IRIS
PALKA, Giandomenico
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 8.725
EU - Europa 6.722
AS - Asia 6.343
SA - Sud America 619
AF - Africa 74
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 6
Totale 22.499
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 8.539
SG - Singapore 2.203
CN - Cina 1.917
UA - Ucraina 1.090
IT - Italia 897
IE - Irlanda 806
GB - Regno Unito 778
TR - Turchia 710
SE - Svezia 706
RU - Federazione Russa 668
DE - Germania 645
FR - Francia 598
IN - India 563
VN - Vietnam 541
BR - Brasile 496
FI - Finlandia 231
CA - Canada 109
BD - Bangladesh 107
AT - Austria 98
PL - Polonia 52
HK - Hong Kong 49
MX - Messico 47
JP - Giappone 42
AR - Argentina 41
IQ - Iraq 35
NL - Olanda 34
KR - Corea 30
ZA - Sudafrica 30
EC - Ecuador 26
BE - Belgio 22
ES - Italia 22
GR - Grecia 19
CZ - Repubblica Ceca 17
IL - Israele 17
ID - Indonesia 16
PK - Pakistan 16
VE - Venezuela 16
IR - Iran 15
CO - Colombia 11
KE - Kenya 11
PY - Paraguay 11
RO - Romania 11
LT - Lituania 10
EU - Europa 9
PE - Perù 9
SA - Arabia Saudita 9
MY - Malesia 8
UZ - Uzbekistan 8
MA - Marocco 7
PH - Filippine 7
AU - Australia 6
DO - Repubblica Dominicana 6
JO - Giordania 6
LB - Libano 6
OM - Oman 6
CL - Cile 5
HN - Honduras 5
JM - Giamaica 5
SY - Repubblica araba siriana 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
CH - Svizzera 4
EG - Egitto 4
MD - Moldavia 4
CR - Costa Rica 3
ET - Etiopia 3
NP - Nepal 3
PA - Panama 3
QA - Qatar 3
SN - Senegal 3
UY - Uruguay 3
BB - Barbados 2
BH - Bahrain 2
CY - Cipro 2
DK - Danimarca 2
DZ - Algeria 2
GE - Georgia 2
MK - Macedonia 2
MU - Mauritius 2
NG - Nigeria 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BS - Bahamas 1
CG - Congo 1
CI - Costa d'Avorio 1
EE - Estonia 1
GD - Grenada 1
GT - Guatemala 1
HU - Ungheria 1
KG - Kirghizistan 1
KH - Cambogia 1
KN - Saint Kitts e Nevis 1
KZ - Kazakistan 1
LY - Libia 1
NO - Norvegia 1
PS - Palestinian Territory 1
Totale 22.494
Salva come PNG Salva come JPEG
Città #
Singapore 1.439
Jacksonville 1.136
San Jose 1.055
Chandler 895
Dublin 804
Ashburn 611
Southend 603
Beijing 473
Princeton 395
Dallas 383
Izmir 383
Nanjing 335
Wilmington 250
Los Angeles 239
Dearborn 237
Cambridge 190
The Dalles 183
Ho Chi Minh City 145
Tongling 143
Chieti 139
Nanchang 138
Santa Clara 130
Grafing 126
New York 124
Council Bluffs 123
Munich 122
Buffalo 117
Hanoi 110
Boardman 104
Altamura 103
Vienna 94
Ann Arbor 88
Moscow 86
Dong Ket 76
Woodbridge 76
Shenyang 70
Hebei 66
Kunming 60
Tianjin 59
São Paulo 51
Orem 49
Grevenbroich 45
Jiaxing 44
Washington 44
Hong Kong 41
Pescara 39
Brooklyn 38
Hangzhou 38
Jinan 38
Montreal 38
Rome 36
Tokyo 36
Helsinki 34
Warsaw 34
Milan 33
Hefei 32
Redondo Beach 32
Atlanta 30
Seoul 30
Augusta 29
Chicago 29
Kocaeli 29
San Mateo 29
Houston 28
Norwalk 27
Toronto 27
Seattle 25
Changsha 24
Orange 24
Haiphong 23
Johannesburg 23
Ningbo 23
Stockholm 23
Zhengzhou 23
London 22
Chennai 21
Guangzhou 20
Denver 19
Lanzhou 19
San Francisco 18
Manchester 17
Mexico City 17
Poplar 17
Baghdad 16
Kraków 16
Rio de Janeiro 16
Da Nang 15
Düsseldorf 15
Leawood 15
Brussels 14
Phoenix 14
Auburn Hills 13
Brno 13
Mumbai 13
Amsterdam 12
Boston 12
Changchun 12
Frankfurt am Main 12
Quito 12
Ankara 11
Totale 13.459
Salva come PNG Salva come JPEG
Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 212
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 191
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 188
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 184
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 181
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 179
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 176
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 175
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 175
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 171
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 171
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 170
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 170
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 162
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 160
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 159
A new case of pure partial 7q duplication 158
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 157
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 156
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 154
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 154
[Chromosome anomalies and Waldenström's macroglobulinemia]. 153
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 149
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 149
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 148
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 147
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 147
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 146
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 145
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 145
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 144
Non-invasive prenatal screening: a 20-year experience in Italy 143
X/Y translocation in a family with Leri-Weill dyschondrosteosis 141
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 141
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 141
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 141
[Trisomy 7 in a case of acute myelomonocytic leukemia]. 141
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 140
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 140
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 140
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 140
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 139
I nuovi orizzonti della diagnosi prenatale 138
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 138
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 137
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 136
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 136
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 136
Male infertility: role of genetic background 135
Concerns about using Zn supplementation in Down's syndrome (DS) children. 135
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 135
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 134
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 134
A case of triploidy detected by crosstrimester test. 133
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 133
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 132
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 132
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 132
Allogeneic bone marrow transplantation for Fanconi anemia. 132
[Chromosomal proteins during ontogenesis of Gallus gallus. III. Non-histone proteins in the heart]. 132
Characterization of novel genes in AZF regions 131
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 131
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 130
[Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17]. 130
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 130
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 129
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 128
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 128
Cytogenetic survey of benign prostate hyperplasia 128
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 128
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 127
Karyologic analysis in erythroleukemia 126
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 126
SHOX mutations detected by FISH and direct sequencing in patients with short stature 125
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 124
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 124
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 124
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 124
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 123
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 123
Morphometric and functional study of apoptotic cell chromatin 122
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 122
La parete del tubulo seminifero contorto di ratto in diverse condizioni sperimentali 121
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 120
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 120
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 119
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 118
[Cytogenetics in bone marrow transplantations. II. Acute lymphocytic leukemia]. 118
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 118
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. 117
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 117
[Cytogenetic study of 140 patients with changes in sexual features]. 117
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 116
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 114
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 114
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 114
Different approaches in the molecular analysis of the SHOX gene dysfunctions 114
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 113
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 113
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 113
Totale 13.922
Salva come PNG Salva come JPEG
Categoria #
all - tutte 86.446
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 86.446
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021115 0 0 0 0 0 0 0 0 0 0 0 115
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
2025/20266.664 580 320 669 865 651 439 1.106 433 669 531 269 132
Totale 22.777