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life sciences & biomedicine (20) 20
science & technology (20) 20
humans (15) 15
genomes (12) 12
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european continental ancestry group - genetics (3) 3
fenofibrate (3) 3
general & internal medicine (3) 3
hypertriglyceridemia - drug therapy (3) 3
hypertriglyceridemia - genetics (3) 3
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medicine, general & internal (3) 3
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1. Full Text JEM: A joint test to estimate the effect of multiple genetic variants on DNA methylation
by Sarnowski, Chloe and Huan, Tianxiao and Jain, Deepti and Liu, Chunyu and Yao, Chen and Joehanes, Roby and Levy, Daniel and Dupuis, Josee
Genetic epidemiology, ISSN 0741-0395, 10/2020
Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Mathematical & Computational Biology | Index Medicus
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2. Full Text SigMod: an exact and efficient method to identify a strongly interconnected disease-associated module in a gene network
by Liu, Yuanlong and Brossard, Myriam and Roqueiro, Damian and Margaritte-Jeannin, Patricia and Sarnowski, Chloe and Bouzigon, Emmanuelle and Demenais, Florence
BIOINFORMATICS, ISSN 1367-4803, 05/2017, Volume 33, Issue 10, pp. 1536 - 1544
Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Computational Biology - methods | Genetic Predisposition to Disease | Algorithms | Humans | Polymorphism, Single Nucleotide | Software | Gene Regulatory Networks | Genome-Wide Association Study - methods | Asthma - genetics | Index Medicus
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3. Full Text Impact of Genetic Determinants of HbA1c on Type 2 Diabetes Risk and Diagnosis
by Sarnowski, Chloé and Hivert, Marie-France
Current diabetes reports, ISSN 1534-4827, 8/2018, Volume 18, Issue 8, pp. 1 - 9
Type 2 diabetes | Hemoglobinopathies | GWAS | Medicine & Public Health | Hemoglobin A1c | Erythrocytes | Diabetes | Genetic variants | Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Medical colleges | Genomics | African Americans | Genetic research | Glycosylated hemoglobin | Diagnosis | Risk factors | Medical diagnosis | Genomes | Index Medicus
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4. Full Text Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels
by Sarnowski, Chloé and Lent, Samantha and Dupuis, Josée
BMC genetics, ISSN 1471-2156, 09/2018, Volume 19, Issue Suppl 1, pp. 83 - 83
Hypertriglyceridemia - drug therapy | Hypoglycemic Agents - therapeutic use | Genome-Wide Association Study | Epigenomics | Hypertriglyceridemia - genetics | Humans | Parents | Fenofibrate - therapeutic use | DNA Methylation | Phenotype | Triglycerides - blood | CpG Islands | Polymorphism, Single Nucleotide | Physiological aspects | Epigenetic inheritance | Genetic aspects | Triglycerides | Research | Methylation | Analysis | Single nucleotide polymorphisms | Mediation | Investigations | Phenotypes | Fasting | DNA probes | Lipids | Genomes | Single-nucleotide polymorphism | Gene expression | Metabolic syndrome | Datasets | Studies | Fenofibrate | Genetic variance | Diet | DNA methylation | Epigenetics | Genetics | Software | Heritability | Probes | Deoxyribonucleic acid--DNA | Fenofibrate treatment | Parent-of-origin effects
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5. Full Text DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis
by Sarnowski, Chloé, PhD and Laprise, Catherine, PhD and Malerba, Giovanni, PhD and Moffatt, Miriam F., DPhil and Dizier, Marie-Hélène, PhD and Morin, Andréanne, MSc and Vincent, Quentin B., MD, PhD and Rohde, Klaus, PhD and Esparza-Gordillo, Jorge, PhD and Margaritte-Jeannin, Patricia, PhD and Liang, Liming, PhD and Lee, Young-Ae, MD and Bousquet, Jean, MD and Siroux, Valérie, PhD and Pignatti, Pier Franco, MD and Cookson, William O., MD, DPhil and Lathrop, Mark, PhD and Pastinen, Tomi, MD and Demenais, Florence, MD and Bouzigon, Emmanuelle, MD, PhD
Journal of allergy and clinical immunology, ISSN 0091-6749, 2016, Volume 138, Issue 3, pp. 748 - 753
Allergy and Immunology | parent-of-origin effect | DNA methylation | positional cloning | asthma | allergic rhinitis | Linkage analysis | genetic association study | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Rhinitis, Allergic - genetics | Comorbidity | Humans | Genotype | Rhinitis, Allergic - epidemiology | Receptor, Melatonin, MT1 - genetics | Asthma - genetics | Genetic Variation | DNA Methylation | Alleles | CpG Islands | Paternal Inheritance | Asthma - epidemiology | Allergens | Epigenetic inheritance | Rhinitis | Communicable diseases | DNA | Genetic research | Research institutes | Methylation | Public health | Melatonin | Analysis | Studies | Datasets | Epigenetics | Families & family life | Genomes | Gene expression | Epidemiology | Allergies | Deoxyribonucleic acid--DNA | Asthma | Index Medicus | Abridged Index Medicus | Life Sciences | Allergology
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6. Full Text Whole genome sequence analyses of brain imaging measures in the Framingham Study
by Sarnowski, Chloé and Satizabal, Claudia L and DeCarli, Charles and Pitsillides, Achilleas N and Cupples, L Adrienne and Vasan, Ramachandran S and Wilson, James G and Bis, Joshua C and Fornage, Myriam and Beiser, Alexa S and DeStefano, Anita L and Dupuis, Josée and Seshadri, Sudha and TOPMed Neurocognitive Working Grp and NHLBI Trans-Omics Precision Med TO and NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium and TOPMed Neurocognitive Working Group
Neurology, ISSN 0028-3878, 12/2017, Volume 90, Issue 3, pp. e188 - e196
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Index Medicus | Abridged Index Medicus | 120
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7. Full Text Application of novel and existing methods to identify genes with evidence of epigenetic association: results from GAW20
by Fuady, Angga M and Lent, Samantha and Sarnowski, Chloé and Tintle, Nathan L
BMC genetics, ISSN 1471-2156, 09/2018, Volume 19, Issue Suppl 1, pp. 72 - 72
Hypertriglyceridemia - drug therapy | Hypoglycemic Agents - therapeutic use | DNA Methylation | Genome-Wide Association Study | Hypertriglyceridemia - genetics | Epigenesis, Genetic | Humans | Polymorphism, Single Nucleotide | Physiological aspects | Epigenetic inheritance | Research | Single nucleotide polymorphisms | Identification and classification | Genes | Methylation | Methods | Working groups | Environmental health | Association analysis | Data processing | Lipids | Genomes | Single-nucleotide polymorphism | Studies | Pedigree | Technological change | DNA methylation | Epigenetics | Deoxyribonucleic acid--DNA | Multimarker tests | Methodology | Ascertainment | Single nucleotide polymorphism | GAW20 | Family data
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8. Full Text A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions
by Sugier, Pierre-Emmanuel and Brossard, Myriam and Sarnowski, Chloé and Vaysse, Amaury and Morin, Andréanne and Pain, Lucile and Margaritte-Jeannin, Patricia and Dizier, Marie-Hélène and Cookson, William O.C.M and Lathrop, Mark and Moffatt, Miriam F and Laprise, Catherine and Demenais, Florence and Bouzigon, Emmanuelle
Journal of allergy and clinical immunology, ISSN 0091-6749, 05/2018, Volume 141, Issue 5, pp. 1659 - 1667.e11
ciliary function | genetics | ADGRV1 | DNAH5 | genome-wide association study | asthma | text mining | gene-gene interaction | Atopy | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Anopheles | Analysis | Genes | Genomics | Dynein | Mineral industry | Single nucleotide polymorphisms | Data mining | Mining industry | Epidemiology | Medical research | Filtration | Identification methods | Allergic diseases | Epistasis | Genomes | Single-nucleotide polymorphism | Statistics | Gene polymorphism | Loci | Allergies | Asthma | Datasets | Studies | Councils | Eczema | Genetics | Polymorphism
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9. Full Text Genetic variants associated with earlier age at menopause increase the risk of cardiovascular events in women
by Sarnowski, Chloé and Kavousi, Maryam and Isaacs, Steve and Demerath, Ellen W and Broer, Linda and Muka, Taulant and Franco, Oscar H and Ikram, Mohammad Arfan and Uitterlinden, André and Franceschini, Nora and Lunetta, Kathryn L and Murabito, Joanne M
Menopause (New York, N.Y.), ISSN 1072-3714, 04/2018, Volume 25, Issue 4, pp. 451 - 457
Age-at-natural menopause | Genetic correlation | Cardiovascular disease | Pleiotropy | DNA damage response pathway | Genetic risk score | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Predisposition to Disease | Women's Health | Age Factors | Genetic Association Studies | Humans | Middle Aged | Risk Factors | Menopause, Premature - genetics | Adult | Female | Cardiovascular Diseases - genetics | Genetic aspects | Cardiovascular diseases | Health aspects | Menopause | Risk factors | Index Medicus | cardiovascular disease | genetic risk score | genetic correlation | pleiotropy
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10. Full Text Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families
by Dizier, Marie-Hélène and Margaritte-Jeannin, Patricia and Pain, Lucile and Sarnowski, Chloé and Brossard, Myriam and Mohamdi, Hamida and Lavielle, Nolwenn and Babron, Marie-Claude C and Just, Jocelyne and Lathrop, Mark and Laprise, Catherine and Bouzigon, Emmanuelle and Demenais, Florence and Nadif, Rachel
Thorax, ISSN 0040-6376, 03/2019, Volume 74, Issue 3, pp. 254 - 260
asthma | ETS | ATP | BHR | GxE interaction | FBAT | Life Sciences & Biomedicine | Respiratory System | Science & Technology | Tobacco smoke | Disease | Cloning | Genes | Systematic review | Genomes | Cigarettes | Asthma | Studies | Consortia | Genotype & phenotype | Genetics | Smoking | Index Medicus | Life Sciences | Santé publique et épidémiologie
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11. Full Text Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program
by Sarnowski, Chloé and Leong, Aaron and Raffield, Laura M and Wu, Peitao and de Vries, Paul S and DiCorpo, Daniel and Guo, Xiuqing and Xu, Huichun and Liu, Yongmei and Zheng, Xiuwen and Hu, Yao and Brody, Jennifer A and Goodarzi, Mark O and Hidalgo, Bertha A and Highland, Heather M and Jain, Deepti and Liu, Ching-Ti and Naik, Rakhi P and O’Connell, Jeffrey R and Perry, James A and Porneala, Bianca C and Selvin, Elizabeth and Wessel, Jennifer and Psaty, Bruce M and Curran, Joanne E and Peralta, Juan M and Blangero, John and Kooperberg, Charles and Mathias, Rasika and Johnson, Andrew D and Reiner, Alexander P and Mitchell, Braxton D and Cupples, L. Adrienne and Vasan, Ramachandran S and Correa, Adolfo and Morrison, Alanna C and Boerwinkle, Eric and Rotter, Jerome I and Rich, Stephen S and Manning, Alisa K and Dupuis, Josée and Meigs, James B and TOPMed Diabetes Working Group and TOPMed Hematology Working Group and National Heart, Lung, and Blood Institute TOPMed Consortium and TOPMed Hemostasis Working Group and Natl Heart Lung Blood Inst TOPMed and TOPMed Hemostasis Working Grp and TOPMed Hematology Working Grp and TOPMed Diabet Working Grp
American journal of human genetics, ISSN 0002-9297, 10/2019, Volume 105, Issue 4, pp. 706 - 718
whole-genome sequence association analyses | The Trans-Omics for Precision Medicine (TOPMed) program | multi-ancestry sample | hemoglobin A1c | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Variation | Diabetes Mellitus - genetics | Humans | Population Groups - genetics | Female | Male | Polymorphism, Single Nucleotide | Diabetes Mellitus - diagnosis | Glycated Hemoglobin A - genetics | Cohort Studies | Precision Medicine | Genetic variation | Glycosylated hemoglobin | Genetic aspects | Research | Diabetes | Diagnosis | Health aspects | Index Medicus
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