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Eliana Hechter

Showing results (1-10 of 7) with videos related to

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Genetic Epidemiology|March 19, 2011
Disease model distortion in association studiesDamjan Vukcevic, Eliana Hechter, Chris Spencer, et al.
Plos Genetics|March 26, 2011
Quantifying the underestimation of relative risks from genome-wide association studiesChris Spencer, Eliana Hechter, Damjan Vukcevic, et al.
Hormone Research in Paediatrics|May 9, 2013
Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencingAri J Wassner, Laurie E Cohen, Eliana Hechter, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2012
The mystery of missing heritability: Genetic interactions create phantom heritabilityOr Zuk, Eliana Hechter, Shamil R Sunyaev, et al.
The Journal of Pediatrics|September 15, 2012
Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorderAndrew Dauber, Joan Stoler, Eliana Hechter, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genetic Epidemiology|March 19, 2011
Disease model distortion in association studiesDamjan Vukcevic, Eliana Hechter, Chris Spencer, et al.
Plos Genetics|March 26, 2011
Quantifying the underestimation of relative risks from genome-wide association studiesChris Spencer, Eliana Hechter, Damjan Vukcevic, et al.
Hormone Research in Paediatrics|May 9, 2013
Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencingAri J Wassner, Laurie E Cohen, Eliana Hechter, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2012
The mystery of missing heritability: Genetic interactions create phantom heritabilityOr Zuk, Eliana Hechter, Shamil R Sunyaev, et al.
The Journal of Pediatrics|September 15, 2012
Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorderAndrew Dauber, Joan Stoler, Eliana Hechter, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 21, 2014
Searching for missing heritability: designing rare variant association studiesOr Zuk, Stephen F Schaffner, Kaitlin Samocha, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
Pageof 1