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Rossella Gulli · SciRah

Researcher profile · Semantic Scholar

Rossella Gulli

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Rossella Gulli — researcher profile on SciRah

h-index: 17
Works: 38
Citations: 1,059

Most-cited papers

Endothelial dysfunction in rheumatic autoimmune diseases.
G. Murdaca, B. Colombo, P. Cagnati, Rossella Gulli +2 more
2012Atherosclerosis196 citations
Semantic Scholar
Current views on diagnostic approach and treatment of lymphedema.
G. Murdaca, P. Cagnati, Rossella Gulli, Francesca Spanò +3 more
2012American Journal of Medicine112 citations
Semantic Scholar
TNF-α gene polymorphisms: association with disease susceptibility and response to anti-TNF-α treatment in psoriatic arthritis.
G. Murdaca, Rossella Gulli, Francesca Spanò, F. Lantieri +4 more
2014Journal of Investigative Dermatology111 citations Open access
Semantic Scholar
HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients
Simona Capponi, Alessandro Geroldi, P. Fossa, M. Grandis +5 more
2011Journal of the peripheral nervous system66 citations
Semantic Scholar
Update upon efficacy and safety of TNF-α inhibitors
G. Murdaca, B. Colombo, P. Cagnati, Rossella Gulli +2 more
2012Expert Opinion on Drug Safety64 citations Open access
Semantic Scholar
Therapeutic Effects of Alendronate on Bone Erosion and Atrophy in a Patient with Rheumatoid Arthritis and Hepatitis C Virus Infection
G. Murdaca, P. Cagnati, Rossella Gulli, Matteo Caiti +3 more
2008Journal of Rheumatology58 citations Open access
Semantic Scholar
Genetic factors and systemic sclerosis.
G. Murdaca, M. Contatore, Rossella Gulli, P. Mandich +1 more
2016Autoimmunity Reviews57 citations
Semantic Scholar
Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia: A case‐control study
E. Di Maria, Rossella Gulli, S. Begni, A. De Luca +9 more
2004American Journal of Medical Genetics Part B: Neuropsychiatric Genetics39 citations
Semantic Scholar
Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies
P. Mandich, P. Fossa, Simona Capponi, Alessandro Geroldi +6 more
2009European Journal of Human Genetics38 citations Open access
Semantic Scholar
Update upon efficacy and safety of etanercept for the treatment of spondyloarthritis and juvenile idiopathic arthritis
G. Murdaca, S. Negrini, Ottavia Magnani, Elena Penza +4 more
2018Modern Rheumatology35 citations
Semantic Scholar
Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene
P. Mandich, M. Grandis, A. Varese, Alessandro Geroldi +9 more
2010Journal of Child Neurology34 citations
Semantic Scholar
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
E. Di Maria, Rossella Gulli, P. Balestra, D. Cassandrini +7 more
2004Journal of Neurology Neurosurgery & Psychiatry29 citations Open access
Semantic Scholar
DRD3 Ser9Gly variant is not associated with essential tremor in a series of Italian patients
C. Vitale, Rossella Gulli, P. Ciotti, C. Scaglione +7 more
2008European Journal of Neurology28 citations
Semantic Scholar
GDAP1 mutations in Italian axonal Charcot-Marie-Tooth patients: Phenotypic features and clinical course.
I. Pezzini, Alessandro Geroldi, Simona Capponi, Rossella Gulli +11 more
2016Neuromuscular Disorders21 citations
Semantic Scholar
The spectrum of GNE mutations: allelic heterogeneity for a common phenotype
M. Grandis, Rossella Gulli, D. Cassandrini, E. Gazzerro +10 more
2010Neurological Sciences21 citations
Semantic Scholar
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease.
P. Ciotti, M. Luigetti, Alessandro Geroldi, Simona Capponi +7 more
2014Journal of Neurological Sciences19 citations
Semantic Scholar
Essential tremor is not associated with α‐synuclein gene haplotypes
S. Pigullo, E. Di Maria, R. Marchese, E. Bellone +8 more
200317 citations
Semantic Scholar
Enlarging the clinical spectrum associated with C9orf 72 repeat expansions: Findings in an Italian cohort of patients with Parkinsonian syndromes and relevance for genetic counselling
P. Origone, S. Verdiani, P. Ciotti, Rossella Gulli +4 more
2013Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration16 citations
Semantic Scholar
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease
P. Mandich, M. Grandis, Alessandro Geroldi, M. Acquaviva +4 more
2008Journal of Human Genetics16 citations
Semantic Scholar
Pharmacogenetics and Future Therapeutic Scenarios: What Affects the Prediction of Response to Treatment with Etanercept?
G. Murdaca, Rossella Gulli, Francesca Spanò, P. Mandich +1 more
2014Drug development research (Print)15 citations
Semantic Scholar
Essential tremor is not associated with alpha-synuclein gene haplotypes.
S. Pigullo, E. Di Maria, R. Marchese, E. Bellone +8 more
2003Movement Disorders13 citations
Semantic Scholar
1993–2014: two decades of predictive testing for Huntington's disease at the Medical Genetics Unit of the University of Genoa
P. Mandich, Merit Lamp, Fabio Gotta, Rossella Gulli +5 more
2017Molecular Genetics & Genomic Medicine12 citations Open access
Semantic Scholar
Germline mutations in the von Hippel-Lindau gene in Italian patients.
P. Ciotti, A. Garuti, Rossella Gulli, A. Ballestrero +2 more
2009European Journal of Medical Genetics11 citations
Semantic Scholar
Common mutations in the LRRK2 exon 41 are not responsible for essential tremor in Italian patients.
C. Vitale, P. Ciotti, Rossella Gulli, E. Bellone +5 more
2009Parkinsonism & Related Disorders9 citations
Semantic Scholar
Linkage exclusion in Italian families with hereditary essential tremor
Andrea Novelletto, Rossella Gulli, P. Ciotti, C. Vitale +11 more
2011European Journal of Neurology7 citations
Semantic Scholar
A putative regulatory subunit (NR3A) of the NMDA receptor complex as candidate gene for susceptibility to schizophrenia: a case-control study.
Rossella Gulli, Bianca Masnata, C. Bonvicini, G. B. Tura +7 more
2007Psychiatric Genetics7 citations
Semantic Scholar
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy “in disguise”
M. Grandis, Alessandro Geroldi, Rossella Gulli, F. Manganelli +11 more
2018Orphanet Journal of Rare Diseases4 citations Open access
Semantic Scholar
Contribution of copy number variations in CMT1X: a retrospective study
Simona Capponi, Alessandro Geroldi, I. Pezzini, Rossella Gulli +8 more
2015European Journal of Neurology3 citations
Semantic Scholar
Gene symbol: GNE. Disease: Inclusion body myopathy.
C. Bruno, M. Grandis, D. Cassandrini, E. Bellone +2 more
2008Human Genetics2 citations
Semantic Scholar
Two novel cases of compound heterozygous mutations in mitofusin2: Finding out the inheritance.
Alessandro Geroldi, P. Lastella, M. Patruno, Fabio Gotta +8 more
2017Neuromuscular Disorders1 citations
Semantic Scholar
Nocturia: an uncommon presentation of lower-limb lymphedema.
P. Cagnati, B. Colombo, Rossella Gulli, R. Russo +4 more
2010American Journal of Medicine1 citations Open access
Semantic Scholar
K08 1993–2013: Two Decades of Predictive HD Testing at the Medical Genetics Service of the University Of Genoa
P. Mandich, Merit Lamp, Rossella Gulli, A. Iacometti +4 more
2014Journal of Neurology Neurosurgery & Psychiatry0 citations
Semantic Scholar
LITAF/SIMPLE MUTATION ANALYSIS IN DOMINANT DEMYELINATING CHARCOT- MARIE-TOOTH DISEASE: A NOVEL MUTATION
P. Ciotti, Alessandro Geroldi, Simona Capponi, R. Massa +5 more
20120 citations
Semantic Scholar
Differential diagnosis in recurrent intestinal perforation: Chronic inflammatory disease with intestinal lymphedema or antiphospholipid syndrome?
F. Boccardo, G. Murdaca, P. Cagnati, Rossella Gulli +4 more
20120 citations
Semantic Scholar
Cava: Uncommon Presentation of Antiphospholipid Syndrome Recurrent Intestinal Perforation Associated with Thrombosis of Inferior Vena
Rossella Gulli, Matteo Caiti, F. Boccardo, F. Puppo
20080 citations
Semantic Scholar
Abstracts of the 8th Meeting of the Italian Peripheral Nerve Study Group: 65: Absract
E. Bellone, E. Di Maria, Rossella Gulli, P. Balestra +6 more
20030 citations
Semantic Scholar
Glutamate hypothesis of schizophrenia: No evidence that the N-Methyl-D-Aspartate receptor 2B gene (GRIN2B) is associated with susceptibility to schizophrenia
E. Di Maria, Rossella Gulli, R. Pioli, A. De Luca +3 more
20010 citations
Semantic Scholar
On the role for glutamate in the pathogenesis of schizophrenia; association study with the N-methyl-D-aspartate receptor 2B
E. Ria, Rossella Gulli, S. Begni, R. Pioli +4 more
20010 citations
Semantic Scholar

Frequent co-authors

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P. Mandich×28
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P. Mandich — researcher profile on SciRah
E. Bellone×25
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E. Bellone — researcher profile on SciRah
P. Ciotti×12
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P. Ciotti — researcher profile on SciRah
F. Puppo×11
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×10

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G. Murdaca — researcher profile on SciRah

Alessandro Geroldi×10

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Alessandro Geroldi — researcher profile on SciRah

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M. Grandis — researcher profile on SciRah

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E. Di Maria — researcher profile on SciRah

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P. Cagnati — researcher profile on SciRah

Simona Capponi×6

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Simona Capponi — researcher profile on SciRah

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Francesca Spanò×5

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Francesca Spanò — researcher profile on SciRah