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Alberto Magi, Tania Giangregorio, Roberto Semeraro, Giulia Carangelo, Flavia Palombo, Giovanni Cara Romeo, Marco Seri, Tommaso Pippucci
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10.1038/nature11632
10.1038/nature11632
10.1007/s00439-013-1344-x
10.1007/s00439-013-1344-x
10.1371/journal.pgen.1004030
10.1371/journal.pgen.1004030
Evolution in health and medicine Sackler colloquium: consanguinity, human evolution, and complex diseases
10.1073/pnas.0906079106 · 2010
10.1073/pnas.1606460113
10.1073/pnas.1606460113
10.1086/302661
10.1086/302661
10.1002/humu.20383
10.1002/humu.20383
10.1038/nrg.2017.109
10.1038/nrg.2017.109
10.1016/j.ajhg.2015.06.001
10.1016/j.ajhg.2015.06.001
10.1093/bioinformatics/btr330
10.1093/bioinformatics/btr330
10.1093/bioinformatics/btu149
10.1093/bioinformatics/btu149
Genome-wide inbreeding estimation within Lebanese communities using SNP arrays
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
europepmc
Confidence 96%
openalex
Confidence 95%
unpaywall
Confidence 95%
doaj
Confidence 92%
datacite
Confidence 0%
10.1038/ejhg.2015.17 · 2015
10.1038/nature14618
10.1038/nature14618
10.1016/j.ajhg.2016.08.007
10.1016/j.ajhg.2016.08.007
10.1371/journal.pgen.1000353
10.1371/journal.pgen.1000353
Schizophrenia Psychiatric Genome-Wide Association Study Consortium. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
10.1371/journal.pgen.1002656 · 2012
10.1371/journal.pone.0013996
10.1371/journal.pone.0013996
10.1073/pnas.0710021104
10.1073/pnas.0710021104
10.1093/bioinformatics/btu401
10.1093/bioinformatics/btu401
10.1016/j.ajhg.2008.08.007
10.1016/j.ajhg.2008.08.007
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
10.1371/journal.pgen.1000415 · 2009
10.1007/s10048-009-0182-4
10.1007/s10048-009-0182-4
10.1093/bioinformatics/btw044
10.1093/bioinformatics/btw044
10.1038/jhg.2016.120
10.1038/jhg.2016.120
Genomic patterns of homozygosity in worldwide human populations
10.1016/j.ajhg.2012.06.014 · 2012
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
10.1371/journal.pone.0082154
10.1371/journal.pone.0082154
10.1086/519795
10.1086/519795
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
10.1093/nar/gkp369
10.1093/nar/gkp369
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome
10.1371/journal.pgen.1005097 · 2015
10.1371/journal.pone.0028787
10.1371/journal.pone.0028787
10.1002/mgg3.115
10.1002/mgg3.115
10.1016/j.ajhg.2013.05.003
10.1016/j.ajhg.2013.05.003
10.1002/humu.22728
10.1002/humu.22728
10.1101/gr.168393.113
10.1101/gr.168393.113
10.1086/503875
10.1086/503875
10.1002/humu.21432
10.1002/humu.21432
No additional external references are available.