J. Andresen

发表

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

C. Disteche, F. Behm, D. Horsman, 1996, Nature Genetics.

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.

Karen Marder, Norman Arnheim, Ira Shoulson, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Phosphorylation of ATXN1 at Ser776 in the cerebellum

H. Zoghbi, H. Orr, P. Jafar-Nejad, 2009, Journal of neurochemistry.

Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model

H. Zoghbi, H. Orr, L. Duvick, 2011, Human molecular genetics.

Genome-Wide Linkage Analysis of Obsessive-Compulsive Disorder Implicates Chromosome 1p36

E. Cook, J. Grant, J. Badner, 2012, Biological Psychiatry.

The Relationship Between CAG Repeat Length and Age of Onset Differs for Huntington's Disease Patients with Juvenile Onset or Adult Onset

L. Cardon, M. MacDonald, D. Housman, 2007, Annals of human genetics.

The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36.

X. Wu, T. Hudson, D. Housman, 1997, Human molecular genetics.

The Gene for Schnyder's Crystalline Corneal Dystrophy Maps to Human Chromosome 1p34.1–p36

T. Hudson, D. Housman, F. Haluska, 1996 .

Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31.

X. Chen, J. Korenberg, J. Andresen, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Replication of twelve association studies for Huntington’s disease residual age of onset in large Venezuelan kindreds

L. Cardon, D. Housman, S. Cherny, 2006, Journal of Medical Genetics.

Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds

L. Cardon, D. Housman, S. Cherny, 2008, Genetic epidemiology.

RORα-Mediated Purkinje Cell Development Determines Disease Severity in Adult SCA1 Mice

H. Zoghbi, H. Orr, H. G. Serra, 2006, Cell.

Emerging pathogenic pathways in the spinocerebellar ataxias.

H. Orr, J. Andresen, Kerri M. Carlson, 2009, Current opinion in genetics & development.

Spinocerebellar ataxia type 1 (SCA1) is caused by the expansion of a cytosine-adenosine-guanosine trinucleotide repeat that encodes a polyglutamine tract in the ataxin-1

H. Zoghbi, H. Orr, P. Jafar-Nejad, 2009 .

Hsp70/Hsc70 regulates the effect phosphorylation has on stabilizing ataxin‐1

H. Zoghbi, H. Orr, J. Andresen, 2007, Journal of neurochemistry.

UvA-DARE ( Digital Academic Repository ) Symptom Dimensions in OCD : Item-Level Factor Analysis and Heritability Estimates

Dan J Stein, M. Jenike, J. Grant, 2010 .

Venezuelan kindreds Huntington's disease residual age of onset in large Replication of twelve association studies for

L. Cardon, D. Housman, S. Cherny, 2007 .

Repeat instability in the 27–39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications

L. Cardon, J. Penney, S. Cherny, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.