J. F. Gusella

发表

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ‐1 (T497C) genes in familial Parkinson's disease from the GenePD study

Mark Guttman, R H Myers, P P Pramstaller, 2005, Movement disorders : official journal of the Movement Disorder Society.

Neurofibromatosis type 2 appears to be a genetically homogeneous disease.

J. Haines, R. Martuza, G. Lenoir, 1992, American journal of human genetics.

Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease

J. Haines, M. Pericak-Vance, A. Roses, 1995, Neurology.

Identification and characterization of two novel tetratricopeptide repeat-containing genes.

D. Church, J. Gusella, J. Wasmuth, 1996, DNA and cell biology.

A novel G protein-coupled receptor kinase gene cloned from 4p16.3.

D. Church, M. MacDonald, C. Ambrose, 1992, Human molecular genetics.

Inflammatory bowel disease: is it in the genes?

Daniel K. Podolsky, J. F. Gusella, 1998, Gastroenterology.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Amyloid β protein gene: cDNA, mRNA distribution and genetic linkage near the Alzheimer locus

R. Tanzi, J. Gusella, R. Neve, 1988 .

Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1

M. MacDonald, J. Gusella, C. Morton, 2005, Journal of Medical Genetics.

A haplotype at the PARK3 locus influences onset age for Parkinson’s disease

J. Growdon, C. Singer, M. Stacy, 2003, Neurology.

Accumulation of wild type p53 protein in human astrocytomas.

D. Louis, J. Gusella, A. von Deimling, 1993, Cancer research.

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas.

R. Martuza, M. Sanson, O. Delattre, 1991, Genomics.

Molecular genetics of human chromosome 21.

R. Tanzi, J. Gusella, P. Watkins, 1986, Journal of medical genetics.

A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene.

M. MacDonald, J. Gusella, S. Baxendale, 1990, American journal of human genetics.

An index marker map of chromosome 9 provides strong evidence for positive interference.

J. Haines, S. Povey, C. Dib, 1993, American journal of human genetics.

A tiger behind many doors: multiple genetic pathways to malignant glioma.

D. Louis, J. Gusella, David N. Louis, 1995, Trends in genetics : TIG.

Sequence analysis and mapping of a novel human mitochondrial ATP synthase subunit 9 cDNA (ATP5G3).

J. Haines, T. Lerner, J. Gusella, 1994, Genomics.

The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family.

N. Risch, M. Brin, J. Penney, 1998, Advances in neurology.

Genome-wide scan for Parkinson's disease

M. MacDonald, J. Growdon, J. Hubble, 2001, Neurology.

Heterogeneous Topographic and Cellular Distribution of Huntingtin Expression in the Normal Human Neostriatum

M. MacDonald, S. Hersch, J. Gusella, 1997, The Journal of Neuroscience.

Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age

M. MacDonald, H. Shill, J. Growdon, 2006, Neurology.

Towards Standardizing Nomenclature in Huntington’s Disease Research

M. MacDonald, B. Leavitt, Emily C. Gantman, 2024, Journal of Huntington's disease.

Molecular genetics of Huntington's disease.

M. MacDonald, M. Duyao, M. Macdonald, 1993, Results and problems in cell differentiation.

BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study

H. Shill, S. Sherman, D. Burn, 2005, Neurology.

The putative glioma tumor suppressor gene on chromosome 19q maps between APOC2 and HRC.

D. Louis, H. Mohrenweiser, J. Gusella, 1994, Cancer research.

Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndrome.

V. P. Johnson, J. Gusella, J. Wasmuth, 1992, American journal of medical genetics.

Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region.

F. Collins, M. MacDonald, J. Gusella, 1992, Genomics.