User profiles for Francesco Cali

Francesco Calì

Associazione 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

…, F Berrada, CM Bravi, F Brisighelli, GBJ Busby, F Cali… - Nature, 2014 - nature.com
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 …

[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 …

[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, …

[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 …

[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 …

Dramatic brain aminergic deficit in a genetic mouse model of phenylketonuria

…, S Cabib, T Pascucci, R Ventura, F Cali… - …, 2000 - journals.lww.com
Clinical data suggest that brain catecholamines and serotonin are deficient in phenylketonuria
(PKU), an inherited metabolic disorder that causes severe mental retardation and …

Population structure in the Mediterranean basin: AY chromosome perspective

C Capelli, N Redhead, V Romano, F Calì… - Annals of Human …, 2006 - Wiley Online Library
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 …

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 …

[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 …

A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy

L Vetri, F Calì, M Vinci, C Amato, M Roccella… - European Journal of …, 2020 - Elsevier
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 …