IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
NA - Nord America 7.052
EU - Europa 6.107
AS - Asia 5.436
SA - Sud America 570
AF - Africa 56
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 4
Totale 19.235
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Nazione #
US - Stati Uniti d'America 6.899
CN - Cina 1.839
SG - Singapore 1.838
UA - Ucraina 1.088
IT - Italia 829
IE - Irlanda 805
GB - Regno Unito 768
TR - Turchia 705
SE - Svezia 704
DE - Germania 639
FR - Francia 587
IN - India 537
BR - Brasile 473
VN - Vietnam 290
FI - Finlandia 231
RU - Federazione Russa 172
AT - Austria 98
CA - Canada 94
PL - Polonia 51
MX - Messico 40
JP - Giappone 37
AR - Argentina 34
KR - Corea 30
ZA - Sudafrica 28
NL - Olanda 26
BD - Bangladesh 25
EC - Ecuador 23
BE - Belgio 21
HK - Hong Kong 21
ES - Italia 20
GR - Grecia 19
IQ - Iraq 19
CZ - Repubblica Ceca 17
IL - Israele 15
IR - Iran 15
ID - Indonesia 13
PY - Paraguay 11
LT - Lituania 10
RO - Romania 10
EU - Europa 9
VE - Venezuela 9
PK - Pakistan 8
CO - Colombia 7
KE - Kenya 7
PE - Perù 7
MY - Malesia 6
DO - Repubblica Dominicana 5
MA - Marocco 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
CL - Cile 4
EG - Egitto 4
HN - Honduras 4
LB - Libano 4
ET - Etiopia 3
JO - Giordania 3
MD - Moldavia 3
OM - Oman 3
BH - Bahrain 2
CR - Costa Rica 2
DK - Danimarca 2
DZ - Algeria 2
GE - Georgia 2
MK - Macedonia 2
NP - Nepal 2
QA - Qatar 2
SA - Arabia Saudita 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BB - Barbados 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CY - Cipro 1
GD - Grenada 1
GT - Guatemala 1
HU - Ungheria 1
JM - Giamaica 1
KN - Saint Kitts e Nevis 1
KZ - Kazakistan 1
NO - Norvegia 1
PA - Panama 1
PH - Filippine 1
PS - Palestinian Territory 1
RS - Serbia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TG - Togo 1
TW - Taiwan 1
UY - Uruguay 1
Totale 19.235
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Città #
Singapore 1.223
Jacksonville 1.136
Chandler 895
Dublin 803
Southend 603
Beijing 468
Ashburn 459
Princeton 395
Izmir 383
Dallas 376
Nanjing 335
Wilmington 250
Dearborn 237
Los Angeles 220
Cambridge 190
The Dalles 183
Tongling 143
Chieti 138
Nanchang 138
Grafing 126
Munich 122
Santa Clara 121
Buffalo 114
Boardman 104
Altamura 103
New York 100
Vienna 94
Ann Arbor 88
Dong Ket 76
Woodbridge 76
Ho Chi Minh City 73
Shenyang 70
Hebei 66
Kunming 60
Tianjin 59
Hanoi 47
São Paulo 47
Grevenbroich 45
Jiaxing 44
Washington 42
Hangzhou 38
Jinan 38
Brooklyn 37
Pescara 37
Helsinki 34
Montreal 33
Tokyo 33
Warsaw 33
Hefei 32
Redondo Beach 32
Rome 30
Seoul 30
Augusta 29
Kocaeli 29
San Mateo 29
Chicago 28
Houston 27
Norwalk 27
Council Bluffs 26
Toronto 25
Changsha 24
Orange 24
Seattle 24
Ningbo 23
Zhengzhou 23
Johannesburg 22
Atlanta 21
Stockholm 21
Hong Kong 20
Milan 20
Denver 19
Guangzhou 19
Lanzhou 19
London 19
Orem 19
San Francisco 18
Mexico City 17
Kraków 16
Poplar 16
Chennai 15
Düsseldorf 15
Leawood 15
Manchester 15
Brussels 14
Rio de Janeiro 14
Auburn Hills 13
Brno 13
Changchun 12
Ankara 11
Ardabil 11
Boston 11
Campinas 11
Haiphong 11
Moscow 11
Phoenix 11
Quito 11
Turku 11
Belo Horizonte 10
Brasília 10
Mumbai 10
Totale 11.518
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 181
The Italian multi-centre project on evaluation of MRI and other imaging modalities in early detection of breast cancer in subjects at high genetic risk 171
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 166
Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer 164
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 161
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 159
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 158
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 156
Widening of a Y-chromosome interval 6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to RBM1 and DAZ genes 155
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 155
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 155
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 150
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 145
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 143
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 140
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 138
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 134
A new case of pure partial 7q duplication 134
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 134
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 133
[Chromosome anomalies and Waldenström's macroglobulinemia]. 131
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 129
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 129
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 128
Human second trimester amniotic fluid cells are able to create embryoid body-like structures in vitro and to show typical expression profiles of embryonic and primordial germ cells 128
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 127
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 126
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 126
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 126
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 125
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 124
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 124
X/Y translocation in a family with Leri-Weill dyschondrosteosis 123
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 122
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 122
Concerns about using Zn supplementation in Down's syndrome (DS) children. 120
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 120
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 119
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 119
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 119
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 119
I nuovi orizzonti della diagnosi prenatale 118
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 118
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 118
Characterization of novel genes in AZF regions 116
Allogeneic bone marrow transplantation for Fanconi anemia. 116
Karyologic analysis in erythroleukemia 115
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 115
A case of triploidy detected by crosstrimester test. 115
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 115
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 114
SHOX mutations detected by FISH and direct sequencing in patients with short stature 114
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 114
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 114
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 113
[Chromosomal proteins during ontogenesis of Gallus gallus. III. Non-histone proteins in the heart]. 113
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 113
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 113
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 112
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 112
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 111
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 110
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 110
Cytogenetic survey of benign prostate hyperplasia 110
Male infertility: role of genetic background 109
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 109
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 108
[Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17]. 108
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 107
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 107
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 106
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 106
Non-invasive prenatal screening: a 20-year experience in Italy 106
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 105
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization 105
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 105
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 104
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 104
[Cytogenetics in bone marrow transplantations. II. Acute lymphocytic leukemia]. 104
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 104
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 104
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 104
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 102
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 102
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 102
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 102
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 101
Different approaches in the molecular analysis of the SHOX gene dysfunctions 101
Morphometric and functional study of apoptotic cell chromatin 100
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid leukemia. 100
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. 100
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 99
[Cytogenetic study of 140 patients with changes in sexual features]. 99
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 99
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 98
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 98
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 98
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 97
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 96
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 96
Totale 11.952
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Categoria #
all - tutte 74.811
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 74.811
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021987 0 0 0 0 0 250 16 20 282 218 86 115
2021/2022850 22 10 3 140 83 136 10 57 50 10 104 225
2022/20232.746 228 362 182 277 261 575 173 209 324 20 69 66
2023/20241.177 80 35 100 31 68 393 237 52 6 31 13 131
2024/20252.994 227 412 360 98 86 46 80 105 383 183 373 641
2025/20263.382 580 320 669 865 651 297 0 0 0 0 0 0
Totale 19.495