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Miriam F. Moffatt

Researcher at National Institutes of Health

Publications -  19
Citations -  7794

Miriam F. Moffatt is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Genome-wide association study & Gene expression profiling. The author has an hindex of 17, co-authored 19 publications receiving 7001 citations. Previous affiliations of Miriam F. Moffatt include Imperial College London.

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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Elizabeth K. Speliotes, +413 more
- 01 Nov 2010 - 
TL;DR: Genetic loci associated with body mass index map near key hypothalamic regulators of energy balance, and one of these loci is near GIPR, an incretin receptor, which may provide new insights into human body weight regulation.
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Reagent and laboratory contamination can critically impact sequence-based microbiome analyses

TL;DR: It is demonstrated that contaminating DNA is ubiquitous in commonly used DNA extraction kits and other laboratory reagents, varies greatly in composition between different kits and kit batches, and that this contamination critically impacts results obtained from samples containing a low microbial biomass.
Journal ArticleDOI

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Sonja I. Berndt, +385 more
- 01 May 2013 - 
TL;DR: A genome-wide search for loci associated with the upper versus the lower 5th percentiles of body mass index, height and waist-to-hip ratio as well as clinical classes of obesity, including up to 263,407 individuals of European ancestry finds a large overlap in genetic structure and the distribution of variants between traits based on extremes and the general population and little etiological heterogeneity between obesity subgroups.

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Sonja I. Berndt, +321 more
Journal ArticleDOI

Seventy-five genetic loci influencing the human red blood cell

Pim van der Harst, +194 more
- 20 Dec 2012 - 
TL;DR: A genome-wide association study of haemoglobin concentration and related parameters in up to 135,367 individuals identifies 75 independent genetic loci associated with one or more red blood cell phenotypes at P < 10−8, which together explain 4–9% of the phenotypic variance per trait.