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1. Full Text Association Between APOE Alleles and Change of Neuropsychological Tests in the Long Life Family Study
by Du, Mengtian and Andersen, Stacy L and Schupf, Nicole and Feitosa, Mary F and Barker, Megan S and Perls, Thomas T and Sebastiani, Paola
Journal of Alzheimer's disease, ISSN 1387-2877, 01/2021, Volume 79, Issue 1, pp. 117 - 125
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory | Cognitive ability | Risk analysis | Risk factors | Apolipoprotein E | Older people | Alleles | Aging | Adults | Mathematical models | Bayesian analysis | Cross sections | Genotypes | Index Medicus
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2. Full Text A bivariate genome-wide approach to metabolic syndrome: STAMPEED Consortium
by Kraja, Aldi T and Vaidya, Dhananjay and Pankow, James S and Goodarzi, Mark O and Assimes, Themistocles L and Kullo, Iftikhar J and Sovio, Ulla and Mathias, Rasika A and Sun, Yan V and Franceschini, Nora and Absher, Devin and Li, Guo and Zhang, Qunyuan and Feitosa, Mary F and Glazer, Nicole L and Haritunians, Talin and Hartikainen, Anna-Liisa and Knowles, Joshua W and North, Kari E and Iribarren, Carlos and Kral, Brian and Yanek, Lisa and O'Reilly, Paul F and McCarthy, Mark I and Jaquish, Cashell and Couper, David J and Chakravarti, Aravinda and Psaty, Bruce M and Becker, Lewis C and Province, Michael A and Boerwinkle, Eric and Quertermous, Thomas and Palotie, Leena and Jarvelin, Marjo-Riitta and Becker, Diane M and Kardia, Sharon L. R and Rotter, Jerome I and Chen, Yii-Der Ida and Borecki, Ingrid B
Diabetes (New York, N.Y.), ISSN 0012-1797, 04/2011, Volume 60, Issue 4, pp. 1329 - 1339
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Diabetes. Impaired glucose tolerance | Miscellaneous | Other metabolic disorders | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Metabolic diseases | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Middle Aged | Genotype | Male | Phenotype | Metabolic Syndrome - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Complications and side effects | Genetic aspects | Research | Metabolic syndrome X | Genetic variation | Health aspects | Index Medicus | Abridged Index Medicus | Genetics
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3. Full Text Deriving stratified effects from joint models investigating gene-environment interactions
by Laville, Vincent and Majarian, Timothy and de Vries, Paul S and Bentley, Amy R and Feitosa, Mary F and Sung, Yun J and Rao, D. C and Manning, Alisa and Aschard, Hugues and CHARGE Gene-Lifestyle Interactions and on behalf of the CHARGE Gene-Lifestyle Interactions Working Group
BMC bioinformatics, ISSN 1471-2105, 06/2020, Volume 21, Issue 1, pp. 1 - 251
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Biochemical Research Methods | Science & Technology | Mathematical & Computational Biology | Consortia | Models | Genes | Analysis | Investigations | Working groups | Computer simulation | Bias | Estimation | Exposure | Single-nucleotide polymorphism | Environmental statistics | Statistical tests | Statistics | Generalized linear models | Programming languages | Accuracy | Simulation | Environment models | Genetics | Estimators | Genotypes | Index Medicus | Binary exposure | Stratified analysis | Gene-environment interaction | Summary statistics
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4. Full Text Prevalence, Incidence, and Risk Factors for Overall, Physical, and Cognitive Independence Among Those From Exceptionally Long-Lived Families: The Long Life Family Study
by Santanasto, Adam J and Marron, Megan M and Boudreau, Robert M and Feitosa, Mary F and Wojczynski, Mary K and Arbeev, Konstantin G and Thyagarajan, Bharat and Schupf, Nicole and Stallard, Eric and Sebastiani, Paola and Cosentino, Stephanie and Christensen, Kaare and Newman, Anne B
The journals of gerontology. Series A, Biological sciences and medical sciences, ISSN 1079-5006, 04/2020, Volume 75, Issue 5, pp. 899 - 905
Disability | Oldest old | Compression of morbidity | Dementia | Gerontology | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Activities of Daily Living | Prevalence | Humans | Risk Factors | Aged, 80 and over | Female | Male | Cognition | Longevity | Disabled Persons | Incidence | Respiratory function | Demography | Activities of daily living | Older people | Body weight | Cognitive ability | Families & family life | Glycosylation | Risk factors | Index Medicus | Abridged Index Medicus | THE JOURNAL OF GERONTOLOGY | Medical Sciences | MED00280 | SCI00960 | AcademicSubjects
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5. Full Text Characterization of european ancestry nonalcoholic fatty liver disease‐associated variants in individuals of african and hispanic descent
by Palmer, Nicholette D and Musani, Solomon K and Yerges‐Armstrong, Laura M and Feitosa, Mary F and Bielak, Lawrence F and Hernaez, Ruben and Kahali, Bratati and Carr, J. Jeffrey and Harris, Tamara B and Jhun, Min A and Kardia, Sharon L.R and Langefeld, Carl D and Mosley, Thomas H and Norris, Jill M and Smith, Albert V and Taylor, Herman A and Wagenknecht, Lynne E and Liu, Jiankang and Borecki, Ingrid B and Peyser, Patricia A and Speliotes, Elizabeth K
Hepatology (Baltimore, Md.), ISSN 0270-9139, 09/2013, Volume 58, Issue 3, pp. 966 - 975
Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Gene Frequency - genetics | Chondroitin Sulfate Proteoglycans - genetics | African Continental Ancestry Group - ethnology | Humans | Middle Aged | Male | European Continental Ancestry Group - ethnology | Lectins, C-Type - genetics | Fatty Liver - ethnology | Lysophospholipase - genetics | Non-alcoholic Fatty Liver Disease | Adult | Female | Hispanic Americans - ethnology | African Continental Ancestry Group - genetics | Fatty Liver - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Hispanic Americans - genetics | Membrane Proteins - genetics | Nerve Tissue Proteins - genetics | Phosphoprotein Phosphatases - genetics | Adaptor Proteins, Signal Transducing - genetics | Genetic Predisposition to Disease - ethnology | Aged | Genetic Variation - genetics | Cohort Studies | Lipase - genetics | African Americans | Genealogy | Liver diseases | Diet | Liver cirrhosis | Hepatology | Index Medicus
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6. Full Text HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype
by Malhotra, Rajeev and Mauer, Andreas C and Cardenas, Christian L. Lino and Guo, Xiuqing and Yao, Jie and Zhang, Xiaoling and Wunderer, Florian and Smith, Albert and Wong, Quenna and Pechlivanis, Sonali and Hwang, Shih-Jen and Wang, Judy and Lu, Lingyi and Nicholson, Christopher J and Shelton, Georgia and Buswell, Mary D and Barnes, Hanna J and Sigurslid, Haakon H and Slocum, Charles and O'Rourke, Caitlin and Rhee, David K and Bagchi, Aranya and Nigwekar, Sagar U and Buys, Emmanuel S and Campbell, Catherine Y and Harris, Tamara and Budoff, Matthew and Criqui, Michael H and Rotter, Jerome and Johnson, Andrew D and Song, Ci and Franceschini, Nora and Debette, Stephanie and Hoffmann, Udo and Kaelsch, Hagen and Noethen, Markus M and Sigurdsson, Sigurdur and Freedman, Barry and Bowden, Donald W and Jckel, Karl-Heinz and Moebus, Susanne and Erbel, Raimund and Feitosa, Mary F and Gudnason, Vilmundur and Thanassoulis, George and Zapol, Warren M and Lindsay, Mark E and Bloch, Donald B and Post, Wendy S and O'Donnell, Christopher J
Nature genetics, ISSN 1061-4036, 11/2019, Volume 51, Issue 11, pp. 1580 - 1587
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Muscle, Smooth, Vascular - metabolism | Atherosclerosis - genetics | Humans | Middle Aged | Vascular Calcification - genetics | Male | Aorta - metabolism | GTPase-Activating Proteins - metabolism | Repressor Proteins - physiology | Vascular Calcification - metabolism | Female | Repressor Proteins - metabolism | Atherosclerosis - pathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Histone Deacetylases - genetics | Mice, Inbred C57BL | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Vascular Calcification - pathology | Atherosclerosis - metabolism | Mice, Knockout | Aorta - pathology | Muscle, Smooth, Vascular - pathology | Phenotype | Animals | Muscle Contraction | Aged | Mice | Polymorphism, Single Nucleotide | GTPase-Activating Proteins - genetics | Histone Deacetylases - physiology | Cohort Studies | Evaluation | Genome-wide association studies | Smooth muscle | Genetic aspects | Single nucleotide polymorphisms | Cardiovascular diseases | Health aspects | Risk factors | Calcification (ectopic) | Heart | Phenotypes | Hispanic Americans | Muscles | African Americans | Genomes | Thorax | Single-nucleotide polymorphism | Gene expression | Muscle contraction | Loci | Abdomen | Meta-analysis | Proteins | Signal transduction | Arteriosclerosis | Coronary vessels | Atherosclerosis | Calcification | Aorta | Gene loci | Inhibition | Index Medicus
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7. Full Text Independent associations of TOMM40 and APOE variants with body mass index
by Kulminski, Alexander M and Loika, Yury and Culminskaya, Irina and Huang, Jian and Arbeev, Konstantin G and Bagley, Olivia and Feitosa, Mary F and Zmuda, Joseph M and Christensen, Kaare and Yashin, Anatoliy I and Long Life Family Study Res Grp and Long Life Family Study Research Group
Aging cell, ISSN 1474-9718, 02/2019, Volume 18, Issue 1, pp. e12869 - n/a
age‐dependent effect | TOMM40 | body mass index | lifespan | ApoE polymorphism | aging | health span | age-dependent effect | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Cell Biology | Body Mass Index | Multivariate Analysis | Genetic Association Studies | Humans | Middle Aged | Linkage Disequilibrium - genetics | Genotype | Aging - genetics | Membrane Transport Proteins - genetics | Apolipoproteins E - genetics | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Cohort Studies | Body mass index | Apolipoproteins | Analysis | Body weight | Genetic polymorphisms | Neurodegenerative diseases | Apolipoprotein E | Alleles | Heterozygotes | Alzheimers disease | Gene polymorphism | Alzheimer's disease | Age | Polymorphism | Index Medicus | Original Papers | Original Paper
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8. Full Text An exome-wide sequencing study of lipid response to high-fat meal and fenofibrate in Caucasians from the GOLDN cohort
by Geng, Xin and Irvin, Marguerite R and Hidalgo, Bertha and Aslibekyan, Stella and Srinivasasainagendra, Vinodh and An, Ping and Frazier-Wood, Alexis C and Tiwari, Hemant K and Dave, Tushar and Ryan, Kathleen and Ordovas, Jose M and Straka, Robert J and Feitosa, Mary F and Hopkins, Paul N and Borecki, Ingrid and Province, Michael A and Mitchell, Braxton D and Arnett, Donna K and Zhi, Degui
Journal of lipid research, ISSN 0022-2275, 2018, Volume 59, Issue 4, pp. 722 - 729
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Exome | Lipids - genetics | Sequence Analysis, RNA | Humans | Dietary Fats - administration & dosage | Fenofibrate - administration & dosage | European Continental Ancestry Group | DNA Methylation - genetics | Fenofibrate - therapeutic use | Cohort Studies | Fenofibrate | Lipoproteins (low density) | Genetic variance | Phenotypes | Transcription | Lipids | Digital divide | Cholesterol | Index Medicus | triglyceride | epidemiology | Patient-Oriented and Epidemiological Research | genetics | high-density lipoprotein | cholesterol | whole-exome sequencing | rare variant | low-density lipoprotein | postprandial lipemia
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9. Full Text An exome-wide sequencing study of the GOLDN cohort reveals novel associations of coding variants and fasting plasma lipids
by Geng, Xin and Irvin, Marguerite R and Hidalgo, Bertha and Aslibekyan, Stella and Srinivasasainagendra, Vinodh and An, Ping and Frazier-Wood, Alexis C and Tiwari, Hemant K and Dave, Tushar and Ryan, Kathleen and Ordovas, Jose M and Straka, Robert J and Feitosa, Mary F and Hopkins, Paul N and Borecki, Ingrid and Province, Michael A and Mitchell, Braxton D and Arnett, Donna K and Zhi, Degui
Frontiers in genetics, ISSN 1664-8021, 2019, Volume 10, pp. 158 - 158
HDL | Rare variant | LDL | Whole exome sequencing | Genetics | Triglyceride | Epidemiology | Cholesterol | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Usage | Fasting | Research | Blood lipids | Genetic variation | Exome sequencing | triglyceride | cholesterol | rare variant | whole exome sequencing
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10. Full Text Composite Measure of Physiological Dysregulation as a Predictor of Mortality: The Long Life Family Study
by Arbeev, Konstantin G and Bagley, Olivia and Ukraintseva, Svetlana V and Duan, Hongzhe and Kulminski, Alexander M and Stallard, Eric and Wu, Deqing and Christensen, Kaare and Feitosa, Mary F and Thyagarajan, Bharat and Zmuda, Joseph M and Yashin, Anatoliy I and Long Life Family Study
Frontiers in public health, ISSN 2296-2565, 03/2020, Volume 8, pp. 56 - 56
Long Life Family Study | statistical distance | deficits index | mortality | prediction | physiological dysregulation | aging | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Physiological aspects | Mortality
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