Publications by authors named "Eliana Hechter"

7Publications

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.

Nature 2015 Feb 10;518(7537):102-6. Epub 2014 Dec 10.

1] Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. [2] Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. [3] Department of Medicine, Harvard Medical School, Boston, Massachusetts 02114, USA. [4] Program in Medical and Population Genetics, Broad Institute, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA.

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http://kooperberg.fhcrc.org/papers/2015do.pdf
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http://www.nature.com/doifinder/10.1038/nature13917
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http://dx.doi.org/10.1038/nature13917DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319990PMC
February 2015

Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing.

Horm Res Paediatr 2013 3;79(6):379-86. Epub 2013 May 3.

Division of Endocrinology, Boston Children's Hospital, Boston, MA 02115, USA.

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http://dx.doi.org/10.1159/000350013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3788832PMC
February 2014

Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorder.

J Pediatr 2013 Jan 10;162(1):202-4.e1. Epub 2012 Sep 10.

Division of Endocrinology, Children's Hospital Boston, Boston, MA, 02115, USA.

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http://dx.doi.org/10.1016/j.jpeds.2012.07.055DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524393PMC
January 2013

The mystery of missing heritability: Genetic interactions create phantom heritability.

Proc Natl Acad Sci U S A 2012 Jan 5;109(4):1193-8. Epub 2012 Jan 5.

Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.

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http://dx.doi.org/10.1073/pnas.1119675109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268279PMC
January 2012

Quantifying the underestimation of relative risks from genome-wide association studies.

PLoS Genet 2011 Mar 17;7(3):e1001337. Epub 2011 Mar 17.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1371/journal.pgen.1001337DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060077PMC
March 2011

Disease model distortion in association studies.

Genet Epidemiol 2011 May 17;35(4):278-90. Epub 2011 Mar 17.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.

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http://dx.doi.org/10.1002/gepi.20576DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110308PMC
May 2011