يعرض 1 - 10 نتائج من 757 نتيجة بحث عن '"Ollila, A. M"', وقت الاستعلام: 0.90s تنقيح النتائج
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    دورية أكاديمية

    المؤلفون: Ollila, Hanna M, Sharon, Eilon, Lin, Ling, Sinnott-Armstrong, Nasa, Ambati, Aditya, Yogeshwar, Selina M, Hillary, Ryan P, Jolanki, Otto, Faraco, Juliette, Einen, Mali, Luo, Guo, Zhang, Jing, Han, Fang, Yan, Han, Dong, Xiao Song, Li, Jing, Zhang, Jun, Hong, Seung-Chul, Kim, Tae Won, Dauvilliers, Yves, Barateau, Lucie, Lammers, Gert Jan, Fronczek, Rolf, Mayer, Geert, Santamaria, Joan, Arnulf, Isabelle, Knudsen-Heier, Stine, Bredahl, May Kristin Lyamouri, Thorsby, Per Medbøe, Plazzi, Giuseppe, Pizza, Fabio, Moresco, Monica, Crowe, Catherine, Van den Eeden, Stephen K, Lecendreux, Michel, Bourgin, Patrice, Kanbayashi, Takashi, Martínez-Orozco, Francisco J, Peraita-Adrados, Rosa, Benetó, Antonio, Montplaisir, Jacques, Desautels, Alex, Huang, Yu-Shu, Jennum, Poul, Nevsimalova, Sona, Kemlink, David, Iranzo, Alex, Overeem, Sebastiaan, Wierzbicka, Aleksandra, Geisler, Peter, Sonka, Karel, Honda, Makoto, Högl, Birgit, Stefani, Ambra, Coelho, Fernando Morgadinho, Mantovani, Vilma, Feketeova, Eva, Wadelius, Mia, Eriksson, Niclas, Smedje, Hans, Hallberg, Pär, Hesla, Per Egil, Rye, David, Pelin, Zerrin, Ferini-Strambi, Luigi, Bassetti, Claudio L, Mathis, Johannes, Khatami, Ramin, Aran, Adi, Nampoothiri, Sheela, Olsson, Tomas, Kockum, Ingrid, Partinen, Markku, Perola, Markus, Kornum, Birgitte R, Rueger, Sina, Winkelmann, Juliane, Miyagawa, Taku, Toyoda, Hiromi, Khor, Seik-Soon, Shimada, Mihoko, Tokunaga, Katsushi, Rivas, Manuel, Pritchard, Jonathan K, Risch, Neil, Kutalik, Zoltan, O’Hara, Ruth, Hallmayer, Joachim, Ye, Chun Jimmie, Mignot, Emmanuel J

    المصدر: Nature Communications. 14(1)

    وصف الملف: application/pdf

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    دورية أكاديمية

    المساهمون: Genomics and Computational Biology, Program in Molecular Medicine

    المصدر: Nature microbiology ; 9 ; 3 ; 751 ; 762 ; United States ; England

    العلاقة: Nature Microbiology; https://doi.org/10.1038/s41564-023-01589-3Test; Kotliar D, Raju S, Tabrizi S, Odia I, Goba A, Momoh M, Sandi JD, Nair P, Phelan E, Tariyal R, Eromon PE, Mehta S, Robles-Sikisaka R, Siddle KJ, Stremlau M, Jalloh S, Gire SK, Winnicki S, Chak B, Schaffner SF, Pauthner M, Karlsson EK, Chapin SR, Kennedy SG, Branco LM, Kanneh L, Vitti JJ, Broodie N, Gladden-Young A, Omoniwa O, Jiang PP, Yozwiak N, Heuklom S, Moses LM, Akpede GO, Asogun DA, Rubins K, Kales S, Happi AN, Iruolagbe CO, Dic-Ijiewere M, Iraoyah K, Osazuwa OO, Okonkwo AK, Kunz S, McCormick JB, Khan SH, Honko AN, Lander ES, Oldstone MBA, Hensley L, Folarin OA, Okogbenin SA, Günther S, Ollila HM, Tewhey R, Okokhere PO, Schieffelin JS, Andersen KG, Reilly SK, Grant DS, Garry RF, Barnes KG, Happi CT, Sabeti PC. Genome-wide association study identifies human genetic variants associated with fatal outcome from Lassa fever. Nat Microbiol. 2024 Mar;9(3):751-762. doi:10.1038/s41564-023-01589-3. Epub 2024 Feb 7. PMID: 38326571; PMCID: PMC10914620.; http://hdl.handle.net/20.500.14038/53260Test

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    دورية أكاديمية

    المساهمون: Institute for Molecular Medicine Finland, STEMM - Stem Cells and Metabolism Research Program, Helsinki Institute of Life Science HiLIFE, Clinicum, Children's Hospital, HUS Children and Adolescents, Faculty Common Matters (Faculty of Medicine), Medicum, Centre of Excellence in Complex Disease Genetics, Research Programs Unit, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders

    وصف الملف: application/pdf

    العلاقة: Open Access funding provided by University of Helsinki (including Helsinki University Central Hospital). This work was funded by grants from the Finnish Cultural Foundation (EH, TO and MB), Finnish Foundation for Pediatric Research (EH, TO and MB.), the Finnish Medical Foundation (EH), Sigrid Juselius Foundation (EH), Helsinki University (EH), and The Academy of Finland (EH).; Broberg , M , Ampuja , M , Jones , S , Ojala , T , Rahkonen , O , Kivelä , R , Priest , J , Palotie , A , Ollila , H M & Helle , E 2024 , ' Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects ' , BMC Genomics , vol. 25 , no. 1 , 256 . https://doi.org/10.1186/s12864-024-10172-xTest; ORCID: /0000-0003-0153-922X/work/157593800; ORCID: /0000-0002-2686-8890/work/157593934; ORCID: /0000-0002-2527-5874/work/157598047; ORCID: /0000-0002-5419-9479/work/157599035; ORCID: /0000-0002-5302-6429/work/157599585; ORCID: /0000-0001-9092-7763/work/157600076; http://hdl.handle.net/10138/574231Test; 4aa2ff7e-d653-47b5-8880-e649375d00a1; 85186899509; 001181195800001

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    دورية أكاديمية

    المساهمون: Institute for Molecular Medicine Finland

    وصف الملف: application/pdf

    العلاقة: Kalinowski , A , Tian , L , Pattni , R , Ollila , H M , Khan , M , Manko , C , Silverman , M , Ma , M , Columbo , L , Farhadian , B , Swedo , S , Murphy , T , Johnson , M , Fernell , E , Gillberg , C , Thienemann , M , Mellins , E D , Levinson , D F , Urban , A E & Frankovich , J 2023 , ' Evaluation of C4 gene copy number in Pediatric Acute Neuropsychiatric Syndrome ' , Developmental Neuroscience , vol. 45 , no. 6 , pp. 315 - 324 . https://doi.org/10.1159/000531707Test; ORCID: /0000-0002-5302-6429/work/152353819; ba0c92a2-782f-46ae-ba4d-d36289f2fc03; http://hdl.handle.net/10138/570654Test; 001018232500001

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    دورية أكاديمية

    المساهمون: Institute for Molecular Medicine Finland

    وصف الملف: application/pdf

    العلاقة: This work was supported by the National Institute of Health grants R01HL153814 (to H.W.), National Heart, Lung, and Blood Institute R35HL135818 (to S.R.), and National Institute for Health and Care Research Manchester Biomedical Research Centre.; Goodman , M O , Dashti , H S , Lane , J M , Windred , D P , Burns , A , Jones , S E , Sofer , T , Purcell , S M , Zhu , X , Ollila , H M , Kyle , S D , Spiegelhalder , K , Peker , Y , Huang , T , Cain , S W , Phillips , A J K , Saxena , R , Rutter , M K , Redline , S & Wang , H 2023 , ' Causal Association Between Subtypes of Excessive Daytime Sleepiness and Risk of Cardiovascular Diseases ' , Journal of the American Heart Association , vol. 12 , no. 24 , e030568 . https://doi.org/10.1161/JAHA.122.030568Test; ORCID: /0000-0003-0153-922X/work/152342833; ORCID: /0000-0002-5302-6429/work/152353820; 0daed711-7b6a-43c6-bde0-747888df11e2; http://hdl.handle.net/10138/570431Test; 001127622000002

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    دورية أكاديمية

    المساهمون: Institute for Molecular Medicine Finland, Helsinki Institute of Life Science HiLIFE, HUS Head and Neck Center, Clinicum, Korva-, nenä- ja kurkkutautien klinikka, HUS Neurocenter, Department of Neurosciences

    وصف الملف: application/pdf

    العلاقة: FinnGen , Jones , S E , Maisha , F I , Strausz , S J , Lammi , V , Cade , B E , Tervi , A , Helaakoski , V , Broberg , M E , Lane , J M , Redline , S , Saxena , R , Ollila , H M , Kaprio , J , Mäkitie , A & Tienari , P 2023 , ' The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections ' , EBioMedicine , vol. 93 , 104630 . https://doi.org/10.1016/j.ebiom.2023.104630Test; ORCID: /0000-0002-3256-5239/work/142009184; ORCID: /0000-0002-5302-6429/work/142009640; ORCID: /0000-0002-5419-9479/work/142010025; ORCID: /0000-0003-0153-922X/work/142010966; ORCID: /0000-0002-9857-2132/work/142011084; 62a26b6d-9033-41c7-976e-2bfc1ad6960f; http://hdl.handle.net/10138/569583Test; 001045040400001

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    دورية أكاديمية

    المساهمون: Helsinki Institute of Life Science HiLIFE, Joint Activities, Institute for Molecular Medicine Finland, University of Helsinki, Genomic Discoveries and Clinical Translation, HUS Heart and Lung Center, Department of Medicine, Helsinki University Hospital Area, Keuhkosairauksien yksikkö

    وصف الملف: application/pdf

    العلاقة: Business Finland (HUS 4685/31/2016 and UH4386/31/2016); AbbVie Inc.; AstraZeneca UK Ltd.; BiogenMA Inc.; Bristol Myers Squibb; Genentech Inc.; Merck Sharp Dohme Corp; Pfizer Inc.; Glaxo-SmithKline Intellectual Property Development Ltd; Sanofi US Services Inc.; Maze Therapeuticslnc.; Janssen Biotech Inc; Novartis Pharma AG and Boehringer Ingelheim. Following biobanks are acknowledged for delivering biobank samples to FinnGen: Auria Biobank (wwv.T.auria.fi/biopankki), THL Biobank (,,www.thl.fi/biobank), Helsinki Biobank (www.helsinginbiopankki.fi), Biobank Borealis of Northern Finland (https:www.ppshp.fil Tutkimus-ja-opetus/Biopankki/Pages/Biobank-Borealis-bi efly in En Tx), Finnish Clinical Biobank Tampere (wwwLays. S/Research/and/dev,eloprnent)Einnish/Clinical/Biobanki re), Biobank of Eastern Finland (ww ila suornenbiopankki. filen), Central Finland Biobank (www.ksshp.filfi-FI/Potilaallel Bio_.ankki), Finnish Red Cross Blood Service Biobank (\ARARAr. veripalvelufilverenluovutus/biopankkitoiminta) and Terveystalo Biobank (www.terveystalo.comlfi/YrybistietoalTerveysLalo Riopankki/Biopankki/). All Finnish biobanks are members of BBMRI.fi infrastructure (www.bbrnrifi), and FINBB Biobank Cooperative (https://finbbfiTest/) is the coordinator of the BBMRIERIC operations in Finland covering all Finnish biobanks.; FinnGen , Tervi , A , Junna , N , Broberg , M , Jones , S E , Strausz , S , Kreivi , H-R , Heckman , C A & Ollila , H M 2023 , ' Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA ' , Human Molecular Genetics , vol. 32 , no. 1 , pp. 161–171 . https://doi.org/10.1093/hmg/ddac212Test; ORCID: /0000-0002-5302-6429/work/127508093; ORCID: /0000-0002-5953-5523/work/127508101; ORCID: /0000-0002-5419-9479/work/127508398; ORCID: /0000-0003-0153-922X/work/127509926; ORCID: /0000-0002-9857-2132/work/127510036; c005c1d5-3d0b-482f-9b96-ed14e06fba81; http://hdl.handle.net/10138/569554Test; 000866202200001

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    دورية أكاديمية