PALKA, Giandomenico
 Distribuzione geografica
Continente #
EU - Europa 5.619
NA - Nord America 4.830
AS - Asia 2.565
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 5
OC - Oceania 3
AF - Africa 1
Totale 13.033
Nazione #
US - Stati Uniti d'America 4.805
CN - Cina 1.249
UA - Ucraina 1.088
IE - Irlanda 842
IT - Italia 812
GB - Regno Unito 697
SE - Svezia 697
TR - Turchia 688
FR - Francia 557
IN - India 510
DE - Germania 502
FI - Finlandia 194
AT - Austria 92
VN - Vietnam 76
BE - Belgio 45
CA - Canada 23
RU - Federazione Russa 22
GR - Grecia 18
PL - Polonia 16
IR - Iran 15
IL - Israele 13
NL - Olanda 13
RO - Romania 10
EU - Europa 9
CZ - Repubblica Ceca 5
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
SG - Singapore 1
SK - Slovacchia (Repubblica Slovacca) 1
TW - Taiwan 1
Totale 13.033
Città #
Jacksonville 1.151
Chandler 913
Dublin 840
Southend 607
Princeton 402
Izmir 384
Nanjing 340
Wilmington 253
Dearborn 237
Beijing 221
Ashburn 217
Cambridge 192
Chieti 147
Nanchang 138
Grafing 127
Altamura 104
Vienna 92
Ann Arbor 88
Dong Ket 76
Woodbridge 76
Shenyang 71
Boardman 69
Hebei 66
Kunming 61
Tianjin 58
Grevenbroich 45
Jiaxing 44
Washington 41
Hangzhou 39
Brussels 38
Jinan 38
Kocaeli 29
New York 29
Pescara 29
San Mateo 29
Norwalk 27
Augusta 26
Changsha 26
Orange 24
Ningbo 23
Zhengzhou 22
Lanzhou 21
Rome 21
Houston 18
Guangzhou 16
Kraków 16
Düsseldorf 15
Leawood 15
Auburn Hills 13
Toronto 13
Changchun 12
Hefei 12
Seattle 12
Ardabil 11
Milan 11
Helsinki 10
Los Angeles 9
Teramo 9
Sartrouville 8
Atessa 7
Bangalore 7
Mumbai 7
Vasto 7
Montesilvano Marina 6
Taizhou 6
Waanrode 6
Bellante 5
Caserta 5
Fuzhou 5
L'aquila 5
Tortoreto 5
Andover 4
Bari 4
Bologna 4
Brno 4
Campobasso 4
Chicago 4
Cluj-napoca 4
Collecorvino 4
Edinburgh 4
Falls Church 4
Florence 4
London 4
Ottawa 4
Redwood City 4
Roseto Degli Abruzzi 4
Walnut 4
Agnone 3
Alingsås 3
Bucharest 3
Chisinau 3
Genova 3
Haikou 3
Kagoshima 3
Kuala Lumpur 3
L’Aquila 3
Melendugno 3
Montesilvano 3
Naples 3
Notaresco 3
Totale 7.855
Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 141
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 139
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. 133
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 128
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis. 114
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 114
Hsa-miR-155-5p drives aneuploidy at early stages of cellular transformation 110
Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion. 109
Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis 108
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 107
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 105
Two novel mutations affecting splicing in the IRF6 gene associated with van der Woude syndrome 101
Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women 101
Deregulation of Sertoli and Leyding cells function in patients with Klinefelter Syndrome as evidenced by testis transcriptome analysis. 99
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 98
BRCA1 AND BRCA2 MUTATION IN BREAST/OVARIAN CANCER PATIENTS FROM CENTRAL ITALY 97
A new case of "de novo" BRCA1 mutation in a patient with early-onset breast cancer 96
X/Y translocation in a family with Leri-Weill dyschondrosteosis 95
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 94
An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations 94
Y-chromosomal DNA haplotype differences in control and infertile Italian subpopulations. 93
Mutations of APC and MYH in unrelated Italian patients with adenomatous polyposis coli 91
Use of the MLPA Assay in the Molecular Diagnosis of GeneCopy Number Alterations in Human Genetic Diseases 91
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 90
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 90
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 89
A new case of pure partial 7q duplication 89
BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Italy 88
[Chromosome anomalies and Waldenström's macroglobulinemia]. 88
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 86
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 86
I nuovi orizzonti della diagnosi prenatale 85
SHOX mutations detected by FISH and direct sequencing in patients with short stature 85
Karyologic analysis in erythroleukemia 84
Relationship between Y-chromosomal DNA haplotype and sperm count in Italy. 84
Human amniotic fluid stem cells culture onto titanium screws: a new perspective for bone engineering. 84
Characterization of novel genes in AZF regions 84
Male infertility: role of genetic background 83
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 83
Karyotype in chronic myeloid leukemia in a blastic crisis. II. Trisomy 17 82
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 82
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 81
Correlation between mutations and mRNA expression of APC and MUTYH genes: New insight into hereditary colorectal polyposis predisposition 81
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 81
Trisomy 18 fetuses with cystic hygroma linked to positive maternal serum Down's syndrome Triple test screening result. 80
Concerns about using Zn supplementation in Down's syndrome (DS) children. 80
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 80
Different approaches in the molecular analysis of the SHOX gene dysfunctions 80
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. 79
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 79
Is zinc deficiency a cause of subclinical hypothyroidism in Down syndrome? 79
Germline allele-specific expression of APC and MUTYH in mutation-negative patients with multiple colorectal adenomas and/ or colorectal cancer 78
Vitamin E induction of experimental allergic encephalomyelitis in the Lewis rat. 78
Correlation Between Down's Syndrome and Malformations of Pediatric Surgical Interest 77
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 77
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 77
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 76
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 76
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 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 75
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 75
[Analysis of cellular components in immunocompetent organs treated with ionizing radiations]. 75
Hnrnpl restrains MIR-155 targeting of BUB1 to stabilize aberrant karyotypes of transformed cells in chronic lymphocytic leukemia 75
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 74
High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. 73
Espressione allelica del gene MYH in pazienti con poliposi, APC-negativi 73
A case of triploidy detected by crosstrimester test. 73
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 72
Prenatal diagnosis using the triple test 72
Cytogenetic survey of benign prostate hyperplasia 72
[Analysis of nonhistone chromosomal proteins during ontogenesis. II. NHCP of the neck muscle in Gallus gallus]. 72
Van der Woude syndrome: variable expressivity through four generations 71
Morphometric and functional study of apoptotic cell chromatin 71
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 71
Polymorphisms of chemokine receptor genes in Alzheimer's and Parkinson's Patients 71
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 71
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 70
Correlation between apoptosis and TP53 status in osteosarcoma 69
Gene expression modifications in Wharton's Jelly mesenchymal stem cells promoted by prolonged in vitro culturing 69
Detection of pre-apoptotic stage by "in situ" nick translation in peripheral blood leucocyte of patients with Down syndrome and HIV infection 68
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 68
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 68
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 68
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 68
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 67
Immature granulocytic precursors are present in the peripheral blood of Down's subjects and disappear after zinc therapy 67
Growth delay in Down syndrome and zinc sulphate supplementation 67
Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome. 67
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 67
Molecular studies in three patients with isodicentric Y chromosome 67
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 67
[Analysis of the nonhistone chromosomal proteins during ontogenesis. I. NHCP of the leg muscle in Gallus gallus]. 67
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 67
Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3 67
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 67
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 66
Genetic testing in couples undergoing assisted reproduction technique protocols 66
Gemelli Down con pluri-malformazioni. Rilievi sulla "concordanza" delle anomalie 66
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 66
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 66
Totale 8.266
Categoria #
all - tutte 37.024
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 37.024


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019610 0 0 0 0 0 0 0 0 21 26 15 548
2019/20202.590 802 189 10 73 222 184 350 250 58 183 260 9
2020/20211.505 199 9 201 9 70 263 20 22 284 225 86 117
2021/2022890 22 14 6 147 86 137 15 60 55 11 106 231
2022/20232.862 234 368 186 284 263 585 204 223 337 26 78 74
2023/20241.044 85 39 103 33 81 404 239 53 7 0 0 0
Totale 13.314