MARTORANA, DAVIDE
 Distribuzione geografica
Continente #
NA - Nord America 372
EU - Europa 304
AS - Asia 119
AF - Africa 8
Continente sconosciuto - Info sul continente non disponibili 1
Totale 804
Nazione #
US - Stati Uniti d'America 371
IE - Irlanda 80
IT - Italia 80
SE - Svezia 80
CN - Cina 78
DE - Germania 22
SG - Singapore 21
TR - Turchia 18
FI - Finlandia 12
CI - Costa d'Avorio 8
BE - Belgio 7
UA - Ucraina 6
CZ - Repubblica Ceca 5
GB - Regno Unito 3
FR - Francia 2
NL - Olanda 2
PL - Polonia 2
BG - Bulgaria 1
CA - Canada 1
EU - Europa 1
JP - Giappone 1
PK - Pakistan 1
RO - Romania 1
RS - Serbia 1
Totale 804
Città #
Chandler 103
Dublin 80
Ann Arbor 55
Parma 25
Boardman 24
Ashburn 22
Shanghai 21
Dearborn 19
Izmir 18
Nanjing 18
Bremen 13
Princeton 12
Singapore 11
New York 10
Abidjan 8
Wilmington 8
Brussels 7
Ravenna 7
Beijing 6
Helsinki 5
Verona 5
Cascina 4
Jacksonville 4
Los Angeles 4
Zhengzhou 4
Cornaredo 3
Dallas 3
Des Moines 3
Fremont 3
Hefei 3
Jiaxing 3
Kunming 3
Modena 3
Rio Saliceto 3
Seattle 3
Bologna 2
Chicago 2
Guangzhou 2
Hebei 2
Jinan 2
Latina 2
Quattro Castella 2
Redwood City 2
Romainville 2
Terracina 2
Woodbridge 2
Amsterdam 1
Belgrade 1
Brno 1
Changsha 1
Clifton 1
Dortmund 1
Fairfield 1
Falls Church 1
Focsani 1
Genoa 1
Houston 1
Huizen 1
Manchester 1
Milan 1
Nanchang 1
Olomouc 1
Prague 1
Quzhou 1
Rho 1
San Mateo 1
Shenyang 1
Sofia 1
Somma Vesuviana 1
Tianjin 1
Toronto 1
Warsaw 1
Washington 1
Totale 572
Nome #
Neurofibromatosis type I and multiple myeloma coexistence: A possible link? 92
Monogenic autoinflammatory diseases with mendelian inheritance: Genes, mutations, and genotype/phenotype correlations 82
Spectrum of X-linked intellectual disabilities and psychiatric symptoms in a family harbouring a Xp22.12 microduplication encompassing the RPS6KA3 gene 80
Combination of ultrasound and molecular testing in malignancy risk estimate of Bethesda category IV thyroid nodules: results from a single-institution prospective study 75
Discrimination of FCGR2B polymorphism without coamplification of FCGR2A and FCGR2C genes 74
Combined genetic variants of human cytomegalovirus envelope glycoproteins as congenital infection markers 59
A large-scale genetic analysis reveals an autoimmune origin of idiopathic retroperitoneal fibrosis 58
Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I 55
Patterns of novel alleles and genotype/phenotype correlations resulting from the analysis of 108 previously undetected mutations in patients affected by neurofibromatosis type I 54
F7 gene variants modulate protein levels in a large cohort of patients with factor VII deficiency: Results from a genotype-phenotype study 50
A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever 45
Clinical and genetic findings in a series of eight families with arthrogryposis 35
Genetic Basis of Breast and Ovarian Cancer: Approaches and Lessons Learnt from Three Decades of Inherited Predisposition Testing 32
ANCA-Associated Vasculitis 24
Success and Pitfalls of Genetic Testing in Undiagnosed Diseases: Whole Exome Sequencing and Beyond 13
Reassessment of the NF1 variants of unknown significance found during the 20-year activity of a genetics diagnostic laboratory 2
Phenotypic Expansion of Autosomal Dominant LZTR1-Related Disorders with Special Emphasis on Adult-Onset Features 1
Totale 831
Categoria #
all - tutte 3.762
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 3.762


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202069 0 0 0 3 8 23 15 2 7 6 3 2
2020/202168 2 2 6 6 7 2 6 3 5 10 13 6
2021/202283 10 3 5 6 4 0 8 12 0 4 4 27
2022/2023325 30 39 24 36 38 33 3 17 92 2 11 0
2023/2024138 8 19 4 0 7 22 6 14 1 22 16 19
2024/202548 18 30 0 0 0 0 0 0 0 0 0 0
Totale 831