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by Gottlieb, Daniel J and Hek, Karin and Chen, T.-H and Watson, N.F and Eiriksdottir, Gudny and Byrne, E.M and Cornelis, Marilyn and Warby, S.C and Bandinelli, S and Cherkas, Lynn and Evans, Daniel and Grabe, Hans Jörgen and Lahti, Jari and Li, Man and Lehtimäki, Terho and Lumley, Thomas and Marciante, Kristin and Perusse, Louis and Psaty, Bruce and Robbins, J and Tranah, Gregory and Vink, J.M and Wilk, J.B and Stafford, J.M and Bellis, Claire and Biffar, R and Bouchard, Claude and Cade, B and Curhan, Gary and Eriksson, J and Ewert, R and Ferrucci, Luigi and Fülöp, T and Gehrman, Philip and Goodloe, Robert and Harris, Tamara and Heath, Anew C and Hernandez, Dena and Hofman, Albert and Hottenga, Jouke Jan and Hunter, David and Jensen, Majken K and Johnson, Anew and Kähönen, Mika and Kao, Wen and Kraft, Peter and Larkin, E.K and Lauderdale, D.S and Luik, Annemarie and Medici, M and Montgomery, Grant W and Palotie, A and Patel, Sanjay and Pistis, Giorgio and Porcu, E and Quaye, Lydia and Raitakari, Olli and Redline, Susan and Rimm, Eric B and Rotter, J.I and Smith, Albert and Spector, Timothy and Teumer, Alexander and Uitterlinden, Ané and Vohl, Marie-Claude and Widen, E and Willemsen, Gonneke and Young, Terri L and Zhang, X and Liu, Y and Blangero, John and Boomsma, Dorret and Gudnason, Vilmundur and Hu, F and Mangino, M and Martin, Nicholas and O'Connor, George and Stone, Katie L and Tanaka, T and Viikari, Jorma and Gharib, Sina and Punjabi, Naresh and Räikkönen, Katri and Völzke, Henry and Mignot, E and Tiemeier, Henning
Molecular Psychiatry, ISSN 1359-4184, 01/2015, Volume 20, Issue 10, pp. 1232 - 1239
Journal Article
Neurology, ISSN 0028-3878, 03/2012, Volume 78, Issue 10, pp. 690 - 695
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The... 
HOMOZYGOSITY | ALLELE | OF-ONSET | GENE | LENGTH | MUTATION | CHROMOSOMES | CLINICAL NEUROLOGY | TRINUCLEOTIDE REPEAT | Humans | Age of Onset | Alleles | Huntington Disease - genetics | Adult | Female | Genotype | Huntington Disease - diagnosis | Male | Trinucleotide Repeat Expansion | 164
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2015, Volume 20, pp. 1232 - 1239
Usual sleep duration is a heritable trait correlated with psychiatric morbidity, cardiometabolic disease and mortality, although little is known about the... 
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 2015, Volume 20, Issue 10, pp. 1232 - 1239
Usual sleep duration is a heritable trait correlated with psychiatric morbidity, cardiometabolic disease and mortality, although little is known about the... 
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2011, Volume 43, Issue 1, pp. 66 - 71
Journal Article
Soil Science Society of America Journal, ISSN 0361-5995, 07/2012, Volume 76, Issue 4, pp. 1407 - 1417
Forty to fifty percent decreases in acidic deposition through the 1980s and 1990s led to partial recovery of acidified surface waters in the northeastern... 
TEMPORAL VARIATION | HUBBARD-BROOK | SOIL SCIENCE | WINTER INJURY | DISSOLVED ORGANIC-CARBON | PICEA-RUBENS | ATMOSPHERIC DEPOSITION | CHEMISTRY | NORTHEASTERN UNITED-STATES | CALCIUM ADDITION | BROOK-EXPERIMENTAL-FOREST | Trees | Studies | Soils | Chemistry | Decomposition | Trends | Deposition
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
Journal Article
Journal of Computational and Applied Mathematics, ISSN 0377-0427, 1996, Volume 74, Issue 1, pp. 313 - 329
Mathematical models for treating problems of linear viscoelasticity involving hereditary constitutive relations for compressible solids are presented, and... 
Finite element method | Error estimates | Linear viscoelasticity | Nonlinear viscoelasticity | MATHEMATICS, APPLIED | VOLTERRA INTEGRAL-EQUATIONS | finite element method | nonlinear viscoelasticity | SOLIDS | linear viscoelasticity | CRACK INITIATION | COMPUTATION | DYNAMIC FRACTURE | 2ND KIND | error estimates
Journal Article
Journal of Computational and Applied Mathematics, ISSN 0377-0427, 1995, Volume 63, Issue 1, pp. 91 - 107
Mathematical models for treating problems of linear viscoelasticity involving hereditary constitutive relations for compressible solids are discussed, and... 
Viscoelasticity | Finite element method | Volterra equations | MATHEMATICS, APPLIED | COMPUTATION | VOLTERRA EQUATIONS | EQUATION | FINITE ELEMENT METHOD | VISCOELASTICITY
Journal Article
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