المؤلفون: Frahm N, Geraghty DE, Casimiro DR, McElrath J, Cirulli ET, Shianna KV, Fellay J, Goldstein DB

المصدر: Retrovirology, Vol 6, Iss Suppl 3, p P398 (2009)

مصطلحات موضوعية: Immunologic diseases. Allergy, RC581-607

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1742-4690

URL الوصول: https://doaj.org/article/909e9ce3dcec41a3a840def5611ac436

المؤلفون: Need, AC, McEvoy, JP, Gennarelli, M, Heinzen, EL, Ge, DL, Maia, JM, Shianna, KV, He, M, Cirulli, ET, Gumbs, CE, Zhao, Q, Campbell, CR, Hong, L, Rosenquist, P, Putkonen, A, Hallikainen, T, Repo-Tiihonen, E, Tiihonen, J, Levy, DL, Meltzer, HY, Goldstein, DB

المصدر: American journal of human genetics. 91(2):303-312

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:125072836

المؤلفون: Stefansson, H, Ophoff, RA, Steinberg, S, Andreassen, OA, Cichon, S, Rujescu, D, Werge, T, Pietilainen, OPH, Mors, O, Mortensen, PB, Sigurdsson, E, Gustafsson, O, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Suvisaari, J, Lonnqvist, J, Paunio, T, Borglum, AD, Hartmann, A, Fink-Jensen, A, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Bottcher, Y, Olesen, J, Breuer, R, Moller, HJ, Giegling, I, Rasmussen, HB, Timm, S, Mattheisen, M, Bitter, I, Rethelyi, JM, Magnusdottir, BB, Sigmundsson, T, Olason, P, Mason, G, Gulcher, JR, Haraldsson, M, Fossdal, R, Thorgeirsson, TE, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Franke, B, Strengman, E, Kiemeney, LA, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Sanjuan, J, de Frutos, R, Bramon, E, Vassos, E, Fraser, G, Ettinger, U, Picchioni, M, Walker, N, Toulopoulou, T, Need, AC, Ge, D, Yoon, JL, Shianna, KV, Freimer, NB, Cantor, RM, Murray, R, Kong, A, Golimbet, V, Carracedo, A, Arango, C, Costas, J, Jonsson, EG, Terenius, L, Agartz, I, Petursson, H, Nothen, MM, Rietschel, M, Matthews, PM, Muglia, P, Peltonen, L, St Clair, D, Goldstein, DB, Stefansson, K, Collier, DA

المصدر: Nature. 460(7256):744-U99

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:119170676

المؤلفون: Heinzen EL, Swoboda KJ, Hitomi Y, Gurrieri F, Nicole S, de Vries B, Tiziano FD, Fontaine B, Walley NM, Heavin S, Panagiotakaki E, European Alternating Hemiplegia of Childhood Genetics Consortium, Neri G, Koelewijn S, Kamphorst J, Geilenkirchen M, Pelzer N, Laan L, Haan J, Ferrari M, van den Maagdenberg A, Biobanca e. Registro Clinico per l'Emiplegia Alternante Consortium, Zucca C, Bassi MT, Franchini F, Vavassori R, Giannotta M, Gobbi G, Granata T, Nardocci N, De Grandis E, Veneselli E, Stagnaro M, Vigevano F, European Network for Research on Alternating Hemiplegia for Small, Medium sized Enterpriese Consortium, Oechsler C, Arzimanoglou A, Ninan M, Neville B, Ebinger F, Fons C, Campistol J, Kemlink D, Nevsimalova S, Peeters Scholte C, Casaer P, Sange G, Spiel G, Martinelli Boneschi F, Schyns T, Crawley F, Poncelin D, Fiori S, Abiusi E, Di Pietro L, Sweney MT, Newcomb TM, Viollet L, Huff C, Jorde LB, Reyna SP, Murphy KJ, Shianna KV, Gumbs CE, Little L, Silver K, Ptáček LJ, Ferrari MD, Bye AM, Herkes GK, Whitelaw CM, Webb D, Lynch BJ, Uldall P, King MD, Scheffer IE, van den Maagdenberg AM, Sisodiya SM, Mikati MA, Goldstein D.B., CASARI , GIORGIO NEVIO

المساهمون: Heinzen, El, Swoboda, Kj, Hitomi, Y, Gurrieri, F, Nicole, S, de Vries, B, Tiziano, Fd, Fontaine, B, Walley, Nm, Heavin, S, Panagiotakaki, E, European Alternating Hemiplegia of Childhood Genetics, Consortium, Neri, G, Koelewijn, S, Kamphorst, J, Geilenkirchen, M, Pelzer, N, Laan, L, Haan, J, Ferrari, M, van den Maagdenberg, A, Biobanca e., Registro Clinico per l'Emiplegia Alternante Consortium, Zucca, C, Bassi, Mt, Franchini, F, Vavassori, R, Giannotta, M, Gobbi, G, Granata, T, Nardocci, N, De Grandis, E, Veneselli, E, Stagnaro, M, Vigevano, F, European Network for Research on Alternating Hemiplegia for, Small, Medium sized Enterpriese, Consortium, Oechsler, C, Arzimanoglou, A, Ninan, M, Neville, B, Ebinger, F, Fons, C, Campistol, J, Kemlink, D, Nevsimalova, S, Peeters Scholte, C, Casaer, P, Casari, GIORGIO NEVIO, Sange, G, Spiel, G, Martinelli Boneschi, F, Schyns, T, Crawley, F, Poncelin, D, Fiori, S, Abiusi, E, Di Pietro, L, Sweney, Mt, Newcomb, Tm, Viollet, L, Huff, C, Jorde, Lb, Reyna, Sp, Murphy, Kj, Shianna, Kv, Gumbs, Ce, Little, L, Silver, K, Ptáček, Lj, Ferrari, Md, Bye, Am, Herkes, Gk, Whitelaw, Cm, Webb, D, Lynch, Bj, Uldall, P, King, Md, Scheffer, Ie, van den Maagdenberg, Am, Sisodiya, Sm, Mikati, Ma, Goldstein, D. B.

المصدر: Nature Genetics, 44(9), 1030
Nature genetics

مصطلحات موضوعية: Nonsynonymous substitution, Genetics, 0303 health sciences, Mutation, Alternating hemiplegia of childhood, Neurological disorder, Biology, Settore MED/03 - GENETICA MEDICA, medicine.disease, medicine.disease_cause, Alternating Hemiplegia, Article, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, ATP1A3, medicine, Etiology, 030217 neurology & neurosurgery, Alternating hemiplegia, Exome sequencing, 030304 developmental biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5340c120e42b07a60df6c472c9cc43da

المؤلفون: Urban, TJ, Shen, YF, Stolz, A, Chalasani, N, Fontana, RJ, Rochon, J, Ge, DL, Shianna, KV, Daly, AK, Lucena, MI, Nelson, MR, Molokhia, M, Aithal, GP, Floratos, A, Pe'er, I, Serrano, J, Bonkovsky, H, Davern, TJ, Lee, WM, Navarro, VJ, Talwalkar, JA, Goldstein, DB, Watkins, PB, Guarner C., Soriano G., Román E.M., Drug-Induced Liver Injury Network

المصدر: Pharmacogenetics and Genomics
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

مصطلحات موضوعية: genome-wide association study, drug-induced liver injury, pharmacogenetics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::87bd6a8c2571a5d450750aa757abce92
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=11066

المؤلفون: Need, Ac, Ge, D, Weale, Me, Maia, J, Feng, S, Heinzen, El, Shianna, Kv, Yoon, W, Kasperavici, Te, D, Gennarelli, Massimo, Strittmatter, Wj, Bonvicini, C, Rossi, G, Jayathilake, K, Cola, Pa, Mcevoy, Jp, Keefe, Rs, Fisher, Em, ST JEAN PL, Giegling, I, Hartmann, Am, Möller, Hj, Ruppert, A, Fraser, G, Crombie, C, Middleton, Lt, ST CLAIR, D, Roses, Ad, Muglia, P, Francks, C, Rujescu, D, Meltzer, Hy, Goldstein, Db

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3662::abce0d4354cee2d9ba7eeff108f87d43
http://hdl.handle.net/11379/21829

المؤلفون: Toulopoulou, T, Franke, B, Crombie, C, Fossdal, R, Sigmundsson, T, BuizerVoskamp, JE, Hansen, T, Jakobsen, KD, Muglia, P, Francks, C, Matthews, PM, Murray, R, Ruggeri, M, Sabatti, C, Gylfason, A, Halldorsson, BV, Vassos, E, Tosato, S, Walshe, M, Freimer, NB, Gulcher, JR, Gudbjartsson, D, Thorsteinsdottir, U, Kong, A, Thorgeirsson, TE, Olesen, J, Vasilescu, C, Andreassen, OA, Melle, I, Mühleisen, TW, Wang, AG, Ullum, H, Need, AC, Sigurdsson, A, Jonasdottir, A, Djurovic, S, Ophoff, RA, Georgi, A, Rietschel, M, Werge, T, Bjornsson, A, Mattiasdottir, S, Blondal, T, Haraldsson, M, Petursson, H, MyinGermeys, I, Krabbendam, L, De Haan, L, Cahn, W, Bruggeman, R, Wiersma, D, Goldstein, DB, Nöthen, MM, Peltonen, L, Van Os, J, Linszen, DH, Kahn, RS, Stefansson, K, Magnusdottir, BB, Di Forti, M, Bramon, E, Paunio, T, TuulioHenriksson, A, Giegling, I, Möller, HJ, Suvisaari, J, Hartmann, A, Shianna, KV, Ge, D, Lonnqvist, J, Collier, DA, Walker, N, Li, T, Fraser, G, Ingason, A, Steinberg, S, Sigurdsson, E, St Clair, D, Kiemeney, LA, Stefansson, H, Rujescu, D, Cichon, S, Pietiläinen, OPH

المساهمون: ANS - Amsterdam Neuroscience, Adult Psychiatry

المصدر: Nature, 455, 7210, pp. 232-6
Nature, 455, 232-6
Nature, 455(7210), 232-236. Nature Publishing Group

مصطلحات موضوعية: Schizophrenia/genetics, Genetics and epigenetic pathways of disease [NCMLS 6], Loss of Heterozygosity, Aetiology, screening and detection [ONCOL 5], Bioinformatics, China, Chromosomes, Human, Pair 1/genetics, Pair 15/genetics, Europe, Gene Dosage/genetics, Genetic Predisposition to Disease/genetics, Genome, Human/genetics, Genotype, Models, Genetic, Polymorphism, Single Nucleotide/genetics, Psychotic Disorders/genetics, Sequence Deletion/genetics, Perception and Action [DCN 1], Determinants in Health and Disease [EBP 1], Copy-number variation, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], Genetics, education.field_of_study, Multidisciplinary, biology, CHRNA7, Fragile X syndrome, References (31) View In Table Layout, Schizophrenia, Functional Neurogenomics [DCN 2], Psychosis, Population, Single-nucleotide polymorphism, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Cognitive neurosciences [UMCN 3.2], Translational research [ONCOL 3], mental disorders, medicine, education, Hereditary cancer and cancer-related syndromes [ONCOL 1], medicine.disease, Genetic defects of metabolism [UMCN 5.1], biology.protein, Autism

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abe93dab86948eaa9355e125d23ef45b
http://hdl.handle.net/10722/141844

المؤلفون: Fellay, J, Shianna, Kv, Ge, Dl, Colombo, S, Ledergerber, B, Weale, M, Zhang, Kl, Gumbs, C, Castagna, A, Cossarizza, A, Cozzi Lepri, A, DE LUCA, Andrea, Easterbrook, P, Francioli, P, Mallal, S, Martinez Picado, J, Miro, Jm, Obel, N, Smith, Jp, Wyniger, J, Descombes, P, Antonarakis, Se, Letvin, Nl, Mcmichael, Aj, Haynes, Bf, Telenti, A, Goldstein, Db

مصطلحات موضوعية: Male, Genome, HIV Infections, HLA-C Antigens, Single Nucleotide, Viral Load, DNA-Binding Proteins, Female, Genes, MHC Class I, Genome, Human, Haplotypes, HIV-1, HLA-B Antigens, Humans, Immediate-Early Proteins, Major Histocompatibility Complex, Polymorphism, Single Nucleotide, Regression Analysis, MHC Class I, Genes, Polymorphism, Human

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1820::fe5a2ef83500364b05f71acb1cdf561b
https://hdl.handle.net/11365/1011687

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