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Wyświetlanie 1-20 z 61
Podgląd okładki
Tytuł :
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity
Index Terms :
Asian Continental Ancestry Group/genetics
Chromosome Mapping
European Continental Ancestry Group/genetics
Female
Gene Frequency
Genetic Predisposition to Disease/ethnology
Genotype
HLA Antigens/genetics
Humans
Lung Neoplasms/ethnology
Major Histocompatibility Complex/genetics
Male
Middle Aged
Peptides/genetics
Polymorphism, Single Nucleotide
dk/atira/pure/researchoutput/pubmedpublicationtype/D016428
Journal Article
dk/atira/pure/researchoutput/pubmedpublicationtype/D052061
Research Support, N.I.H., Extramural
dk/atira/pure/researchoutput/pubmedpublicationtype/D013485
Research Support, Non-U.S. Gov't
article
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Polygenic hazard score to guide screening for aggressive prostate cancer:development and validation in large scale cohorts
Index Terms :
Age of Onset
Aged
Cohort Studies
Disease-Free Survival
Early Detection of Cancer/methods
European Continental Ancestry Group/genetics
Genotype
Humans
Kallikreins/analysis
Male
Middle Aged
Outcome Assessment (Health Care)
Polymorphism, Single Nucleotide/genetics
Predictive Value of Tests
Prostate-Specific Antigen/analysis
Prostatic Neoplasms/blood
Risk Assessment
Survival Analysis
dk/atira/pure/researchoutput/pubmedpublicationtype/D003160
Comparative Study
dk/atira/pure/researchoutput/pubmedpublicationtype/D016428
Journal Article
dk/atira/pure/researchoutput/pubmedpublicationtype/D013485
Research Support, Non-U.S. Gov't
dk/atira/pure/researchoutput/pubmedpublicationtype/D013486
Research Support, U.S. Gov't, Non-P.H.S.
article
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes
Index Terms :
Adaptor Proteins, Signal Transducing/genetics
Apolipoproteins E/genetics
Case-Control Studies
Collagen Type IV/genetics
Comorbidity
Coronary Artery Disease/diagnosis
Cyclin-Dependent Kinases/genetics
Diabetes Mellitus, Type 1/diagnosis
Europe/epidemiology
European Continental Ancestry Group/genetics
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Phenotype
Polymorphism, Single Nucleotide
Risk Factors
TRPP Cation Channels/genetics
dk/atira/pure/researchoutput/pubmedpublicationtype/D016428
Journal Article
dk/atira/pure/researchoutput/pubmedpublicationtype/D017418
Meta-Analysis
dk/atira/pure/researchoutput/pubmedpublicationtype/D013485
Research Support, Non-U.S. Gov't
article
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Influence of MCHR2 and MCHR2-AS1 Genetic Polymorphisms on Body Mass Index in Psychiatric Patients and In Population-Based Subjects with Present or Past Atypical Depression.
Index Terms :
Adult; Body Mass Index; Depression/genetics; European Continental Ancestry Group/genetics; Genetic Association Studies; Genetic Predisposition to Disease; Haplotypes/genetics; Humans; Mental Disorders/genetics; Middle Aged; Polymorphism, Single Nucleotide/genetics; RNA, Long Noncoding/genetics; Receptors, G-Protein-Coupled/genetics; Receptors, Pituitary Hormone/genetics; Reproducibility of Results
info:eu-repo/semantics/article
article
URL :
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_200412067B842">http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_200412067B842
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Defining the role of common variation in the genomic and biological architecture of adult human height.
Index Terms :
Adult; Analysis of Variance; Body Height/genetics; European Continental Ancestry Group/genetics; Genetic Variation/genetics; Genetics, Population; Genome-Wide Association Study/methods; Humans; Oligonucleotide Array Sequence Analysis; Polymorphism, Single Nucleotide/genetics
info:eu-repo/semantics/article
article
URL :
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_344F80F34D5F2">http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_344F80F34D5F2
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Index Terms :
Adolescent
Adult
Aged
Aged, 80 and over
Asian Continental Ancestry Group/genetics
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genetic Variation
Genotype
Haplotypes/genetics
Humans
Male
Middle Aged
Parkinson Disease/genetics/prevention & control
Protein-Serine-Threonine Kinases/genetics
Risk
Young Adult
alpha-Synuclein/genetics
tau Proteins/genetics
Genetics
Interaction
LRRK2
MAPT
Parkinson's disease
SNCA
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/17198">http://orbilu.uni.lu/handle/10993/17198
http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf">http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Defining the role of common variation in the genomic and biological architecture of adult human height
Index Terms :
Adult
Analysis of Variance
Body Height/genetics
European Continental Ancestry Group/genetics
Genetic Variation/genetics
Genetics
Genome-Wide Association Study/methods
Humans
Oligonucleotide Array Sequence Analysis
Polymorphism
Population
Single Nucleotide/genetics
Contribution to Journal
URL :
https://eprints.qut.edu.au/91788/1/emss-60217.pdf">https://eprints.qut.edu.au/91788/1/emss-60217.pdf
https://eprints.qut.edu.au/91788/1/emss-60217.pdf">https://eprints.qut.edu.au/91788/1/emss-60217.pdf
DOI:10.1038/ng.3097
Wood, Andrew, Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune, Gustafsson, Stefan, Chu, Audrey, Estrada, Karol, Luan, Jian'an, Nyholt, Dale, & other, and (2014) Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46(11), pp. 1173-1186.
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Index Terms :
Adolescent
Adult
Aged
Aged, 80 and over
Asian Continental Ancestry Group/genetics
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genetic Variation
Genotype
Haplotypes/genetics
Humans
Male
Middle Aged
Parkinson Disease/genetics/prevention & control
Protein-Serine-Threonine Kinases/genetics
Risk
Young Adult
alpha-Synuclein/genetics
tau Proteins/genetics
Genetics
Interaction
LRRK2
MAPT
Parkinson's disease
SNCA
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/17198">http://orbilu.uni.lu/handle/10993/17198
http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf">http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Index Terms :
Adolescent
Adult
Aged
Aged, 80 and over
Asian Continental Ancestry Group/genetics
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genetic Variation
Genotype
Haplotypes/genetics
Humans
Male
Middle Aged
Parkinson Disease/genetics/prevention & control
Protein-Serine-Threonine Kinases/genetics
Risk
Young Adult
alpha-Synuclein/genetics
tau Proteins/genetics
Genetics
Interaction
LRRK2
MAPT
Parkinson's disease
SNCA
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/17198">http://orbilu.uni.lu/handle/10993/17198
http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf">http://orbilu.uni.lu/bitstream/10993/17198/1/Heckman.pdf
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Association of polymorphisms in natural killer cell-related genes with preterm birth.
Autorzy :
Harmon QE
Engel SM
Olshan AF
Moran T
Stuebe AM
Luo J
Wu MC
Avery CL
Pokaż więcej
Źródło :
American journal of epidemiology [Am J Epidemiol] 2013 Oct 15; Vol. 178 (8), pp. 1208-18. Date of Electronic Publication: 2013 Aug 27.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Killer Cells, Natural*/physiology
Polymorphism, Single Nucleotide*
Premature Birth/*genetics
African Americans/genetics ; Case-Control Studies ; Colony-Stimulating Factors/genetics ; European Continental Ancestry Group/genetics ; Female ; Genetic Association Studies ; Genotyping Techniques ; Humans ; Interleukins/genetics ; Linkage Disequilibrium ; Pregnancy ; Premature Birth/ethnology ; Receptors, Interferon/genetics ; Receptors, KIR3DL2/genetics ; T-Lymphocytes
Czasopismo naukowe
Szczegóły
Podgląd okładki
Tytuł :
Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry. : combined analysis of 111,421 individuals of European ancestry
Index Terms :
Endocrinology and Diabetes
Adult
Alleles
Body Mass Index
European Continental Ancestry Group/genetics
Female
Genetic Association Studies
Genetic Predisposition to Disease
Humans
Logistic Models
Male
Motor Activity/genetics
Obesity/epidemiology
Polymorphism, Single Nucleotide
Risk Factors
Surveys and Questionnaires
contributiontojournal/article
info:eu-repo/semantics/article
text
URL :
http://dx.doi.org/10.1371/journal.pgen.1003607">http://dx.doi.org/10.1371/journal.pgen.1003607
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
A mega-analysis of genome-wide association studies for major depressive disorder
Index Terms :
Bipolar Disorder/genetics
Case-Control Studies
Depressive Disorder
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/*genetics
Genome-Wide Association Study/*statistics & numerical data
Humans
Major/*genetics
Male
Polymorphism
Single Nucleotide/genetics
Contribution to Journal
URL :
https://eprints.qut.edu.au/91824/1/nihms505456.pdf">https://eprints.qut.edu.au/91824/1/nihms505456.pdf
https://eprints.qut.edu.au/91824/1/nihms505456.pdf">https://eprints.qut.edu.au/91824/1/nihms505456.pdf
DOI:10.1038/mp.2012.21
Ripke, Stephan, Wray, Naomi, Lewis, Cathryn, Hamilton, Steven, Weissman, Myrna, Breen, Gerome, Byrne, Enda, Blackwood, Douglas, Boomsma, Dorret, Cichon, Sven, Nyholt, Dale, & other, and (2013) A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18(4), pp. 497-511.
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Glucocerebrosidase mutations in a Serbian Parkinson's disease population.
Index Terms :
Adult
Aged
Aged, 80 and over
Alleles
Case-Control Studies
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genotype
Glucosylceramidase/genetics
Humans
Jews/genetics
Male
Middle Aged
Mutation
Parkinson Disease/genetics
Serbia
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/24440">http://orbilu.uni.lu/handle/10993/24440
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Glucocerebrosidase mutations in a Serbian Parkinson's disease population.
Index Terms :
Adult
Aged
Aged, 80 and over
Alleles
Case-Control Studies
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genotype
Glucosylceramidase/genetics
Humans
Jews/genetics
Male
Middle Aged
Mutation
Parkinson Disease/genetics
Serbia
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/24440">http://orbilu.uni.lu/handle/10993/24440
Zasób elektroniczny
Szczegóły
Podgląd okładki
Tytuł :
Glucocerebrosidase mutations in a Serbian Parkinson's disease population.
Index Terms :
Adult
Aged
Aged, 80 and over
Alleles
Case-Control Studies
European Continental Ancestry Group/genetics
Female
Genetic Predisposition to Disease/genetics
Genotype
Glucosylceramidase/genetics
Humans
Jews/genetics
Male
Middle Aged
Mutation
Parkinson Disease/genetics
Serbia
info:eu-repo/semantics/article
URL :
http://orbilu.uni.lu/handle/10993/24440">http://orbilu.uni.lu/handle/10993/24440
Zasób elektroniczny
Szczegóły
Wyświetlanie 1-20 z 61

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