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1. Full Text A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Paediatric Cohorts
by Middeldorp, Christel M., MD, PhD and Hammerschlag, Anke R., MSc and Ouwens, Klaasjan G., MSc and Groen-Blokhuis, Maria M., MD, PhD and St. Pourcain, Beate, PhD and Greven, Corina U., PhD and Pappa, Irene, MD, PhD and Tiesler, Carla M.T., PhD and Ang, Wei, MSc and Nolte, Ilja M., PhD and Vilor-Tejedor, Natalia, MSc and Bacelis, Jonas, MSc and Ebejer, Jane L., PhD and Zhao, Huiying, PhD and Davies, Gareth E., PhD and Ehli, Erik A., PhD and Evans, David M., PhD and Fedko, Iryna O., MSc and Guxens, Mònica, PhD and Hottenga, Jouke-Jan, PhD and Hudziak, James J., MD and Jugessur, Astanand, PhD and Kemp, John P., PhD and Krapohl, Eva, MSc and Martin, Nicholas G., PhD and Murcia, Mario, MSc and Myhre, Ronny, PhD and Ormel, Johan, PhD and Ring, Susan M., PhD and Standl, Marie, PhD and Stergiakouli, Evie, PhD and Stoltenberg, Camilla, MD, PhD and Thiering, Elisabeth, PhD and Timpson, Nicholas J., PhD and Trzaskowski, Maciej, PhD and van der Most, Peter J., PhD and Wang, Carol, BSc and Nyholt, Dale R., PhD and Medland, Sarah E., PhD and Neale, Benjamin, PhD and Jacobsson, Bo, MD, PhD and Sunyer, Jordi, PhD and Hartman, Catharina A., PhD and Whitehouse, Andrew J.O., PhD and Pennell, Craig E., MBBS, PhD and Heinrich, Joachim, PhD and Plomin, Robert, PhD and Smith, George Davey, PhD and Tiemeier, Henning, MD, PhD and Posthuma, Danielle, PhD and Boomsma, Dorret I., PhD and EArly Genetics Lifecourse and Psychiatric Genomics Consortium and EArly Genetics and Lifecourse Epidemiology (EAGLE) Consortium and Psychiatric Genomics Consortium ADHD Working Group and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Sahlgrenska akademin and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Obstetrics and Gynecology and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för obstetrik och gynekologi
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2016, Volume 55, Issue 10, pp. 896 - 905.e6
Abstract Objective To elucidate the influence of common genetic variants on childhood attention-deficit/hyperactivity disorder (ADHD) symptoms, to identify... 
Pediatrics | Psychiatry | GWA | meta-analysis | ADHD symptoms | attention problems | SNP heritability | ADHD | BEHAVIOR PROBLEMS | PSYCHIATRY | DEFICIT HYPERACTIVITY DISORDER | PSYCHOLOGY, DEVELOPMENTAL | RISK | CHILDHOOD | TWIN | PROFILE | ULTRASOUND | PEDIATRICS | GENETIC INFLUENCES | TRAITS | Genome-Wide Association Study | Genetics, Population - methods | Attention Deficit Disorder with Hyperactivity - genetics | Humans | Adolescent | Attention Deficit Disorder with Hyperactivity - psychology | Female | Male | Child | Case-Control Studies | Cohort Studies | Genome-wide association studies | Analysis | Attention-deficit hyperactivity disorder | Causes of | Heritability | Genetic aspects | Single nucleotide polymorphisms | Diagnosis | Attention deficit disorder | Genotype & phenotype | Genomes | Epidemiology | Meta-analysis | Attention deficit hyperactivity disorder | Genes | Associations | Variants | Lying | Childhood | Genetic factors | Statistical power | Power | Index Medicus | Trastorn per dèficit d'atenció amb hiperactivitat | Genètica | Psykiatri
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2. Full Text Genome-wide association study identifies 74 loci associated with educational attainment
by Okbay, Aysu and Beauchamp, Jonathan and Fontana, M.A and Lee, James J and Pers, Tune and Rietveld, C.A and Turley, Patrick and Chen, G.-B and Emilsson, Valur and Meddens, S.F.W and Oskarsson, S and Pickrell, J.K and Thom, K and Timshel, P and Vlaming, Ronald and Abdellaoui, Abdel and Ahluwalia, Tarunveer Singh and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, G and Brandsma, Johan and Pina Concas, M and Derringer, J and Furlotte, N.A and Galesloot, Tessel and Girotto, S and Gupta, R and Hall, Leanne M and Harris, Sarah and Hofer, E and Horikoshi, M and Huffman, Jennifer E and Kaasik, K and Kalafati, Ioanna-Panagiota and Karlsson, Robert and Kong, Augustine and Lahti, Jari and Lee, Sven and Deleeuw, C and Lind, Penelope and Lindgren, K.-O and Liu, T and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Mike and Most, Peter and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter and Qian, Y and Raitakari, Olli and Rueedi, R and Salvi, E and Schmidt, B and Schraut, K.E and Shi, J and Smith, Albert Vernon and Poot, Raymond and St Pourcain, Beate and Teumer, Alexander and Thorleifsson, Gudmar and Verweij, Niek and Vuckovic, gana and Wellmann, J and Westra, Harm-Jan and Yang, J and Zhao, W and Zhu, Z and Alizadeh, Behrooz and Amin, Najaf and Bakshi, A and Baumeister, Sebastian and Biino, G and Bønnelykke, Klaus and Boyle, Patricia and Campbell, Harry and Cappuccio, F.P and Davies, Gail and Neve, Jan-Emmanuel and Deloukas, Panagiotis and Demuth, Ilja and Ding, J and Eibich, P and Eisele, L and Eklund, Niina and Evans, David and Faul, Jessica D and Feitosa, Mary Furlan and Forstner, Aneas and Gandin, Ilaria and Gunnarsson, B and Halldorsson, Bjarni and Harris, Tamara and Holliday, Elizabeth and Heath, Anew C and Hocking, L.J and Homuth, Georg and Horan, Mike and ... and LifeLines Cohort Study and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 539 - 542
textabstractEducational attainment is strongly influenced by social and other environmental factors, but genetic factors are estimated to account for at least... 
ACHIEVEMENT | TRAITS | MULTIDISCIPLINARY SCIENCES | HERITABILITY | Genome-Wide Association Study | Gene Expression Regulation - genetics | Humans | Molecular Sequence Annotation | Computational Biology | Fetus - metabolism | United Kingdom | Cognition | Educational Status | Bipolar Disorder - genetics | Gene-Environment Interaction | Brain - metabolism | Schizophrenia - genetics | Polymorphism, Single Nucleotide - genetics | Alzheimer Disease - genetics | Quantitative trait loci | Academic achievement | Genome-wide association studies | Genetic aspects | Observations | Studies | Genomes | Gene expression | Genes | Educational attainment | Meta-analysis | Index Medicus | Quantitative Finance | Samhällsvetenskap | Biological Sciences | Social Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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3. Full Text Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
by Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjoerg and Hotze, Melanie and Strachan, David P and Curtin, John A and Bonnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P and den Dekker, Herman T and Ferreira, Manuel A and Altmaier, Elisabeth and Sleiman, Patrick M. A and Xiao, Feng Li and Gonzalez, Juan R and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Chengjian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M and Venturini, Cristina and Pennell, Craig E and Barton, Sheila J and Levin, Albert M and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Moller, Eskil and Lockett, Gabrielle A and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L and Henderson, A. John and Kemp, John P and Zheng, Jie and Smith, George Davey and Rueschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Aneas and Homuth, Georg and Schmidt, Carsten O and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Roiguez, Elke and Peters, Annette and Franke, Ane and Lieb, Wolfgang and Novak, Natalija and Foelster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L and Grarup, Niels and De Jongste, Johan C and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V and Pasmans, Suzanne G. M. A and Elbert, Niels J and Uitterlinden, Ane G and Marks, Guy B and Thompson, Philip J and Matheson, Melanie C and Robertson, Colin F and Ried, Janina S and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong and Sun, Liang Dan and McAleer, Maeve A and O'Regan, Grainne M and Fahy, Caoimhe M. R and Campbell, Linda E and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T and ... and AAGC and EArly Genetics Lifecourse Epidemio and Australian Asthma Genetics Consortium (AAGC) and the EArly Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Obstetrics and Gynecology and Sahlgrenska Academy and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för obstetrik och gynekologi
Nature Genetics, ISSN 1061-4036, 12/2015, Volume 47, Issue 12, pp. 1449 - +
Genetic association studies have identified 21 loci associated with atopic dermatitis risk predominantly in populations of European ancestry. To identify... 
CELLS | METAANALYSIS | VARIANTS | FILAGGRIN | DISEASE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | ASTHMA | SKIN | INTERLEUKIN-7 RECEPTOR | IL-7 | Dermatitis, Atopic - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Risk Factors | Immunity, Innate - genetics | Dermatitis, Atopic - pathology | Genetic Loci | Dermatitis, Atopic - ethnology | Case-Control Studies | Ethnic Groups - genetics | T-Lymphocytes - cytology | T-Lymphocytes - metabolism | Genetic Markers - genetics | Polymorphism, Single Nucleotide - genetics | T-Lymphocytes - immunology | Genome-wide association studies | Immune response | Atopic dermatitis | Development and progression | Genotype | Genetic aspects | Identification and classification | Health aspects | Methods | Studies | Confidence intervals | Inflammatory bowel disease | Genealogy | Disease | Psoriasis | Bias | Eczema | Genomes | Mutation | Dermatitis | Quality of life | Index Medicus | Genètica | Grups ètnics | Dermatitis atòpica | GENETIC ARCHITECTURE | ATES OF AMERICA | Genetics & Heredity | PE1761 | Obstetrics, Gynecology and Reproductive Medicine | INFLAMMATORY-BOWEL-DISEASE | JAPANESE POPULATION | Reproduktionsmedicin och gynekologi | V110 | PSORIASIS
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4. Full Text Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
by Zhang, Ge and Feenstra, Bjarke and Bacelis, Jonas and Liu, Xueping and Muglia, Lisa M and Muglia, Louis J and Juodakis, Julius and Miller, Daniel E and Litterman, Nadia and Jiang, Pan-Pan and Russell, Laura and Hinds, David A and Hu, Youna and Weirauch, Matthew T and Chen, Xiaoting and Chavan, Arun R and Wagner, Günter P and Pavličev, Mihaela and Nnamani, Mauris C and Maziarz, Jamie and Karjalainen, Minna K and Rämet, Mika and Sengpiel, Verena and Geller, Frank and Boyd, Heather A and Palotie, Aarno and Momany, Allison and Bedell, Bruce and Ryckman, Kelli K and Huusko, Johanna M and Forney, Carmy R and Kottyan, Leah C and Hallman, Mikko and Teramo, Kari and Nohr, Ellen A and Davey Smith, George and Melbye, Mads and Jacobsson, Bo and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Obstetrics and Gynecology and Sahlgrenska Academy and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för obstetrik och gynekologi
The New England Journal of Medicine, ISSN 0028-4793, 09/2017, Volume 377, Issue 12, pp. 1156 - 1167
In a genomewide association study, variants at three loci — EBF1, EEFSEC, and AGTR2 — were associated with both gestational duration and preterm birth. 
MEDICINE, GENERAL & INTERNAL | POLYMORPHISMS | VARIANTS | SUSCEPTIBILITY | RISK | LOCI | DIFFERENTIATION | WEIGHT | ENDOMETRIOSIS | GENOME-WIDE ASSOCIATION | AGE | Receptor, Angiotensin, Type 2 - genetics | ras Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Premature Birth - genetics | Datasets as Topic | Humans | Gestational Age | Wnt4 Protein - genetics | Genetic Variation | Pregnancy | Regression Analysis | Phenotype | Trans-Activators - genetics | Female | Polymorphism, Single Nucleotide | Adenylyl Cyclases - genetics | Peptide Elongation Factors - genetics | Genetic variation | Causes of | Reports | Genetic aspects | Research | Premature labor | Haplotypes | Medical research | Pediatrics | Wnt protein | Premature birth | Genomics | Principal components analysis | Genomes | Gestation | Birth | Epidemiology | Obstetrics | Studies | Uterus | Replication | Genetics | Genetic factors | Public health | Polymorphism | Index Medicus | Abridged Index Medicus | differentiation | susceptibility | endometriosis | weight | variants | polymorphisms | Obstetrics, Gynecology and Reproductive Medicine | Reproduktionsmedicin och gynekologi | risk | genome-wide association | loci | General & Internal Medicine | age
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5. Full Text Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
by Lee, James J and Wedow, Robbee and Okbay, Aysu and Kong, Edward and Maghzian, Omeed and Zacher, Meghan and Nguyen-Viet, Tuan Anh and Bowers, Peter and Sidorenko, Julia and Karlsson Linnér, Richard and Fontana, Mark Alan and Kundu, Tushar and Lee, Chanwook and Li, Hui and Li, Ruoxi and Royer, Rebecca and Timshel, Pascal N and Walters, Raymond K and Willoughby, Emily A and Yengo, Loïc and Agee, Michelle and Alipanahi, Babak and Auton, Adam and Bell, Robert K and Bryc, Katarzyna and Elson, Sarah L and Fontanillas, Pierre and Hinds, David A and McCreight, Jennifer C and Huber, Karen E and Litterman, Nadia K and McIntyre, Matthew H and Mountain, Joanna L and Noblin, Elizabeth S and Northover, Carrie A. M and Pitts, Steven J and Sathirapongsasuti, J. Fah and Sazonova, Olga V and Shelton, Janie F and Shringarpure, Suyash and Tian, Chao and Vacic, Vladimir and Wilson, Catherine H and Okbay, Aysu and Beauchamp, Jonathan P and Fontana, Mark Alan and Lee, James J and Pers, Tune H and Rietveld, Cornelius A and Turley, Patrick and Chen, Guo-Bo and Emilsson, Valur and Meddens, S. Fleur W and Oskarsson, Sven and Pickrell, Joseph K and Thom, Kevin and Timshel, Pascal and Vlaming, Ronald de and Abdellaoui, Abdel and Ahluwalia, Tarunveer S and Bacelis, Jonas and Baumbach, Clemens and Bjornsdottir, Gyda and Brandsma, Johannes H and Concas, Maria Pina and Derringer, Jaime and Furlotte, Nicholas A and Galesloot, Tessel E and Girotto, Giorgia and Gupta, Richa and Hall, Leanne M and Harris, Sarah E and Hofer, Edith and Horikoshi, Momoko and Huffman, Jennifer E and Kaasik, Kadri and Kalafati, Ioanna P and Karlsson, Robert and Kong, Augustine and Lahti, Jari and van der Lee, Sven J and Leeuw, Christiaan de and Lind, Penelope A and Lindgren, Karl-Oskar and Liu, Tian and Mangino, Massimo and Marten, Jonathan and Mihailov, Evelin and Miller, Michael B and van der Most, Peter J and Oldmeadow, Christopher and Payton, Antony and Pervjakova, Natalia and Peyrot, Wouter J and Qian, Yong and Raitakari, Olli and Rueedi, Rico and Salvi, Erika and Schmidt, Börge and Schraut, Katharina E and ... and 23Me Res Team and Social Sci Genetic Assoc Consortiu and COGENT Cognitive Genomics Consorti and 23andMe Research Team and COGENT (Cognitive Genomics Consortium) and Social Science Genetic Association Consortium and Humanistisk-samhällsvetenskapliga vetenskapsområdet and Uppsala universitet and Statsvetenskapliga institutionen and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 08/2018, Volume 50, Issue 8, pp. 1112 - 1121
Here we conducted a large-scale genetic association analysis of educational attainment in a sample of approximately 1.1 million individuals and identify 1,271... 
INTELLIGENCE | HUMAN TRAITS | HUMAN BRAIN | METAANALYSIS | GWAS | STATISTICS | GENETICS & HEREDITY | POPULATIONS | LOCI | MAPPING CAUSAL VARIANTS | HERITABILITY | Humans | Middle Aged | Male | Educational Status | Multifactorial Inheritance | Phenotype | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Cohort Studies | Cell interaction | Genome-wide association studies | Usage | Analysis | Multifactorial traits | Research | Health education | Brain | Phenotypes | Dosage compensation | Sample size | Cognitive ability | Association analysis | Genomes | Single-nucleotide polymorphism | Gene expression | Estimates | Environmental effects | Educational attainment | Meta-analysis | Consortia | Education | Genetic analysis | Heritability | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Biological Sciences | Naturvetenskap | Medical and Health Sciences | Medicin och hälsovetenskap | Biologiska vetenskaper | Medicinska och farmaceutiska grundvetenskaper | Natural Sciences
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6. Full Text Assessing the Causal Relationship of Maternal Height on Birth Size and Gestational Age at Birth: A Mendelian Randomization Analysis
by Zhang, Ge and Bacelis, Jonas and Lengyel, Candice and Teramo, Kari and Hallman, Mikko and Helgeland, Øyvind and Johansson, Stefan and Myhre, Ronny and Sengpiel, Verena and Njølstad, Pål Rasmus and Jacobsson, Bo and Muglia, Louis and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Obstetrics and Gynecology and Sahlgrenska Academy and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för obstetrik och gynekologi
PLoS Medicine, ISSN 1549-1277, 08/2015, Volume 12, Issue 8, pp. e1001865 - e1001865
Background Observational epidemiological studies indicate that maternal height is associated with gestational age at birth and fetal growth measures (i.e.,... 
MULTIPLE GENETIC-VARIANTS | MEDICINE, GENERAL & INTERNAL | RISK-FACTORS | DETERMINANTS | INSTRUMENTAL VARIABLES | CHILDHOOD GROWTH | LENGTH | WEIGHT | PRETERM | COMPLEX TRAITS | ASSOCIATION | Phenotype | Pregnant women | Birth size | Genetic aspects | Birth weight | Single nucleotide polymorphisms | Identification and classification | Childbirth | Index Medicus | Obstetrics, Gynecology and Reproductive Medicine | Reproduktionsmedicin och gynekologi | Haplotypes | Disease | Prenatal development | Genomes | Mothers | Studies | Babies | Pregnancy | Genotype & phenotype | Researchers | Influence | Diabetes | Age
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7. Full Text Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: Results from a large prospective observational cohort study
by Sengpiel, Verena and Elind, Elisabeth and Bacelis, Jonas and Nilsson, Staffan and Grove, Jakob and Myhre, Ronny and Haugen, Margaretha and Meltzer, Helle M and Alexander, Jan and Jacobsson, Bo and Brantsæter, Anne-Lise and Department of Mathematical Sciences, Mathematical Statistics and Naturvetenskapliga fakulteten and Faculty of Sciences and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Sahlgrenska akademin and Institutionen för matematiska vetenskaper, matematisk statistik and Institute of Clinical Sciences, Section for the Health of Women and Children, Department of Obstetrics and Gynecology and Institutionen för kliniska vetenskaper, sektionen för kvinnors och barns hälsa, Avdelningen för obstetrik och gynekologi
BMC Medicine, ISSN 1741-7015, 02/2013, Volume 11, Issue 1, pp. 42 - 42
Background: Pregnant women consume caffeine daily. The aim of this study was to examine the association between maternal caffeine intake from different sources... 
birth weight | tea | caffeine | small for gestational age | soft drinks | coffee | growth curve | intrauterine growth restriction | gestational length | preterm delivery | CHILD COHORT | FETAL-GROWTH | PRETERM BIRTH | RISK | PLASMA CAROTENOIDS | MEDICINE, GENERAL & INTERNAL | MEDITERRANEAN-TYPE DIET | SPONTANEOUS-ABORTION | NORWEGIAN MOTHER | AGE BIRTH | Caffeine - metabolism | Pregnancy | Young Adult | Birth Weight | Premature Birth | Norway | Humans | Adult | Female | Diet - methods | Cohort Studies | Pregnant women | Analysis | Premature birth | Birth weight, Low | Coffee | Gestational age | Caffeine | Studies | Womens health | Epidemiology | Index Medicus | Obstetrics, Gynecology and Reproductive Medicine | Reproduktionsmedicin och gynekologi
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8. Full Text A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis
by Bohman, Anton and Juodakis, Julius and Oscarsson, Martin and Bacelis, Jonas and Bende, Mats and Naluai, Åsa Torinsson and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Öron-, näs- och halssjukdomar and Uppsala universitet and Institutionen för kirurgiska vetenskaper
PLoS ONE, ISSN 1932-6203, 12/2017, Volume 12, Issue 12, pp. e0185244 - e0185244
Background The pathogenesis of chronic rhinosinusitis with nasal polyps is largely unknown. Previous studies have given valuable information about genetic... 
SINUSITIS | POPULATION | CELLS | POLYMORPHISMS | MULTIDISCIPLINARY SCIENCES | EXACERBATED RESPIRATORY-DISEASE | CYSTIC-FIBROSIS | PREVALENCE | ASTHMATIC-PATIENTS | IDENTIFICATION | CFTR | Genetic markers | Genome-wide association studies | Usage | Research | gna | Nasal polyps | Sinusitis | Disease | Pathogenesis | Rhinosinusitis | Genes | Genomics | Otolaryngology | Genomes | Single-nucleotide polymorphism | Males | Immunology | Population | Chronic illnesses | Gynecology | Markers | Skewed distributions | Cystic fibrosis | Gene expression | Obstetrics | Loci | Asthma | Quantitative trait loci | Studies | Genetic variance | Hypotheses | Hospitals | Respiratory diseases | Histocompatibility antigen HLA | Females | Polyps | Index Medicus | Clinical Medicine | Otorhinolaryngology | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Oto-rino-laryngologi
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