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European Journal of Human Genetics : EJHG|February 16, 2017
Coffee consumption is associated with DNA methylation levels of human bloodYu-Hsuan Chuang, Austin Quach, Devin Absher, et al.
European Journal of Human Genetics : EJHG|February 23, 2017
Prevalence of congenital amusiaIsabelle Peretz, Dominique T Vuvan
European Journal of Human Genetics : EJHG|March 9, 2017
Genetics of the peloponnesean populations and the theory of extinction of the medieval peloponnesean GreeksGeorge Stamatoyannopoulos, Aritra Bose, Athanasios Teodosiadis, et al.
European Journal of Human Genetics : EJHG|March 9, 2017
Ancient mitochondrial lineages support the prehistoric maternal root of Basques in Northern Iberian PeninsulaLeire Palencia-Madrid, Sergio Cardoso, Christine Keyser, et al.
European Journal of Human Genetics : EJHG|March 16, 2017
A novel recessive TTN founder variant is a common cause of distal myopathy in the Serbian populationStojan Perić, Jelena Nikodinović Glumac, Ana Töpf, et al.
European Journal of Human Genetics : EJHG|March 16, 2017
A mutation in the TMEM65 gene results in mitochondrial myopathy with severe neurological manifestationsAisha Nazli, Adeel Safdar, Ayesha Saleem, et al.
European Journal of Human Genetics : EJHG|March 16, 2017
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden deathNajim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, et al.
European Journal of Human Genetics : EJHG|February 5, 2021
Origins of human genetics. A personal perspectiveEberhard Passarge
European Journal of Human Genetics : EJHG|September 19, 2019
Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variantSunitha Balaraju, Ana Töpf, Grace McMacken, et al.
European Journal of Human Genetics : EJHG|September 19, 2019
Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet databaseStéphanie Nguengang Wakap, Deborah M Lambert, Annie Olry, et al.
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