An Exponential Bound for Cox Regression()

Por Goldberg, Y., Kosorok, M. R.
Publicado em 2012

On the robustness of the adaptive lasso to model misspecification

Por LU, W., GOLDBERG, Y., FINE, J. P.
Publicado em 2012

Increased killer B cells in chronic HCV infection may lead to autoimmunity and increased viral load

Por Eiza, N., Zuckerman, E., Carlebach, M., Rainis, T., Goldberg, Y., Vadasz, Z.
Publicado no Clin Exp Immunol (2018)

Clinical course and outcome of patients with high-level microsatellite instability cancers in a real-life setting: a retrospective analysis

Por Halpern N, Goldberg Y, Kadouri L, Duvdevani M, Hamburger T, Peretz T, Hubert A
Publicado em 2017-03-01

Double heterozygosity in the BRCA1 and BRCA2 genes in the Jewish population

Por Lavie, O., Narod, S., Lejbkowicz, F., Dishon, S., Goldberg, Y., Gemer, O., Rennert, G.
Publicado em 2011

Activation of protein kinase C or cAMP-dependent protein kinase increases phosphorylation of the c-erbA-encoded thyroid hormone receptor and of the v-erbA-encoded protein.

Por Goldberg, Y, Glineur, C, Gesquière, J C, Ricouart, A, Sap, J, Vennström, B, Ghysdael, J
Publicado em 1988

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.

Por Kremer, B, Almqvist, E, Theilmann, J, Spence, N, Telenius, H, Goldberg, Y P, Hayden, M R
Publicado em 1995

Different mechanisms underlie DNA instability in Huntington disease and colorectal cancer.

Por Goellner, G M, Tester, D, Thibodeau, S, Almqvist, E, Goldberg, Y P, Hayden, M R, McMurray, C T
Publicado em 1997

Molecular analysis of late onset Huntington's disease.

Por Kremer, B, Squitieri, F, Telenius, H, Andrew, S E, Theilmann, J, Spence, N, Goldberg, Y P, Hayden, M R
Publicado em 1993

An Alu element retroposition in two families with Huntington disease defines a new active Alu subfamily.

Por Hutchinson, G B, Andrew, S E, McDonald, H, Goldberg, Y P, Graham, R, Rommens, J M, Hayden, M R
Publicado em 1993

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.

Por Goldberg, Y P, Andrew, S E, Theilmann, J, Kremer, B, Squitieri, F, Telenius, H, Brown, J D, Hayden, M R
Publicado em 1993

Hepcidin in iron overload disorders

Por Papanikolaou, George, Tzilianos, Michalis, Christakis, John I., Bogdanos, Dionisios, Tsimirika, Konstantina, MacFarlane, Julie, Goldberg, Y. Paul, Sakellaropoulos, Nikos, Ganz, Tomas, Nemeth, Elizabeta
Publicado em 2005

Sodium channel Na(V)1.9 mutations associated with insensitivity to pain dampen neuronal excitability

Por Huang, Jianying, Vanoye, Carlos G., Cutts, Alison, Goldberg, Y. Paul, Dib-Hajj, Sulayman D., Cohen, Charles J., Waxman, Stephen G., George, Alfred L.
Publicado no J Clin Invest (2017)

Huntington Disease without CAG Expansion: Phenocopies or Errors in Assignment?

Por Andrew, Susan E., Goldberg, Y. Paul, Kremer, Berry, Squitieri, Ferdinando, Theilmann, Jane, Zeisler, Jutta, Telenius, Håkan, Adam, Shelin, Almquist, Elisabeth, Anvret, Maria, Lucotte, Gerard, Stoessl, A. Jon, Campanella, Giuseppe, Hayden, Michael R.
Publicado em 1994

Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

Por Lafrenière, Ronald G., MacDonald, Marcia L. E., Dubé, Marie-Pierre, MacFarlane, Julie, O’Driscoll, Mary, Brais, Bernard, Meilleur, Sébastien, Brinkman, Ryan R., Dadivas, Owen, Pape, Terry, Platon, Christèle, Radomski, Chris, Risler, Jenni, Thompson, Jay, Guerra-Escobio, Ana-Maria, Davar, Gudarz, Breakefield, Xandra O., Pimstone, Simon N., Green, Roger, Pryse-Phillips, William, Goldberg, Y. Paul, Younghusband, H. Banfield, Hayden, Michael R., Sherrington, Robin, Rouleau, Guy A., Samuels, Mark E.
Publicado em 2004