IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
EU - Europa 5.727
NA - Nord America 5.155
AS - Asia 3.184
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 5
OC - Oceania 3
AF - Africa 1
Totale 14.085
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Nazione #
US - Stati Uniti d'America 5.127
CN - Cina 1.255
UA - Ucraina 1.075
IE - Irlanda 804
IT - Italia 795
GB - Regno Unito 694
SE - Svezia 685
TR - Turchia 684
SG - Singapore 622
FR - Francia 569
DE - Germania 530
IN - India 501
FI - Finlandia 219
RU - Federazione Russa 160
AT - Austria 92
VN - Vietnam 78
CA - Canada 26
BE - Belgio 21
GR - Grecia 18
PL - Polonia 17
CZ - Repubblica Ceca 15
IR - Iran 15
IL - Israele 13
NL - Olanda 13
RO - Romania 10
EU - Europa 9
JP - Giappone 5
AU - Australia 3
BR - Brasile 3
MD - Moldavia 3
MY - Malesia 3
LB - Libano 2
MX - Messico 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
BD - Bangladesh 1
CH - Svizzera 1
CL - Cile 1
CY - Cipro 1
EC - Ecuador 1
ES - Italia 1
HK - Hong Kong 1
HU - Ungheria 1
LT - Lituania 1
MK - Macedonia 1
NO - Norvegia 1
PH - Filippine 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 14.085
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Città #
Jacksonville 1.135
Chandler 894
Dublin 802
Southend 603
Singapore 528
Princeton 395
Izmir 382
Nanjing 335
Wilmington 249
Dearborn 237
Beijing 220
Ashburn 214
Cambridge 190
Chieti 138
Nanchang 138
Grafing 126
Boardman 104
Altamura 103
Santa Clara 94
Vienna 92
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 34
Helsinki 33
Munich 32
Kocaeli 29
San Mateo 29
New York 27
Norwalk 27
Augusta 26
Orange 24
Rome 24
Changsha 23
Ningbo 23
Zhengzhou 22
Lanzhou 19
Guangzhou 18
Houston 18
Kraków 16
Düsseldorf 15
Leawood 15
Toronto 15
Brussels 14
Milan 14
Auburn Hills 13
Brno 13
Changchun 12
Hefei 12
Seattle 12
Ardabil 11
Moscow 11
Teramo 10
Romola 8
Sartrouville 8
Atessa 7
Bangalore 7
Mumbai 7
Vasto 7
Fuzhou 6
Montesilvano Marina 6
Naples 6
Taizhou 6
Waanrode 6
Clifton 5
London 5
Ottawa 5
Tortoreto 5
Andover 4
Bologna 4
Cagliari 4
Campobasso 4
Caserta 4
Cluj-napoca 4
Collecorvino 4
Falls Church 4
Florence 4
L'aquila 4
Parma 4
Redwood City 4
Roseto Degli Abruzzi 4
Walnut 4
Agnone 3
Alingsås 3
Bari 3
Bucharest 3
Chengdu 3
Chicago 3
Chisinau 3
Edinburgh 3
Totale 8.497
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 149
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 144
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 136
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 133
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 130
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 127
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 125
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 120
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 119
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 115
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 113
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 111
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 109
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 108
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 107
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 107
X/Y translocation in a family with Leri-Weill dyschondrosteosis 102
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 102
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 102
[Chromosome anomalies and Waldenström's macroglobulinemia]. 101
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 101
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 100
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 97
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 97
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 96
A new case of pure partial 7q duplication 96
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 96
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 96
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 95
Characterization of novel genes in AZF regions 93
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 93
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 93
Karyologic analysis in erythroleukemia 91
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 91
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 91
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 90
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 90
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 90
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 90
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 90
SHOX mutations detected by FISH and direct sequencing in patients with short stature 89
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 89
Concerns about using Zn supplementation in Down's syndrome (DS) children. 88
I nuovi orizzonti della diagnosi prenatale 88
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 88
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 87
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 87
Allogeneic bone marrow transplantation for Fanconi anemia. 87
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 87
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 86
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 86
Male infertility: role of genetic background 85
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 85
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 84
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 84
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 84
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 84
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 84
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 83
Different approaches in the molecular analysis of the SHOX gene dysfunctions 83
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 82
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 82
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 81
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 81
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 81
Cytogenetic survey of benign prostate hyperplasia 81
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 81
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 81
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 81
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 80
A case of triploidy detected by crosstrimester test. 80
Prenatal diagnosis using the triple test 78
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 78
Van der Woude syndrome: variable expressivity through four generations 77
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 77
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 77
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 77
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 77
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 77
Morphometric and functional study of apoptotic cell chromatin 76
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 76
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 76
Molecular studies in three patients with isodicentric Y chromosome 76
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 75
Growth delay in Down syndrome and zinc sulphate supplementation 74
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 74
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 74
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 74
[Analysis of the nonhistone chromosomal proteins during ontogenesis. I. NHCP of the leg muscle in Gallus gallus]. 74
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 74
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 73
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 73
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 73
[Cytogenetic study of 140 patients with changes in sexual features]. 73
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 73
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 73
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 73
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 72
Non-invasive prenatal screening: a 20-year experience in Italy 72
FISH analysis in detecting 9p duplication (p22p24) 71
Totale 9.012
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Categoria #
all - tutte 51.068
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 51.068
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.260 0 0 0 0 0 184 347 244 56 165 255 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
2024/20251.226 227 412 360 98 86 43 0 0 0 0 0 0
Totale 14.345