A. Zanko

发表

A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

Jane S. Paulsen, J. Mysore, M. MacDonald, 2003, American journal of human genetics.

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

Bruce R Korf, Piotr Madanecki, David K Crossman, 2013, Nature Genetics.

Duplication of C7orf58, WNT16 and FAM3C in an Obese Female with a t(7;22)(q32.1;q11.2) Chromosomal Translocation and Clinical Features Resembling Coffin-Siris Syndrome

G. Magrane, M. Golabi, Jun Zhu, 2012, PloS one.

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset

Samuel Frank, Karen Marder, Christopher A. Ross, 2012, Human Genetics.

Interstitial deletions of chromosome 6q: genotype–phenotype correlation utilizing array CGH

K. Rauen, A. Zanko, F. Conte, 2007, Clinical genetics.

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

Jane S. Paulsen, R H Myers, C A Ross, 2012, Neurology.

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16

Jane S. Paulsen, J. Mysore, M. MacDonald, 2004, Neurogenetics.

Speech and language delay are early manifestations of juvenile-onset Huntington disease

S. Lin, A. Boxer, A. Zanko, 2006, Neurology.

Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study

Jane S. Paulsen, T. Gillis, J. Mysore, 2006, BMC Medical Genetics.

Huntington disease: A case study describing the complexities and nuances of predictive testing of monozygotic twins

A. Zanko, A. Heimler, 1995, Journal of Genetic Counseling.

Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.

T. Gillis, J. Mysore, M. MacDonald, 2012, American journal of human genetics.

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset

T. Gillis, J. Mysore, M. MacDonald, 2013, neurogenetics.

Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease

M. MacDonald, M. Hayden, C. Ross, 2003, American journal of medical genetics. Part A.

Psychological impact of news of genetic risk for Huntington disease.

E. F. Donnelly, M. Horowitz, A. Zanko, 2001, American journal of medical genetics.

Coping with grim news from genetic tests.

M. Horowitz, A. Zanko, E. Sundin, 2001, Psychosomatics.

Case Report: Concurrent Wilson Disease and Huntington Disease: Lightning Can Strike Twice

A. Zanko, L. Abrams, 2015, Journal of Genetic Counseling.

TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.

T. Gillis, J. Mysore, M. MacDonald, 2012, Biochemical and biophysical research communications.

Electrophysical properties of vanadium oxide films deposited by reactive magnetron sputtering

D. Golosov, S. Zavadski, S. Melnikov, 2020 .

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

R. Nagy, B. Korf, A. Piotrowski, 2013, Nature Genetics.