E. Stenroos

发表

Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23

M. Polymeropoulos, R. Nussbaum, J. Higgins, 1996, Science.

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Robert L. Nussbaum, Giuseppe Di Iorio, William G. Johnson, 1997 .

Studies of penetrance and anticipation in five autosomal‐dominant restless legs syndrome pedigrees

M. Brin, A. Walters, B. Ehrenberg, 1999, Movement disorders : official journal of the Movement Disorder Society.

Teratogenic Alleles in Autism and Other Neurodevelopmental Disorders

S. Buyske, W. Johnson, E. Stenroos, 2008 .

Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locus.

T. Lehner, D. Mandelbaum, W. Johnson, 1998, American journal of medical genetics.

Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis

Kobert S. Schwartz, W. Brown, W. Johnson, 1998, Annals of neurology.

Neuron‐Like Cells in Culture of Tuberous Sclerosis Tissue

E. Stenroos, M. Davidson, H. Yoshidome, 1991, Annals of the New York Academy of Sciences.

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.

S E Ide, A. Dehejia, M. Polymeropoulos, 1997, Science.

Pelizaeus-Merzbacher-like disease: Exclusion of the proteolipid protein locus and documentation of a new locus on Xq

T. Lehner, W. Johnson, E. Stenroos, 1997, Neurology.

Pedigree analysis in families with febrile seizures.

D. Mandelbaum, W. Johnson, E. Stenroos, 1996, American journal of medical genetics.

HLA-DR4 as a risk allele for autism acting in mothers of probands possibly during pregnancy.

S. Buyske, W. Johnson, E. Stenroos, 2009, Archives of pediatrics & adolescent medicine.

Risk of autistic disorder in affected offspring of mothers with a glutathione S-transferase P1 haplotype.

S. Buyske, W. Johnson, E. Stenroos, 2007, Archives of pediatrics & adolescent medicine.

Genetic variant of glutathione peroxidase 1 in autism

S. Buyske, W. Johnson, E. Stenroos, 2010, Brain and Development.

Ataxin-3 Interactions with Rad23 and Valosin-Containing Protein and Its Associations with Ubiquitin Chains and the Proteasome Are Consistent with a Role in Ubiquitin-Mediated Proteolysis

W. G. Johnson, E. Stenroos, K. Madura, 2003, Molecular and Cellular Biology.

Maternally Acting Alleles in Autism and Other Neurodevelopmental Disorders: The Role of HLA-DR4 Within the Major Histocompatibility Complex

S. Buyske, W. Johnson, E. Stenroos, 2010 .

No evidence for association of familial Parkinson's disease with CAG repeat expansion

K. Lindblad, A. Brice, H. Payami, 1995, Neurology.

Absence of linkage between familial neural tube defects and PAX3 gene.

E. Mariman, Y. Shugart, W. Johnson, 1995, Journal of medical genetics.

Short tandem repeat polymorphism linkage studies in a new family with X-linked mental retardation (MRX20).

J. Ott, T. Lehner, B. Gold, 1995, American journal of medical genetics.

Smoking behavior and the C677T allele of the methylenetetrahydrofolate reductase (MTHFR) gene.

E. Stenroos, C. Schroeder, T. Scholl, 2001, American journal of medical genetics.

Common dihydrofolate reductase 19-base pair deletion allele: a novel risk factor for preterm delivery.

S. Buyske, W. Johnson, E. Stenroos, 2005, The American journal of clinical nutrition.

New 19 bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

S. Buyske, W. Johnson, E. Stenroos, 2004, American journal of medical genetics. Part A.

Analysis of case-parent trios at a locus with a deletion allele: association of GSTM1 with autism

S. Buyske, W. Johnson, E. Stenroos, 2006, BMC Genetics.

Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida.

S. Heath, T. Lehner, W. Johnson, 1999, American journal of medical genetics.

Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele.

J. Ott, W. Johnson, E. Stenroos, 1994, American journal of medical genetics.

Origin of the Neuron‐Like Cells in Tuberous Sclerosis Tissues a

E. Stenroos, H. Yoshidome, W. Johnson, 1991, Annals of the New York Academy of Sciences.

The tau A0 allele in Parkinson's disease

L. Golbe, W. Johnson, E. Stenroos, 2001, Movement Disorders.

Glutathione S‐transferase polymorphisms and onset age in α‐synuclein A53T mutant Parkinson's disease

J. Vance, L. Golbe, W. Johnson, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.