti di Ricovero e Cura a Carattere Scientifico Sapienza University of Rome University of Rome Tor Vergata

About

Alessandro Bruselles is an author at Istituto Superiore di Sanità specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	20	24	1.1K
2	Natural Sciences	4	4	163
3	Social Sciences	2	2	127
4	Engineering	1	1	20
5	Health Sciences	1	1	27

Alessandro Bruselles

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population Elisa Benetti, Rossella Tita, Ottavia Spiga, European Journal of Human Genetics	2020	267
A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer Alessandra Viel, Alessandro Bruselles, Ettore Meccia, EBioMedicine	2017	223
Use of Massively Parallel Ultradeep Pyrosequencing To Characterize the Genetic Diversity of Hepatitis B Virus in Drug-Resistant and Drug-Naive Patients and To Detect Minor Variants in Reverse Transcriptase and Hepatitis B S Antigen Mariacarmela Solmone, Donatella Vincenti, Mattia Prosperi, Journal of Virology Line ProbeGeneticsGenetic EpidemiologyHepatitis BPathology	2008	160
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases Ludovica Grassi, Romina Alfonsi, Federica Francescangeli, Cell Death and Disease	2019	156
p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas Valentina Pinna, Valentina Lanari, Paola Daniele, European Journal of Human Genetics NeurogenomicsMedicineDistinctive Nf1 PhenotypeNeurochemical BiomarkersNeurology	2014	134
Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies Marcello Niceta, Emilia Stellacci, Karen W. Gripp, The American Journal of Human Genetics	2015	113
Massively parallel pyrosequencing highlights minority variants in the HIV-1 env quasispecies deriving from lymphomonocyte sub-populations Gabriella Rozera, Isabella Abbate, Alessandro Bruselles, Retrovirology	2009	107
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum Marialetizia Motta, Luca Pannone, Francesca Pantaleoni, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyGenetic DisorderEnhanced Mapk1 FunctionDegenerative Disease	2020	94
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome Christiane K. Bauer, Paolo Calligari, Francesca Clementina Radio, The American Journal of Human Genetics	2018	91
Combinatorial analysis and algorithms for quasispecies reconstruction using next-generation sequencing Mattia Prosperi, L Prosperi, Alessandro Bruselles, BMC Bioinformatics	2011	87

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