IRIS
PALKA, Giandomenico
 Distribuzione geografica
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Continente #
EU - Europa 5.691
NA - Nord America 4.830
AS - Asia 2.678
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 5
OC - Oceania 3
AF - Africa 1
Totale 13.218
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Nazione #
US - Stati Uniti d'America 4.805
CN - Cina 1.240
UA - Ucraina 1.080
IE - Irlanda 809
IT - Italia 798
GB - Regno Unito 692
SE - Svezia 690
TR - Turchia 686
FR - Francia 558
DE - Germania 515
IN - India 505
FI - Finlandia 195
RU - Federazione Russa 160
SG - Singapore 128
AT - Austria 92
VN - Vietnam 78
CA - Canada 23
BE - Belgio 20
GR - Grecia 18
CZ - Repubblica Ceca 16
PL - Polonia 16
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
BD - Bangladesh 1
CH - Svizzera 1
CL - Cile 1
CY - Cipro 1
EC - Ecuador 1
ES - Italia 1
HU - Ungheria 1
LT - Lituania 1
MK - Macedonia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 13.218
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Città #
Jacksonville 1.141
Chandler 904
Dublin 807
Southend 603
Princeton 397
Izmir 383
Nanjing 338
Wilmington 250
Dearborn 237
Beijing 220
Ashburn 215
Cambridge 191
Chieti 139
Nanchang 138
Grafing 126
Boardman 105
Altamura 104
Vienna 92
Ann Arbor 88
Singapore 79
Dong Ket 76
Woodbridge 76
Shenyang 70
Hebei 66
Kunming 60
Tianjin 57
Grevenbroich 45
Jiaxing 44
Washington 40
Hangzhou 38
Jinan 38
Los Angeles 34
Pescara 34
Kocaeli 29
New York 29
San Mateo 29
Norwalk 27
Augusta 26
Changsha 24
Orange 24
Ningbo 23
Rome 23
Zhengzhou 22
Lanzhou 21
Houston 18
Munich 17
Guangzhou 16
Kraków 16
Düsseldorf 15
Leawood 15
Brno 14
Auburn Hills 13
Brussels 13
Toronto 13
Changchun 12
Hefei 12
Helsinki 12
Seattle 12
Ardabil 11
Milan 11
Moscow 11
Teramo 10
Sartrouville 8
Atessa 7
Bangalore 7
Mumbai 7
Vasto 7
Montesilvano Marina 6
Naples 6
Taizhou 6
Waanrode 6
Bellante 5
Caserta 5
Clifton 5
Fuzhou 5
Tortoreto 5
Andover 4
Bari 4
Bologna 4
Campobasso 4
Cluj-napoca 4
Collecorvino 4
Falls Church 4
Florence 4
L'aquila 4
London 4
Ottawa 4
Parma 4
Redwood City 4
Roseto Degli Abruzzi 4
Walnut 4
Agnone 3
Alingsås 3
Bucharest 3
Chicago 3
Chisinau 3
Edinburgh 3
Genova 3
Haikou 3
Kagoshima 3
Totale 7.925
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Nome #
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 143
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 142
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 135
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 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 115
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 113
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 111
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 110
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 109
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 106
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 102
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 101
BRCA1 AND BRCA2 MUTATION IN BREAST/OVARIAN CANCER PATIENTS FROM CENTRAL ITALY 100
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 99
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 99
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 98
X/Y translocation in a family with Leri-Weill dyschondrosteosis 96
[Chromosome anomalies and Waldenström's macroglobulinemia]. 96
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 95
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 95
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 94
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 93
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 93
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 93
A new case of pure partial 7q duplication 92
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 91
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 90
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 90
Karyologic analysis in erythroleukemia 87
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 87
I nuovi orizzonti della diagnosi prenatale 86
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 86
SHOX mutations detected by FISH and direct sequencing in patients with short stature 86
Characterization of novel genes in AZF regions 86
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 85
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 85
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 85
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 84
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 84
Concerns about using Zn supplementation in Down's syndrome (DS) children. 83
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 83
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 83
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 81
Male infertility: role of genetic background 81
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 81
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 81
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 81
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 81
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 80
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 80
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 80
Different approaches in the molecular analysis of the SHOX gene dysfunctions 80
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 79
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 79
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 78
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 78
A case of triploidy detected by crosstrimester test. 78
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 77
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 77
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 76
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 76
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 76
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 76
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 75
Cytogenetic survey of benign prostate hyperplasia 75
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 74
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 74
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 73
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 73
Prenatal diagnosis using the triple test 73
Van der Woude syndrome: variable expressivity through four generations 72
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 72
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 72
Morphometric and functional study of apoptotic cell chromatin 71
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 71
Growth delay in Down syndrome and zinc sulphate supplementation 71
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 71
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 70
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 70
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 70
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 70
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 70
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 70
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 69
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 69
Correlation between apoptosis and TP53 status in osteosarcoma 69
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 69
Molecular studies in three patients with isodicentric Y chromosome 69
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 69
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 69
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 69
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. 68
Gemelli Down con pluri-malformazioni. Rilievi sulla "concordanza" delle anomalie 68
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 68
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 68
[Analysis of the nonhistone chromosomal proteins during ontogenesis. I. NHCP of the leg muscle in Gallus gallus]. 68
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 67
Genotype-Phenotype Correlations and Clinical Diagnostic Criteria in Wolf-Hirschhorn Syndrome 67
FISH analysis in detecting 9p duplication (p22p24) 67
Genetic testing in couples undergoing assisted reproduction technique protocols 67
Totale 8.374
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Categoria #
all - tutte 43.210
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 43.210
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.753 0 188 10 73 215 184 348 247 57 166 256 9
2020/20211.471 194 7 199 7 67 259 16 20 282 219 86 115
2021/2022860 22 10 3 143 83 136 15 57 50 10 105 226
2022/20232.771 229 365 184 283 262 578 174 211 325 21 72 67
2023/20241.194 81 36 101 32 70 399 238 53 6 31 13 134
2024/2025233 227 6 0 0 0 0 0 0 0 0 0 0
Totale 13.451