IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
EU - Europa 5.780
NA - Nord America 5.355
AS - Asia 3.619
SA - Sud America 129
Continente sconosciuto - Info sul continente non disponibili 10
AF - Africa 7
OC - Oceania 3
Totale 14.903
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Nazione #
US - Stati Uniti d'America 5.324
CN - Cina 1.257
UA - Ucraina 1.076
SG - Singapore 1.022
IT - Italia 814
IE - Irlanda 804
GB - Regno Unito 694
TR - Turchia 689
SE - Svezia 685
FR - Francia 574
DE - Germania 540
IN - India 501
FI - Finlandia 219
RU - Federazione Russa 167
BR - Brasile 115
AT - Austria 95
VN - Vietnam 79
CA - Canada 26
BE - Belgio 21
NL - Olanda 20
GR - Grecia 19
PL - Polonia 17
CZ - Repubblica Ceca 15
IR - Iran 15
HK - Hong Kong 13
IL - Israele 13
RO - Romania 10
EU - Europa 9
JP - Giappone 5
MX - Messico 5
AR - Argentina 4
EC - Ecuador 4
AU - Australia 3
BD - Bangladesh 3
MD - Moldavia 3
MY - Malesia 3
PK - Pakistan 3
LB - Libano 2
MA - Marocco 2
UZ - Uzbekistan 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
CL - Cile 1
CO - Colombia 1
CY - Cipro 1
ES - Italia 1
GE - Georgia 1
HU - Ungheria 1
ID - Indonesia 1
IQ - Iraq 1
KE - Kenya 1
KZ - Kazakistan 1
LT - Lituania 1
MK - Macedonia 1
NO - Norvegia 1
OM - Oman 1
PH - Filippine 1
PS - Palestinian Territory 1
PY - Paraguay 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 14.903
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Città #
Jacksonville 1.135
Chandler 894
Dublin 802
Southend 603
Singapore 570
Princeton 395
Izmir 382
Nanjing 335
Wilmington 249
Dearborn 237
Beijing 220
Ashburn 217
Cambridge 190
The Dalles 178
Chieti 138
Nanchang 138
Grafing 126
Boardman 104
Altamura 103
Santa Clara 94
Vienna 94
Ann Arbor 88
Dong Ket 76
Woodbridge 76
Shenyang 70
Hebei 66
Kunming 60
Tianjin 58
Los Angeles 54
Grevenbroich 45
Jiaxing 44
Washington 40
Hangzhou 38
Jinan 38
Pescara 37
Helsinki 33
Munich 32
Kocaeli 29
San Mateo 29
New York 27
Norwalk 27
Rome 27
Augusta 26
Orange 24
Changsha 23
Ningbo 23
Zhengzhou 22
Guangzhou 19
Lanzhou 19
Houston 18
Milan 17
Kraków 16
Düsseldorf 15
Leawood 15
Toronto 15
Brussels 14
Auburn Hills 13
Brno 13
Changchun 12
Hefei 12
Hong Kong 12
Seattle 12
Ardabil 11
Moscow 11
Teramo 10
Rio de Janeiro 8
Romola 8
Sartrouville 8
São Paulo 8
Atessa 7
Bangalore 7
Mumbai 7
Naples 7
Vasto 7
Fuzhou 6
Montesilvano Marina 6
Taizhou 6
Waanrode 6
Clifton 5
London 5
Ottawa 5
Tortoreto 5
Andover 4
Bologna 4
Cagliari 4
Campinas 4
Campobasso 4
Caserta 4
Cluj-napoca 4
Collecorvino 4
Falls Church 4
Florence 4
L'aquila 4
Mexico City 4
Nuremberg 4
Parma 4
Porto Alegre 4
Redwood City 4
Roseto Degli Abruzzi 4
Walnut 4
Totale 8.753
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 157
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 147
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 146
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 138
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 138
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 133
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 131
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 127
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 125
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 124
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 123
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 120
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 114
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 114
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 111
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 109
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 106
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 106
A new case of pure partial 7q duplication 105
[Chromosome anomalies and Waldenström's macroglobulinemia]. 105
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 105
X/Y translocation in a family with Leri-Weill dyschondrosteosis 104
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 104
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 103
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 103
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 102
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 102
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 100
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 100
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 99
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 98
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 97
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 97
Characterization of novel genes in AZF regions 96
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 96
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 96
Concerns about using Zn supplementation in Down's syndrome (DS) children. 95
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 95
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 95
Allogeneic bone marrow transplantation for Fanconi anemia. 93
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 93
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 93
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 92
Karyologic analysis in erythroleukemia 92
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 92
I nuovi orizzonti della diagnosi prenatale 92
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 92
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 91
SHOX mutations detected by FISH and direct sequencing in patients with short stature 91
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 91
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 91
Male infertility: role of genetic background 90
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 90
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 89
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 88
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 87
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 87
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 87
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 86
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 86
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 86
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 85
A case of triploidy detected by crosstrimester test. 85
Different approaches in the molecular analysis of the SHOX gene dysfunctions 85
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 84
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 84
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 84
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 84
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 84
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 83
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 83
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 83
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 82
Morphometric and functional study of apoptotic cell chromatin 81
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 81
Cytogenetic survey of benign prostate hyperplasia 81
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 80
Van der Woude syndrome: variable expressivity through four generations 79
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 79
Prenatal diagnosis using the triple test 79
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 79
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 78
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 78
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 78
[Analysis of the nonhistone chromosomal proteins during ontogenesis. I. NHCP of the leg muscle in Gallus gallus]. 78
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 78
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 78
Growth delay in Down syndrome and zinc sulphate supplementation 77
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 77
Molecular studies in three patients with isodicentric Y chromosome 77
[Cytogenetic study of 140 patients with changes in sexual features]. 77
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 77
Non-invasive prenatal screening: a 20-year experience in Italy 77
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 76
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. 76
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 76
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 76
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 76
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 76
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 76
Totale 9.452
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Categoria #
all - tutte 59.288
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 59.288
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020264 0 0 0 0 0 0 0 0 0 0 255 9
2020/20211.459 193 7 198 7 67 250 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
2024/20252.044 227 412 360 98 86 46 80 105 383 183 64 0
Totale 15.163