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Genetics and pathogenesis of multiple sclerosis

Seminars in immunology, 2009-12, Vol.21 (6), p.328-333

2009

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Association and gene-gene interaction of SLC6A4 and ITGB3 in autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-03, Vol.153B (2), p.477-483

2010

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Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

Nature genetics, 1996-06, Vol.13 (2), p.189-195

1996

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Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism

American journal of human genetics, 2005-09, Vol.77 (3), p.377-388

2005

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Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes

American journal of human genetics, 2003-03, Vol.72 (3), p.539-548

2003

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Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

Nature genetics, 1994-12, Vol.8 (4), p.345-351

1994

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HLA-DR2 Dose Effect on Susceptibility to Multiple Sclerosis and Influence on Disease Course

American journal of human genetics, 2003-03, Vol.72 (3), p.710-716

2003

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Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families

Science (American Association for the Advancement of Science), 1993-08, Vol.261 (5123), p.921-923

1993

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Genotype-based association test for general pedigrees: The genotype-PDT

Genetic epidemiology, 2003-11, Vol.25 (3), p.203-213

2003

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Variants in several genomic regions associated with asperger disorder

Autism research, 2010-12, Vol.3 (6), p.303-310

2010

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Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder

American journal of medical genetics, 2000-02, Vol.96 (1), p.43-48

2000

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Science (American Association for the Advancement of Science), 2009-02, Vol.323 (5918), p.1205-1208

2009

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GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

Genes and immunity, 2016-07, Vol.17 (5), p.305-312

2016

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Lack of association between UBQLN1 and Alzheimer disease

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-04, Vol.141B (3), p.208-213

2006

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Notch Signaling Is A Potential Novel Target In Atherosclerosis

The Journal of surgical research, 2011, Vol.165 (2), p.326-326

2011

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Longitudinal follow-up of late-onset Alzheimer disease families

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-07, Vol.147B (5), p.571-578

2008

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Examination of association to autism of common genetic variationin genes related to dopamine

Autism research, 2008-12, Vol.1 (6), p.364-369

2008

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Identifying Copy Number Variation influencing risk for Alzheimer's disease in the Amish

Alzheimer's & dementia, 2010-07, Vol.6 (4), p.S202-S202

2010

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Genome-wide linkage study in the Amish shows evidence for a chromosome 3 locus in late-onset Alzheimer's disease

Alzheimer's & dementia, 2010-07, Vol.6 (4), p.S74-S75

2010

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Genome-wide association study for late-onset Alzheimer's disease in the Mid-Western U.S. Amish

Alzheimer's & dementia, 2010-07, Vol.6 (4), p.S203-S203

2010

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Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease

Neuroscience letters, 2017-05, Vol.649, p.124-129

2017

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Ordered-subset analysis of savant skills in autism for 15q11-q13

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-05, Vol.135B (1), p.38-41

2005

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Multiple rare SAPAP3 missense variants in trichotillomania and OCD

Molecular psychiatry, 2009-01, Vol.14 (1), p.6-9

2009

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No association between the APOE gene and autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-02, Vol.125B (1), p.57-60

2004

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Parkinson disease loci in the mid-western Amish

Human genetics, 2013-11, Vol.132 (11), p.1213-1221

2013

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Genetics and pathogenesis of multiple sclerosis

Association and gene-gene interaction of SLC6A4 and ITGB3 in autism

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism

Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

HLA-DR2 Dose Effect on Susceptibility to Multiple Sclerosis and Influence on Disease Course

Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families

Genotype-based association test for general pedigrees: The genotype-PDT

Variants in several genomic regions associated with asperger disorder

Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosis

Lack of association between UBQLN1 and Alzheimer disease

Notch Signaling Is A Potential Novel Target In Atherosclerosis

Longitudinal follow-up of late-onset Alzheimer disease families

Examination of association to autism of common genetic variationin genes related to dopamine

Identifying Copy Number Variation influencing risk for Alzheimer's disease in the Amish

Genome-wide linkage study in the Amish shows evidence for a chromosome 3 locus in late-onset Alzheimer's disease

Genome-wide association study for late-onset Alzheimer's disease in the Mid-Western U.S. Amish

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease

Ordered-subset analysis of savant skills in autism for 15q11-q13

Multiple rare SAPAP3 missense variants in trichotillomania and OCD

No association between the APOE gene and autism

Parkinson disease loci in the mid-western Amish

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