Research graph
References from AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics. Local targets link to admitted publications; unresolved targets remain external evidence.
10.1038/nature11632
10.1038/nature11632 · External reference
10.1007/s00439-013-1344-x
10.1007/s00439-013-1344-x · External reference
10.1371/journal.pgen.1004030
10.1371/journal.pgen.1004030 · External reference
Evolution in health and medicine Sackler colloquium: consanguinity, human evolution, and complex diseases
10.1073/pnas.0906079106 · 2010 · External reference
10.1073/pnas.1606460113
10.1073/pnas.1606460113 · External reference
10.1086/302661
10.1086/302661 · External reference
10.1002/humu.20383
10.1002/humu.20383 · External reference
10.1038/nrg.2017.109
10.1038/nrg.2017.109 · External reference
10.1016/j.ajhg.2015.06.001
10.1016/j.ajhg.2015.06.001 · External reference
10.1093/bioinformatics/btr330
10.1093/bioinformatics/btr330 · External reference
10.1093/bioinformatics/btu149
10.1093/bioinformatics/btu149 · External reference
Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
10.1038/ejhg.2015.17 · 2015 · External reference
10.1038/nature14618
10.1038/nature14618 · External reference
10.1016/j.ajhg.2016.08.007
10.1016/j.ajhg.2016.08.007 · External reference
10.1371/journal.pgen.1000353
10.1371/journal.pgen.1000353 · External reference
Schizophrenia Psychiatric Genome-Wide Association Study Consortium. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
10.1371/journal.pgen.1002656 · 2012 · External reference
10.1371/journal.pone.0013996
10.1371/journal.pone.0013996 · External reference
10.1073/pnas.0710021104
10.1073/pnas.0710021104 · External reference
10.1093/bioinformatics/btu401
10.1093/bioinformatics/btu401 · External reference
10.1016/j.ajhg.2008.08.007
10.1016/j.ajhg.2008.08.007 · External reference
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
10.1371/journal.pgen.1000415 · 2009 · External reference
10.1007/s10048-009-0182-4
10.1007/s10048-009-0182-4 · External reference
10.1093/bioinformatics/btw044
10.1093/bioinformatics/btw044 · External reference
10.1038/jhg.2016.120
10.1038/jhg.2016.120 · External reference
Genomic patterns of homozygosity in worldwide human populations
10.1016/j.ajhg.2012.06.014 · 2012 · External reference
Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies
10.1159/000362412 · 2014 · External reference
10.1371/journal.pone.0082154
10.1371/journal.pone.0082154 · External reference
10.1086/519795
10.1086/519795 · External reference
Greater Middle East Variome Consortium, Alkuraya FS, Casanova JL, Gleeson JG. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
10.1038/ng.3592 · 2016 · External reference
10.1093/nar/gkp369
10.1093/nar/gkp369 · External reference
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome
10.1371/journal.pgen.1005097 · 2015 · External reference
10.1371/journal.pone.0028787
10.1371/journal.pone.0028787 · External reference
10.1002/mgg3.115
10.1002/mgg3.115 · External reference
10.1016/j.ajhg.2013.05.003
10.1016/j.ajhg.2013.05.003 · External reference
10.1002/humu.22728
10.1002/humu.22728 · External reference
10.1101/gr.168393.113
10.1101/gr.168393.113 · External reference
10.1086/503875
10.1086/503875 · External reference
10.1002/humu.21432
10.1002/humu.21432 · External reference
