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Geometriae Dedicata, ISSN 0046-5755, 01/2018, Volume 197, Issue 1, pp. 97 - 106
Inoue constructed the first examples of smooth minimal complex surfaces of general type with pg=0 and K2=7. These surfaces are finite Galois covers of the... 
Loci
Journal Article
by Michailidou, Kyriaki and Hall, Per and Gonzalez-Neira, Anna and Ghoussaini, Maya and Dennis, Joe and Milne, Roger L and Schmidt, Marjanka K and Chang-Claude, Jenny and Bojesen, Stig E and Bolla, Manjeet K and Wang, Qin and Dicks, Ed and Lee, Anew and Turnbull, Clare and Rahman, Nazneen and Fletcher, Olivia and Peto, Julian and Gibson, Lorna and dos Santos Silva, Isabel and Nevanlinna, Heli and Muranen, Taru A and Aittomäki, Kristiina and Blomqvist, Carl and Czene, Kamila and Irwanto, Astrid and Liu, Jianjun and Waisfisz, Quinten and Meijers-Heijboer, Hanne and Adank, Muriel and van der Luijt, Rob B and Hein, Rebecca and Dahmen, Norbert and Beckman, Lars and Meindl, Alfons and Schmutzler, Rita K and Müller-Myhsok, Bertram and Lichtner, Peter and Hopper, John L and Southey, Melissa C and Makalic, Enes and Schmidt, Daniel F and Uitterlinden, Ane G and Hofman, Albert and Hunter, David J and Chanock, Stephen J and Vincent, Daniel and Bacot, François and Tessier, Daniel C and Canisius, Sander and Wessels, Lodewyk F. A and Haiman, Christopher A and Shah, Mitul and Luben, Robert and Brown, Judith and Luccarini, Craig and Schoof, Nils and Humphreys, Keith and Li, Jingmei and Nordestgaard, Børge G and Nielsen, Sune F and Flyger, Henrik and Couch, Fergus J and Wang, Xianshu and Vachon, Celine and Stevens, Kristen N and Lambrechts, Diether and Moisse, Matthieu and Paridaens, Robert and Christiaens, Marie-Rose and Rudolph, Anja and Nickels, Stefan and Flesch-Janys, Dieter and Johnson, Nichola and Aitken, Zoe and Aaltonen, Kirsimari and Heikkinen, Tuomas and Broeks, Annegien and van 't Veer, Laura J and van der Schoot, C. Ellen and Guénel, Pascal and Truong, Thérèse and Laurent-Puig, Pierre and Menegaux, Florence and Marme, Frederik and Schneeweiss, Aneas and Sohn, Christof and Burwinkel, Barbara and Zamora, M. Pilar and Perez, Jose Ignacio Arias and Pita, Guillermo and Alonso, M. Rosario and Cox, Angela and Brock, Ian W and Cross, Simon S and Reed, Malcolm W. R and Sawyer, Elinor J and Tomlinson, Ian and Kerin, Michael J and Miller, Nicola and Henderson, Brian E and ... and kConFab Investigators and GENICA Gene Environm Interaction B and Hereditary Breast Ovarian Canc Res and Australian Ovarian Can Study Grp and Breast Ovarian Canc Susceptibility and Australian Ovarian Cancer Study Group and GENICA (Gene Environment Interaction and Breast Cancer in Germany) Network and Breast and Ovarian Cancer Susceptibility Collaboration and Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and The Breast and Ovarian Cancer Susceptibility Collaboration and The GENICA (Gene Environment Interaction and Breast Cancer in Germany) Network
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 4, pp. 353 - 361
Journal Article
by Elks, Cathy and Perry, John and Sulem, Patrick and Chasman, Daniel and Franceschini, Nora and He, Chunyan and Lunetta, Kathryn and Visser, Jenny and Byrne, Enda and Cousminer, Diana and Gudbjartsson, Daniel and Esko, Tõnu and Feenstra, Bjarke and Hottenga, Jouke Jan and Koller, Daniel and Kutalik, Zoltán and Lin, Peng and Mangino, Massimo and Marongiu, Mara and McArdle, Patrick and Smith, Albert Vernon and Stolk, Lisette and Wingerden, Sophie and Zhao, Jing Hua and Albrecht, Eva and Corre, Tanguy and Ingelsson, Erik and Hayward, Caroline and Magnusson, Patrik and Ulivi, Shelia and Warrington, Nicole and Zgaga, Lina and Alavere, Helene and Amin, Najaf and Aspelund, Thor and Bandinelli, Stefania and Barroso, Inês and Berenson, Gerald and Bergmann, Sven and Blackburn, Hannah and Boerwinkle, Eric and Buring, Julie and Busonero, F and Campbell, Harry and Chanock, Stephen and Chen, Wei and Cornelis, Marilyn and Couper, David and Coviello, Anea and Adamo, Pio and Faire, Ulf and Geus, Eco and Deloukas, Panagiotis and Döring, Angela and Easton, Douglas and Eiriksdottir, Gudny and Emilsson, Valur and Eriksson, Johan and Ferrucci, Luigi and Folsom, Aaron and Foroud, Tatiana and Garcia, Melissa and Gasparini, Paolo and Geller, Frank and Gieger, Christian and Gudnason, Vilmundur and Hall, Alistair and Hankinson, Susan and Ferreli, Liana and Heath, Anew and Hernandez, Dena and Hofman, Albert and Hu, Frank and Illig, Thomas and Järvelin, M.R and Johnson, Anew and Karasik, David and Khaw, Kay-Tee and Kiel, Douglas and Kilpelänen, Tuomas and Kolcic, Ivana and Kraft, Peter and Launer, Lenore and Laven, Joop and Li, Shengxu and Liu, Jianjun and Levy, Daniel and Martin, Nicholas and Melbye, Mads and Mooser, Vincent and Murray, Jeffrey and Nalls, Michael and Navarro, Pau and Nelis, Mari and Ness, Anew and Northstone, Kate and Oostra, Ben and Peacock, Munro and Palmer, Cameron and Palotie, Aarno and ... and GIANT Consortium and The GIANT Consortium
Nature Genetics, ISSN 1061-4036, 12/2010, Volume 42, Issue 12, pp. 1077 - 1085
Journal Article
Nature, ISSN 0028-0836, 07/2017, Volume 547, Issue 7662, pp. 173 - 178
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2013, Volume 8, Issue 2, pp. e57500 - e57500
Journal Article
Journal Article
by Kottgen, A and Albrecht, E and Teumer, A and Vitart, V and Krumsiek, J and Hundertmark, C and Pistis, G and Ruggiero, D and O'Seaghdha, C.M and Haller, T and Yang, Q and Johnson, A.D and Kutalik, Z and Smith, A.V and Shi, J.L and Struchalin, M and Middelberg, R.P.S and Brown, M.J and Gaffo, A.L and Pirastu, N and Li, G and Hayward, C and Zemunik, T and Huffman, J and Yengo, L and Zhao, J.H and Demirkan, A and Feitosa, M.F and Liu, X and Malerba, G and Lopez, L.M and van der Harst, P and Li, X.Z and Kleber, M.E and Hicks, A.A and Nolte, I.M and Johansson, A and Murgia, F and Wild, S.H and Bakker, S.J.L and Peden, J.F and Dehghan, A and Steri, M and Tenesa, A and Lagou, V and Salo, P and Mangino, M and Rose, L.M and Lehtimaki, T and Woodward, O.M and Okada, Y and Tin, A and Muller, C and Oldmeadow, C and Putku, M and Czamara, D and Kraft, P and Frogheri, L and Thun, G.A and Grotevendt, A and Gislason, G.K and Harris, T.B and Launer, L.J and McArdle, P and Shuldiner, A.R and Boerwinkle, E and Coresh, J and Schmidt, H and Schallert, M and Martin, N.G and Montgomery, G.W and Kubo, M and Nakamura, Y and Tanaka, T and Munroe, P.B and Samani, N.J and Jacobs, D.R and Liu, K and d'Adamo, P and Ulivi, S and Rotter, J.I and Psaty, B.M and Vollenweider, P and Waeber, G and Campbell, S and Devuyst, O and Navarro, P and Kolcic, I and Hastie, N and Balkau, B and Froguel, P and Esko, T and Salumets, A and Khaw, K.T and Langenberg, C and Wareham, N.J and Isaacs, A and Kraja, A and Zhang, Q.Y and Penninx, B.W.J.H and ... and DIAGRAM Consortium and MAGIC Consortium and LifeLines Cohort Study and CARDIoGRAM Consortium and ICBP Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm and Genomik and Uppsala universitet and Uppsala kliniska forskningscentrum (UCR)
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 2, pp. 145 - 154
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1371 - 1379
Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present... 
Internal Medicine | POPULATION | DEPRESSION | MEDICINE, GENERAL & INTERNAL | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | METAANALYSIS | GENE-EXPRESSION | SCHIZOPHRENIA | CACNA1C | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | Genome-Wide Association Study | Humans | Attention Deficit Disorder with Hyperactivity | Schizophrenia | Bipolar disorder | Calcium Channels, L-Type | Logistic Models | Genetic Loci | Children & youth | CACNB2 protein, human | Studies | Autism | Age of Onset | Genetics | Adult | Depressive Disorder, Major | Polymorphism, Single Nucleotide | CACNA1C protein, human | Child Development Disorders, Pervasive | Child | Attention deficit disorder | Enrichment | Brain | Calcium | Disease | Mental disorders | Hyperactivity | Genes | Mental health | Disorders | Genomes | Single-nucleotide polymorphism | Consortia | Datasets | Calcium signalling | Genetic effects | Signal transduction | Regression models | Autopsy | Classification | Psychopathology | Children | Chromosomes | Genotypes | Phenotypes | Channel gating | Attention deficit hyperactivity disorder | Calcium channels (voltage-gated) | Depression | Behavior disorders | Regression analysis | Risk analysis | Loci | Quantitative trait loci | Government grants | Calcium channels (L-type) | Diagnostic systems | Polygenic inheritance | Psychiatry | Polymorphism | Child Development Disorders, Pervasive - epidemiology | Genetic Loci - genetics | Bipolar Disorder - genetics | Depressive Disorder, Major - epidemiology | Schizophrenia - epidemiology | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Depressive Disorder, Major - genetics | Polymorphism, Single Nucleotide - genetics | Bipolar Disorder - epidemiology | Attention Deficit Disorder with Hyperactivity - epidemiology | Physiological aspects | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Medical research | Calcium channels | Depression, Mental | Genomics | Child psychopathology | Quantitative genetics | Medicine, Experimental | Genetic research | Single nucleotide polymorphisms | Index Medicus | Abridged Index Medicus | Neurosciences | Calcium Channels | Pervasive | L-Type | Child Development Disorders | Depressive Disorder | Single Nucleotide | epidemiology | genetics | Bipolar Disorder | Major | Neurovetenskaper
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