Catalogo dei prodotti della ricerca

DEVOTO, MARCELLA
 Distribuzione geografica
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Continente #
NA - Nord America 7.276
EU - Europa 1.135
AS - Asia 1.007
SA - Sud America 31
AF - Africa 10
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 9.463
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Nazione #
US - Stati Uniti d'America 7.229
CN - Cina 352
IT - Italia 330
IN - India 329
SG - Singapore 280
UA - Ucraina 235
FI - Finlandia 184
SE - Svezia 78
GB - Regno Unito 72
DE - Germania 53
RU - Federazione Russa 49
IE - Irlanda 42
CA - Canada 40
NL - Olanda 32
IL - Israele 31
BE - Belgio 29
AR - Argentina 17
BR - Brasile 14
RO - Romania 13
ID - Indonesia 9
ZA - Sudafrica 8
FR - Francia 7
MX - Messico 7
CH - Svizzera 6
PK - Pakistan 3
BG - Bulgaria 2
NZ - Nuova Zelanda 2
AU - Australia 1
EG - Egitto 1
ES - Italia 1
EU - Europa 1
HU - Ungheria 1
KR - Corea 1
PL - Polonia 1
SC - Seychelles 1
TR - Turchia 1
UZ - Uzbekistan 1
Totale 9.463
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Città #
Fairfield 1.423
Woodbridge 715
Houston 598
Ashburn 572
Seattle 571
Cambridge 450
Wilmington 429
Beijing 343
Chandler 301
Ann Arbor 300
Princeton 199
Boston 185
Plano 183
Singapore 163
Rome 151
Santa Clara 113
San Paolo di Civitate 95
Jacksonville 85
San Diego 79
Andover 68
Lawrence 61
Dublin 42
Millbury 37
Des Moines 33
Toronto 32
Norwalk 31
Falls Church 25
Boardman 23
Waanrode 20
Moscow 18
Philadelphia 18
Federal 17
Mannheim 15
Falkenstein 13
Bühl 12
New York 12
Brighton 11
Buffalo 11
Auburn Hills 10
San Mateo 10
Brussels 9
Jakarta 9
Indiana 7
Milan 7
Muizenberg 7
London 6
Ottawa 6
Phoenix 6
Laurel 5
Springfield 5
Dearborn 4
Florence 4
Jundiaí 4
Lappeenranta 4
Las Vegas 4
Loughborough 4
Lucé 4
Mexico City 4
Naples 4
Provo 4
Redmond 4
Cagliari 3
Fort Worth 3
Southend 3
Verona 3
Westminster 3
Zurich 3
Arnsberg 2
Bern 2
Chicago 2
Cincinnati 2
Dallas 2
Galatina 2
Genoa 2
Grosseto 2
Kilburn 2
Kunming 2
Lewisham 2
Napoli 2
Noida 2
Norristown 2
Nuremberg 2
Prineville 2
Riva 2
Seversk 2
Sialkot 2
Sofia 2
Suceava 2
Amsterdam 1
Auckland 1
Budapest 1
Cairo 1
Cary 1
Catania 1
Centrale 1
Chapel Hill 1
Chiswick 1
Coominya 1
Den Haag 1
Deruta 1
Totale 7.657
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Nome #
Variants of ST8SIA1 Are Associated with Risk of Developing Multiple Sclerosis 143
CARD15 genotyping in inflammatory bowel disease patients by multiplex pyrosequencing 112
Genetic loci linked to type 1 diabetes and multiple sclerosis families in Sardinia 96
Integrative genomics identifies LMO1 as a neuroblastoma oncogene 92
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma 91
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma 91
Univariate and bivariate variance component linkage analysis of a whole genome scan for loci contributing to bone mineral density 89
Phenotype-specific association of the TGFBR3 locus with nonsyndromic cryptorchidism 87
High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral density 87
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism 82
THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome 81
Incorporating prior biological information in linkage studies increases power and limits multiple testing 80
Exome sequencing reveals compound heterozygous mutations in ATP8B1 in a JAG1/NOTCH2 mutation-negative patient with clinically diagnosed Alagille syndrome 79
Linkage of ulcerative colitis to the pericentromeric region of chromosome 16 in Italian inflammatory bowel disease families is independent of the presence of common CARD15 mutations 77
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2. 77
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome 77
Weak linkage at 4p16 to predisposition for human neuroblastoma 76
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family 75
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: Suggestive association signals in ADRA1A 75
Expanding the spectrum of genes responsible for hereditary motor neuropathies 75
Estimates of genetic and environmental contribution to 43 quantitative traits support sharing of a homogeneous environment in an isolated population from South Tyrol, Italy 73
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma 73
Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease 73
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes 73
Copy number variation at 1q21.1 associated with neuroblastoma 73
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations 73
Genetic mapping of quantitative trait loci for disease-related phenotypes. 72
A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease 72
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions 71
Statistical tools for linkage analysis and genetic association studies 70
ADHD genetics: 2007 update 70
Heterogeneity in the magnitude of the insulin gene effect on HLA risk in type 1 diabetes 70
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder 70
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients. 69
Integration of Omics Data in Genetic Epidemiology 68
A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 67
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study 66
Polygenic inheritance of cryptorchidism susceptibility in the LE/orl rat 66
Polymorphic changes in the 5' flanking region of factor VII have a combined effect on promoter strength. 66
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction 65
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene 65
Common genetic variants in NEFL influence gene expression and neuroblastoma risk 65
Phenylketonuria mutation in southern Europeans. 64
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease. 64
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum 64
A common molecular basis for three inherited kidney stone diseases. 64
A common haplotype at the 5′ end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression 64
IRAK-M is involved in the pathogenesis of early-onset persistent asthma 64
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles 63
Exploring shared susceptibility between two neural crest cells originating conditions: neuroblastoma and congenital heart disease 63
A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study 63
Association analysis of bone mineral density and single nucleotide polymorphisms in two candidate genes on chromosome 1p36 62
Genetic predisposition to familial neuroblastoma: Identification of two novel genomic regions at 2p and 12p 62
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressor 62
Comparison of sib pair-based approaches for identifying quantitative trait loci underlying asthma in the Busselton families. 62
Single nucleotide polymorphic alleles in the 5' region of the RET proto-oncogene define a risk haplotype in Hirschsprung's disease. 61
Identification of ALK as a major familial neuroblastoma predisposition gene 60
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder 60
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene 59
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. 58
Why is the cystic fibrosis gene so frequent? 58
Association of Variants of the Interleukin-23 Receptor Gene With Susceptibility to Pediatric Crohn’s Disease 58
Novel ZBTB24 Mutation Associated with Immunodeficiency, Centromere Instability, and Facial Anomalies Type-2 Syndrome Identified in a Patient with Very Early Onset Inflammatory Bowel Disease 58
Five families with arginine519-cysteine mutation in COL2A1: Evidence for three distinct founders 57
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome 57
Suggestive linkage of situs inversus and other left-right axis anomalies to chromosome 6p. 57
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations 57
Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease 56
Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12 56
Association of Crohn's disease and ulcerative colitis with haplotypes of the MLH1 gene in Italian inflammatory bowel disease patients. 55
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B 55
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. 55
A second genetic locus for autosomal dominant polycystic kidney disease. 55
Rare Variants in TP53 and Susceptibility to Neuroblastoma 55
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation. 55
Compound heterozygous mutations in NEK8 in siblings with end-stage renal disease with hepatic and cardiac anomalies 55
Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn's disease 54
Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity. 54
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. 54
A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A----G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene. 54
Linkage analysis in families with recurrent neuroblastoma 54
Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and At-Risk for psychosis 54
New locus for autosomal dominant high myopia maps to the long arm of chromosome 17 53
A linkage study of schizophrenia to markers within Xp11 near the MAOB gene. 53
Haplotypes in cystic fibrosis patients with or without pancreatic insufficiency from four European populations. 53
Gender-dependent disease severity in autosomal polycystic kidney disease of rats. 53
Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets. 53
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome. 53
A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report 53
Next-generation linkage analysis. 53
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients 53
Contribution of IBD5 locus to clinical features of IBD patients 52
Segregation analysis of migraine in 128 families. 52
Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population. 52
Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36. 52
Integration of Linkage Analysis and Next-Generation Sequencing Data 51
Novel X-linked mental retardation syndrome with short stature maps to Xq24. 51
Replication of Neuroblastoma SNP Association at the BARD1 Locus in African-Americans 51
Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy. 51
An exploratory association analysis of the insulin gene region with diabetes mellitus in two dog breeds 51
Totale 6.554
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Categoria #
all - tutte 29.566
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 29.566
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.661 0 0 0 0 0 0 341 329 306 350 255 80
2020/2021799 96 135 84 94 11 33 26 83 86 95 51 5
2021/20221.854 38 94 176 36 283 36 42 197 110 145 213 484
2022/20231.104 361 218 59 62 104 100 5 44 82 15 37 17
2023/2024515 44 95 16 39 28 20 7 10 1 75 85 95
2024/2025338 35 12 81 35 116 59 0 0 0 0 0 0
Totale 9.754