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Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 2, p. 135, doi. 10.1002/ajmg.b.32289
By:
- Ramos, Eliana Marisa;
- Gillis, Tammy;
- Mysore, Jayalakshmi S.;
- Lee, Jong‐Min;
- Gögele, Martin;
- D'Elia, Yuri;
- Pichler, Irene;
- Sequeiros, Jorge;
- Pramstaller, Peter P.;
- Gusella, James F.;
- MacDonald, Marcy E.;
- Alonso, Isabel
Publication type:
Article
Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset.
Published in:
Human Genetics, 2012, v. 131, n. 12, p. 1833, doi. 10.1007/s00439-012-1205-z
By:
- Ramos, Eliana;
- Latourelle, Jeanne;
- Lee, Ji-Hyun;
- Gillis, Tammy;
- Mysore, Jayalakshmi;
- Squitieri, Ferdinando;
- Pardo, Alba;
- Donato, Stefano;
- Hayden, Michael;
- Morrison, Patrick;
- Nance, Martha;
- Ross, Christopher;
- Margolis, Russell;
- Gomez-Tortosa, Estrella;
- Ayuso, Carmen;
- Suchowersky, Oksana;
- Trent, Ronald;
- McCusker, Elizabeth;
- Novelletto, Andrea;
- Frontali, Marina
Publication type:
Article
Huntington's disease–like 2 (HDL2) in North America and Japan.
Published in:
Annals of Neurology, 2004, v. 56, n. 5, p. 670
By:
- Russell L. Margolis;
- Susan E. Holmes;
- Adam Rosenblatt;
- Lisa Gourley;
- Elizabeth O'Hearn;
- Christopher A. Ross;
- William K. Seltzer;
- Ruth H. Walker;
- Tetsuo Ashizawa;
- Astrid Rasmussen;
- Michael Hayden;
- Elisabeth W. Almqvist;
- Juliette Harris;
- Stanley Fahn;
- Marcy E. MacDonald;
- Jayalakshmi Mysore;
- Takayoshi Shimohata;
- Shoji Tsuji;
- Nicholas Potter;
- Kazuhiro Nakaso
Publication type:
Article
Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs.
Published in:
Human Molecular Genetics, 2021, v. 30, n. 3/4, p. 135, doi. 10.1093/hmg/ddaa283
By:
- Jung, Roy;
- Lee, Yejin;
- Barker, Douglas;
- Correia, Kevin;
- Shin, Baehyun;
- Loupe, Jacob;
- Collins, Ryan L;
- Lucente, Diane;
- Ruliera, Jayla;
- Gillis, Tammy;
- Mysore, Jayalakshmi S;
- Rodan, Lance;
- Picker, Jonathan;
- Lee, Jong-Min;
- Howland, David;
- Lee, Ramee;
- Kwak, Seung;
- MacDonald, Marcy E;
- Gusella, James F;
- Seong, Ihn Sik
Publication type:
Article
Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington's disease knock-in mice is blocked by Mlh1 knock-out.
Published in:
Human Molecular Genetics, 2020, v. 29, n. 18, p. 3044, doi. 10.1093/hmg/ddaa196
By:
- Loupe, Jacob M;
- Pinto, Ricardo Mouro;
- Kim, Kyung-Hee;
- Gillis, Tammy;
- Mysore, Jayalakshmi S;
- Andrew, Marissa A;
- Kovalenko, Marina;
- Murtha, Ryan;
- Seong, IhnSik;
- Gusella, James F;
- Kwak, Seung;
- Howland, David;
- Lee, Ramee;
- Lee, Jong-Min;
- Wheeler, Vanessa C;
- MacDonald, Marcy E
Publication type:
Article
Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
Published in:
Human Molecular Genetics, 2020, v. 29, n. 15, p. 2551, doi. 10.1093/hmg/ddaa139
By:
- Pinto, Ricardo Mouro;
- Arning, Larissa;
- Giordano, James V;
- Razghandi, Pedram;
- Andrew, Marissa A;
- Gillis, Tammy;
- Correia, Kevin;
- Mysore, Jayalakshmi S;
- Urtubey, Debora-M Grote;
- Parwez, Constanze R;
- Hein, Sarah M von;
- Clark, H Brent;
- Nguyen, Huu Phuc;
- Förster, Eckart;
- Beller, Allison;
- Jayadaev, Suman;
- Keene, C Dirk;
- Bird, Thomas D;
- Lucente, Diane;
- Vonsattel, Jean-Paul
Publication type:
Article
High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington's disease CAG knock-in mice across multiple genetic backgrounds.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 5, p. 913, doi. 10.1093/hmg/ddx006
By:
- Ament, Seth A.;
- Pearl, Jocelynn R.;
- Grindeland, Andrea;
- Claire, Jason St.;
- Earls, John C.;
- Kovalenko, Marina;
- Gillis, Tammy;
- Mysore, Jayalakshmi;
- Gusella, James F.;
- Jong-Min Lee;
- Seung Kwak;
- Howland, David;
- Min Young Lee;
- Baxter, David;
- Scherler, Kelsey;
- Kai Wang;
- Geman, Donald;
- Carroll, Jeffrey B.;
- MacDonald, Marcy E.;
- Carlson, George
Publication type:
Article
Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 16, p. 3227, doi. 10.1093/hmg/ddt176
By:
- Lee, Jong-Min;
- Galkina, Ekaterina I.;
- Levantovsky, Rachel M.;
- Fossale, Elisa;
- Anne Anderson, Mary;
- Gillis, Tammy;
- Srinidhi Mysore, Jayalakshmi;
- Coser, Kathryn R.;
- Shioda, Toshi;
- Zhang, Bin;
- Furia, Matthew D.;
- Derry, Jonathan;
- Kohane, Isaac S.;
- Seong, Ihn Sik;
- Wheeler, Vanessa C.;
- Gusella, James F.;
- MacDonald, Marcy E.
Publication type:
Article
Chromosome substitution strain assessment of a Huntington's disease modifier locus.
Published in:
Mammalian Genome, 2015, v. 26, n. 3/4, p. 119, doi. 10.1007/s00335-014-9552-9
By:
- Ramos, Eliana;
- Kovalenko, Marina;
- Guide, Jolene;
- St. Claire, Jason;
- Gillis, Tammy;
- Mysore, Jayalakshmi;
- Sequeiros, Jorge;
- Wheeler, Vanessa;
- Alonso, Isabel;
- MacDonald, Marcy
Publication type:
Article
Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder.
Published in:
Bipolar Disorders, 2015, v. 17, n. 4, p. 403, doi. 10.1111/bdi.12289
By:
- Ramos, Eliana Marisa;
- Gillis, Tammy;
- Mysore, Jayalakshmi S;
- Lee, Jong‐Min;
- Alonso, Isabel;
- Gusella, James F;
- Smoller, Jordan W;
- Sklar, Pamela;
- MacDonald, Marcy E;
- Perlis, Roy H
Publication type:
Article
Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 16, p. 3039, doi. 10.1093/hmg/ddp242
By:
- Swami, Meera;
- Hendricks, Audrey E.;
- Gillis, Tammy;
- Massood, Tiffany;
- Mysore, Jayalakshmi;
- Myers, Richard H.;
- Wheeler, Vanessa C.
Publication type:
Article
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 19, p. 2233, doi. 10.1093/hmg/11.19.2233
By:
- Fossale, Elisa;
- Wheeler, Vanessa C.;
- Vrbanac, Vladimir;
- Lebel, Lori-Anne;
- Teed, Allison;
- Mysore, Jayalakshmi S.;
- Gusella, James F.;
- MacDonald, Marcy E.;
- Persichetti, Francesca
Publication type:
Article
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset.
Published in:
Neurogenetics, 2013, v. 14, n. 3/4, p. 173, doi. 10.1007/s10048-013-0364-y
By:
- Ramos, Eliana;
- Latourelle, Jeanne;
- Gillis, Tammy;
- Mysore, Jayalakshmi;
- Squitieri, Ferdinando;
- Pardo, Alba;
- Donato, Stefano;
- Gellera, Cinzia;
- Hayden, Michael;
- Morrison, Patrick;
- Nance, Martha;
- Ross, Christopher;
- Margolis, Russell;
- Gomez-Tortosa, Estrella;
- Ayuso, Carmen;
- Suchowersky, Oksana;
- Trent, Ronald;
- McCusker, Elizabeth;
- Novelletto, Andrea;
- Frontali, Marina
Publication type:
Article

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