UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Genetically meaningful phenotypic subgroups in autism spectrum disorders

Genes, brain and behavior, 2014-03, Vol.13 (3), p.276-285

2014

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Patterns of Brain Activation in People at Risk for Alzheimer's Disease

The New England journal of medicine, 2000-08, Vol.343 (7), p.450-456

2000

Volltextzugriff (PDF)

Analysis of the RELN gene as a genetic risk factor for autism

Molecular psychiatry, 2005-06, Vol.10 (6), p.563-571

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Genetics and pathogenesis of multiple sclerosis

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

2009

Volltextzugriff (PDF)

Multiple rare SAPAP3 missense variants in trichotillomania and OCD

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

2009

Volltextzugriff (PDF)

Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

Clinical genetics, 2011-06, Vol.79 (6), p.523-530

2011

Volltextzugriff (PDF)

Genetic basis for clinical expression in multiple sclerosis

Brain (London, England : 1878), 2002, Vol.125 (Pt 1), p.150-158

2002

Volltextzugriff (PDF)

Examination of association of genes in the serotonin system to autism

Neurogenetics, 2009-07, Vol.10 (3), p.209-216

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Apolipoprotein E controls the risk and age at onset of Parkinson disease

Neurology, 2004-06, Vol.62 (11), p.2005-2009

2004

Volltextzugriff (PDF)

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

Translational psychiatry, 2013-05, Vol.3 (5), p.e256-e256

2013

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2003

Volltextzugriff (PDF)

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

Neurology, 2006-05, Vol.66 (9), p.1373-1383

2006

Volltextzugriff (PDF)

Increased Amyloid β-Peptide Deposition in Cerebral Cortex as a Consequence of Apolipoprotein E Genotype in Late-Onset Alzheimer Disease

Proceedings of the National Academy of Sciences - PNAS, 1993-10, Vol.90 (20), p.9649-9653

1993

Volltextzugriff (PDF)

SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease

American journal of human genetics, 2000-08, Vol.67 (2), p.383-394

2000

Volltextzugriff (PDF)

Parkinson disease loci in the mid-western Amish

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

2013

Volltextzugriff (PDF)

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

Nature genetics, 1994-06, Vol.7 (2), p.180-184

1994

Volltextzugriff (PDF)

Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3

Annals of human genetics, 2008-11, Vol.72 (6), p.725-731

2008

Volltextzugriff (PDF)

Genome-wide association study of Alzheimer's disease

Translational psychiatry, 2012-05, Vol.2 (5), p.e117-e117

2012

Volltextzugriff (PDF)

1 – 25 von 992

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(956)
Mit Volltextzugriff
(874)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Alzheimer's & Dementia
(251)
American Journal Of Human Genetics
(58)
Human Molecular Genetics
(34)
Neurology
(33)
Nature Genetics
(32)
Genomics
(25)
Neurogenetics
(25)
Annals Of Neurology
(21)
Neurobiology Of Aging
(20)
American Journal Of Medical Genetics
(18)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

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

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

Genetically meaningful phenotypic subgroups in autism spectrum disorders

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

Patterns of Brain Activation in People at Risk for Alzheimer's Disease

Analysis of the RELN gene as a genetic risk factor for autism

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

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

Genetics and pathogenesis of multiple sclerosis

Multiple rare SAPAP3 missense variants in trichotillomania and OCD

Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

Genetic basis for clinical expression in multiple sclerosis

Examination of association of genes in the serotonin system to autism

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

Apolipoprotein E controls the risk and age at onset of Parkinson disease

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

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

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

APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers

Increased Amyloid β-Peptide Deposition in Cerebral Cortex as a Consequence of Apolipoprotein E Genotype in Late-Onset Alzheimer Disease

SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease

Parkinson disease loci in the mid-western Amish

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease

Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3

Genome-wide association study of Alzheimer's disease

Suchergebnisse filtern