IRIS
PALKA, Giandomenico
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 6.958
EU - Europa 6.089
AS - Asia 5.371
SA - Sud America 550
AF - Africa 45
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 4
Totale 19.027
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.812
SG - Singapore 1.835
CN - Cina 1.834
UA - Ucraina 1.087
IT - Italia 829
IE - Irlanda 805
GB - Regno Unito 763
TR - Turchia 705
SE - Svezia 701
DE - Germania 639
FR - Francia 587
IN - India 533
BR - Brasile 455
VN - Vietnam 261
FI - Finlandia 231
RU - Federazione Russa 171
AT - Austria 97
CA - Canada 91
PL - Polonia 46
MX - Messico 37
AR - Argentina 34
JP - Giappone 33
KR - Corea 30
NL - Olanda 26
ZA - Sudafrica 26
BD - Bangladesh 23
EC - Ecuador 22
BE - Belgio 21
HK - Hong Kong 21
ES - Italia 20
GR - Grecia 19
CZ - Repubblica Ceca 17
IR - Iran 15
IL - Israele 14
IQ - Iraq 14
ID - Indonesia 12
PY - Paraguay 11
RO - Romania 10
EU - Europa 9
LT - Lituania 8
VE - Venezuela 8
CO - Colombia 7
PE - Perù 7
PK - Pakistan 7
DO - Repubblica Dominicana 5
MA - Marocco 5
MY - Malesia 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
CL - Cile 4
HN - Honduras 4
UZ - Uzbekistan 4
KE - Kenya 3
LB - Libano 3
MD - Moldavia 3
CR - Costa Rica 2
DK - Danimarca 2
DZ - Algeria 2
EG - Egitto 2
GE - Georgia 2
MK - Macedonia 2
NP - Nepal 2
OM - Oman 2
SA - Arabia Saudita 2
SN - Senegal 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CH - Svizzera 1
CY - Cipro 1
ET - Etiopia 1
GD - Grenada 1
HU - Ungheria 1
JM - Giamaica 1
JO - Giordania 1
KN - Saint Kitts e Nevis 1
KZ - Kazakistan 1
NO - Norvegia 1
PA - Panama 1
PH - Filippine 1
PS - Palestinian Territory 1
RS - Serbia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TG - Togo 1
TW - Taiwan 1
UY - Uruguay 1
Totale 19.027
Salva come PNG Salva come JPEG
Città #
Singapore 1.220
Jacksonville 1.136
Chandler 895
Dublin 803
Southend 603
Beijing 468
Ashburn 421
Princeton 395
Izmir 383
Dallas 376
Nanjing 335
Wilmington 250
Dearborn 237
Los Angeles 212
Cambridge 190
The Dalles 183
Tongling 143
Chieti 138
Nanchang 138
Grafing 126
Munich 122
Santa Clara 119
Buffalo 114
Boardman 104
Altamura 103
Vienna 94
New York 91
Ann Arbor 88
Dong Ket 76
Woodbridge 76
Shenyang 70
Hebei 66
Ho Chi Minh City 64
Kunming 60
Tianjin 59
Grevenbroich 45
Jiaxing 44
Washington 42
Hanoi 41
São Paulo 41
Hangzhou 38
Jinan 38
Pescara 37
Brooklyn 35
Helsinki 34
Hefei 32
Redondo Beach 32
Montreal 30
Rome 30
Seoul 30
Augusta 29
Kocaeli 29
San Mateo 29
Tokyo 29
Warsaw 28
Chicago 27
Norwalk 27
Council Bluffs 26
Houston 25
Toronto 25
Changsha 24
Orange 24
Seattle 24
Ningbo 23
Zhengzhou 23
Atlanta 20
Hong Kong 20
Johannesburg 20
Milan 20
Guangzhou 19
Lanzhou 19
London 18
San Francisco 18
Stockholm 18
Denver 17
Kraków 16
Mexico City 16
Orem 16
Düsseldorf 15
Leawood 15
Manchester 15
Brussels 14
Chennai 14
Rio de Janeiro 14
Auburn Hills 13
Brno 13
Changchun 12
Poplar 12
Ankara 11
Ardabil 11
Boston 11
Campinas 11
Moscow 11
Phoenix 11
Quito 11
Turku 11
Belo Horizonte 10
Brasília 10
Teramo 10
Frankfurt am Main 9
Totale 11.400
Salva come PNG Salva come JPEG
Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 179
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 169
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 165
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 162
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 160
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 158
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 157
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 155
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 154
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 154
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 153
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 148
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 143
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 142
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 138
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 138
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 134
A new case of pure partial 7q duplication 134
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 132
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 132
[Chromosome anomalies and Waldenström's macroglobulinemia]. 129
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 128
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 127
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 127
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 127
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 126
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 125
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 125
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 124
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 123
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 123
X/Y translocation in a family with Leri-Weill dyschondrosteosis 122
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 122
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 122
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 119
Concerns about using Zn supplementation in Down's syndrome (DS) children. 118
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 118
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 118
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 118
I nuovi orizzonti della diagnosi prenatale 117
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 117
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 117
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 117
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 117
Characterization of novel genes in AZF regions 116
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 115
Allogeneic bone marrow transplantation for Fanconi anemia. 114
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 114
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 113
Karyologic analysis in erythroleukemia 113
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 113
SHOX mutations detected by FISH and direct sequencing in patients with short stature 113
A case of triploidy detected by crosstrimester test. 113
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 113
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 113
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 112
[Chromosomal proteins during ontogenesis of Gallus gallus. III. Non-histone proteins in the heart]. 112
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 112
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 111
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 110
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 110
Male infertility: role of genetic background 109
Cytogenetic survey of benign prostate hyperplasia 109
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 108
Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease 108
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 108
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 107
[Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17]. 107
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 106
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 106
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 105
Non-invasive prenatal screening: a 20-year experience in Italy 105
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 104
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 104
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 104
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 103
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 103
[Characterization of proteases contained in the non-histone protein fraction of the chromatin in human lymphocytes]. 103
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 102
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 102
[Cytogenetics in bone marrow transplantations. II. Acute lymphocytic leukemia]. 102
[Karyotype in chronic myeloid leukemia in a blastic crisis. I. Monosomy 16]. 102
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 102
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 102
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 102
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 101
Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH: a useful lesson. 101
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. 100
Different approaches in the molecular analysis of the SHOX gene dysfunctions 100
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. 99
MS-MLPA analysis for FMR1 gene: evaluation in a routine diagnostic setting 99
Morphometric and functional study of apoptotic cell chromatin 98
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 98
[Cytogenetic study of 140 patients with changes in sexual features]. 98
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 97
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 97
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 96
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 95
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 95
Van der Woude syndrome: variable expressivity through four generations 94
Totale 11.831
Salva come PNG Salva come JPEG
Categoria #
all - tutte 74.478
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 74.478
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021987 0 0 0 0 0 250 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
2024/20252.994 227 412 360 98 86 46 80 105 383 183 373 641
2025/20263.174 580 320 669 865 651 89 0 0 0 0 0 0
Totale 19.287