المؤلفون: Teresa Fazia, Daria Marzanati, Anna Laura Carotenuto, Ashley Beecham, Athena Hadjixenofontos, Jacob L. McCauley, Valeria Saddi, Marialuisa Piras, Luisa Bernardinelli, Davide Gentilini

المصدر: Current Issues in Molecular Biology, Vol 43, Iss 3, Pp 1778-1793 (2021)

مصطلحات موضوعية: multiplex families, Sardinian population, WES data, rare variants, low-frequency variants, Homozygosity Haplotype analysis, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/1467-3045/43/3/125Test; https://doaj.org/toc/1467-3037Test; https://doaj.org/toc/1467-3045Test

الوصول الحر: https://doaj.org/article/8a57d49e240f42eaabb0d4badb50bb82Test

المؤلفون: Ashley Beecham, Daria Marzanati, Athena Hadjixenofontos, Anna Laura Carotenuto, Luisa Bernardinelli, Valeria Saddi, Jacob L. McCauley, Teresa Fazia, Davide Gentilini, Marialuisa Piras

المصدر: Current Issues in Molecular Biology
Volume 43
Issue 3
Pages 125-1793
Current Issues in Molecular Biology, Vol 43, Iss 125, Pp 1778-1793 (2021)

مصطلحات موضوعية: Male, Microbiology (medical), QH301-705.5, Region form Common Ancestor (RCA), Biology, multiple sclerosis, Polymorphism, Single Nucleotide, Microbiology, Exon, multiplex families, Exome Sequencing, medicine, Humans, Genetic Predisposition to Disease, Multiplex, Sardinian population, Biology (General), Molecular Biology, Genotyping, Alleles, Exome sequencing, Genetics, Multiple sclerosis, Homozygote, Haplotype, Genetic Variation, rare variants, General Medicine, Heritability, medicine.disease, Pedigree, Haplotypes, Italy, RNA splicing, WES data, Female, Homozygosity Haplotype analysis, low-frequency variants, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c6c6ccba65151254b04a0a4ff0398e9Test

المؤلفون: Ashley Beecham, Anna Ticca, Roberta Pastorino, Teresa Fazia, Carlo Berzuini, Luisa Bernardinelli, Mark Abney, Pier Paolo Bitti, Luisa Foco, Davide Gentilini, Lide Han, Hui Guo, Charalampos Papachristou, Jacob L. McCauley, Athena Hadjixenofontos

المصدر: Fazia, T, Pastorino, R, Foco, L, Han, L, Abney, M, Beecham, A, Hadjixenofontos, A, Guo, H, Gentilini, D, Papachristou, C, Bitti, P P, Ticca, A, Berzuini, C, McCauley, J & Bernardinelli, L 2017, ' Investigating Multiple Sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci ', Multiple Sclerosis Journal . https://doi.org/10.1177/1352458517732841Test

مصطلحات موضوعية: 0301 basic medicine, Genetics, Linkage (software), Multiple Sclerosis, biology, Genetic Linkage, Multiple sclerosis, Single-nucleotide polymorphism, medicine.disease, Major histocompatibility complex, Polymorphism, Single Nucleotide, 03 medical and health sciences, 030104 developmental biology, Italy, Neurology, Genetic linkage, medicine, biology.protein, Genetic predisposition, Humans, SNP, Genetic Predisposition to Disease, Neurology (clinical), Alleles, Founder effect

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d3ae5b288898c6f8a2851518727c6eTest
https://doi.org/10.1177/1352458517732841Test

المؤلفون: Chantal M. E. Tallaksen, Byung-Woo Yoon, Erik H. Niks, Valery L. Feigin, Alexander F. Lipka, Maziar Moradi-Lakeh, Kelly Jones, Cathrine Brunborg, Angelina H. Maniaol, Kathryn M. McPherson, Ashley Beecham, John F. Kurtzke, Moon-Ku Han, Clara P. Manrique, Alice Theadom, Mohammad Ali Sahraian, Braden Te Ao, Leticia Tornes, Seung-Mi Lee, Jong-Moo Park, Tomas Kalincik, Sylvia R. Delgado, Margaret A. Pericak-Vance, Suzanne Barker-Collo, J.J.G. Verschuuren, Anthony Dowell, Pouria Heydarpour, Druckerei Stückle, Wan-Chun Huang, Luuk Dekker, Solomon Chih-Cheng Chen, Byung Joo Park, Shabnam Abtahi, Anne T. Heldal, Jacob L. McCauley, Martin Tobias, Shayan Khoshkish, Athena Hadjixenofontos, Trine Haug Popperud, Chin-Li Lu, Paul Brown, Melissa R. Ortega, Nicola J. Starkey, Marion I. Boldingh, Nam Kyong Choi, Kottil Rammohan, Shanthi Ameratunga

المصدر: Neuroepidemiology. 44:I-IV

مصطلحات موضوعية: Traditional medicine, Epidemiology, business.industry, Medicine, Neurology (clinical), business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::308d73fdabb5f31027c3bbdb672ea849Test
https://doi.org/10.1159/000437404Test

المؤلفون: Michael A. Schmidt, Patrice L. Whitehead, Dale J. Hedges, Jonathan L. Haines, Scott M. Williams, Harry H. Wright, Michael L. Cuccaro, Ruth K. Abramson, Athena Hadjixenofontos, Ramkumar Menon, John R. Gilbert, Ioanna Konidari, Eden R. Martin, Jacob L. McCauley, Margaret A. Pericak-Vance

المصدر: Annals of Human Genetics. 77:9-21

مصطلحات موضوعية: Proband, Genetics, Mitochondrial DNA, Haplotype, Single-nucleotide polymorphism, Genome-wide association study, Biology, medicine.disease, behavioral disciplines and activities, mental disorders, Genetic variation, medicine, Autism, Genetics (clinical), Genetic association

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::44232254d4aa0c1dfd43d8dfa37ec992Test
https://doi.org/10.1111/j.1469-1809.2012.00736.xTest

المؤلفون: Bénédicte Dubois, Lucia Corrado, Deborah F. Mason, Allan G. Kermode, Pentti J. Tienari, Annette Bang Oturai, Charles Hillier, Adrian J. Ivinson, Stephen L. Hauser, Ashley Beecham, Jeannette Lechner-Scott, Vincent Thijs, Jonathan L. Haines, Sarah Edkins, Alexander T. Dilthey, Daniele Cusi, Guy Nagels, David A. Hafler, Mark Slee, Petra Nilsson, James S. Wiley, Lou Brundin, Amy Strange, Elizabeth Visser, Mireia Sospedra, Athena Hadjixenofontos, Sergio E. Baranzini, Jenny Link, Robert Andrews, Viola Biberacher, Helle Bach Søndergaard, Vittorio Martinelli, Tomas Olsson, Gillian L Hall, Stephen Sawcer, Stacy J. Caillier, Per Soelberg Sørensen, Céline Bellenguez, Cornelia M. van Duijn, Frauke Zipp, Nikolaos A. Patsopoulos, Cristin McCabe, Colin Freeman, Simon Broadley, Luisa Bernardinelli, Margaret A. Pericak-Vance, Jan Hillert, Wassila Carpentier, Sandip Shaunak, Anne Spurkland, Barnaby Fiddes, Judith Field, Jan Lycke, Christina M. Lill, Federica Esposito, Ioanna Konidari, Elisabeth Gulowsen Celius, Christian Gieger, Helmut Butzkueven, Ling Shen, James F. Wilson, Magdalena Lindén, Tejas S. Shah, Amie Baker, Dionysia K. Xifara, Hong Quach, Laura Bergamaschi, Rogier Q. Hintzen, Jacob L. McCauley, Janna Saarela, J W Thorpe, Christine Lebrun-Frenay, Felix Luessi, Sandra D'Alfonso, B. E. Kendall, Helga Westerlind, Giancarlo Comi, Nathalie Schnetz-Boutaud, Paola Brambilla, Chris Cotsapas, Anders Hamsten, William Camu, Achim Berthele, Kjell-Morten Myhr, Clive Hawkins, Richard Nicholas, James Harley, Carl A. Anderson, Keijo Koivisto, Irene Coman, Neil Robertson, Hakon Hakonarson, Finn Sellebjerg, Fredrik Piehl, Alessia Di Sapio, Loukas Moutsianas, Mehdi Alizadeh, Lars Alfredsson, Catherine Schaefer, David Rog, Virpi Leppa, C. Martin, Bruce A.C. Cree, Christopher Halfpenny, Irina Elovaara, Filippo Martinelli-Boneschi, Cordelia Langford, Hanne F. Harbo, Wim Robberecht, Isabelle Cournu-Rebeix, Steve Vucic, Izaura Lima Bomfim, Irene Y. Frohlich, Michelle Lee, Bertrand Fontaine, Bernhard Hemmer, Eva Zindler, Chris C. A. Spencer, Malin Larsson, Simon Shields, Ilijas Jelcic, Juliane Winkelmann, Jorge R. Oksenberg, Alastair Wilkins, Silvia Delgado, Volker Siffrin, Helena C. Kronsbein, Bruno Brochet, Panos Deloukas, Daniela Galimberti, Nikos Evangelou, Rebecca C. Selter, Maja Jagodic, Martin Duddy, Timothy Harrower, Per Hall, Nadia Barizzone, Siân Price, Matti Pirinen, Pierre-Antoine Gourraud, Thomas M.C. Binder, Giuseppe Liberatore, Mark Lathrop, M.-M. Hoshi, Garrett Hellenthal, Melissa Sorosina, Thomas Korn, Clara Guaschino, Roland Martin, Jeremy Hobart, Marco Salvetti, Peter Donnelly, Ingrid Kockum, An Goris, Alastair Compston, Mariaemma Rodegher, Dorothea Buck, Clara P. Manrique, Christiane Graetz, Benedicte A. Lie, Trevor J. Kilpatrick, Andrew Graham, Anu Kemppinen, Maria Ban, Gil McVean, John Zajicek, Hannah Blackburn, Mary F. Davis, Emilie Sundqvist, Bruce V. Taylor, Maurizio Leone, Lisa F. Barcellos, Fabio Macciardi, Gilles Defer, Vincent Damotte, Satu Männistö, Graeme J. Stewart, Gordon Mazibrada, Inger Lise Mero, Andre Franke, Philip L. De Jager, Verena Grummel, Mauri Reunanen, David R. Booth, Anna Ticca, Angela Jochim, Leentje Cosemans, Julia Y Mescheriakova, Cristina Agliardi, Paola Cavalla, Jeffrey C. Barrett, Sarah E. Hunt, Gavin Band

المساهمون: School of Life Sciences, University of Technology Sydney (UTS), Catholic University of Leuven - Katholieke Universiteit Leuven (KU Leuven), Profium Oy [Helsinki], Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-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 la Recherche Scientifique (CNRS), Institute of Clinical Medicine [Oslo], Faculty of Medicine [Oslo], University of Oslo (UiO)-University of Oslo (UiO), Michigan Technological University (MTU), The Wellcome Trust Centre for Human Genetics [Oxford], University of Oxford [Oxford], The Wellcome Trust Sanger Institute [Cambridge], Génétique épidémiologique et structures des populations humaines (Inserm U535), Epidémiologie, sciences sociales, santé publique (IFR 69), Université Paris 1 Panthéon-Sorbonne (UP1)-Université Paris-Sud - Paris 11 (UP11)-École des hautes études en sciences sociales (EHESS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris 1 Panthéon-Sorbonne (UP1)-Université Paris-Sud - Paris 11 (UP11)-École des hautes études en sciences sociales (EHESS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), UNIROUEN - UFR Santé (UNIROUEN UFR Santé), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU), Service de neurologie [Bordeaux], CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Karolinska Institutet [Stockholm], Institut des Neurosciences de Montpellier - Déficits sensoriels et moteurs (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Plateforme Post-génomique de la Pitié-Salpêtrière (P3S), UMS omique (OMIQUE), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Pierre et Marie Curie - Paris 6 - UFR de Médecine Pierre et Marie Curie (UPMC), Université Pierre et Marie Curie - Paris 6 (UPMC), Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CRICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Service de Neurologie [CHU Caen], Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), Department of Statistics [Oxford], Centro Dino Ferrari [Milano], Università degli Studi di Milano [Milano] (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Epidémiologie et Analyses en Santé Publique : risques, maladies chroniques et handicap (LEASP), Institut National de la Santé et de la Recherche Médicale (INSERM), Department of Medical Epidemiology and Biostatistics (MEB), University College of London [London] (UCL), Fondation Jean Dausset CEPH, Centre Hospitalier Universitaire de Nice (CHU Nice), Dublin Institute of Technology (DIT), University of California [Irvine] (UCI), University of California, Géosciences Environnement Toulouse (GET), Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Observatoire Midi-Pyrénées (OMP), Institut de Recherche pour le Développement (IRD)-Météo France-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Université Fédérale Toulouse Midi-Pyrénées-Institut de Recherche pour le Développement (IRD)-Météo France-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS), Kaiser Permanente, Universität Zürich [Zürich] = University of Zurich (UZH), University Hospitals Leuven [Leuven], Department Biostatistics University of North Carolina, University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC)-University of North Carolina System (UNC), Institute of Bioinformatics and Systems Biology [München], Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Yale University School of Medicine, Big Data Institute, Department of Clinical Neurosciences [Cambridge], University of Cambridge [UK] (CAM), Faculty of Engineering, Neuroprotection & Neuromodulation, Internal Medicine Specializations, Neurology, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Centre National de la Recherche Scientifique (CNRS), Institut des Neurosciences de Montpellier (INM), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire Midi-Pyrénées (OMP), Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Université Fédérale Toulouse Midi-Pyrénées-Météo-France -Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National d'Études Spatiales [Toulouse] (CNES)-Centre National de la Recherche Scientifique (CNRS)-Météo-France -Centre National de la Recherche Scientifique (CNRS), Yale School of Medicine [New Haven, Connecticut] (YSM), University of Oxford, Università degli Studi di Milano = University of Milan (UNIMI)-Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, University of California [Irvine] (UC Irvine), University of California (UC), Cardiology, Epidemiology, Oral and Maxillofacial Surgery, International Multiple Sclerosis Genetics, Consortium, Beecham, Ah, Patsopoulos, Na, Xifara, Dk, Davis, Mf, Kemppinen, A, Cotsapas, C, Shah, T, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli Boneschi, F, Taylor, B, Harbo, Hf, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, Jr, Hintzen, R, Barcellos, Lf, Wellcome Trust Case Control Consortium, 2, International IBD Genetics, Consortium, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, Hb, Baker, A, Band, G, Baranzini, Se, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, Tm, Blackburn, H, Bomfim, Il, Brambilla, P, Broadley, S, Brochet, B, Brundin, L, Buck, D, Butzkueven, H, Caillier, Sj, Camu, W, Carpentier, W, Cavalla, P, Celius, Eg, Coman, I, Comi, Giancarlo, Corrado, L, Cosemans, L, Cournu Rebeix, I, Cree, Ba, Cusi, D, Damotte, V, Defer, G, Delgado, Sr, Deloukas, P, di Sapio, A, Dilthey, At, Donnelly, P, Dubois, B, Duddy, M, Edkins, S, Elovaara, I, Esposito, F, Evangelou, N, Fiddes, B, Field, J, Franke, A, Freeman, C, Frohlich, Iy, Galimberti, D, Gieger, C, Gourraud, Pa, Graetz, C, Graham, A, Grummel, V, Guaschino, C, Hadjixenofontos, A, Hakonarson, H, Halfpenny, C, Hall, G, Hall, P, Hamsten, A, Harley, J, Harrower, T, Hawkins, C, Hellenthal, G, Hillier, C, Hobart, J, Hoshi, M, Hunt, Se, Jagodic, M, Jelčić, I, Jochim, A, Kendall, B, Kermode, A, Kilpatrick, T, Koivisto, K, Konidari, I, Korn, T, Kronsbein, H, Langford, C, Larsson, M, Lathrop, M, Lebrun Frenay, C, Lechner Scott, J, Lee, Mh, Leone, Ma, Leppä, V, Liberatore, G, Lie, Ba, Lill, Cm, Lindén, M, Link, J, Luessi, F, Lycke, J, Macciardi, F, Männistö, S, Manrique, Cp, Martin, R, Martinelli, V, Mason, D, Mazibrada, G, Mccabe, C, Mero, Il, Mescheriakova, J, Moutsianas, L, Myhr, Km, Nagels, G, Nicholas, R, Nilsson, P, Piehl, F, Pirinen, M, Price, Se, Quach, H, Reunanen, M, Robberecht, W, Robertson, Np, Rodegher, M, Rog, D, Salvetti, M, Schnetz Boutaud, Nc, Sellebjerg, F, Selter, Rc, Schaefer, C, Shaunak, S, Shen, L, Shields, S, Siffrin, V, Slee, M, Sorensen, P, Sorosina, M, Sospedra, M, Spurkland, A, Strange, A, Sundqvist, E, Thijs, V, Thorpe, J, Ticca, A, Tienari, P, van Duijn, C, Visser, Em, Vucic, S, Westerlind, H, Wiley, J, Wilkins, A, Wilson, Jf, Winkelmann, J, Zajicek, J, Zindler, E, Haines, Jl, Pericak Vance, Ma, Ivinson, Aj, Stewart, G, Hafler, D, Hauser, Sl, Compston, A, Mcvean, G, De Jager, P, Sawcer, Sj, Mccauley, J. L.

المصدر: Nature Genetics
Nature Genetics, Nature Publishing Group, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩
Beecham, A H, Patsopoulos, N A, Xifara, D K, Davis, M F, Kemppinen, A, Cotsapas, C, Shah, T S, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli-Boneschi, F, Taylor, B, Harbo, H F, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, J R, Hintzen, R, Barcellos, L F, Agliardi, C, Alfredsson, L, Alizadeh, M, Anderson, C, Andrews, R, Søndergaard, H B, Baker, A, Band, G, Baranzini, S E, Barizzone, N, Barrett, J, Bellenguez, C, Bergamaschi, L, Bernardinelli, L, Berthele, A, Biberacher, V, Binder, T M C, Blackburn, H, Bomfim, I L, Brambilla, P, Broadley, S, Wilson, J F & Henderson, P 2013, ' Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis ', Nature Genetics, vol. 45, no. 11, pp. 1353-60 . https://doi.org/10.1038/ng.2770Test
Nature genetics
Nature Genetics, 2013, 45 (11), pp.1353-1360. ⟨10.1038/ng.2770⟩
Nature Genetics, 45(11), 1353-+. Nature Publishing Group

مصطلحات موضوعية: Multiple Sclerosis, Genotype, [SDV]Life Sciences [q-bio], European Continental Ancestry Group, Genome-wide association study, CLEC16A, Biology, multiple sclerosis, Major histocompatibility complex, Polymorphism, Single Nucleotide, Article, White People, 03 medical and health sciences, 0302 clinical medicine, Research Support, N.I.H., Extramural, Gene Frequency, Polymorphism (computer science), Journal Article, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Genotyping, Allele frequency, 030304 developmental biology, 0303 health sciences, Research Support, Non-U.S. Gov't, Multiple sclerosis, Chromosome Mapping, Genetic Variation, medicine.disease, 3. Good health, Genetic Loci, biology.protein, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaed6c6a6596c74a380f29f543038e03Test
https://doi.org/10.1038/ng.2770Test

المؤلفون: Ashley Beecham, Sylvia R. Delgado, Athena Hadjixenofontos, Leticia Tornes, Jacob L. McCauley, Clara P. Manrique, Melissa R. Ortega, Margaret A. Pericak-Vance, Kottil Rammohan

المصدر: Neuroepidemiology. 44(4)

مصطلحات موضوعية: Oncology, Adult, Male, medicine.medical_specialty, Pathology, Multiple Sclerosis, Epidemiology, business.industry, Multiple sclerosis, Age Factors, Hispanic or Latino, medicine.disease, White People, Phenotype, Expression (architecture), Caribbean Region, Disease Presentation, Internal medicine, medicine, Humans, Hispanic population, Female, Neurology (clinical), business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04db957ea8e676df4be8356e98ec81f5Test
https://pubmed.ncbi.nlm.nih.gov/26184860Test

المؤلفون: International Multiple Sclerosis Genetics Consortium, Ashley H. Beecham, Nikolaos A. Patsopoulos, Dionysia K. Xifara, Mary F. Davis, Anu Kemppinen, Chris Cotsapas, Tejas S. Shah, Chris Spencer, David Booth, An Goris, Annette Oturai, Janna Saarela, Bertrand Fontaine, Bernhard Hemmer, Claes Martin, Frauke Zipp, Sandra D'Alfonso, Filippo Martinelli Boneschi, Bruce Taylor, Hanne F. Harbo, Ingrid Kockum, Jan Hillert, Tomas Olsson, Maria Ban, Jorge R. Oksenberg, Rogier Hintzen, Barcellos Lf 2. Wellcome Trust Case Control Consortium, International Ibd Genetics Consortium, Cristina Agliardi, Lars Alfredsson, Mehdi Alizadeh, Carl Anderson, Robert Andrews, Helle Bach Søndergaard, Amie Baker, Gavin Band, Sergio E. Baranzini, Nadia Barizzone, Jeffrey Barrett, Celine Bellenguez, Laura Bergamaschi, Luisa Bernardinelli, Achim Berthele, Viola Biberacher, Thomas M. C. Binder, Hannah Blackburn, Izaura L. Bomfim, Paola Brambilla, Simon Broadley, Bruno Brochet, Lou Brundin, Dorothea Buck, Helmut Butzkueven, Stacy J. Caillier, William Camu, Wassila Carpentier, Paola Cavalla, Elisabeth G. Celius, Irene Coman, Giancarlo Comi, Lucia Corrado, Leentje Cosemans, Isabelle Cournu Rebeix, Bruce A. C. Cree, Daniele Cusi, Vincent Damotte, Gilles Defer, Silvia R. Delgado, Panos Deloukas, A. Di Sapio, Alexander T. Dilthey, Peter Donnelly, Benedicte Dubois, Martin Duddy, Sarah Edkins, Irina Elovaara, Federica Esposito, Nikos Evangelou, Barnaby Fiddes, Judith Field, Andre Franke, Colin Freeman, Irene Y. Frohlich, Daniela Galimberti, Christian Gieger, Pierre Antoine Gourraud, Christiane Graetz, Andrew Graham, Verena Grummel, Clara Guaschino, Athena Hadjixenofontos, Hakon Hakonarson, Christopher Halfpenny, Gillian Hall, Per Hall, Anders Hamsten, James Harley, Timothy Harrower, Clive Hawkins, Garrett Hellenthal, Charles Hillier, Jeremy Hobart, Muni Hoshi, Sarah E. Hunt, Maja Jagodic, Ilijas Jelcic, Angela Jochim, Brian Kendall, Allan Kermode, Trevor Kilpatrick, Keijo Koivisto, Ioanna Konidari, Thomas Korn, Helena Kronsbein, Cordelia Langford, Malin Larsson, Mark Lathrop, Christine Lebrun Frenay, Jeannette Lechner Scott, Michelle H. Lee, Maurizio A. Leone, Virpi Leppa, Giuseppe Liberatore, Benedicte A. Lie, Christina M. Lill, Magdalena Linden, Jenny Link, Felix Luessi, Jan Lycke, Fabio Macciardi, Satu Mannisto, Clara P. Manrique, Roland Martin, Vittorio Martinelli, Deborah Mason, Gordon Mazibrada, Cristin Mccabe, Inger Lise Mero, Julia Mescheriakova, Loukas Moutsianas, Kjell Morten Myhr, Guy Nagels, Richard Nicholas, Petra Nilsson, Fredrik Piehl, Matti Pirinen, Sian E. Price, Hong Quach, Mauri Reunanen, Wim Robberecht, Neil P. Robertson, Mariaemma Rodegher, David Rog, Nathalie C. Schnetz Boutaud, Finn Sellebjerg, Rebecca C. Selter, Catherine Schaefer, Sandip Shaunak, Ling Shen, Simon Shields, Volker Siffrin, Mark Slee, Per Soelberg Sorensen, Melissa Sorosina, Mireia Sospedra, Anne Spurkland, Amy Strange, Emilie Sundqvist, Vincent Thijs, John Thorpe, Anna Ticca, Pentti Tienari, Cornelia Van Duijn, Elizabeth M. Visser, Steve Vucic, Helga Westerlind, James S. Wiley, Alastair Wilkins, James F. Wilson, Juliane Winkelmann, John Zajicek, Eva Zindler, Jonathan L. Haines, Margaret A. Pericak Vance, Adrian J. Ivinson, Graeme Stewart, David Hafler, Stephen L. Hauser, Alastair Compston, Gil Mcvean, Philip De Jager, Stephen J. Sawcer, Jacob L. Mccauley, SALVETTI, Marco

المساهمون: International Multiple Sclerosis Genetics, Consortium, Ashley H., Beecham, Nikolaos A., Patsopoulo, Dionysia K., Xifara, Mary F., Davi, Anu, Kemppinen, Chris, Cotsapa, Tejas S., Shah, Chris, Spencer, David, Booth, An, Gori, Annette, Oturai, Janna, Saarela, Bertrand, Fontaine, Bernhard, Hemmer, Claes, Martin, Frauke, Zipp, Sandra, D'Alfonso, Filippo Martinelli, Boneschi, Bruce, Taylor, Hanne F., Harbo, Ingrid, Kockum, Jan, Hillert, Tomas, Olsson, Maria, Ban, Jorge R., Oksenberg, Rogier, Hintzen, Barcellos Lf 2., Wellcome Trust Case Control Consortium, International Ibd Genetics, Consortium, Cristina, Agliardi, Lars, Alfredsson, Mehdi, Alizadeh, Carl, Anderson, Robert, Andrew, Helle Bach, Søndergaard, Amie, Baker, Gavin, Band, Sergio E., Baranzini, Nadia, Barizzone, Jeffrey, Barrett, Celine, Bellenguez, Laura, Bergamaschi, Luisa, Bernardinelli, Achim, Berthele, Viola, Biberacher, Thomas M. C., Binder, Hannah, Blackburn, Izaura L., Bomfim, Paola, Brambilla, Simon, Broadley, Bruno, Brochet, Lou, Brundin, Dorothea, Buck, Helmut, Butzkueven, Stacy J., Caillier, William, Camu, Wassila, Carpentier, Paola, Cavalla, Elisabeth G., Celiu, Irene, Coman, Giancarlo, Comi, Lucia, Corrado, Leentje, Coseman, Isabelle Cournu, Rebeix, Bruce A. C., Cree, Daniele, Cusi, Vincent, Damotte, Gilles, Defer, Silvia R., Delgado, Panos, Delouka, A., Di Sapio, Alexander T., Dilthey, Peter, Donnelly, Benedicte, Duboi, Martin, Duddy, Sarah, Edkin, Irina, Elovaara, Federica, Esposito, Nikos, Evangelou, Barnaby, Fidde, Judith, Field, Andre, Franke, Colin, Freeman, Irene Y., Frohlich, Daniela, Galimberti, Christian, Gieger, Pierre Antoine, Gourraud, Christiane, Graetz, Andrew, Graham, Verena, Grummel, Clara, Guaschino, Athena, Hadjixenofonto, Hakon, Hakonarson, Christopher, Halfpenny, Gillian, Hall, Per, Hall, Anders, Hamsten, James, Harley, Timothy, Harrower, Clive, Hawkin

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24076602; info:eu-repo/semantics/altIdentifier/wos/WOS:000326384100016; volume:45; issue:11; firstpage:1353; lastpage:+; numberofpages:10; journal:NATURE GENETICS; http://hdl.handle.net/11573/557110Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84887058596

الإتاحة: https://doi.org/10.1038/ng.2770Test
http://hdl.handle.net/11573/557110Test

المؤلفون: Athena, Hadjixenofontos, Michael A, Schmidt, Patrice L, Whitehead, Ioanna, Konidari, Dale J, Hedges, Harry H, Wright, Ruth K, Abramson, Ramkumar, Menon, Scott M, Williams, Michael L, Cuccaro, Jonathan L, Haines, John R, Gilbert, Margaret A, Pericak-Vance, Eden R, Martin, Jacob L, McCauley

المصدر: Annals of human genetics. 77(1)

مصطلحات موضوعية: Adult, Adolescent, Genetic Variation, behavioral disciplines and activities, DNA, Mitochondrial, Polymorphism, Single Nucleotide, Article, Young Adult, Haplotypes, Child Development Disorders, Pervasive, Child, Preschool, mental disorders, Mutation, Humans, Child, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f6d840130542620b4e8539a6c11c30a7Test
https://pubmed.ncbi.nlm.nih.gov/23130936Test