Mental disorders
|
0.100 |
GeneticVariation
|
group |
GWASDB |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
|
20889312 |
2010 |
Forced expiratory volume function
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
|
23284291 |
2012 |
Psychotic Disorders
|
0.100 |
GeneticVariation
|
group |
GWASDB |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
|
20889312 |
2010 |
Pulmonary function
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
|
20010835 |
2010 |
Pulmonary function
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study identifies five loci associated with lung function.
|
20010834 |
2010 |
Pulmonary function (finding)
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
|
20010835 |
2010 |
Pulmonary function (finding)
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association study identifies five loci associated with lung function.
|
20010834 |
2010 |
Colorectal Carcinoma
|
0.310 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Pancreatic Ductal Adenocarcinoma
|
0.300 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
ovarian neoplasm
|
0.020 |
PosttranslationalModification
|
disease |
LHGDN |
Given the emerging role of ADAMs family proteins in growth factor regulation in normal cells, we suggest that epigenetic dysregulation of ADAM19 may contribute to the neoplastic process in ovarian cancer.
|
18714391 |
2008 |
Mental disorders
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
|
20889312 |
2010 |
Forced expiratory volume function
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
|
30804560 |
2019 |
Chronic Obstructive Airway Disease
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis.
|
28166215 |
2017 |
Chronic Obstructive Airway Disease
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.
|
30804561 |
2019 |
Psychotic Disorders
|
0.100 |
GeneticVariation
|
group |
GWASCAT |
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
|
20889312 |
2010 |
Respiratory Function Tests
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.
|
20010835 |
2010 |
Respiratory Function Tests
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.
|
23284291 |
2012 |
peak expiratory flow (procedure)
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.
|
30804560 |
2019 |
Blood Protein Measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Co-regulatory networks of human serum proteins link genetics to disease.
|
30072576 |
2018 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Genotype and Anterior Segment Phenotype in a Cohort of Turkish Patients with Lamellar Ichthyosis.
|
24397709 |
2015 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Whole-exome sequencing in patients with ichthyosis reveals modifiers associated with increased IgE levels and allergic sensitizations.
|
25458912 |
2015 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.
|
15317751 |
2004 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
|
17557927 |
2007 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
Role of molecular testing in the multidisciplinary diagnostic approach of ichthyosis.
|
26762237 |
2016 |
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
NIPAL4/ichthyin is expressed in the granular layer of human epidermis and mutated in two Pakistani families with autosomal recessive ichthyosis.
|
20016120 |
2010 |