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Warrington, N.M.* et al.: Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Nat. Genet. 51, 804-814 (2019)
Bustamante, M.* et al.: A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. Hum. Mol. Genet. 25, 4127-4142 (2016)
Marinelli, M.* et al.: Heritability and genome-wide association analyses of sleep duration in children: The EAGLE Consortium. Sleep 39, 1859-1869 (2016)
Schulte, E.C. et al.: Rare variants in β-Amyloid Precursor Protein (APP) and Parkinson's disease. Eur. J. Hum. Genet. 23, 1328-1333 (2015)
van der Valk, R.J.* et al.: A novel common variant in DCST2 is associated with length in early life and height in adulthood. Hum. Mol. Genet. 24, 1155-1168 (2015)
Almouzni, G.* et al.: Relationship between genome and epigenome - challenges and requirements for future research. BMC Genomics 15:487 (2014)
Boraska, V.* et al.: A genome-wide association study of anorexia nervosa. Mol. Psychiatry 19, 1085-1094 (2014)
Esko, T.* et al.: Genetic characterization of Northeastern Italian population isolates in the context of broader European genetic diversity. Eur. J. Hum. Genet. 21, 659-665 (2013)
Horikoshi, M.* et al.: New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Nat. Genet. 45, 76-82 (2013)
Lappalainen, T.* et al.: Transcriptome and genome sequencing uncovers functional variation in humans. Nature 501, 506-511 (2013)
Müller, T.D. et al.: Fat mass and obesity-associated gene (FTO) in eating disorders: Evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa. Obes. Facts 5, 408-419 (2012)
Taal, H.R.* et al.: Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat. Genet. 44, 532-538 (2012)
Tsoi, L.C.* et al.: Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat. Genet. 44, 1341-1348 (2012)
Jacquemont, S.* et al.: Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 478, 97-102 (2011)
Rebordosa, C.* et al.: ADRB2 Gly16Arg polymorphism, asthma control and lung function decline. Eur. Respir. J. 38, 1029-1035 (2011)
Bergboer, J.G.M.* et al.: Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis. J. Invest. Dermatol. 130, 2057-2061 (2010)
Castro-Giner, F.* et al.: Positionally cloned genes and age-specific effects in asthma and atopy: An international population-based cohort study (ECRHS). Thorax 65, 124-131 (2010)
Castro-Giner, F.* et al.: A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS). BMC Med. Genet. 10:128 (2009)
Castro-Giner, F.* et al.: Joint effect of obesity and TNFA variability on asthma: Two international cohort studies. Eur. Respir. J. 33, 1003-1009 (2009)
Castro-Giner, F.* et al.: Traffic-related air pollution, oxidative stress genes, and asthma (ECHRS). Environ. Health Perspect. 117, 1919-1924 (2009)