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발행년	- (예 : 2010-2015)

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

Academic Journal

Do, R.; Won, H.-H.; Peloso, G.M.; Altshuler, D.; Kathiresan, S.; Kiezun, A.; Zuk, O.; Farlow, D.N.; DePristo, M.A.; Hechter, E.; Lander, E.S.; Sunyaev, S.R.; Gabriel, S.; Stitziel, N.O.; Cresci, S.; Jørgensen, A.B.; Tybjaerg-Hansen, A.; Duga, S.; Guella, I.; Asselta, R.; Merlini, P.A.; Farrall, M.; Goel, A.; Watkins, H.; Lange, L.A.; Lange, E.M.; Auer, P.L.; Reiner, A.P.; Carlson, C.S.; Kooperberg, C.; Schwartz, S.M.; Girelli, D.; Martinelli, N.; Olivieri, O.; Roberts, R.; Stewart, A.F.R.; Saleheen, D.; Danesh, J.; Epstein, S.E.; Sivapalaratnam, S.; Hovingh, G.K.; Kastelein, J.J.; Samani, N.J.; Schunkert, H.; Erdmann, J.; Shah, S.H.; Kraus, W.E.; Davies, R.; Nikpay, M.; McPherson, R.; Johansen, C.T.; Wang, J.; Hegele, R.A.; Marz, W.; Kleber, M.E.; Huang, J.; O'Donnell, C.J.; Johnson, A.D.; Li, M.; Burke, G.L.; Gross, M.; Liu, Y.; Assimes, T.L.; Heiss, G.; Folsom, A.R.; Taylor, H.A.; Hamsten, A.; Clarke, R.; Reilly, D.F.; Yin, W.; Rivas, M.A.; Donnelly, P.; Rossouw, J.E.; Psaty, B.M.; Herrington, D.M.; Wilson, J.G.; Rich, S.S.; Bamshad, M.J.; Nickerson, D.A.; Tracy, R.P.; Cupples, L.A.; Rader, D.J.; Reilly, M.P.; Spertus, J.A.; Hartiala, J.; Allayee, H.; Tang, W.H.W.; Hazen, S.L.; Siscovick, D.S.; Jackson, R.D.; Boerwinkle, E.; Abecasis, G.R.; Ardissino, D.

In: Nature. (Nature, 5 February 2015, 518(7537):102-106)

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Searching for missing heritability: Designing rare variant association studies

Academic Journal

Zuk, O.; Schaffner, S.F.; Samocha, K.; Do, R.; Hechter, E.; Kathiresan, S.; Daly, M.J.; Neale, B.M.; Sunyaev, S.R.; Lander, E.S.

In: Proceedings of the National Academy of Sciences of the United States of America. (Proceedings of the National Academy of Sciences of the United States of America, 28 January 2014, 111(4):E455-E464)

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

Academic Journal

Wassner, A.J.; Cohen, L.E.; Dauber, A.; Hechter, E.

In: Hormone Research in Paediatrics. (Hormone Research in Paediatrics, July 2013, 79(6):379-386)

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Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing

Academic Journal

Wassner, A.J.; Cohen, L.E.; Hechter, E.; Dauber, A.

In: Hormone Research in Paediatrics. (Hormone Research in Paediatrics, In Press, 3 May 2013)

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

Academic Journal

Dauber, A.; Safer, J.; Hirschhorn, J.N.; Hechter, E.; Stoler, J.

In: Journal of Pediatrics. (Journal of Pediatrics, January 2013, 162(1):202-204e1)

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The mystery of missing heritability: Genetic interactions create phantom heritability

Academic Journal

Zuk, O.; Hechter, E.; Sunyaev, S.R.; Lander, E.S.

In: Proceedings of the National Academy of Sciences of the United States of America. (Proceedings of the National Academy of Sciences of the United States of America, 24 January 2012, 109(4):1193-1198)

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

Academic Journal

Spencer, C.; Vukcevic, D.; Donnelly, P.; Hechter, E.

In: PLoS Genetics. (PLoS Genetics, March 2011, 7(3))

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Disease model distortion in association studies

Academic Journal

Vukcevic, D.; Spencer, C.; Donnelly, P.; Hechter, E.

In: Genetic Epidemiology. (Genetic Epidemiology, 2011, 35(4):278-290)

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Extremities

Academic Journal

Hechter, E.

In: Ploughshares. (Ploughshares, 1 June 2015, 41(2):42-51)

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