LAINO, LUIGI
 Distribuzione geografica
Continente #
NA - Nord America 172
EU - Europa 41
AS - Asia 3
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 219
Nazione #
US - Stati Uniti d'America 169
IT - Italia 27
FR - Francia 10
CA - Canada 3
CN - Cina 2
DE - Germania 2
AU - Australia 1
CL - Cile 1
FI - Finlandia 1
IN - India 1
UA - Ucraina 1
ZA - Sudafrica 1
Totale 219
Città #
Santa Cruz 20
Rome 17
Fairfield 16
Ashburn 14
Buffalo 12
Chicago 11
Houston 8
Seattle 7
Woodbridge 7
Cambridge 5
New York 4
Wilmington 3
Boardman 2
Dallas 2
Des Moines 2
Los Angeles 2
Paris 2
San Diego 2
San Jose 2
Andover 1
Ann Arbor 1
Atlanta 1
Bellevue 1
Büdelsdorf 1
Helsinki 1
Henderson 1
Honolulu 1
Kaveripatnam 1
Las Vegas 1
Melbourne 1
Miami 1
Milan 1
Milpitas 1
Muizenberg 1
Omaha 1
Ottawa 1
Phoenix 1
Provo 1
Reston 1
Saint Cloud 1
Tortoreto 1
Washington 1
Totale 161
Nome #
c-MET receptor as potential biomarker and target molecule for malignant testicular germ cell tumors, file e383531d-4766-15e8-e053-a505fe0a3de9 117
Prenatal diagnosis and post-mortem examination in a fetus with thrombocytopenia-absent radius (TAR) syndrome due to compound heterozygosity for a 1q21.1 microdeletion and a RBM8A hypomorphic allele: a case report, file e383531e-8e04-15e8-e053-a505fe0a3de9 75
Identification of a variant hotspot in MYBPC3 and of a novel CSRP3 autosomal recessive alteration in a cohort of Polish patients with hypertrophic cardiomyopathy, file e383532e-1460-15e8-e053-a505fe0a3de9 15
Variability in a three-generation family with pierre robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16, file e383531f-6a15-15e8-e053-a505fe0a3de9 7
Disorders of sex development: a genetic study of patients in a multidisciplinary clinic., file e3835312-6ecc-15e8-e053-a505fe0a3de9 5
An Additional Patient With 3q27.3 Microdeletion Syndrome., file e3835314-2691-15e8-e053-a505fe0a3de9 3
Clinical and molecular characterization of a boy with intellectual disability, facial dysmorphism, minor digital anomalies and a complex IL1RAPL1 intragenic rearrangement, file e3835315-6bf1-15e8-e053-a505fe0a3de9 2
Oropharyngeal teratoma, oral duplication, cervical diplomyelia and anencephaly in a 22-week fetus: A review of the craniofacial teratoma syndrome, file e3835312-46d5-15e8-e053-a505fe0a3de9 1
Autism spectrum disorder in a patient with a genomic rearrangement that only involves the EPHA5 gene, file e383532e-07a5-15e8-e053-a505fe0a3de9 1
Congenital heart defects in the recurrent 2q13 deletion syndrome, file e383532e-1fca-15e8-e053-a505fe0a3de9 1
Totale 227
Categoria #
all - tutte 466
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 466


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201915 0 0 0 0 0 0 0 0 0 0 8 7
2019/202038 4 3 3 2 3 1 3 5 3 5 5 1
2020/202126 1 1 1 2 2 1 5 0 3 4 3 3
2021/202252 1 4 2 3 4 1 0 3 4 4 17 9
2022/202359 3 1 13 5 1 5 1 2 24 2 2 0
2023/202427 1 0 4 4 5 3 5 2 2 1 0 0
Totale 227