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Pharmacogenomics|July 11, 2013
Functional diversity of the glutathione peroxidase gene family among human populations: implications for genetic predisposition to disease and drug responseRenato Polimanti, Maria Fuciarelli, Giovanni Destro-Bisol, et al.
Journal of Anthropological Sciences = Rivista Di Antropologia : JASS|December 24, 2021
The emerging complexity of Open Science: assessing Intelligent Data Openness in Genomic Anthropology and Human GenomicsPaolo Anagnostou, Marco Capocasa, Francesca Brisighelli, et al.
Plos One|March 24, 2015
When data sharing gets close to 100%: what human paleogenetics can teach the open science movementPaolo Anagnostou, Marco Capocasa, Nicola Milia, et al.
Human Biology|July 15, 2014
Reevaluating a model of gender-biased gene flow among Sub-Saharan Hunter-gatherers and farmersPaolo Anagnostou, Cinzia Battaggia, Marco Capocasa, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council|December 25, 2008
Tracing the distribution and evolution of lactase persistence in Southern Europe through the study of the T(-13910) variantPaolo Anagnostou, Cinzia Battaggia, Valentina Coia, et al.
American Journal of Physical Anthropology|May 17, 2005
Brief communication: mtDNA variation in North Cameroon: lack of Asian lineages and implications for back migration from Asia to sub-Saharan AfricaValentina Coia, Giovanni Destro-Bisol, Fabio Verginelli, et al.
Molecular Phylogenetics and Evolution|November 17, 2006
Phylogeography of the human mitochondrial L1c haplogroup: genetic signatures of the prehistory of Central AfricaChiara Batini, Valentina Coia, Cinzia Battaggia, et al.
Forensic Science International. Genetics|May 19, 2012
Using forensic microsatellites to decipher the genetic structure of linguistic and geographic isolates: A survey in the eastern Italian AlpsFrancesco Montinaro, Ilaria Boschi, Federica Trombetta, et al.
Plos One|February 19, 2013
Detecting genetic isolation in human populations: a study of European language minoritiesMarco Capocasa, Cinzia Battaggia, Paolo Anagnostou, et al.
Human Mutation|February 3, 2007
Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitisOrsolya Király, Arnaud Boulling, Heiko Witt, et al.
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