IRIS PubliCatt

Zollino, Marcella
 Distribuzione geografica
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Continente #
NA - Nord America 610
EU - Europa 131
AS - Asia 26
SA - Sud America 5
AF - Africa 4
OC - Oceania 1
Totale 777
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Nazione #
US - Stati Uniti d'America 607
IT - Italia 56
FI - Finlandia 33
DE - Germania 17
CN - Cina 13
VN - Vietnam 8
PL - Polonia 6
RU - Federazione Russa 4
ZA - Sudafrica 4
AE - Emirati Arabi Uniti 3
BR - Brasile 3
CA - Canada 3
CZ - Repubblica Ceca 3
FR - Francia 3
CL - Cile 2
GB - Regno Unito 2
IE - Irlanda 2
SK - Slovacchia (Repubblica Slovacca) 2
AU - Australia 1
GR - Grecia 1
ID - Indonesia 1
NL - Olanda 1
SA - Arabia Saudita 1
UA - Ucraina 1
Totale 777
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Città #
Fairfield 102
Santa Cruz 66
Ashburn 65
Seattle 43
Cambridge 38
Woodbridge 36
Houston 35
Lappeenranta 31
Buffalo 29
Wilmington 28
Cattolica 26
Ann Arbor 14
Dong Ket 8
Los Angeles 8
Santa Maria 8
San Diego 7
Warsaw 6
Busto Arsizio 5
Boardman 4
Chicago 4
Las Vegas 4
Muizenberg 4
Phoenix 4
Henderson 3
Milpitas 3
Ottawa 3
Recife 3
Saint Petersburg 3
Auburn 2
Beijing 2
Clearwater 2
Dublin 2
Guangzhou 2
Helsinki 2
Lake Forest 2
Milan 2
Mountain View 2
Nové Zámky 2
Rome 2
Amsterdam 1
Austin 1
Bellevue 1
Boston 1
Büdelsdorf 1
Chesapeake 1
Crugers 1
Dallas 1
Esslingen am Neckar 1
Fiumicino 1
Jakarta 1
Kenmore 1
Lincoln 1
Magenta 1
Provo 1
San Francisco 1
San Jose 1
Santa Rosa 1
Santiago 1
Scarsdale 1
Scranton 1
Shanghai 1
Siena 1
Sydney 1
Taizhou 1
University Park 1
Wuhan 1
Yellow Springs 1
Totale 640
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Nome #
Pembrolizumab as first-line treatment for metastatic uveal melanoma, file e309db6d-e534-0599-e053-3705fe0a55db 209
The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use, file e309db6d-01ff-0599-e053-3705fe0a55db 182
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene, file e309db6d-e257-0599-e053-3705fe0a55db 146
The chromosome analysis of the miscarriage tissue. Miscarried embryo/fetal crown rump length (CRL) measurement: A practical use, file e309db6e-d47e-0599-e053-3705fe0a55db 58
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis, file e309db6d-ec34-0599-e053-3705fe0a55db 57
Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly, file e309db6e-a97b-0599-e053-3705fe0a55db 36
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency, file e309db6e-eadb-0599-e053-3705fe0a55db 32
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes, file e309db6e-8b60-0599-e053-3705fe0a55db 29
LETM1 couples mitochondrial DNA metabolism and nutrient preference, file e309db6f-60de-0599-e053-3705fe0a55db 20
High-throughput genetic testing in ALS: The challenging path of variant classification considering the acmg guidelines, file e309db6f-6744-0599-e053-3705fe0a55db 13
Primary fibroblasts cultures reveal TDP-43 abnormalities in amyotrophic lateral sclerosis patients with and without SOD1 mutations, file e309db6c-8323-0599-e053-3705fe0a55db 4
New ALS-related genes expand the spectrum paradigm of amyotrophic lateral sclerosis, file e309db6d-2d0b-0599-e053-3705fe0a55db 3
Matrin 3 variants are frequent in Italian ALS patients, file e309db6c-aea1-0599-e053-3705fe0a55db 2
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis, file e309db6d-4930-0599-e053-3705fe0a55db 2
Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder, file 3907cb52-eea9-4d23-ad81-1d109bc0034f 1
The HFE p.H63D (p.His63Asp) Polymorphism Is a Modifier of ALS Outcome in Italian and French Patients with SOD1 Mutations, file 3c0fc86c-cee6-4672-959c-95513825f85c 1
Investigating the "Fetal Side" in Recurrent Pregnancy Loss: Reliability of Cell-Free DNA Testing in Detecting Chromosomal Abnormalities of Miscarriage Tissue, file 605ed276-785b-4ffb-8a23-4429cfde9d2f 1
Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome, file 92323f39-13ae-43be-9475-b3f7635bbd88 1
Case Report: Challenges of Non-Invasive Prenatal Testing (NIPT): A Case Report of Confined Placental Mosaicism and Clinical Considerations, file b0d2f96a-5ee1-42f0-b3d2-7fd58a1b89ac 1
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome, file e309db6d-3d55-0599-e053-3705fe0a55db 1
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene, file e309db6d-cede-0599-e053-3705fe0a55db 1
Complex Muco-cutaneous Manifestations of CARMIL2-associated Combined Immunodeficiency: A Novel Presentation of Dysfunctional Epithelial Barriers, file e309db6e-2b87-0599-e053-3705fe0a55db 1
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS, file e309db6e-8ec0-0599-e053-3705fe0a55db 1
A deep phenotyping experience: up to date in management and diagnosis of Malan syndrome in a single center surveillance report, file eed57c9d-4211-4dc4-afaa-bc990c5d6514 1
Totale 803
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Categoria #
all - tutte 3.075
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 3.075
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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
2019/2020229 11 28 27 86 10 14 8 11 13 5 9 7
2020/2021142 9 4 9 2 8 12 18 5 8 31 22 14
2021/2022178 11 10 8 8 19 3 5 9 10 4 66 25
2022/2023117 3 4 45 27 2 7 3 1 2 1 13 9
2023/202475 2 6 13 3 3 5 1 5 5 31 1 0
Totale 803