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by Sonnenschein-van der Voort, Agnes M.M., PhD and Arends, Lidia R., PhD and de Jongste, Johan C., MD, PhD and Annesi-Maesano, Isabella, MD, PhD and Arshad, S. Hasan, DM and Barros, Henrique, MD, PhD and Basterrechea, Mikel, MD and Bisgaard, Hans, MD, DMSci and Chatzi, Leda, MD, PhD and Corpeleijn, Eva, PhD and Correia, Sofia, PharmD, MSc and Craig, Leone C., MD, PhD and Devereux, Graham, MD, PhD and Dogaru, Cristian, MD, PhD and Dostal, Miroslav, MD, DSc and Duchen, Karel, MD and Eggesbø, Merete, MD, PhD and van der Ent, C. Kors, MD, PhD and Fantini, Maria P., MD and Forastiere, Francesco, MD, PhD and Frey, Urs, MD, PhD and Gehring, Ulrike, PhD and Gori, Davide, MD and van der Gugten, Anne C., MD, PhD and Hanke, Wojciech, MD, PhD and Henderson, A. John, MD, PhD and Heude, Barbara, PhD and Iñiguez, Carmen, PhD and Inskip, Hazel M., MSc, PhD and Keil, Thomas, MD, MScPH and Kelleher, Cecily C., MD, MPH and Kogevinas, Manolis, MD, PhD and Kreiner-Møller, Eskil, MD and Kuehni, Claudia E., MD, PhD and Küpers, Leanne K., MSc and Lancz, Kinga, PhD and Larsen, Pernille S., MSc and Lau, Susanne, MD, PhD and Ludvigsson, Johnny, MD, PhD and Mommers, Monique, PhD and Nybo Andersen, Anne-Marie, MD, PhD and Palkovicova, Lubica, MD, PhD and Pike, Katharine C., MD, PhD and Pizzi, Costanza, MSc and Polanska, Kinga, PhD and Porta, Daniela, MSc and Richiardi, Lorenzo, MD, PhD and Roberts, Graham, DM and Schmidt, Anne, MD and Sram, Radim J., MD, DSc and Sunyer, Jordi, MD, PhD and Thijs, Carel, MD, PhD and Torrent, Maties, MD, PhD and Viljoen, Karien, MBChB, MSc and Wijga, Alet H., PhD and Vrijheid, Martine, PhD and Jaddoe, Vincent W.V., MD, PhD and Duijts, Liesbeth, MD, PhD and Barn- och ungdomskliniken i Linköping and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Avdelningen för kliniska vetenskaper and Barn- och kvinnocentrum and Östergötlands Läns Landsting and Hälsouniversitetet and Kvinnokliniken i Linköping
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 133, Issue 5, pp. 1317 - 1329
Background Preterm birth, low birth weight, and infant catch-up growth seem associated with an increased risk of respiratory diseases in later life, but... 
Allergy and Immunology | epidemiology | children | cohort studies | asthma | infant growth | low birth weight | wheezing | Gestational age | ADULT LUNG-FUNCTION | HE-3 MAGNETIC-RESONANCE | IMMUNOLOGY | PRESCHOOL-CHILDREN | GESTATIONAL-AGE | ALLERGY | GROWTH | BODY-MASS INDEX | COHORT | GENERATION R | RESPIRATORY SYMPTOMS | OBSTRUCTIVE AIRWAYS DISEASE | Asthma - physiopathology | Humans | Risk Factors | Europe - epidemiology | Infant | Male | Premature Birth - epidemiology | Gestational Age | Birth Weight | Premature Birth - pathology | Premature Birth - physiopathology | Female | Weight Gain | Asthma - pathology | Infant, Newborn | Asthma - epidemiology | Asthma in children | Infants (Premature) | Risk factors | Babies | Studies | Birth weight | Chronic obstructive pulmonary disease | Questionnaires | Infants prematurs | Asma infantil | Low birth weight | Cohort studies | Asma | Wheezing | Infant growth | Children | Epidemiologia | Epidemiology | Asthma | SDS, Standard deviation scores | pOR, Pooled odds ratio | BMI, Body mass index | Asthma and Lower Airway Disease | ISAAC, International Study on Asthma and Allergy in Childhood | OR, Odds ratio | Clinical Medicine | Gestational age; low birth weight; infant growth; wheezing; asthma; children; cohort studies; epidemiology | Medical and Health Sciences | Medicin och hälsovetenskap | MEDICIN | Klinisk medicin | MEDICINE
Journal Article
Nature Communications, ISSN 2041-1723, 03/2014, Volume 5, Issue 1, p. 3339
Bipolar disorder (BD) is a common and highly heritable mental illness and genome-wide association studies (GWAS) have robustly identified the first common... 
IMPUTATION | METAANALYSIS | DIAGNOSTIC INTERVIEW | RATIONALE | GENETICS | ANNOTATION | MULTIDISCIPLINARY SCIENCES | GENES | DISEASE | SCHIZOPHRENIA | LINKAGE | Genetic Predisposition to Disease - genetics | Humans | Polymorphism, Single Nucleotide - genetics | Female | Male | Adenylyl Cyclases - genetics | Genome-Wide Association Study - methods | Bipolar Disorder - genetics
Journal Article
by Jacobs, Kevin B and Yeager, Meredith and Zhou, Weiyin and Wacholder, Sholom and Wang, Zhaoming and Rodriguez-Santiago, Benjamin and Hutchinson, Amy and Deng, Xiang and Liu, Chenwei and Horner, Marie-Josephe and Cullen, Michael and Epstein, Caroline G and Burdett, Laurie and Dean, Michael C and Chatterjee, Nilanjan and Sampson, Joshua and Chung, Charles C and Kovaks, Joseph and Gapstur, Susan M and Stevens, Victoria L and Teras, Lauren T and Gaudet, Mia M and Albanes, Demetrius and Weinstein, Stephanie J and Virtamo, Jarmo and Taylor, Philip R and Freedman, Neal D and Abnet, Christian C and Goldstein, Alisa M and Hu, Nan and Yu, Kai and Yuan, Jian-Min and Liao, Linda and Ding, Ti and Qiao, You-Lin and Gao, Yu-Tang and Koh, Woon-Puay and Xiang, Yong-Bing and Tang, Ze-Zhong and Fan, Jin-Hu and Aldrich, Melinda C and Amos, Christopher and Blot, William J and Bock, Cathryn H and Gillanders, Elizabeth M and Harris, Curtis C and Haiman, Christopher A and Henderson, Brian E and Kolonel, Laurence N and Le Marchand, Loic and McNeill, Lorna H and Rybicki, Benjamin A and Schwartz, Ann G and Signorello, Lisa B and Spitz, Margaret R and Wiencke, John K and Wrensch, Margaret and Wu, Xifeng and Zanetti, Krista A and Ziegler, Regina G and Figueroa, Jonine D and Garcia-Closas, Montserrat and Malats, Nuria and Marenne, Gaelle and Prokunina-Olsson, Ludmila and Baris, Dalsu and Schwenn, Molly and Johnson, Alison and Landi, Maria Teresa and Goldin, Lynn and Consonni, Dario and Bertazzi, Pier Alberto and Rotunno, Melissa and Rajaraman, Preetha and Andersson, Ulrika and Freeman, Laura E. Beane and Berg, Christine D and Buring, Julie E and Butler, Mary A and Carreon, Tania and Feychting, Maria and Ahlbom, Anders and Gaziano, J Michael and Giles, Graham G and Hallmans, Goran and Hankinson, Susan E and Hartge, Patricia and Henriksson, Roger and Inskip, Peter D and Johansen, Christoffer and Landgren, Annelie and McKean-Cowdin, Roberta and Michaud, Dominique S and Melin, Beatrice S and Peters, Ulrike and Ruder, Avima M and Sesso, Howard D and Severi, Gianluca and Shu, Xiao-Ou and Visvanathan, Kala and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Institutionen för strålningsvetenskaper and Näringsforskning and Onkologi and Umeå universitet
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 651 - 658
Journal Article
by Wolpin, Brian M and Rizzato, Cosmeri and Kraft, Peter and Kooperberg, Charles and Petersen, Gloria M and Wang, Zhaoming and Arslan, Alan A and Beane-Freeman, Laura and Bracci, Paige M and Buring, Julie and Canzian, Federico and Duell, Eric J and Gallinger, Steven and Giles, Graham G and Goodman, Gary E and Goodman, Phyllis J and Jacobs, Eric J and Kamineni, Aruna and Klein, Alison P and Kolonel, Laurence N and Kulke, Matthew H and Li, Donghui and Malats, Núria and Olson, Sara H and Risch, Harvey A and Sesso, Howard D and Visvanathan, Kala and White, Emily and Zheng, Wei and Abnet, Christian C and Albanes, Demetrius and Andreotti, Gabriella and Austin, Melissa A and Barfield, Richard and Basso, Daniela and Berndt, Sonja I and Boutron-Ruault, Marie-Christine and Brotzman, Michelle and Büchler, Markus W and Bueno-De-Mesquita, H Bas and Bugert, Peter and Burdette, Laurie and Campa, Daniele and Caporaso, Neil E and Capurso, Gabriele and Chung, Charles and Cotterchio, Michelle and Costello, Eithne and Elena, Joanne and Funel, Niccola and Gaziano, J Michael and Giese, Nathalia A and Giovannucci, Edward L and Goggins, Michael and Gorman, Megan J and Gross, Myron and Haiman, Christopher A and Hassan, Manal and Helzlsouer, Kathy J and Henderson, Brian E and Holly, Elizabeth A and Hu, Nan and Hunter, David J and Innocenti, Federico and Jenab, Mazda and Kaaks, Rudolf and Key, Timothy J and Khaw, Kay-Tee and Klein, Eric A and Kogevinas, Manolis and Krogh, Vittorio and Kupcinskas, Juozas and Kurtz, Robert C and Lacroix, Andrea and Landi, Maria T and Landi, Stefano and Le Marchand, Loic and Mambrini, Andrea and Mannisto, Satu and Milne, Roger L and Nakamura, Yusuke and Oberg, Ann L and Owzar, Kouros and Patel, Alpa V and Peeters, Petra H.M and Peters, Ulrike and Pezzilli, Raffaele and Piepoli, Ada and Porta, Miquel and Real, Francisco X and Riboli, Elio and Rothman, Nathaniel and Scarpa, Aldo and Shu, Xiao-Ou and Silverman, Debra T and Soucek, Pavel and Sund, Malin and Talar-Wojnarowska, Renata and Taylor, Philip R and Theodoropoulos, George E and ... and Medicinska fakulteten and Institutionen för kirurgisk och perioperativ vetenskap and Umeå universitet
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 9, pp. 994 - 1000
Journal Article
Lancet Respiratory Medicine, The, ISSN 2213-2600, 2013, Volume 1, Issue 9, pp. 695 - 704
Journal Article
by Garcia-Closas, M and Chatterjee, N and Malats, N and Wu, X and Figueroa, J.D and Real, F.X and Berg, D. Van den and Matullo, G and Baris, D and Thun, M and Kiemeney, L.A.L.M and Vilneis, P and De Vivo, I and Albanes, D and Purdue, M and Rafnar, T and Hildebrandt, M.A.T and Kiltie, A.E and Cussenot, O and Golka, K and Kumar, R and Taylor, J.A and Mayordomo, J.I and Jacobs, K.B and Kogevinas, M and Hutchinson, A and Wang, Z and Fu, Y and Prokunina-Olsson, L and Burdett, L and Yeager, M and Wheeler, W and Tardon, A and Serra, C and Carrato, A and Garcia-Closas, R and Lloreta, J and Johnson, A and Schwenn, M and Karagas, M.R and Schned, A and Aniole, G.L and Grubb, R and Black, A and Jacobs, E.J and Diver, W.R and Gapstur, S.M and Weinstein, S.J and Virtamo, J and Cortessis, V.K and Gago-Dominguez, M and Pike, M.C and Stern, M.C and Yuan, J.M and Hunter, D.J and McGrath, M and Dinney, C.P and Czerniak, B and Chen, M and Yang, H and Vermeulen, S and Aben, K.K.H and Witjes, J.A and Makkinje, R.R and Sulem, P and Besenbacher, S and Riboli, E and Brennan, P and Panico, S and Navarro, C and Allen, N.E and Bueno-De-Mesquita, H.B and Trichopoulos, D and Caporaso, N and Landi, M.T and Canzian, F and Ljungberg, B and Tjonneland, A and Clavel-Chapelon, F and Bishop, D.T and Teo, M.T and Knowles, M.A and Guarrera, S and Polidoro, S and Ricceri, F and Sacerdote, C and Allione, A and Cancel-Tassin, G and Selinski, S and Hengstler, J.G and Dietrich, H and Fletcher, T and Rudnai, P and Gurzau, E and Koppova, K and Bolick, S.C and Godfrey, A and Xu, Z and Medicinska fakulteten and Urologi och andrologi and Institutionen för kirurgisk och perioperativ vetenskap and Umeå universitet
Nature Genetics, ISSN 1061-4036, 2010, Volume 42, Issue 11, pp. 978 - 984
We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120... 
CONFERS SUSCEPTIBILITY | CHROMOSOME 8Q24 | COMMON VARIANTS | UDP-GLUCURONOSYLTRANSFERASES | SEQUENCE VARIANT | TELOMERASE MUTATIONS | GENETICS & HEREDITY | DOWN-REGULATION | RECOMBINATION HOTSPOTS | PULMONARY-FIBROSIS | CELL-CARCINOMA | Smoking - adverse effects | United States - epidemiology | Arylamine N-Acetyltransferase - metabolism | Humans | Male | Incidence | Chromosomes, Human, Pair 2 - genetics | Chromosomes, Human, Pair 22 - genetics | Urinary Bladder Neoplasms - genetics | Chromosome Mapping - methods | Urinary Bladder Neoplasms - pathology | Female | Urinary Bladder Neoplasms - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Risk Assessment | Risk Factors | Europe - epidemiology | Sex Characteristics | Spain - epidemiology | Family | Arylamine N-Acetyltransferase - genetics | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 18 - genetics | Neoplasm Staging | Quantitative trait loci | Genetic aspects | Disease susceptibility | Research | Bladder cancer | Studies | Genotype & phenotype | Family medical history | Chromosomes | Cancer | Tumors | Index Medicus | Genome-wide association studies | Psychology | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | confers susceptibility; udp-glucuronosyltransferases; recombination hotspots; telomerase mutations; pulmonary-fibrosis; sequence variant; common variants; chromosome 8q24; down-regulation; cell-carcinoma
Journal Article