Luca Bello

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 11 papers. Top paper: “Genetic modifiers of respiratory function in Duchenne muscular dystrophy”.

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51046

N/A

0DataRank · unranked

45 citations

Maria Grazia D’Angelo, Matteo Villa, Aurora Fusto, Sara Vianello, Beatrice Merlo +36 more

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy

European Journal of Human Genetics(2020)10.1038/s41431-019-0563-6

N/A

0DataRank · unranked

41 citations

Pietro Spitali, Irina Zaharieva, Stefan Böhringer, Monika Hiller, Amina Chaouch +19 more

Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis

Neurology(2021)10.1212/wnl.0000000000011626

N/A

0DataRank · unranked

37 citations

Michael G. Hanna, Pedro Machado, Umesh A. Badrising, Hector Chinoy, Olivier Benvéniste +93 more

Longitudinal motor function in proximal versus distal DMD pathogenic variants

Muscle & Nerve(2021)10.1002/mus.27371

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0DataRank · unranked

6 citations

Luca Bello, Heather Gordish‐Dressman, CINRG‐DNHS Investigators, Mathula Thangarajh

Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy

Neuromuscular Disorders(2021)10.1016/j.nmd.2021.06.001

N/A

0DataRank · unranked

8 citations

Elaine McColl, Michael McDermott, William B. Martens, Michela Guglieri, Robert C. Griggs +42 more

Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

medRxiv(2021)10.1101/2021.04.08.21254942

N/A

0DataRank · unranked

2 citations

Payam Mohassel, Sandra Donkervoort, Lin Guo, Kevin J. O’Donovan, Maura Coughlin +53 more

Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

Nature Communications(2022)10.1038/s41467-022-30015-1

N/A

0DataRank · unranked

44 citations

Payam Mohassel, Sandra Donkervoort, Lin Guo, Kevin O’Donovan, Maura Coughlin +53 more

Genetic modifiers of upper limb function in Duchenne muscular dystrophy

Journal of Neurology(2022)10.1007/s00415-022-11133-8

N/A

0DataRank · unranked

7 citations

Aurora Fusto, Sara Vianello, Matteo Villa, J.A. Janik, Grazia D’Angelo +28 more

Influence of β2 adrenergic receptor genotype on longitudinal measures of forced vital capacity in patients with Duchenne muscular dystrophy

Neuromuscular Disorders(2022)10.1016/j.nmd.2021.12.006

N/A

0DataRank · unranked

4 citations

Troy J. Cross, Craig M. McDonald, Eric P. Hoffman, Luca Bello, Eli F. Kelley

The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy

Journal of Neuromuscular Diseases(2024)10.3233/jnd-230129

N/A

0DataRank · unranked

4 citations

Daniele Sabbatini, Aurora Fusto, Domenico Gorgoglione, Giovanni Umberto Borin, Martina Penzo +34 more

Assessing Pharmacogenomic loci Associated with the Pharmacokinetics of Vamorolone in Boys with Duchenne Muscular Dystrophy

The Journal of Clinical Pharmacology(2024)10.1002/jcph.2446

N/A

0DataRank · unranked

2 citations

Daniele Sabbatini, Elena Pegoraro, Luca Bello, Paula R. Clemens, Michela Guglieri +7 more