The genomic history of southeastern Europe

I Mathieson, S Alpaslan-Roodenberg, C Posth… - Nature, 2018 - nature.com
Farming was first introduced to Europe in the mid-seventh millennium bc, and was
associated with migrants from Anatolia who settled in the southeast before spreading …

[图书][B] Human evolutionary genetics: origins, peoples and disease

M Jobling, C Tyler-Smith - 2019 - taylorfrancis.com
Human Evolutionary Genetics is a groundbreaking text which for the first time brings
together molecular genetics and genomics to the study of the origins and movements of …

Association of a germline copy number polymorphism of APOBEC3A and APOBEC3B with burden of putative APOBEC-dependent mutations in breast cancer

S Nik-Zainal, DC Wedge, LB Alexandrov, M Petljak… - Nature …, 2014 - nature.com
The somatic mutations in a cancer genome are the aggregate outcome of one or more
mutational processes operative through the lifetime of the individual with cancer,,. Each …

[HTML][HTML] CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank

T Fitzgerald, E Birney - Cell Genomics, 2022 - cell.com
Copy number variation (CNV) is known to influence human traits, having a rich history of
research into common and rare genetic disease, and although CNV is accepted as an …

More evidence for widespread antagonistic pleiotropy in polymorphic disease alleles

C Lockwood, AS Vo, H Bellafard, AJR Carter - Frontiers in Genetics, 2024 - frontiersin.org
Introduction Many loci segregate alleles classified as “genetic diseases” due to their
deleterious effects on health. However, some disease alleles have been reported to show …

RHD PCR of D-Negative Blood Donors

FF Wagner - Transfusion Medicine and Hemotherapy, 2013 - karger.com
RHD PCR of blood donors may be used to reveal weak D, partial D, DEL and chimeric D+/D-
donors among presumed D-negative blood donors. Units donated by such donors pose a …

Sequence diversity of the Rh blood group system in Basques

A Flores-Bello, D Mas-Ponte, ME Rosu… - European Journal of …, 2018 - nature.com
Basques show specific cultural, demographic, and genetic characteristics that have placed
them as an isolated and unique population within Europe, such as their non-Indo-European …

Noninvasive fetal blood group typing

CE van der Schoot, D Winkelhorst… - … Prenatal Testing (NIPT), 2018 - Elsevier
Noninvasive fetal genotyping for alloantigens of blood cells is indicated in relation to
hemolytic disease of the fetus and newborn (HDFN) and fetal neonatal alloimmune …

Copy number variation in human genomes from three major ethno-linguistic groups in Africa

OA Nyangiri, H Noyes, J Mulindwa, H Ilboudo… - BMC genomics, 2020 - Springer
Background Copy number variation is an important class of genomic variation that has been
reported in 75% of the human genome. However, it is underreported in African populations …

[图书][B] Les groupes sanguins érythrocytaires

P Bailly, J Chiaroni, F Roubinet - 2015 - researchgate.net
Attention cet ouvrage est important. Par l'originalité de son sujet, la qualité de ses auteurs,
son apport à la médecine, il est une référence en la matière. Je suis fier que l'Établissement …