Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases
about
Estimating the inbreeding depression on cognitive behavior: a population based study of child cohortConsanguineous marriages : Preconception consultation in primary health care settingsThe Impact of Evolutionary Driving Forces on Human Complex Diseases: A Population Genetics ApproachImportance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene FunctionsPairomics, the omics way to mate choiceImplementing risk-stratified screening for common cancers: a review of potential ethical, legal and social issuesIdentifying disease mutations in genomic medicine settings: current challenges and how to accelerate progressGenotype-phenotype correlations in a mountain population community with high prevalence of Wilson's disease: genetic and clinical homogeneityObserved and expected frequencies of structural hemoglobin variants in newborn screening surveys in Africa and the Middle East: deviations from Hardy-Weinberg equilibriumRoyal dynasties as human inbreeding laboratories: the HabsburgsThe emergence of human-evolutionary medical genomicsThe existence of species rests on a metastable equilibrium between inbreeding and outbreeding. An essay on the close relationship between speciation, inbreeding and recessive mutations.Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia.Genetics of consanguinity and inbreeding in health and disease.Origin and schizophrenia in young refugees and inter-country adoptees from Latin America and East Africa in Sweden: a comparative study.Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmesThe low frequency of recessive disease: insights from ENU mutagenesis, severity of disease phenotype, GWAS associations, and demography: an analytical review.Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy.Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study.Fitness consequences of spousal relatedness in 46 small-scale societies.Random inbreeding, isonymy, and population isolates in Argentina.Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?Evolution in health and medicine Sackler colloquium: Evolutionary perspectives on health and medicine.Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi familiesQuantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism dataPopulation-genetic influences on genomic estimates of the inbreeding coefficient: a global perspectiveRuns of homozygosity implicate autozygosity as a schizophrenia risk factor.Biased gene conversion skews allele frequencies in human populations, increasing the disease burden of recessive allelesIs consanguinity prevalence decreasing in Saudis?: A study in two generations.Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant BehaviorUnexpected relationships and inbreeding in HapMap phase III populations.Impact of consanguineous marriages and degrees of inbreeding on fertility, child mortality, secondary sex ratio, selection intensity, and genetic load: a cross-sectional study from Northern India.Impact of consanguinity on cardio-metabolic health and other diseases: findings from an Afro-Indian tribal communityAssessing the influence of consanguinity on congenital heart disease.How obedience of marriage rules may counteract genetic drift.A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka.Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families.The shifting geography and language of cell biology.Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.UK Pakistani views on the adverse health risks associated with consanguineous marriages.
P2860
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P2860
Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Evolution in health and medici ...... volution, and complex diseases
@ast
Evolution in health and medici ...... volution, and complex diseases
@en
Evolution in health and medici ...... volution, and complex diseases
@nl
type
label
Evolution in health and medici ...... volution, and complex diseases
@ast
Evolution in health and medici ...... volution, and complex diseases
@en
Evolution in health and medici ...... volution, and complex diseases
@nl
prefLabel
Evolution in health and medici ...... volution, and complex diseases
@ast
Evolution in health and medici ...... volution, and complex diseases
@en
Evolution in health and medici ...... volution, and complex diseases
@nl
P2860
P3181
P356
P1476
Evolution in health and medici ...... volution, and complex diseases
@en
P2093
A H Bittles
P2860
P304
P3181
P356
10.1073/PNAS.0906079106
P407
P433
P478
107 Suppl 1
P577
2010-01-26T00:00:00Z