User profiles for Francesco Cali
Francesco CalìAssociazione OASI M SS IRCCS Troina EN Italy Verified email at oasi.en.it Cited by 4646 |
Ancient human genomes suggest three ancestral populations for present-day Europeans
We sequenced the genomes of a ∼7,000-year-old farmer from Germany and eight ∼8,000-year-old
hunter-gatherers from Luxembourg and Sweden. We analysed these and other …
hunter-gatherers from Luxembourg and Sweden. We analysed these and other …
[PDF][PDF] Tracing European founder lineages in the Near Eastern mtDNA pool
M Richards, V Macaulay, E Hickey, E Vega… - The American Journal of …, 2000 - cell.com
Founder analysis is a method for analysis of nonrecombining DNA sequence data, with the
aim of identification and dating of migrations into new territory. The method picks out founder …
aim of identification and dating of migrations into new territory. The method picks out founder …
[HTML][HTML] Phylogeographic analysis of haplogroup E3b (E-M215) Y chromosomes reveals multiple migratory events within and out of Africa
F Cruciani, R La Fratta, P Santolamazza… - The American Journal of …, 2004 - cell.com
We explored the phylogeography of human Y-chromosomal haplogroup E3b by analyzing
3,401 individuals from five continents. Our data refine the phylogeny of the entire haplogroup, …
3,401 individuals from five continents. Our data refine the phylogeny of the entire haplogroup, …
[PDF][PDF] The role of recent admixture in forming the contemporary West Eurasian genomic landscape
…, D Nesheva, P Anagnostou, F Cali… - Current biology, 2015 - cell.com
Over the past few years, studies of DNA isolated from human fossils and archaeological
remains have generated considerable novel insight into the history of our species. Several …
remains have generated considerable novel insight into the history of our species. Several …
[HTML][HTML] Identification of human D lactate dehydrogenase deficiency
GR Monroe, AM van Eerde, F Tessadori… - Nature …, 2019 - nature.com
Phenotypic and biochemical categorization of humans with detrimental variants can provide
valuable information on gene function. We illustrate this with the identification of two …
valuable information on gene function. We illustrate this with the identification of two …
Dramatic brain aminergic deficit in a genetic mouse model of phenylketonuria
Clinical data suggest that brain catecholamines and serotonin are deficient in phenylketonuria
(PKU), an inherited metabolic disorder that causes severe mental retardation and …
(PKU), an inherited metabolic disorder that causes severe mental retardation and …
Population structure in the Mediterranean basin: AY chromosome perspective
The Mediterranean region has been characterised by a number of pre‐historical and historical
demographic events whose legacy on the current genetic landscape is still a matter of …
demographic events whose legacy on the current genetic landscape is still a matter of …
Cell line DNA typing in forensic genetics—the necessity of reliable standards
R Szibor, J Edelmann, S Hering, I Plate, H Wittig… - Forensic science …, 2003 - Elsevier
The incorporation of reference DNA is crucial to the validation of any DNA typing protocol.
This paper aims to provide a panel of reference DNAs for actual forensic profiling strategies, ie …
This paper aims to provide a panel of reference DNAs for actual forensic profiling strategies, ie …
[HTML][HTML] Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome
…, PA Underhill, RJ King, V Romano, F Cali… - European Journal of …, 2009 - nature.com
The presence or absence of genetic heterogeneity in Sicily has long been debated.
Through the analysis of the variation of Y-chromosome lineages, using the combination of …
Through the analysis of the variation of Y-chromosome lineages, using the combination of …
A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy
An increasing number of developmental and epileptic encephalopathies have been correlated
with variants of ion channel genes, and in particular of potassium channels genes, such …
with variants of ion channel genes, and in particular of potassium channels genes, such …