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European Journal of Medical Genetics|July 22, 2018
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variantValtter B Virtanen, Perttu P Salo, Jia Cao, et al.
European Heart Journal|October 4, 2020
Development and validation of two SCORE-based cardiovascular risk prediction models for Eastern Europe: a multicohort studyTaavi Tillmann, Kristi Läll, Oliver Dukes, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 31, 2010
Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palateTiit Nikopensius, Triin Jagomägi, Kaarel Krjutskov, et al.
European Journal of Human Genetics : EJHG|November 20, 2014
BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert CentresGert-Jan B van Ommen, Outi Törnwall, Christian Bréchot, et al.
Public Health Nutrition|March 10, 2011
Feasibility of innovative dietary assessment in epidemiological studies using the approach of combining different assessment instrumentsAnne-Kathrin Illner, Ulrich Harttig, Gianluca Tognon, et al.
Plos Genetics|March 2, 2017
Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cellsSilva Kasela, Kai Kisand, Liina Tserel, et al.
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
Epigenetics|December 2, 2014
Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placentaTauno Metsalu, Triin Viltrop, Airi Tiirats, et al.
International Journal of Obesity (2005)|May 30, 2020
Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolomeYu-Han H Hsu, Christina M Astley, Joanne B Cole, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 5, 2011
Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palateTiit Nikopensius, Inga Kempa, Laima Ambrozaitytė, et al.
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