IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
NA - Nord America 10.431
EU - Europa 6.959
AS - Asia 6.418
SA - Sud America 651
Continente sconosciuto - Info sul continente non disponibili 297
AF - Africa 82
OC - Oceania 6
Totale 24.844
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Nazione #
US - Stati Uniti d'America 10.053
SG - Singapore 2.217
CN - Cina 1.935
UA - Ucraina 1.093
IT - Italia 1.060
IE - Irlanda 806
GB - Regno Unito 792
TR - Turchia 714
SE - Svezia 708
RU - Federazione Russa 684
DE - Germania 652
FR - Francia 604
IN - India 563
VN - Vietnam 545
BR - Brasile 511
FI - Finlandia 231
CA - Canada 185
BD - Bangladesh 113
AT - Austria 98
MX - Messico 55
PL - Polonia 54
HK - Hong Kong 50
JP - Giappone 45
AR - Argentina 44
NL - Olanda 39
IQ - Iraq 35
EC - Ecuador 30
KR - Corea 30
ZA - Sudafrica 30
IL - Israele 28
ES - Italia 27
CR - Costa Rica 23
BE - Belgio 22
GR - Grecia 20
HN - Honduras 19
PK - Pakistan 19
VE - Venezuela 18
CZ - Repubblica Ceca 17
ID - Indonesia 16
CO - Colombia 15
IR - Iran 15
SV - El Salvador 14
MY - Malesia 13
GT - Guatemala 12
JM - Giamaica 12
TT - Trinidad e Tobago 12
KE - Kenya 11
PY - Paraguay 11
RO - Romania 11
SA - Arabia Saudita 11
LT - Lituania 10
PE - Perù 10
PR - Porto Rico 10
EU - Europa 9
NI - Nicaragua 9
SC - Seychelles 9
CL - Cile 8
PH - Filippine 8
UZ - Uzbekistan 8
CW - ???statistics.table.value.countryCode.CW??? 7
GP - Guadalupe 7
MA - Marocco 7
AU - Australia 6
DO - Repubblica Dominicana 6
EE - Estonia 6
JO - Giordania 6
LB - Libano 6
OM - Oman 6
SY - Repubblica araba siriana 6
CH - Svizzera 5
TN - Tunisia 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
BB - Barbados 4
EG - Egitto 4
MD - Moldavia 4
NP - Nepal 4
DK - Danimarca 3
ET - Etiopia 3
PA - Panama 3
QA - Qatar 3
SN - Senegal 3
UY - Uruguay 3
AL - Albania 2
BH - Bahrain 2
BS - Bahamas 2
CY - Cipro 2
DZ - Algeria 2
GD - Grenada 2
GE - Georgia 2
HU - Ungheria 2
MK - Macedonia 2
MU - Mauritius 2
NG - Nigeria 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
BO - Bolivia 1
Totale 24.548
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Città #
Singapore 1.447
San Jose 1.188
Jacksonville 1.140
Chandler 895
Dublin 804
Ashburn 651
Southend 603
Beijing 483
Princeton 395
Dallas 394
Izmir 383
Council Bluffs 365
Nanjing 335
Los Angeles 252
Wilmington 251
Dearborn 237
Cambridge 190
The Dalles 183
Santa Clara 164
Buffalo 153
Ho Chi Minh City 147
Tongling 143
Chieti 139
Nanchang 138
New York 131
Grafing 126
Munich 122
Hanoi 111
Boardman 104
Altamura 103
Vienna 94
Ann Arbor 88
Moscow 86
Woodbridge 77
Dong Ket 76
Shenyang 70
Hebei 66
Milan 64
Kunming 60
Tianjin 59
Orem 53
Columbus 52
São Paulo 52
Rome 51
Brooklyn 47
Montreal 47
Washington 46
Grevenbroich 45
Jiaxing 44
Atlanta 42
Hong Kong 42
Houston 42
Phoenix 42
Pescara 41
Tokyo 39
Toronto 39
Chicago 38
Hangzhou 38
Jinan 38
North Bergen 35
Helsinki 34
Warsaw 34
Hefei 32
Redondo Beach 32
Seoul 30
Augusta 29
Kocaeli 29
San Mateo 29
Norwalk 28
Seattle 28
London 27
Denver 25
Changsha 24
Kimball 24
Orange 24
Haiphong 23
Johannesburg 23
Ningbo 23
Stockholm 23
Zhengzhou 23
Chennai 21
Naples 21
Guangzhou 20
Mexico City 20
Philadelphia 20
Lanzhou 19
San Francisco 19
Manchester 18
Charlotte 17
Poplar 17
Rio de Janeiro 17
San José 17
Baghdad 16
Kraków 16
Boston 15
Da Nang 15
Düsseldorf 15
Frankfurt am Main 15
Leawood 15
Brussels 14
Totale 14.281
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 226
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 214
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 200
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 198
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 191
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 191
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 188
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 185
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 185
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 184
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 182
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 181
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 180
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 179
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 178
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 175
A new case of pure partial 7q duplication 169
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 169
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 167
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 167
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 166
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 165
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 164
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 164
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 163
[Chromosome anomalies and Waldenström's macroglobulinemia]. 162
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 161
Non-invasive prenatal screening: a 20-year experience in Italy 159
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 157
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 156
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 156
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 155
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 155
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 155
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 154
X/Y translocation in a family with Leri-Weill dyschondrosteosis 153
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 152
Male infertility: role of genetic background 151
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 151
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 151
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 150
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 150
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 149
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 149
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 148
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 148
[Trisomy 7 in a case of acute myelomonocytic leukemia]. 147
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 146
Concerns about using Zn supplementation in Down's syndrome (DS) children. 145
I nuovi orizzonti della diagnosi prenatale 145
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 144
Allogeneic bone marrow transplantation for Fanconi anemia. 144
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 144
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 143
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 143
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 142
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 141
A case of triploidy detected by crosstrimester test. 141
Characterization of novel genes in AZF regions 140
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 140
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 139
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 139
Karyologic analysis in erythroleukemia 138
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 138
[Chromosomal proteins during ontogenesis of Gallus gallus. III. Non-histone proteins in the heart]. 138
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 138
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 138
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 137
[Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17]. 137
Cytogenetic survey of benign prostate hyperplasia 136
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 136
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 136
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 136
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 135
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 135
SHOX mutations detected by FISH and direct sequencing in patients with short stature 134
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 134
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 134
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 133
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 132
[Cytogenetic study of 140 patients with changes in sexual features]. 132
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 132
Morphometric and functional study of apoptotic cell chromatin 131
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. 131
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 130
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 130
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 130
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 130
La parete del tubulo seminifero contorto di ratto in diverse condizioni sperimentali 130
Correlation between apoptosis and TP53 status in osteosarcoma 128
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 128
[Cytogenetics in bone marrow transplantations. II. Acute lymphocytic leukemia]. 128
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 128
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 127
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 126
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 125
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 124
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 124
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 123
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 123
Totale 15.041
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Categoria #
all - tutte 97.457
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 97.457
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022675 0 0 0 0 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
2025/20266.685 580 320 669 865 651 439 1.106 433 669 531 269 153
2026/20272.046 115 381 307 864 379 0 0 0 0 0 0 0
Totale 24.844