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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.Clinical Research in Cardiology : Official Journal of the German Cardiac Society|August 20, 2022
Genetic and modifiable risk factors combine multiplicatively in common diseaseShichao Pang, Loic Yengo, Christopher P Nelson, et al.Nature|February 28, 2014
Detection and replication of epistasis influencing transcription in humansGibran Hemani, Konstantin Shakhbazov, Harm-Jan Westra, et al.Pageof 42