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PLoS genetics, ISSN 1553-7404, 04/2019, Volume 15, Issue 4, pp. e1007739 - e1007739
Sleep disordered breathing (SDB)-related overnight hypoxemia is associated with cardiometabolic disease and other comorbidities. Understanding the genetic... 
INTERMITTENT HYPOXIA | OXYGEN DESATURATION | HEART-FAILURE | GENETICS & HEREDITY | OSTEOPOROTIC FRACTURES | COGNITIVE IMPAIRMENT | APNEA-HYPOPNEA | NLRP3 INFLAMMASOME | SEX-DIFFERENCES | PULMONARY-FIBROSIS | GENOME-WIDE ASSOCIATION | Humans | Middle Aged | Male | Gene Regulatory Networks | Genetic Variation | NLR Family, Pyrin Domain-Containing 3 Protein - genetics | Young Adult | Interleukin-18 Receptor alpha Subunit - genetics | Serine Endopeptidases - genetics | Aged, 80 and over | Adult | Female | Hexokinase - genetics | Genome-Wide Association Study | Oxyhemoglobins - metabolism | Extracellular Matrix Proteins - genetics | Computational Biology | Sleep Apnea Syndromes - blood | Sleep Apnea Syndromes - genetics | Sleep - genetics | Nerve Tissue Proteins - genetics | Cell Adhesion Molecules, Neuronal - genetics | Oxygen - blood | Hypoxia - blood | Hypoxia - genetics | Adolescent | Aged | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Physiological aspects | Sleep disorders | Genetic aspects | Oxyhemoglobin | Interleukins | Genomics | Mortality | Genomes | Health aspects | Funding | Critical care | Single-nucleotide polymorphism | Epidemiology | Population genetics | Reelin protein | Consortia | Hypoxemia | Interleukin 1 | Bioinformatics | Public health | Phenotypes | Inflammation | Genetic diversity | Gene expression | Hexokinase | Interleukin 18 | Medicine | Nutrition research | Genetic variance | Sleep | Hospitals | Womens health | Replication | Respiration | Oxygenation | Index Medicus
Journal Article
American Journal of Respiratory Cell and Molecular Biology, ISSN 1044-1549, 03/2018, Volume 58, Issue 3, pp. 391 - 401
Obstructive sleep apnea (OSA) is a common heritable disorder displaying marked sexual dimorphism in disease prevalence and progression. Previous genetic... 
Genetics | Genome-wide association studies | Sexual dimorphism | Multiethnic | Obstructive sleep apnea | obstructive sleep apnea | DISTURBANCES | 17P11.2 | HIGH-DENSITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | OBESITY | genetics | GENE | RESPIRATORY SYSTEM | DISEASE | GENDER | DUPLICATION | multiethnic | genome-wide association studies | ASSOCIATION | sexual dimorphism | SEVERITY | ras Proteins - genetics | Genome-Wide Association Study | Sleep, REM - physiology | Humans | Middle Aged | Sleep Apnea, Obstructive - genetics | Male | Sex Characteristics | Transcription Factors - genetics | Phosphatidylethanolamine N-Methyltransferase - genetics | Sterol Regulatory Element Binding Protein 1 - genetics | Adult | Female | Aged | Quantitative Trait Loci - genetics | Genomics | Sex | Hispanic Americans | African Americans | Lipids | Cardiovascular disease | Sleep (REM) | Genomes | Dimorphism | Sleep apnea | Eye movements | Consortia | Body mass index | Sleep disorders | Mens health | Apnea | Sleep (NREM) | Atherosclerosis | Physiology | Lipid metabolism | Heart diseases | Chromosome 17 | Ethnic studies | Coronary artery | Gender differences | Metabolism | Minority & ethnic groups | Chronic fatigue syndrome | Meta-analysis | Quantitative trait loci | Studies | Genetic variance | Sleep | Womens health | Coronary vessels | Gene loci | Heritability | Asian Americans | Index Medicus | Original Research
Journal Article
Diabetes, ISSN 0012-1797, 05/2015, Volume 64, Issue 5, pp. 1853 - 1866
Journal Article
by Pollack, Samuela and Igo, Robert P and Igo, Robert P and Jensen, Richard A and Christiansen, Mark and Christiansen, Mark and Li, Xiaohui and Li, Xiaohui and Cheng, Ching-Yu and Cheng, Ching-Yu and Ng, Maggie C Y and Ng, Maggie C.Y and Smith, Albert V and Smith, Albert V and Rossin, Elizabeth J and Segrè, Ayellet V and Davoudi, Samaneh and Tan, Gavin S and Chen, Yii-Der Ida and Kuo, Jane Z and Kuo, Jane Z and Dimitrov, Latchezar M and Stanwyck, Lynn K and Meng, Weihua and Meng, Weihua and Hosseini, S. Mohsen and Hosseini, S Mohsen and Imamura, Minako and Imamura, Minako and Nousome, Darryl and Kim, Jihye and Hai, Yang and Jia, Yucheng and Jia, Yucheng and Ahn, Jeeyun and Leong, Aaron and Shah, Kaanan and Park, Kyu Hyung and Park, Kyu Hyung and Guo, Xiuqing and Ipp, Eli and Ipp, Eli and Taylor, Kent D and Adler, Sharon G and Sedor, John R and Sedor, John R and Freedman, Barry I and Freedman, Barry I and Lee, I-Te and Sheu, Wayne H.-H and Lee, I-Te and Sheu, Wayne H-H and Kubo, Michiaki and Takahashi, Atsushi and Kubo, Michiaki and Hadjadj, Samy and Takahashi, Atsushi and Marre, Michel and Hadjadj, Samy and Tregouet, David-Alexandre and Marre, Michel and Mckean-Cowdin, Roberta and Tregouet, David-Alexandre and Mckean-Cowdin, Roberta and Varma, Rohit and Varma, Rohit and McCarthy, Mark I and Groop, Leif and McCarthy, Mark I and Groop, Leif and Ahlqvist, Emma and Ahlqvist, Emma and Lyssenko, Valeriya and Lyssenko, Valeriya and Agardh, Elisabet and Morris, Andrew and Agardh, Elisabet and Doney, Alex S.F and Morris, Andrew and Doney, Alex S F and Colhoun, Helen M and Colhoun, Helen M and Toppila, Iiro and Sandholm, Niina and Toppila, Iiro and Sandholm, Niina and Groop, Per-Henrik and Maeda, Shiro and Groop, Per-Henrik and Maeda, Shiro and Hanis, Craig L and Hanis, Craig L and Penman, Alan and Chen, Ching J and Penman, Alan and Hancock, Heather and Chen, Ching J and Hancock, Heather and Mitchell, Paul and Craig, Jamie E and ... and DCCT EDIC Res Grp and Family Invest Nephropathy Diabet-E and Family Investigation of Nephropathy and Diabetes-Eye Research Group, DCCT/EDIC Research Group
Diabetes, ISSN 0012-1797, 02/2019, Volume 68, Issue 2, pp. 441 - 456
To identify genetic variants associated with diabetic retinopathy (DR), we performed a large multiethnic genome-wide association study. Discovery included... 
RISK-FACTORS | METAANALYSIS | POLYMORPHISMS | VARIANTS | ENDOCRINOLOGY & METABOLISM | LOCI | PREVALENCE | CHINESE PATIENTS | SEVERITY | RESOURCE | REVEALS | Proteins | Diabetic retinopathy | Genetic variance | Retinopathy | Diabetes mellitus | Genetic analysis | Replication | Genomes | Genetic diversity | Diabetes
Journal Article
Diabetes, ISSN 0012-1797, 12/2017, Volume 66, Issue 12, pp. 3130 - 3141
Journal Article