The genomic history of southeastern Europe
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 …
associated with migrants from Anatolia who settled in the southeast before spreading …
[КНИГА][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 …
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
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 …
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
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 …
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 …
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 …
donors among presumed D-negative blood donors. Units donated by such donors pose a …
Sequence diversity of the Rh blood group system in Basques
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 …
them as an isolated and unique population within Europe, such as their non-Indo-European …
Noninvasive fetal blood group ty**
CE van der Schoot, D Winkelhorst… - … Prenatal Testing (NIPT), 2018 - Elsevier
Noninvasive fetal genoty** for alloantigens of blood cells is indicated in relation to
hemolytic disease of the fetus and newborn (HDFN) and fetal neonatal alloimmune …
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
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 …
reported in 75% of the human genome. However, it is underreported in African populations …
Variation of rhesus haplotype frequencies in North Africans and in worldwide population analyses
AB Halima, R Bahri, E Esteban, P Moral… - International Journal of …, 2015 - Taylor & Francis
Abstract The Rhesus (Rh) blood group system is one of the most highly polymorphic genetic
systems used in the investigation of human genetic relationships. In this paper the …
systems used in the investigation of human genetic relationships. In this paper the …