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1دورية أكاديمية
المؤلفون: Gina M. Peloso, Sven J. van derLee, International Genomics of Alzheimer's Project (IGAP), R. Sims, S.J. van derLee, A.C. Naj, C. Bellenguez, N. Badarinarayan, J. Jakobsdottir, B.W. Kunkle, A. Boland, R. Raybould, J.C. Bis, E.R. Martin, B. Grenier‐Boley, S. Heilmann‐Heimbach, V. Chouraki, A.B. Kuzma, K. Sleegers, M. Vronskaya, A. Ruiz, R.R. Graham, R. Olaso, P. Hoffmann, M.L. Grove, B.N. Vardarajan, M. Hiltunen, M.M. Nöthen, C.C. White, K.L. Hamilton‐Nelson, J. Epelbaum, W. Maier, S.H. Choi, G.W. Beecham, C. Dulary, S. Herms, A.V. Smith, C.C. Funk, Derbois, A.J. Forstner, S. Ahmad, H. Li, D. Bacq, D. Harold, C.L. Satizabal, O. Valladares, A. Squassina, R. Thomas, J.A. Brody, L. Qu, P. Sánchez‐Juan, T. Morgan, F.J. Wolters, Y. Zhao, F.S. Garcia, N. Denning, M. Fornage, J. Malamon, M.C.D. Naranjo, E. Majounie, T.H. Mosley, B. Dombroski, D. Wallon, M.K. Lupton, J. Dupuis, P. Whitehead, L. Fratiglioni, C. Medway, X. Jian, S. Mukherjee, L. Keller, K. Brown, H. Lin, L.B. Cantwell, F. Panza, B. McGuinness, S. Moreno‐Grau, J.D. Burgess, V. Solfrizzi, P. Proitsi, H.H. Adams, M. Allen, D. Seripa, P. Pastor, L.A. Cupples, N.D. Price, D. Hannequin, A. Frank‐García, D. Levy, P. Chakrabarty, P. Caffarra, I. Giegling, A.S. Beiser, V. Giedraitis, H. Hampel, M.E. Garcia, X. Wang, L. Lannfelt, P. Mecocci, G. Eiriksdottir, P.K. Crane, F. Pasquier, V. Boccardi, I. Henández, R.C. Barber, M. Scherer, L. Tarraga, P.M. Adams, M. Leber, Y. Chen, M.S. Albert, S. Riedel‐Heller, V. Emilsson, D. Beekly, A. Braae, R. Schmidt, D. Blacker, C. Masullo, H. Schmidt, R.S. Doody, G. Spalletta, W.T. Longstreth Jr., T.J. Fairchild, P. Bossù, O.L. Lopez, M.P. Frosch, E. Sacchinelli, B. Ghetti, Q. Yang, R.M. Huebinger, F. Jessen, S. Li, M.I. Kamboh, J. Morris, O. Sotolongo‐Grau, M.J. Katz, C. Corcoran, M. Dunstan, A. Braddel, C. Thomas, A. Meggy, R. Marshall, A. Gerrish, J. Chapman, M. Aguilar, S. Taylor, M. Hill, M.D. Fairén, A. Hodges, B. Vellas, H. Soininen, I. Kloszewska, M. Daniilidou, J. Uphill, Y. Patel, J.T. Hughes, J. Lord, J. Turton, A.M. Hartmann, R. Cecchetti, C. Fenoglio, M. Serpente, M. Arcaro, C. Caltagirone, M.D. Orfei, A. Ciaramella, S. Pichler, M. Mayhaus, W. Gu, A. Lleó, J. Fortea, R. Blesa, I.S. Barber, K. Brookes, C. Cupidi, R.G. Maletta, D. Carrell, S. Sorbi, S. Moebus, M. Urbano, A. Pilotto, J. Kornhuber, P. Bosco, S. Todd, D. Craig, J. Johnston, M. Gill, B. Lawlor, A. Lynch, N.C. Fox, J. Hardy, ARUK Consortium, R.L. Albin, L.G. Apostolova, S.E. Arnold, S. Asthana, C.S. Atwood, C.T. Baldwin, L.L. Barnes, S. Barral, T.G. Beach, J.T. Becker, E.H. Bigio, T.D. Bird, B.F. Boeve, J.D. Bowen, A. Boxer, J.R. Burke, J.M. Burns, J.D. Buxbaum, N.J. Cairns, C. Cao, C.S. Carlson, C.M. Carlsson, R.M. Carney, M.M. Carrasquillo, S.L. Carroll, C.C. Diaz, H.C. Chui, D.G. Clark, D.H. Cribbs, E.A. Crocco, C. DeCarli, M. Dick, R. Duara, D.A. Evans, K.M. Faber, K.B. Fallon, D.W. Fardo, M.R. Farlow, S. Ferris, T.M. Foroud, D.R. Galasko, M. Gearing, D.H. Geschwind, J.R. Gilbert, N.R. Graff‐Radford, R.C. Green, J.H. Growdon, R.L. Hamilton, L.E. Harrell, L.S. Honig, M.J. Huentelman, C.M. Hulette, B.T. Hyman, G.P. Jarvik, E. Abner, L.W. Jin, G. Jun, A. Karydas, J.A. Kaye, R. Kim, N.W. Kowall, J.H. Kramer, F.M. LaFerla, J.J. Lah, J.B. Leverenz, A.I. Levey, G. Li, A.P. Lieberman, K.L. Lunetta, C.G. Lyketsos, D.C. Marson, F. Martiniuk, D.C. Mash, E. Masliah, W.C. McCormick, S.M. McCurry, A.N. McDavid, A.C. McKee, M. Mesulam, B.L. Miller, C.A. Miller, J.W. Miller, J.C. Morris, J.R. Murrell, A.J. Myers, S. O'Bryant, J.M. Olichney, V.S. Pankratz, J.E. Parisi, H.L. Paulson, W. Perry, E. Peskind, A. Pierce, W.W. Poon, H. Potter, J.F. Quinn, A. Raj, M. Raskind, B. Reisberg, C. Reitz, J.M. Ringman, E.D. Roberson, E. Rogaeva, H.J. Rosen, R.N. Rosenberg, M.A. Sager, A.J. Saykin, J.A. Schneider, L.S. Schneider, W.W. Seeley, A.G. Smith, J.A. Sonnen, S. Spina, R.A. Stern, R.H. Swerdlow, R.E. Tanzi, T.A. Thornton‐Wells, J.Q. Trojanowski, J.C. Troncoso, V.M. Van Deerlin, L.J. Van Eldik, H.V. Vinters, J.P. Vonsattel, S. Weintraub, K.A. Welsh‐Bohmer, K.C. Wilhelmsen, J. Williamson, T.S. Wingo, R.L. Woltjer, C.B. Wright, C.E. Yu, L. Yu, F. Garzia, F. Golamaully, G. Septier, S. Engelborghs, R. Vandenberghe, P.P. De Deyn, C.M. Fernadez, Y.A. Benito, H. Thonberg, C. Forsell, L. Lilius, A. Kinhult‐Stählbom, L. Kilander, R. Brundin, L. Concari, S. Helisalmi, A.M. Koivisto, A. Haapasalo, V. Dermecourt, N. Fievet, O. Hanon, C. Dufouil, A. Brice, K. Ritchie, B. Dubois, J.J. Himali, C.D. Keene, J. Tschanz, A.L. Fitzpatrick, W.A. Kukull, M. Norton, T. Aspelund, E.B. Larson, R. Munger, J.I. Rotter, R.B. Lipton, M.J. Bullido, A. Hofman, T.J. Montine, E. Coto, E. Boerwinkle, R.C. Petersen, V. Alvarez, F. Rivadeneira, E.M. Reiman, M. Gallo, C.J. O'Donnell, J.S. Reisch, A.C. Bruni, D.R. Royall, M. Dichgans, M. Sano, D. Galimberti, P. St George‐Hyslop, E. Scarpini, D.W. Tsuang, M. Mancuso, U. Bonuccelli, A.R. Winslow, A. Daniele, C.K. Wu, GERAD/PERADES, CHARGE, ADGC, EADI, O. Peters, B. Nacmias, M. Riemenschneider, R. Heun, C. Brayne, D.C. Rubinsztein, J. Bras, R. Guerreiro, A. Al‐Chalabi, C.E. Shaw, J. Collinge, D. Mann, M. Tsolaki, J. Clarimón, R. Sussams, S. Lovestone, M.C. O'Donovan, M.J. Owen, T.W. Behrens, S. Mead, A.M. Goate, A.G. Uitterlinden, C. Holmes, C. Cruchaga, M. Ingelsson, D.A. Bennett, J. Powell, T.E. Golde, C. Graff, P.L. De Jager, K. Morgan, N. Ertekin‐Taner, O. Combarros, B.M. Psaty, P. Passmore, S.G. Younkin, C. Berr, V. Gudnason, D. Rujescu, D.W. Dickson, J.F. Dartigues, A.L. DeStefano, S. Ortega‐Cubero, H. Hakonarson, D. Campion, M. Boada, J.K. Kauwe, L.A. Farrer, C. Van Broeckhoven, M.A. Ikram, L. Jones, J.L. Haines, C. Tzourio, L.J. Launer, V. Escott‐Price, R. Mayeux, J.F. Deleuze, N. Amin, P.A. Holmans, M.A. Pericak‐Vance, P. Amouyel, C.M. vanDuijn, A. Ramirez, L.S. Wang, J.C. Lambert, S. Seshadri, J. Williams, G.D. Schellenberg, Anita L. Destefano, Sudha Seshardi
المصدر: Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 10, Iss 1, Pp 595-598 (2018)
مصطلحات موضوعية: Genetics, HDL‐C, Single nucleotide polymorphisms, Instrumental variables, Cholesteryl ester transfer protein, Neurology. Diseases of the nervous system, RC346-429, Geriatrics, RC952-954.6
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2352-8729Test
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2دورية أكاديمية
المؤلفون: AL Soilly, C Robert-Viard, C Besse, AL Bruel, B Gerard, A Boland, A Piton, Y Duffourd, J Muller, C Poë, T Jouan, S El Doueiri, L Faivre, D Bacq-Daian, B Isidor, D Genevieve, S Odent, N Philip, M Doco-Fenzy, D Lacombe, ML Asensio, JF Deleuze, C Binquet, DISSEQ Investigators Group, C Thauvin-Robinet, C Lejeune
المصدر: BMC Health Services Research, Vol 23, Iss 1, Pp 1-11 (2023)
مصطلحات موضوعية: Intellectual disability, Exome sequencing, Micro-costing, Cost analysis, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1472-6963Test
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المؤلفون: D. Bacq-Daian, A. Briand, L. Allanore, Michel Vidaud, A. Boland-Auge, Audrey Sabbagh, S. Ferkal, Laurence Pacot, Réseau Nf-France, Ingrid Laurendeau, Eric Pasmant, Jean-François Deleuze, Dominique Vidaud, Pierre Wolkenstein, Béatrice Parfait
المصدر: Annales de Dermatologie et de Vénéréologie. 146:A111-A112
مصطلحات موضوعية: Dermatology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::081612e9ac2438e7c200086ef1732f33Test
https://doi.org/10.1016/j.annder.2019.09.121Test -
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المؤلفون: Jean-François Deleuze, Eva Pipiras, Brigitte Benzacken, P Bitoun, V. Renault, D. Bacq Daian, S. Kuzbari, B. Parfait, A. Boland Auge
المصدر: Acta Ophthalmologica. 95
مصطلحات موضوعية: Proband, Sanger sequencing, Genetics, Optic nerve hypoplasia, Candidate gene, General Medicine, Micropenis, Biology, medicine.disease, Bioinformatics, Ophthalmology, symbols.namesake, symbols, medicine, SNP, Missense mutation, Exome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5e8f2c3cdc1921c71a54dd250901440dTest
https://doi.org/10.1111/j.1755-3768.2017.02781Test -
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المؤلفون: Dominique Vidaud, Jean-François Deleuze, A. Boland-Auge, L. Allanore, Audrey Sabbagh, D. Bacq-Daian, Eric Pasmant, S. Ferkal, Michel Vidaud, Béatrice Parfait, Pierre Wolkenstein
المصدر: Annales de Dermatologie et de Vénéréologie. 144:S94
مصطلحات موضوعية: Dermatology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f03986d21414152682e4e20d14bf7391Test
https://doi.org/10.1016/j.annder.2017.09.101Test -
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المؤلفون: Frank Bellivier, Andrej Marusic, Hugh Gurling, R Abou Jamra, Johannes Schumacher, Margot Albus, D Bacq, Céline Charon, Walter J. Muir, François Ferrero, Douglas Blackwood, Thomas G. Schulze, Margitta Borrmann-Hassenbach, S. Roche, A. Malafosse, Bruno Giros, Patrick McKeon, M. Rietschel, Sven Cichon, Bruno Etain, Carmel Kealey, Markus M. Nöthen, Flavie Mathieu, Christian Dina, Arnaud Lemainque, Mark Lathrop, Stephanie Ohlraun, Sophie Gallina, Wolfgang Maier, C. Henry, Thomas Bourgeron, Z M Dernovsek, C Betard, Martin Preisig, Marion Leboyer, Peter Propping
المساهمون: Neurobiologie et Psychiatrie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de psychiatrie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Hôpital Albert Chenevier, Division Genetic Epidemiology in Psychiatry, Central Institute of Mental Health [Mannheim], University Hospital Mannheim | Universitätsmedizin Mannheim-University Hospital Mannheim | Universitätsmedizin Mannheim, Department of Psychiatry, Rheinische Friedrich-Wilhelms-Universität Bonn, Department of Psychiatry and Psychotherapy, District Hospital Haar, Smurfit Institute of Genetics, Trinity College Dublin, Department of Pharmacology, University of Pennsylvania, Département de psychiatrie, Centre hospitalier Charles Perrens [Bordeaux], Génétique des maladies multifactorielles (GMM), Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS), Molecular Psychiatry Laboratory - Department of Psychiatry and Behavioural Sciences, Windeyer Institute for Medical Sciences-Royal Free Hospital [London, UK], Pôle de Psychiatrie, Faculté de Médecine-IFR10-Groupe hospitalier Henri Mondor-Albert Chenevier, Department of psychiatry, Lausanne University Hospital, Geneva University Hospital (HUG), Life & Brain Center - Department of Genomics, Institute of Human Genetics, Institute of Public Health of the Republic of Slovenia, University Psychiatric Hospital, Génomique fonctionnelle et développement, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre National de Génotypage (CNG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Guellaen, Georges, Medical Faculty [Mannheim]-Medical Faculty [Mannheim], Windeyer Institute for Medical Sciences-Royal Free and University College London Medical School, University of Pennsylvania [Philadelphia], Hôpital Charles Perrens, University Hospital - Lausanne, Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)
المصدر: Molecular Psychiatry
Molecular Psychiatry, 2006, 11 (7), pp.685-94. ⟨10.1038/sj.mp.4001815⟩
Molecular Psychiatry, no. 11, pp. 685-694
Molecular Psychiatry, Nature Publishing Group, 2006, 11 (7), pp.685-94. ⟨10.1038/sj.mp.4001815⟩مصطلحات موضوعية: Male, Proband, Bipolar Disorder, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, 0302 clinical medicine, MESH: Bipolar Disorder, MESH: Child, Chromosomes, Human, Age of Onset, Child, Genetics, Chromosome Mapping, 3. Good health, Europe, Psychiatry and Mental health, Phenotype, Schizophrenia, Microsatellite, Female, Chromosomes, Human, Pair 3, Psychology, Adult, Adolescent, MESH: Age of Onset, MESH: Chromosomes, Human, Pair 3, MESH: Phenotype, MESH: Chromosomes, Human, Statistics, Nonparametric, Article, Genetic determinism, Genomic Imprinting, 03 medical and health sciences, Cellular and Molecular Neuroscience, Genetic linkage, medicine, Humans, Bipolar disorder, Molecular Biology, MESH: Genome, Human, MESH: Adolescent, Linkage (software), MESH: Humans, Genome, Human, MESH: Adult, medicine.disease, MESH: Male, MESH: Genomic Imprinting, 030227 psychiatry, MESH: Lod Score, [SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, MESH: Statistics, Nonpar, MESH: Microsatellite Repeats, MESH: Europe, Lod Score, Age of onset, MESH: Chromosome Mapping, MESH: Female, 030217 neurology & neurosurgery, Microsatellite Repeats
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0df74283d6632fa31ef8569e45d0b0fTest
https://doi.org/10.1038/sj.mp.4001815Test -
7دورية أكاديمية
المؤلفون: H. C. Stanescu, M. Arcos-Burgos, A. Medlar, D. Bockenhauer, A. Kottgen, L. Dragomirescu, C. Voinescu, N. Patel, K. Pearce, M. Hubank, H. A. Stephens, V. Laundy, S. Padmanabhan, A. Zawadzka, J. M. Hofstra, M. J. Coenen, M. den Heijer, L. A. Kiemeney, D. Bacq-Daian, B. Stengel, S. H. Powis, P. Brenchley, J. Feehally, A. J. Rees, H. Debiec, J. F. Wetzels, P. Ronco, P. W. Mathieson, R. Kleta
مصطلحات موضوعية: Uncategorized, Alleles, Chromosomes, Human, Pair 2, Pair 6, Europe, European Continental Ancestry Group, Female, Genome-Wide Association Study, Genotype, Glomerulonephritis, Membranous, HLA-DQ Antigens, HLA-DQ alpha-Chains, Humans, Male, Odds Ratio, Polymorphism, Single Nucleotide, Receptors, Phospholipase A2
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المؤلفون: V. Laundy, Julia M. Hofstra, Detlef Bockenhauer, M. den Heijer, A. Zawadzka, Peter W. Mathieson, L. Dragomirescu, J. Feehally, Alan Medlar, C. Voinescu, Sandosh Padmanabhan, Horia Stanescu, Robert Kleta, Anna Köttgen, Marieke J H Coenen, D. Bacq-Daian, Bénédicte Stengel, H.A.F. Stephens, Hanna Debiec, Pierre Ronco, N. Patel, Mike Hubank, Paul Brenchley, Lambertus A. Kiemeney, Mauricio Arcos-Burgos, S. H. Powis, Andrew J. Rees, Jack F.M. Wetzels, K. Pearce
المصدر: The New England Journal of Medicine, 364, 7, pp. 616-26
New England Journal of Medicine; Vol 364
The New England Journal of Medicine, 364, 616-26
New England Journal of Medicineمصطلحات موضوعية: Male, Genotype, Genetics and epigenetic pathways of disease [NCMLS 6], 030232 urology & nephrology, Human leukocyte antigen, medicine.disease_cause, Glomerulonephritis, Membranous, Polymorphism, Single Nucleotide, HLA-DQ alpha-Chains, White People, Autoimmunity, Molecular epidemiology [NCEBP 1], 03 medical and health sciences, 0302 clinical medicine, Polymorphism (computer science), HLA-DQ Antigens, medicine, Odds Ratio, Humans, Hormonal regulation Molecular epidemiology [IGMD 6], Allele, Genomic disorders and inherited multi-system disorders Molecular epidemiology [IGMD 3], Alleles, 030304 developmental biology, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], Renal disorder [IGMD 9], 0303 health sciences, HLA-DQ Antigen, business.industry, Receptors, Phospholipase A2, Glomerulonephritis, General Medicine, medicine.disease, Idiopathic Membranous Nephropathy, 3. Good health, Europe, Chromosomes, Human, Pair 2, Immunology, Chromosomes, Human, Pair 6, Female, business, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::273f00d0aa874368557eeb87e6315b7fTest
https://hdl.handle.net/2066/97321Test -
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المؤلفون: Marc Fellous, Sandrine Caburet, Philippe Bouchard, Ziva Ben-Neriah, M. Lathrop, Sophie Christin-Maitre, S. Heath, Reiner A. Veitia, Stavit A. Shalev, D. Bacq, N. Bourcigaux
المصدر: Annales d'Endocrinologie. 67:391
مصطلحات موضوعية: Endocrinology, Endocrinology, Diabetes and Metabolism, General Medicine
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::fe83c351a8b5e7a4bdb599f2c990b0fcTest
https://doi.org/10.1016/s0003-4266Test(06)72639-7 -
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المؤلفون: G Mollet, R Salomon, O Gribouval, F Silbermann, D Bacq, G Landthaler, D Milford, A Nayir, G Rizzoni, C Antignac, S Saunier
المصدر: Nature Genetics. 32:459-459
مصطلحات موضوعية: Genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3a63202e76448f809c91aaa9dd5e6e98Test
https://doi.org/10.1038/ng1102-459cTest
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