المؤلفون: Ollila, H.M., Sharon, E., Lin, L., Sinnott-Armstrong, N., Ambati, A., Yogeshwar, S.M., Hillary, R.P., Jolanki, O., Faraco, J., Einen, M., Luo, G., Zhang, J., Han, F., Yan, H., Dong, X.S., Li, J., Hong, S.C., Kim, T.W., Dauvilliers, Y., Barateau, L., Lammers, G.J., Fronczek, R., Mayer, G., Santamaria, J., Arnulf, I., Knudsen-Heier, S., Bredahl, MKL, Thorsby, P.M., Plazzi, G., Pizza, F., Moresco, M., Crowe, C., Van den Eeden, S.K., Lecendreux, M., Bourgin, P., Kanbayashi, T., Martínez-Orozco, F.J., Peraita-Adrados, R., Benetó, A., Montplaisir, J., Desautels, A., Huang, Y.S., Jennum, P., Nevsimalova, S., Kemlink, D., Iranzo, A., Overeem, S., Wierzbicka, A., Geisler, P., Sonka, K., Honda, M., Högl, B., Stefani, A., Coelho, F.M., Mantovani, V., Feketeova, E., Wadelius, M., Eriksson, N., Smedje, H., Hallberg, P., Hesla, P.E., Rye, D., Pelin, Z., Ferini-Strambi, L., Bassetti, C.L., Mathis, J., Khatami, R., Aran, A., Nampoothiri, S., Olsson, T., Kockum, I., Partinen, M., Perola, M., Kornum, B.R., Rueger, S., Winkelmann, J., Miyagawa, T., Toyoda, H., Khor, S.S., Shimada, M., Tokunaga, K., Rivas, M., Pritchard, J.K., Risch, N., Kutalik, Z., O'Hara, R., Hallmayer, J., Ye, C.J., Mignot, E.J.

المساهمون: FinnGen, Als, T.D., Ziemann, A., Abbasi, A., Lehtonen, A., Lertratanakul, A., Riley-Gillis, B., Rahimov, F., Jacob, H., Waring, J., Liu, M., Smaoui, N., Popovic, R., Platt, A., Matakidou, A., Challis, B., Paul, D., Lassi, G., Tachmazidou, I., Hakanen, A., Schleutker, J., Pitkänen, N., Terho, P., Virolainen, P., Mannermaa, A., Kosma, V.M., Chen, C.Y., Runz, H., John, S., Lahdenperä, S., Loomis, S., Eaton, S., Okafo, G., Salminen-Mankonen, H., Jung, M., Lawless, N., Ding, Z., Maranville, J., Hochfeld, M., Plenge, R., Biswas, S., Kanai, M., Maasha, M., Zhou, W., Tuovila, O., Pakkanen, R., Laukkanen, J., Kuopio, T., Aittomäki, K., Mäkitie, A., Pujol, N., Laisk, T., Aalto-Setälä, K., Mäkelä, J., Hautalahti, M., Smith, S., Southerington, T., Kangasniemi, E., Palin, H., Kähönen, M., Siltanen, S., Laitinen, T., Vaura, F., Suvisaari, J., Niiranen, T., Salomaa, V., Partanen, J., Arvas, M., Ritari, J., Hyvärinen, K., Choy, D., Teng, E., Strauss, E., Chen, H., Schutzman, J., Hunkapiller, J., McCarthy, M., Bowers, N., Pendergrass, R., Lu, T., Chu, A., Kulkarni, D., Xu, F., Betts, J., Eicher, J., Gordillo, J.E., Addis, L., McCarthy, L., Mishra, R., Kumar, J., Ehm, M.G., Auro, K., Pulford, D., Pitkäranta, A., Loukola, A., Punkka, E., Linna, M.M., Carpén, O., Raivio, T.

المصدر: Nature communications, vol. 14, no. 1, pp. 2709

مصطلحات موضوعية: Humans, Autoimmunity/genetics, Influenza, Human/epidemiology, Human/genetics, Influenza A Virus, H1N1 Subtype/genetics, Autoimmune Diseases/epidemiology, Autoimmune Diseases/genetics, Influenza Vaccines/adverse effects, Narcolepsy/chemically induced, Narcolepsy/genetics

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37188663; info:eu-repo/semantics/altIdentifier/eissn/2041-1723; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_57D392F74F523; https://serval.unil.ch/notice/serval:BIB_57D392F74F52Test; urn:issn:2041-1723; https://serval.unil.ch/resource/serval:BIB_57D392F74F52.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_57D392F74F523Test

الإتاحة: https://doi.org/10.1038/s41467-023-36120-zTest
https://serval.unil.ch/notice/serval:BIB_57D392F74F52Test
https://serval.unil.ch/resource/serval:BIB_57D392F74F52.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_57D392F74F523Test

المؤلفون: Luo G., Lin L., Jacob L., Bonvalet M., Ambati A., Plazzi G., Pizza F., Leib R., Adams C. M., Partinen M., Mignot E. J. -M.

المساهمون: Luo G., Lin L., Jacob L., Bonvalet M., Ambati A., Plazzi G., Pizza F., Leib R., Adams C.M., Partinen M., Mignot E.J.-M.

مصطلحات موضوعية: anti-hypocretin receptor 2 autoantibodie, narcolepsy

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30921380; info:eu-repo/semantics/altIdentifier/wos/WOS:000462594000057; volume:14; issue:3; firstpage:1; lastpage:5; numberofpages:5; journal:PLOS ONE; http://hdl.handle.net/11585/697597Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85063628909; https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0214340&type=printableTest

الإتاحة: https://doi.org/10.1371/journal.pone.0214340Test
http://hdl.handle.net/11585/697597Test
https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0214340&type=printableTest

المؤلفون: Natan Gadoth, Birgit Högl, Rosa Hasan, G. Plazzi, Andrea N. Goldstein-Piekarski, Makrina Daniilidou, Thomas J Rico, Smaranda Leu-Semenescu, Ryan P. Hillary, Neal M. Farber, Guy D. Leschziner, Emmanuel Mignot, Yakov Sivan, Michel Lecendreux, José L. Vicario, Hanna Ollila, Juliette Faraco, Sona Nevsimalova, Isabelle Arnulf, Fang Han, Francesca Canellas, Pauline Dodet, Patrice Bourgin, Geert Mayer, Fabio Pizza, Makoto Honda, Yu-Shu Huang, Kazuhiko Kume, Rosa Peraita-Adrados, Ling Lin, David B. Rye, Takashi Kanbayashi, Eileen B. Leary, Seung Chul Hong, Emmanuel H. During, Anne-Marie Landtblom, Yves Dauvilliers, Aditya Ambati

المساهمون: Ambati A., Hillary R., Leu-Semenescu S., Ollila H.M., Lin L., During E.H., Farber N., Rico T.J., Faraco J., Leary E., Goldstein-Piekarski A.N., Huang Y.-S., Han F., Sivan Y., Lecendreux M., Dodet P., Honda M., Gadoth N., Nevsimalova S., Pizza F., Kanbayashi T., Peraita-Adrados R., Leschziner G.D., Hasan R., Canellas F., Kume K., Daniilidou M., Bourgin P., Rye D., Vicario J.L., Hogl B., Hong S.C., Plazzi G., Mayer G., Landtblom A.M., Dauvilliers Y., Arnulf I., Mignot E.J.-M., Retiveau, Nolwenn, Stanford University, Service de Pathologies du sommeil [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre National de Référence pour les Maladies Rares : narcolepsie, hypersomnie idiopathique et syndrome de Kleine-Levin [CHU Pitié-Salpêtrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-CHU Pitié-Salpêtrière [AP-HP], Veterans Affairs Palo Alto Healthcare System, Chang Gung Memorial Hospital [Taipei] (CGMH), Peking University [Beijing], Sackler Faculty of Medicine, Tel Aviv University (TAU), Hôpital Robert Debré, Hôpital Robert Debré-Centre Hospitalier Universitaire de Reims (CHU Reims), Tokyo Metropolitan Institute of Medical Science (TMIMS), Tel Aviv Sourasky Medical Center [Te Aviv], Charles University [Prague] (CU), University of Bologna/Università di Bologna, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Université de Tsukuba = University of Tsukuba, Hospital General Universitario 'Gregorio Marañón' [Madrid], Guy's Hospital [London], King‘s College London, Universidade de São Paulo = University of São Paulo (USP), Nagoya City University [Nagoya, Japan], Uppsala University Hospital, Linköping university hospital, CHU Strasbourg, Emory University [Atlanta, GA], Innsbruck Medical University = Medizinische Universität Innsbruck (IMU), Catholic University of Korea, Philipps Universität Marburg = Philipps University of Marburg, Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Institut des Neurosciences de Montpellier (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)

المصدر: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (12), pp.e2005753118. ⟨10.1073/pnas.2005753118⟩

مصطلحات موضوعية: Male, Pediatrics, Bipolar Disorder, [SDV]Life Sciences [q-bio], Genome-wide association study, MESH: Risk Assessment, MESH: Pregnancy, MESH: Risk Factors, Pregnancy, MESH: Bipolar Disorder, Birth difficultie, Odds Ratio, GWAS, Apathy, MESH: Genetic Variation, Obstetric Labor Complication, MESH: Genetic Association Studies, MESH: Cytokines, Hypersomnia, Multidisciplinary, MESH: Genetic Predisposition to Disease, Pathophysiology, [SDV] Life Sciences [q-bio], Schizophrenia, Female, Disease Susceptibility, medicine.symptom, MESH: Kleine-Levin Syndrome, Human, medicine.medical_specialty, MESH: Obstetric Labor Complications, MESH: Disease Susceptibility, Birth difficulties, Disorders of Excessive Somnolence, Genetic Association Studie, Kleine-Levin Syndrome, Risk Assessment, MESH: Polymorphism, Genetic, medicine, Genetic Predisposition to Disease, Bipolar disorder, Cytokine, MESH: Humans, Polymorphism, Genetic, business.industry, Risk Factor, Genetic Variation, Odds ratio, medicine.disease, MESH: Male, MESH: Odds Ratio, Kleine–Levin syndrome, Kleine-Levin syndrome, bipolar disorder, birth difficulties, hypersomnia, Disinhibition, business, MESH: Female, MESH: Disorders of Excessive Somnolence

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a628f3bc4473a79bda8966a1c1b669c7Test
https://doi.org/10.1073/pnas.2005753118Test

المؤلفون: Ambati A., Hillary R., Leu-Semenescu S., Ollila H. M., Lin L., During E. H., Farber N., Rico T. J., Faraco J., Leary E., Goldstein-Piekarski A. N., Huang Y. -S., Han F., Sivan Y., Lecendreux M., Dodet P., Honda M., Gadoth N., Nevsimalova S., Pizza F., Kanbayashi T., Peraita-Adrados R., Leschziner G. D., Hasan R., Canellas F., Kume K., Daniilidou M., Bourgin P., Rye D., Vicario J. L., Hogl B., Hong S. C., Plazzi G., Mayer G., Landtblom A. M., Dauvilliers Y., Arnulf I., Mignot E. J. -M.

المساهمون: Ambati A., Hillary R., Leu-Semenescu S., Ollila H.M., Lin L., During E.H., Farber N., Rico T.J., Faraco J., Leary E., Goldstein-Piekarski A.N., Huang Y.-S., Han F., Sivan Y., Lecendreux M., Dodet P., Honda M., Gadoth N., Nevsimalova S., Pizza F., Kanbayashi T., Peraita-Adrados R., Leschziner G.D., Hasan R., Canellas F., Kume K., Daniilidou M., Bourgin P., Rye D., Vicario J.L., Hogl B., Hong S.C., Plazzi G., Mayer G., Landtblom A.M., Dauvilliers Y., Arnulf I., Mignot E.J.-M.

مصطلحات موضوعية: Bipolar disorder, Birth difficultie, GWAS, Hypersomnia, Kleine-Levin syndrome, Cytokine, Disorders of Excessive Somnolence, Female, Genetic Association Studie, Genetic Predisposition to Disease, Human, Male, Obstetric Labor Complication, Odds Ratio, Polymorphism, Genetic, Pregnancy, Risk Assessment, Risk Factor, Disease Susceptibility, Genetic Variation

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33737391; info:eu-repo/semantics/altIdentifier/wos/WOS:000631868600003; volume:118; issue:12; firstpage:e2005753118; lastpage:e2005753118; numberofpages:11; journal:PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA; http://hdl.handle.net/11585/859863Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103146380

الإتاحة: https://doi.org/10.1073/PNAS.2005753118Test
http://hdl.handle.net/11585/859863Test

المؤلفون: Guo Luo, Ling Lin, Louis Jacob, Mélodie Bonvalet, Aditya Ambati, Giuseppe Plazzi, Fabio Pizza, Ryan Leib, Christopher M Adams, Markku Partinen, Emmanuel Jean-Marie Mignot, and the PLOS ONE Editors

المساهمون: Luo G., Lin L., Jacob L., Bonvalet M., Ambati A., Plazzi G., Pizza F., Leib R., Adams C.M., Partinen M., Mignot E.J.-M.

المصدر: PLoS ONE, Vol 14, Iss 3, p e0214340 (2019)

مصطلحات موضوعية: anti-hypocretin receptor 2 autoantibodies, narcolepsy, Multidisciplinary, business.industry, lcsh:R, Autoantibody, lcsh:Medicine, anti-hypocretin receptor 2 autoantibodie, medicine.disease, Immunology, medicine, Pandemrix, lcsh:Q, lcsh:Science, Receptor, business, Narcolepsy

وصف الملف: ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab43c5102c334f7bf375daeacfc8572Test
https://doi.org/10.1371/journal.pone.0214340Test