IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
NA - Nord America 8.346
EU - Europa 6.674
AS - Asia 6.264
SA - Sud America 617
AF - Africa 74
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 6
Totale 21.991
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Nazione #
US - Stati Uniti d'America 8.171
SG - Singapore 2.198
CN - Cina 1.909
UA - Ucraina 1.090
IT - Italia 853
IE - Irlanda 806
GB - Regno Unito 777
TR - Turchia 710
SE - Svezia 706
RU - Federazione Russa 668
DE - Germania 643
FR - Francia 598
IN - India 563
VN - Vietnam 540
BR - Brasile 496
FI - Finlandia 231
CA - Canada 100
AT - Austria 98
PL - Polonia 52
HK - Hong Kong 47
MX - Messico 47
BD - Bangladesh 44
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
IR - Iran 15
VE - Venezuela 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
JM - Giamaica 5
SY - Repubblica araba siriana 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
EG - Egitto 4
HN - Honduras 4
MD - Moldavia 4
CH - Svizzera 3
CR - Costa Rica 3
ET - Etiopia 3
NP - Nepal 3
PA - Panama 3
QA - Qatar 3
SN - Senegal 3
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
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BB - Barbados 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 21.986
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Città #
Singapore 1.437
Jacksonville 1.136
San Jose 916
Chandler 895
Dublin 804
Southend 603
Ashburn 599
Beijing 470
Princeton 395
Izmir 383
Dallas 378
Nanjing 335
Wilmington 250
Dearborn 237
Los Angeles 234
Cambridge 190
The Dalles 183
Ho Chi Minh City 145
Tongling 143
Chieti 139
Nanchang 138
Santa Clara 127
Grafing 126
Munich 122
Buffalo 116
Hanoi 110
New York 106
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 42
Hong Kong 39
Pescara 39
Hangzhou 38
Jinan 38
Brooklyn 37
Montreal 37
Tokyo 36
Helsinki 34
Warsaw 34
Council Bluffs 32
Hefei 32
Redondo Beach 32
Milan 30
Rome 30
Seoul 30
Augusta 29
Kocaeli 29
San Mateo 29
Chicago 28
Houston 27
Norwalk 27
Toronto 27
Atlanta 25
Changsha 24
Orange 24
Seattle 24
Haiphong 23
Johannesburg 23
Ningbo 23
Stockholm 23
Zhengzhou 23
Chennai 21
London 21
Denver 19
Guangzhou 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
Auburn Hills 13
Brno 13
Mumbai 13
Amsterdam 12
Changchun 12
Frankfurt am Main 12
Phoenix 12
Quito 12
Ankara 11
Ardabil 11
Totale 13.152
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 210
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 189
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 186
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 179
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 179
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 176
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 173
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 173
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 171
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 171
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 170
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 169
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 169
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 158
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 157
A new case of pure partial 7q duplication 156
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 153
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 152
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 152
[Chromosome anomalies and Waldenström's macroglobulinemia]. 151
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 150
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 149
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 147
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 146
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 146
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 145
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 144
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 142
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 142
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 142
Non-invasive prenatal screening: a 20-year experience in Italy 142
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 141
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 139
X/Y translocation in a family with Leri-Weill dyschondrosteosis 138
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 138
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 138
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 137
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 137
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 136
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 136
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 135
I nuovi orizzonti della diagnosi prenatale 135
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 135
Concerns about using Zn supplementation in Down's syndrome (DS) children. 134
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 133
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 133
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 133
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 133
Male infertility: role of genetic background 132
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 132
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 131
[Chromosomal proteins during ontogenesis of Gallus gallus. III. Non-histone proteins in the heart]. 131
A case of triploidy detected by crosstrimester test. 131
Allogeneic bone marrow transplantation for Fanconi anemia. 130
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 130
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 130
Characterization of novel genes in AZF regions 129
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 128
Cytogenetic survey of benign prostate hyperplasia 128
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 127
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 127
[Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17]. 127
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 127
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 126
Karyologic analysis in erythroleukemia 126
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 125
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
SHOX mutations detected by FISH and direct sequencing in patients with short stature 124
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 124
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 123
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 123
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 122
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 122
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 121
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 120
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 120
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 120
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 119
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 119
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 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
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 118
Morphometric and functional study of apoptotic cell chromatin 117
[Cytogenetic study of 140 patients with changes in sexual features]. 116
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 115
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 115
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 115
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 115
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 113
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 113
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. 112
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 112
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 111
[Trisomy 7 in a case of acute myelomonocytic leukemia]. 111
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 111
Different approaches in the molecular analysis of the SHOX gene dysfunctions 111
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 110
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. 110
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 109
Totale 13.587
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Categoria #
all - tutte 80.489
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 80.489
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021419 0 0 0 0 0 0 0 0 0 218 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
2025/20266.138 580 320 669 865 651 439 1.106 433 669 406 0 0
Totale 22.251