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Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twin...
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Identification of common genetic variants influencing spontaneous dizygotic twin...
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Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twin...
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Two newly identified genetic determinants of pigmentation in Europeans.
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The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Proper...
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Support for involvement of the AHI1 locus in schizophrenia
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Variant in the sequence of the LINGO1 gene confers risk of essential tremor
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Variant of TREM2 associated with the risk of Alzheimer's disease.
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Disruption of the neurexin 1 gene is associated with schizophrenia
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Genetic determinants of hair, eye and skin pigmentation in Europeans
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Disruption of the neurexin 1 gene is associated with schizophrenia
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Disruption of the neurexin 1 gene is associated with schizophrenia
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Disruption of the neurexin 1 gene is associated with schizophrenia
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
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Disruption of the neurexin 1 gene is associated with schizophrenia
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Rate of de novo mutations and the importance of father's age to disease risk.
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Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large Euro...
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Genome-wide association study of panic disorder reveals geneticoverlap with neur...
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Genome-wide association study of panic disorder reveals genetic overlap with neu...
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Identification of common genetic variants influencing spontaneous dizygotic twin...
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Article in Journal/Newspaper
27
Text
3
Author
Steinberg, Stacy
Stefansson, Kari
25
Werge, Thomas
16
Rujescu, Dan
14
Ingason, Andres
13
Stefansson, Hreinn
12
Tosato, Sarah
12
Hoffmann, Per
11
Sigurdsson, Engilbert
10
Djurovic, Srdjan
9
Giegling, Ina
9
Gustafsson, Omar
9
Petursson, Hannes
9
Sigmundsson, Thordur
9
Bonetto, Chiara
8
Bramon, Elvira
8
Cichon, Sven
8
Crombie, Caroline
8
Ettinger, Ulrich
8
Fossdal, Ragnheidur
8
Franke, Barbara
8
Fraser, Gillian
8
Gylfason, Arnaldur
8
Hansen, Thomas
8
Hardarsson, Gudmundur
8
Kiemeney, Lambertus A
8
Lonnqvist, Jouko
8
Mbarek, Hamdi
8
Melle, Ingrid
8
Murray, Robin
8
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Topic
Humans
9
Iceland
9
Female
8
Male
7
Case-Control Studies
5
Polymorphism
5
Single Nucleotide
5
Adult
4
AADAC
3
Association study
3
CNV
3
Copy number variation
3
Genetic Predisposition to Disease
3
Genome-Wide Association Study
3
Gilles de la Tourette syndrome
3
Human
3
Neuropsychiatric disorder
3
Risk Factors
3
Schizophrenia
3
Young Adult
3
AUTISM SPECTRUM DISORDER
2
Adolescent
2
Aged
2
Article
2
COPY-NUMBER VARIATION
2
Chromosomes
2
DNA
2
Dizygotic
2
European Continental Ancestry Group
2
Eye Color
2
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Content Provider
Hirsla - Landspítali University Hospital research archive
11
King's College, London: Research Portal
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HighWire Press (Stanford University)
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University of Copenhagen: Research
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University of Groningen research database
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Aarhus University: Research
1
Apollo - University of Cambridge Repository
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Mannheim University: MADOC
1
PubMed Central (PMC)
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Queensland University of Technology: QUT ePrints
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SAGE Publications
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The University of Queensland: UQ eSpace
1
Università degli Studi di Verona: Catalogo dei Prodotti della Ricerca (IRIS)
1
Utrecht University Repository
1
Vrije Universiteit Amsterdam (VU): Research Portal
1
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Norway
8
Language
English
28
unknown
2
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Iceland
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