IRIS
Straniero, Letizia
 Distribuzione geografica
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Continente #
NA - Nord America 455
EU - Europa 123
AS - Asia 75
AF - Africa 15
SA - Sud America 1
Totale 669
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Nazione #
US - Stati Uniti d'America 454
SG - Singapore 49
FI - Finlandia 30
IE - Irlanda 24
CN - Cina 21
NG - Nigeria 15
DE - Germania 14
FR - Francia 12
IT - Italia 11
NL - Olanda 8
SE - Svezia 7
BE - Belgio 3
CH - Svizzera 3
GB - Regno Unito 3
IL - Israele 3
JP - Giappone 2
RO - Romania 2
AL - Albania 1
AT - Austria 1
CA - Canada 1
CL - Cile 1
CZ - Repubblica Ceca 1
MD - Moldavia 1
NO - Norvegia 1
UA - Ucraina 1
Totale 669
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Città #
Wilmington 92
Chandler 64
San Mateo 36
Helsinki 30
Ann Arbor 29
Singapore 29
Dublin 24
New York 22
Boardman 20
Shanghai 20
Lawrence 18
Princeton 18
Leawood 17
Benin City 15
Fairfield 11
Paris 11
Woodbridge 10
Amsterdam 8
Ashburn 8
Abbiategrasso 5
Norwalk 5
Brussels 3
Milan 3
Seattle 3
Zurich 3
Anzio 2
Redmond 2
Borås 1
Boulder 1
Brno 1
Cambridge 1
Chisinau 1
Clearwater 1
Falkenstein 1
Greifswald 1
Leeds 1
London 1
Muenster 1
Mutters 1
Nuremberg 1
Phoenix 1
Redwood City 1
San Diego 1
San Nicola Manfredi 1
Tappahannock 1
Toronto 1
Zhengzhou 1
Totale 528
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Nome #
2,6-Difluorobenzamide Inhibitors of Bacterial Cell Division Protein FtsZ: Design, Synthesis, and Structure-Activity Relationships 71
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. 61
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. *Shared first authorship 57
A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest. 51
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II 50
DNAJC12 and dopa-responsive nonprogressive parkinsonism 49
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 39
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p. 38
Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders 33
Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites 33
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP plus Treatment by Altering LRRK2 Binding to DRP1 29
Saposin D variants are not a common cause of familial Parkinson's disease among Italians. 28
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations 27
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants 26
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy 24
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A 18
The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD 16
β-Glucocerebrosidase Deficiency Activates an Aberrant Lysosome-Plasma Membrane Axis Responsible for the Onset of Neurodegeneration 12
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk 11
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease 4
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis-like syndrome 4
The Interaction between HLA‐DRB and Smoking in Parkinson's Disease Revisited 3
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease 2
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers 2
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors 2
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study 2
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease 2
Capture-seq protocol and TE-reX pipeline guidelines for detection of recombination of repeat elements in short- and long-DNA reads libraries 2
A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia 2
Two novel splicing mutations in the OTUD6B gene associated with intellectual disability and seizures 2
Screening of LRP10 mutations in Parkinson's disease patients from Italy 1
Totale 701
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Categoria #
all - tutte 6.254
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 6.254
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 0 0 0 0 0 0 0 0 0 0 1
2020/2021185 4 3 8 4 0 51 22 14 36 22 1 20
2021/202292 0 0 3 18 0 5 4 13 12 13 17 7
2022/2023231 39 5 19 27 20 21 0 15 47 19 18 1
2023/2024149 12 14 30 5 2 23 12 13 1 3 12 22
2024/202543 7 11 3 22 0 0 0 0 0 0 0 0
Totale 701