statistiche ricercatore

BALDASSARRI, MARGHERITA

Distribuzione geografica

Continente	#
EU - Europa	575
NA - Nord America	512
AS - Asia	79
OC - Oceania	6
AF - Africa	5
Totale	1.177

Salva come PNG Salva come JPEG

Nazione	#
US - Stati Uniti d'America	500
IT - Italia	257
IE - Irlanda	96
FR - Francia	55
GB - Regno Unito	34
SE - Svezia	26
DE - Germania	24
NL - Olanda	18
VN - Vietnam	18
ES - Italia	17
CN - Cina	14
IR - Iran	13
UA - Ucraina	12
CA - Canada	10
CZ - Repubblica Ceca	8
IN - India	8
JP - Giappone	7
HK - Hong Kong	5
TR - Turchia	5
CH - Svizzera	4
NZ - Nuova Zelanda	4
AE - Emirati Arabi Uniti	3
BE - Belgio	3
DK - Danimarca	3
FI - Finlandia	3
IL - Israele	3
ZA - Sudafrica	3
AU - Australia	2
GR - Grecia	2
MX - Messico	2
RO - Romania	2
RS - Serbia	2
RU - Federazione Russa	2
SI - Slovenia	2
AM - Armenia	1
AT - Austria	1
LT - Lituania	1
LU - Lussemburgo	1
LY - Libia	1
MA - Marocco	1
PL - Polonia	1
PT - Portogallo	1
QA - Qatar	1
UZ - Uzbekistan	1
Totale	1.177

Salva come PNG Salva come JPEG

Città	#
Siena	106
Dublin	88
Ashburn	65
Fairfield	55
Santa Cruz	38
Florence	32
Houston	26
Buffalo	25
Stockholm	23
Seattle	19
Cambridge	18
Dong Ket	18
Woodbridge	18
Southend	14
Shanghai	12
Wilmington	12
Chicago	11
Santa Cruz de Tenerife	11
Ann Arbor	10
San Diego	9
Arezzo	8
Boardman	8
Milan	8
Rome	8
Amsterdam	7
Brescia	7
La Gacilly	7
Cedar Knolls	6
Mold	6
Prato	6
Chester	5
Dallas	5
Los Angeles	5
Council Bluffs	4
London	4
Naples	4
New York	4
Paris	4
Provo	4
Toronto	4
Brussels	3
Crugers	3
Dunedin	3
Kyoto	3
Muizenberg	3
Ottawa	3
Palma	3
Pisa	3
Pune	3
Verona	3
Atlanta	2
Bengaluru	2
Bergamo	2
Capel Curig	2
Central	2
Florissant	2
Frederiksberg	2
Henderson	2
Huixquilucan de Degollado	2
Istanbul	2
Kollam	2
Lake Forest	2
Landstuhl	2
Lappeenranta	2
Las Vegas	2
Lawrenceville	2
Lucerne	2
Malmo	2
Palermo	2
Phoenix	2
Rockville	2
Saint Petersburg	2
San Jose	2
San Maurizio D'opaglio	2
Scranton	2
Tel Aviv	2
Viareggio	2
Yellow Springs	2
Zurich	2
Ankara	1
Asciano	1
Bari	1
Boiling Springs	1
Boulder	1
Bracke	1
Campi Bisenzio	1
Castelfiorentino	1
Christchurch	1
Clearwater	1
College Park	1
Collegeville	1
Columbus	1
Deeside	1
Denver	1
Diyarbakır	1
Doha	1
Dulles	1
Edmonton	1
Foresto Sparso	1
Frankfurt am Main	1
Totale	833

Salva come PNG Salva come JPEG

Nome	#
Usefulness and limitations of comprehensive characterization of mRNA splicing profiles in the definition of the clinical relevance of BRCA1/2 variants of uncertain significance, file e0feeaa8-3583-44d2-e053-6605fe0a8db0	162
Omic Approach in Non-Smoker Female with Lung Squamous Cell Carcinoma Pinpoints to Germline Susceptibility and Personalized Medicine, file e0feeaa6-8085-44d2-e053-6605fe0a8db0	153
null, file e0feeaaa-249a-44d2-e053-6605fe0a8db0	108
Alport syndrome: impact of digenic inheritance in patients management, file e0feeaab-67e0-44d2-e053-6605fe0a8db0	107
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population, file e0feeaa8-ceda-44d2-e053-6605fe0a8db0	89
Two-point-NGS analysis of cancer genes in cell-free DNA of metastatic cancer patients, file e0feeaa8-527c-44d2-e053-6605fe0a8db0	67
null, file e0feeaaa-1f34-44d2-e053-6605fe0a8db0	67
null, file e0feeaaa-52ef-44d2-e053-6605fe0a8db0	63
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability., file e0feeaab-b7d2-44d2-e053-6605fe0a8db0	49
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males., file e8887f01-8ecd-408c-a6e4-5b1d8e6d5c42	38
Expanding the clinical spectrum associated with the PACS1 p.Arg203Trp mutational hot-spot: Two additional Italian patients, file 0d4aac84-4a5c-4047-b15a-0985b9a24b17	33
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19, file 96f4df86-86ac-462c-8a12-3ca958289b45	28
null, file e0feeaab-b657-44d2-e053-6605fe0a8db0	21
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues, file b27bf0e9-010f-47e6-a116-48649af66e36	20
null, file e0feeaaa-063d-44d2-e053-6605fe0a8db0	18
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients, file e0feeaab-0e66-44d2-e053-6605fe0a8db0	18
Mapping the human genetic architecture of COVID-19, file e0feeaab-73d3-44d2-e053-6605fe0a8db0	15
Clinical and molecular characterization of COVID-19 hospitalized patients, file 125e504f-f9c2-4d04-8ea6-eb60ed7246fe	14
C9orf72 intermediate repeats confer genetic risk for severe covid-19 pneumonia independently of age, file 530676af-72b7-4a15-b48a-51204a80e40d	12
Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes, file ebc57d5c-8d48-406c-b361-06dd583c7b6b	12
An explainable model of host genetic interactions linked to COVID-19 severity, file a40b8f9e-8132-42fb-ba8e-085aaa454eda	11
Whole-genome sequencing reveals host factors underlying critical COVID-19, file b47ac884-9c8d-4cf9-84ab-2c6dfbaa52e5	10
Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males, file 434b66aa-b383-4316-9027-8d28bd50a93f	9
Identification of a Novel Pathogenic Variant in the NAGLU Gene in a Child with Neurodevelopmental Delay., file e0feeaab-6df6-44d2-e053-6605fe0a8db0	9
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor, file e0feeaab-b43d-44d2-e053-6605fe0a8db0	9
null, file e0feeaa9-7c6e-44d2-e053-6605fe0a8db0	8
SELP Asp603Asn and severe thrombosis in COVID-19 males, file e0feeaaa-35ce-44d2-e053-6605fe0a8db0	8
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues, file 4b6371f4-5458-443b-941a-cf972c6ace63	6
PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis, file d3e278d5-ea93-4501-8e66-9ffa44309c22	6
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity, file d7cf9e79-1409-43ab-b33c-176302109711	5
Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research, file 2280e542-6881-4bb1-813e-9235d2285d2d	4
Host genetic basis of COVID-19: from phenotype to genes., file 48738bf1-79a3-44cb-a680-58134c9cc408	3
13q Deletion Syndrome Involving RB1: Characterization of a New Minimal Critical Region for Psychomotor Delay, file 5ed185b5-d73e-435b-bd2a-6d488d221ce8	3
null, file e0feeaa7-e022-44d2-e053-6605fe0a8db0	3
Association of toll-like receptor 7 variants with life-threatening COVID-19 disease in males: Findings from a nested case-control study, file 512d6119-39f2-474c-a2fd-045eb023d546	2
Pathogen-sugar interactions revealed by universal saturation transfer analysis, file 83e3ea53-7dd8-465d-985b-a21f380e98c4	2
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor, file e0feeaa5-679d-44d2-e053-6605fe0a8db0	2
Severe COVID-19 in hospitalized carriers of single CFTR pathogenic variants, file e0feeaaa-3c01-44d2-e053-6605fe0a8db0	2
Genetic mechanisms of critical illness in COVID-19, file e0feeaaa-50e1-44d2-e053-6605fe0a8db0	2
Alport syndrome: impact of digenic inheritance in patients management, file e0feeaab-67e1-44d2-e053-6605fe0a8db0	2
Detection of cryptic mosaicism in X-linked alport syndrome prompts to re-evaluate living-donor kidney transplantation, file eee44607-ca6d-454e-bc12-500bf1e1b82d	2
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women, file c44a78e1-66be-49a4-a3e1-68030161493b	1
Revealing the complexity of a monogenic disease: rett syndrome exome sequencing, file e0feeaa5-8d1f-44d2-e053-6605fe0a8db0	1
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability., file e0feeaaa-145b-44d2-e053-6605fe0a8db0	1
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality, file e0feeaab-0fea-44d2-e053-6605fe0a8db0	1
A pilot study of next generation sequencing–liquid biopsy on cell-free DNA as a novel non-invasive diagnostic tool for Klippel–Trenaunay syndrome, file fa0345e7-a40b-401f-ba2a-349831c18220	1
Totale	1.207

Salva come PNG Salva come JPEG

Categoria	#
all - tutte	4.941
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	4.941

Salva come PNG Salva come JPEG

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2018/2019	17	0	0	0	0	0	0	0	0	0	3	9	5
2019/2020	82	3	3	1	13	10	7	8	8	11	4	7	7
2020/2021	169	9	5	11	3	8	10	8	20	5	30	29	31
2021/2022	255	16	17	4	10	19	11	16	11	19	17	82	33
2022/2023	392	14	15	59	48	40	59	29	42	23	24	32	7
2023/2024	288	13	16	14	28	17	47	64	31	7	51	0	0
Totale													1.207