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1. Full Text Identification of DNA methylation changes in newborns related to maternal smoking during pregnancy
by Markunas, Christina A and Xu, Zongli and Harlid, Sophia and Wade, Paul A and Lie, Rolv T and Taylor, Jack A and Wilcox, Allen J
Environmental health perspectives, ISSN 0091-6765, 10/2014, Volume 122, Issue 10, pp. 1147 - 1153
Public, Environmental & Occupational Health | Environmental Sciences & Ecology | Toxicology | Life Sciences & Biomedicine | Science & Technology | Environmental Sciences | Smoking - adverse effects | Infant, Newborn - blood | Genome-Wide Association Study | Prenatal Exposure Delayed Effects - epidemiology | Epigenesis, Genetic | Humans | Male | Smoking - genetics | Maternal Exposure - statistics & numerical data | Pregnancy | Prenatal Exposure Delayed Effects - genetics | Smoking - epidemiology | Norway - epidemiology | CpG Islands | Maternal Exposure - adverse effects | Adult | Female | Pregnancy Trimester, First - drug effects | DNA Methylation - drug effects | Prenatal Exposure Delayed Effects - chemically induced | Cohort Studies | Medical research | DNA | Physiological aspects | Medicine, Experimental | Research | Methylation | Smoking in pregnancy | Studies | DNA methylation | Tobacco smoke | Genes | Index Medicus | Health | Deoxyribonucleic acid | Exposure | Infants | Smoke | Smoking | Children's Health
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2. Full Text Human Genetics of Addiction: New Insights and Future Directions
by Hancock, Dana B and Markunas, Christina A and Bierut, Laura J and Johnson, Eric O
Current psychiatry reports, ISSN 1523-3812, 2/2018, Volume 20, Issue 2, pp. 1 - 17
Drugs | Brain | Nicotine/smoking | GWAS | Medicine & Public Health | Omics | Alcohol | Psychiatry | Life Sciences & Biomedicine | Science & Technology | Illegal drugs | Behavioral health care | Genetic aspects | Analysis | Genomics | Public health | Genomes | Gene loci | Addictions | Index Medicus
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3. Full Text Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
by Gregory, Simon G and Connelly, Jessica J and Towers, Aaron J and Johnson, Jessica and Biscocho, Dhani and Markunas, Christina A and Lintas, Carla and Abramson, Ruth K and Wright, Harry H and Ellis, Peter and Langford, Cordelia F and Worley, Gordon and Delong, G. Robert and Murphy, Susan K and Cuccaro, Michael L and Persico, Antonello and Pericak-Vance, Margaret A
BMC medicine, ISSN 1741-7015, 10/2009, Volume 7, Issue 1, pp. 62 - 62
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Autistic Disorder - genetics | Sequence Deletion | Receptors, Oxytocin - deficiency | Humans | Child, Preschool | Male | DNA - metabolism | DNA - genetics | Young Adult | DNA Methylation | Comparative Genomic Hybridization | Microarray Analysis | Adolescent | Adult | Female | Child | Autism | Genetic aspects | Research | Oxytocin | Genomics | Index Medicus
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4. Full Text Comprehensive evaluation of disease- and trait-specific enrichment for eight functional elements among GWAS-identified variants
by Markunas, Christina A and Johnson, Eric O and Hancock, Dana B
Human genetics, ISSN 0340-6717, 07/2017, Volume 136, Issue 7, pp. 911 - 919
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Promoter Regions, Genetic | Genome-Wide Association Study | Diabetes Mellitus - genetics | Anthropometry | Gene Frequency | Humans | Mutation, Missense | Nervous System Diseases - genetics | Cardiovascular Diseases - genetics | Linkage Disequilibrium | Autoimmune Diseases - genetics | Mental Disorders - genetics | Phenotype | Neoplasms - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Type 2 diabetes | Quantitative genetics | Nervous system diseases | Analysis | Genomics | Protection and preservation | Single nucleotide polymorphisms | Cardiovascular diseases | Protein binding | Deoxyribonuclease | Statistical analysis | Diabetes mellitus | Linkage disequilibrium | Amino acid sequence | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Promoters | Quantitative trait loci | Enhancers | Conserved sequence | Gene frequency | Cancer | Index Medicus
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5. DNA methylation and microRNA-based biomarkers for risk of type 2 diabetes
by O’Connell, Thomas M and Markunas, Christina A
Current diabetes reviews, ISSN 1573-3998, 10/2016, Volume 12, Issue 1, pp. 20 - 29
Biomarker | GWAS | MicroRNA | Pre-diabetes | Epigenetics | Genetics | Diabetes
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6. Full Text Genome-wide DNA methylation differences in nucleus accumbens of smokers vs. nonsmokers
by Markunas, Christina A and Semick, Stephen A and Quach, Bryan C and Tao, Ran and Deep-Soboslay, Amy and Carnes, Megan U and Bierut, Laura J and Hyde, Thomas M and Kleinman, Joel E and Johnson, Eric O and Jaffe, Andrew E and Hancock, Dana B
Neuropsychopharmacology (New York, N.Y.), ISSN 0893-133X, 2020, Volume 46, Issue 3, pp. 554 - 560
Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Genomes | Regression analysis | Cigarette smoking | Nucleus accumbens | Genetic variance | Addiction | Autopsy | Peripheral blood | DNA methylation | Biomarkers | Deoxyribonucleic acid--DNA | Genotypes | Smoking
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7. Full Text Developmental effects of maternal smoking during pregnancy on the human frontal cortex transcriptome
by Semick, Stephen A and Collado-Torres, Leonardo and Markunas, Christina A and Shin, Joo Heon and Deep-Soboslay, Amy and Tao, Ran and Huestis, Marilyn A and Bierut, Laura J and Maher, Brion S and Johnson, Eric O and Hyde, Thomas M and Weinberger, Daniel R and Hancock, Dana B and Kleinman, Joel E and Jaffe, Andrew E
Molecular psychiatry, ISSN 1359-4184, 12/2020, Volume 25, Issue 12, pp. 3267 - 3277
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Nervous system diseases | Cerebral cortex | Child development | Development and progression | Genetic aspects | Mental illness | Health aspects | Risk factors | Smoking in pregnancy | Mental disorders | Genomes | Ribonucleic acid--RNA | Gene expression | Cigarette smoking | Intrauterine exposure | Pregnancy | Autism | Addiction | Autopsy | Cortex (frontal) | Prenatal experience | Public health | Age | Smoking | Index Medicus
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8. Full Text Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits
by Quach, Bryan C and Bray, Michael J and Gaddis, Nathan C and Liu, Mengzhen and Palviainen, Teemu and Minica, Camelia C and Zellers, Stephanie and Sherva, Richard and Aliev, Fazil and Nothnagel, Michael and Young, Kena A and Marks, Jesse A and Young, Hannah and Carnes, Megan U and Guo, Yuelong and Walop, Alex and Sey, Nancy Y.A and Landi, Maria T and McNeil, Daniel W and chel, Dmitriy and Farrer, Lindsay A and Markunas, Christina A and Vink, Jacqueline M and Hottenga, Jouke Jan and Iacono, William G and Kranzler, Henry R and Saccone, Nancy L and Neale, Michael C and Madden, Pamela and Rietschel, Marcella and Marazita, Mary L and McGue, Matthew and Won, Hyejung and Winterer, Georg and Grucza, Richard and Dick, Danielle M and Gelernter, Joel and Caporaso, Neil E and Baker, Timothy B and Boomsma, Dorret I and Kaprio, Jaakko and Hokanson, John E and Vrieze, Scott and Bierut, Laura J and Johnson, Eric O and Hancock, Dana B
Nature communications, ISSN 2041-1723, 11/2020, Volume 11, Issue 1, pp. 1 - 13
Chemistry(all) | Biochemistry, Genetics and Molecular Biology(all) | Physics and Astronomy(all) | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Phenotype | Quantitative Trait, Heritable | Humans | Molecular Sequence Annotation | Inheritance Patterns - genetics | Linkage Disequilibrium - genetics | Polymorphism, Single Nucleotide - genetics | Tobacco Use Disorder - genetics | Genetic Loci | Cerebellum | Phenotypes | Genomes | Single-nucleotide polymorphism | Genetic diversity | Gene expression | Cigarette smoking | Loci | Morbidity | Dependence | Genetics | Heritability | Drug dependence | Nicotine | Smoking | Index Medicus | Behavioural genetics | Genome-wide association studies
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9. Full Text Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation
by Markunas, Christina A and Enterline, David S and Dunlap, Kaitlyn and Soldano, Karen and Cope, Heidi and Stajich, Jeffrey and Grant, Gerald and Fuchs, Herbert and Gregory, Simon G and Ashley‐Koch, Allison E
Annals of human genetics, ISSN 0003-4800, 01/2014, Volume 78, Issue 1, pp. 1 - 12
ordered subset analysis | Posterior cranial fossa | Chiari Type I Malformation | endophenotypes | heritability | Heritability | Ordered subset analysis | Endophenotypes | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Quantitative Trait, Heritable | Humans | Middle Aged | Male | Young Adult | Cranial Fossa, Posterior - abnormalities | Arnold-Chiari Malformation - diagnosis | Arnold-Chiari Malformation - genetics | Adolescent | Adult | Female | Child | Principal Component Analysis | Genetic Linkage | Genetic research | Chromosomes | Genomics | Index Medicus
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