المؤلفون: Geissler, Julia M, Romanos, Marcel, Sheerin, Una-Marie, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Saad, Mohamad, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, Simón-Sánchez, Javier, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Schulte, Claudia, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Gerlach, Manfred, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, members, International Parkinson Disease Genomics Consortium, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, Nalls, Mike, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Plagnol, Vincent, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Hernandez, Dena G, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Sharma, Manu, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony

المساهمون: Human genetics, Neurology, Amsterdam Neuroscience - Neurodegeneration, Geissler, Julia M [0000-0003-1878-9647], Apollo - University of Cambridge Repository

المصدر: ADHD Attention Deficit and Hyperactivity Disorders, 9(2), 121-127
ADHD Attention Deficit and Hyperactivity Disorders 9(2), 121-127 (2017). doi:10.1007/s12402-017-0219-8
ADHD Attention Deficit and Hyperactivity Disorders, 9(2), 121-127. Springer Wien
Attention Deficit and Hyperactivity Disorders, 9, 121-127
Geissler, J M, Schulte, C, Berg, D & International Parkinson Disease Genomics Consortium members 2017, ' No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs ', ADHD Attention Deficit and Hyperactivity Disorders, vol. 9, no. 2, pp. 121-127 . https://doi.org/10.1007/s12402-017-0219-8Test
Attention Deficit and Hyperactivity Disorders, 9, 2, pp. 121-127

مصطلحات موضوعية: 0301 basic medicine, Parkinson's disease, Single-nucleotide polymorphism, Genome-wide association study, genetics [Attention Deficit Disorder with Hyperactivity], Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, genetics [Parkinson Disease], medicine, Attention deficit hyperactivity disorder, ADHD, GWAS, Humans, Genetic Predisposition to Disease, ddc:610, genetics [Genetic Predisposition to Disease], Genetic Association Studies, Genetic association, Dopamine transporter, Genetics, TPH2, biology, Parkinson Disease, General Medicine, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], medicine.disease, Psychiatry and Mental health, Clinical Psychology, 030104 developmental biology, Norepinephrine transporter, Attention Deficit Disorder with Hyperactivity, biology.protein, genetics [Polymorphism, Single Nucleotide], Parkinson’s disease, Psychology, 030217 neurology & neurosurgery, CDH13, SNPs

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64dc92688c2a4ae8420a2ef6ebe5479Test

المؤلفون: Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw R., Williams, Nigel M., Arepalli, Sampath, Barker, Roger, Barrett, Jeffrey, Ben-Shlomo, Yoav, Berendse, Henk W., Berg, Daniela, Bhatia, Kailash, de Bie, Rob M.A., Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J., Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F., Chong, Sean, Clarke, Carl E., Cookson, Mark R., Cooper, Jonathan M., Corvol, Jen-Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean Francois, Deloukas, Panagiotis, Deuschl, Günther, Dexter, David T., van Dijk, Karin D., Dillman, Allissa, Durif, Frank, Edkins, Sarah, Evans, Jonathan R., Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Gray, Emma, Gústafsson, Ómar, Harris, Clare, Hernandez, Dena G., van Hilten, Jacobus J., Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E., Huttenlocher, Johanna, Illig, Thomas, Langford, Cordelia, Lees, Andrew, Lesage, Suzanne, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E., Mudanohwo, Ese, Pearson, Justin, Perlmutter, Joel S., Pétursson, Hjörvar, Plagnol, Vincent, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Saad, Mohamad, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Sheerin, Una-Marie, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Stefánsson, Kári, Steinberg, Stacy, Stockton, Joanna D., Sveinbjornsdottir, Sigurlaug, Talbot, Kevin, Tanner, Carlie M., Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J., Uitterlinden, André G., Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Wood, Nicholas

المساهمون: Internal Medicine, Functional Genomics, Neuroscience Campus Amsterdam - Neurodegeneration, Neuroscience Campus Amsterdam - Brain Mechanisms in Health & Disease, Human genetics, NCA - Brain mechanisms in health and disease, NCA - neurodegeneration, ANS - Amsterdam Neuroscience, Neurology, Graduate School, Pollak, Pierre

المصدر: Human molecular genetics 22(5), 1039-1049 (2012). doi:10.1093/hmg/dds492
Human Molecular Genetics, 22, 5, pp. 1039-49
Holmans, P, Moskvina, V, Jones, L, Sharma, M, Vedernikov, A, Buchel, F, Sadd, M, Bras, J M, Bettella, F, Nicolaou, N, Simon Sanchez, J, Mittag, F, Gibbs, J R, Schulte, C, Durr, A, Guerreiro, R, Hernandez, D, Brice, A, Stefánsson, H, Majamaa, K, Gasser, T, Heutink, P, Wood, N W, Martinez, M, Singleton, A B, Nalls, M A, Hardy, J, Morris, H R, Williams, N M & Bochdanovits, Z 2013, ' A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease ', Human Molecular Genetics, vol. 22, no. 5, pp. 1039-1049 . https://doi.org/10.1093/hmg/dds492Test
Human Molecular Genetics, 22(5), 1039-1049. Oxford University Press
Human Molecular Genetics, 22, 1039-49
Human molecular genetics, 22(5), 1039-1049. Oxford University Press
Human Molecular Genetics, Vol. 22, No 5 (2013) pp. 1039-49

مصطلحات موضوعية: Parkinson's disease, Genome-wide association study, Genome, Parkinson Disease/genetics/immunology/metabolism, 0302 clinical medicine, genetics [Parkinson Disease], HLA Antigens, Genetics (clinical), Genetics, 0303 health sciences, biology, Association Studies Articles, Parkinson Disease, HLA Antigens/genetics, General Medicine, genetics [Metabolic Networks and Pathways], Human Movement & Fatigue [DCN MP - Plasticity and memory NCEBP 10], HMG-CoA reductase, immunology [Metabolic Networks and Pathways], Corrigendum, Metabolic Networks and Pathways, Risk, medicine.medical_specialty, DCN MP - Plasticity and memory, metabolism [Parkinson Disease], Single-nucleotide polymorphism, Locus (genetics), Human leukocyte antigen, Polymorphism, Single Nucleotide, 03 medical and health sciences, Immune system, immunology [Parkinson Disease], SDG 3 - Good Health and Well-being, Molecular genetics, ddc:570, medicine, Genetic predisposition, Humans, Genetic Predisposition to Disease, Allele, Gene, Molecular Biology, Alleles, 030304 developmental biology, Metabolic Networks and Pathways/genetics/immunology, medicine.disease, ddc:616.8, genetics [HLA Antigens], biology.protein, 030217 neurology & neurosurgery, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628f9e0180872fd9a3a4c2ad9663ef23Test
https://doi.org/10.1093/hmg/dds492Test

المؤلفون: Nalls, Mike A, Saad, Mohamad, Morris, Huw R, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Williams, Nigel, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Gasser, Thomas, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Heutink, Peter, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams-Gray, Caroline H, Wood, Nick, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Hardy, John, Brice, Alexis, Singleton, Andrew B, Wood, Nicholas W, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard, Su, Zhan, Vukcevic, Damjan, Consortium, International Parkinson's Disease Genomics, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, 2, Wellcome Trust Case Control Consortium, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Noyce, Alastair J, Consortium, North American Brain Expression, McCarthy, Mark I, Cookson, Mark R, Consortium, United Kingdom Brain Expression, Gibbs, J Raphael, Hernandez, Dena G, Dillman, Allissa, Nalls, Michael A, Zonderman, Alan B, Arepalli, Sampath, Ferrucci, Luigi, Johnson, Robert, Longo, Dan L, O'Brien, Richard, Nalls, Mike, Traynor, Bryan, Troncoso, Juan, van der Brug, Marcel, Zielke, Ronald H, Weale, Michael E, Ramasamy, Adaikalavan, Plagnol, Vincent, Walker, Rober, Sharma, Manu, Sheerin, Una-Marie, Simón-Sánchez, Javier, Schulte, Claudia, Keller, Margaux F, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Schrag, Anette, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Bestwick, Jonathan P, Chong, Sean, Clarke, Carl E, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Durif, Frank, Dürr, Alexandra, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morrison, Karen E

المساهمون: ANS - Amsterdam Neuroscience, Neurology, Graduate School, Erasmus MC other

المصدر: Human Molecular Genetics, 23, 3, pp. 831-41
Human Molecular Genetics, 23, 831-41
Human molecular genetics, 23(3), 831-841. Oxford University Press
Human Molecular Genetics, 23(3), 831-841
Human molecular genetics 23(3), 831-841 (2013). doi:10.1093/hmg/ddt465
Human Molecular Genetics, 23(3), 831-841. Oxford University Press

مصطلحات موضوعية: genetics [Crohn Disease], epidemiology [Schizophrenia], Single-nucleotide polymorphism, Genome-wide association study, Disease, Comorbidity, Biology, Bioinformatics, Inflammatory bowel disease, Polymorphism, Single Nucleotide, Crohn Disease, genetics [Parkinson Disease], Risk Factors, ddc:570, Mendelian randomization, mental disorders, Genetics, medicine, Humans, Genetic Predisposition to Disease, genetics [Schizophrenia], Molecular Biology, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Genetics (clinical), Genetic association, epidemiology [Crohn Disease], Association Studies Articles, Parkinson Disease, General Medicine, DNA Methylation, medicine.disease, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], 3. Good health, Schizophrenia, CpG Islands, epidemiology [Parkinson Disease], Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcaffb53f0053f5b20f6016b2dc6fbb8Test
https://hdl.handle.net/2066/138086Test

المؤلفون: Keller, Margaux F, Saad, Mohamad, Schulte, Claudia, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Moskvina, Valentina, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Durr, Alexandra, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Holmans, Peter, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Kilarski, Laura L, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Guerreiro, Rita, Martinez, Maria, Sabatier, Paul, Hardy, John, Brice, Alexis, Singleton, Andrew B, Wood, Nicholas W, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Hernandez, Dena G, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Ylikotila, Pauli, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Bras, Jose, Majamaa, Kari, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Gasser, Thomas, Heutink, Peter, Nalls, Michael A, Bettella, Francesco, Consortium, International Parkinson's Disease Genomics, 2, Wellcome Trust Case Control Consortium, Plagnol, Vincent, Sheerin, Una-Marie, Simón-Sánchez, Javier, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Nicolaou, Nayia, Arepalli, Sampath, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Mittag, Florian, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Segalen, Victor, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Büchel, Finja, Dillman, Allissa, Durif, Frank, Montpied, Gabriel, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Sharma, Manu, Gústafsson, Omar, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Lees, Andrew, Lichtner, Peter

المساهمون: ANS - Amsterdam Neuroscience, Neurology, ACS - Amsterdam Cardiovascular Sciences, Graduate School, Human genetics, NCA - Neurodegeneration

المصدر: Human Molecular Genetics, 21, 22, pp. 4996-5009
Keller, M F, Saad, M, Bras, J, Bettella, F, Nicolaou, N, Simon-Sanchez, J, Mittag, F, Buchel, F, Sharma, M, Gibbs, J R, Schulte, C, Moskvina, V, Durr, A, Holmans, P, Kilarski, L L, Guerreiro, R, Hernandez, D G, Brice, A, Ylikotila, P, Stefansson, H, Majamaa, K, Morris, H R, Williams, N, Gasser, T, Heutink, P, Wood, N W, Hardy, J, Martinez, M, Singleton, A B & Nalls, M A 2012, ' Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease ', Human Molecular Genetics, vol. 21, no. 22, pp. 4996-5009 . https://doi.org/10.1093/hmg/dds335Test
Human molecular genetics, 21(22), 4996-5009. Oxford University Press
Human molecular genetics 21(22), 4996-5009 (2012). doi:10.1093/hmg/dds335
Human Molecular Genetics, 21(22), 4996-5009. Oxford University Press
Human Molecular Genetics, 21, 4996-5009

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Multifactorial Inheritance, Parkinson's disease, Functional Neurogenomics Human Movement & Fatigue [DCN 2], Single-nucleotide polymorphism, Genome-wide association study, Quantitative trait locus, Biology, Genome, White People, 03 medical and health sciences, Quantitative Trait, Heritable, 0302 clinical medicine, genetics [Parkinson Disease], Missing heritability problem, Molecular genetics, ddc:570, medicine, Genetics, Humans, Genetic Predisposition to Disease, Molecular Biology, Genetics (clinical), Aged, 030304 developmental biology, Genetic association, Aged, 80 and over, 0303 health sciences, Association Studies Articles, Genetic Variation, Family aggregation, Parkinson Disease, General Medicine, Middle Aged, Heritability, medicine.disease, Corrigenda, 3. Good health, genetics [European Continental Ancestry Group], Human Movement & Fatigue [DCN MP - Plasticity and memory NCEBP 10], Female, Trait analysis, 030217 neurology & neurosurgery, Imputation (genetics), Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f05a64c4ccd93447b089c81c44ddea71Test
https://hdl.handle.net/2066/110130Test

المؤلفون: Consortium, International Parkinson Disease Genomics, Nalls, Michael A, Sveinbjörnsdóttir, Sigurlaug, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Stefánsson, Kári, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Martinez, Maria, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Utterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Hardy, John, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W, Plagnol, Vincent, Hernandez, Dena G, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, Javier, Schulte, Claudia, Lesage, Suzanne, Arepalli, Sampath, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Sharma, Manu, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Alissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Simón-Sánchez, J., Gústafsson, Ómar, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar

المساهمون: ANS - Amsterdam Neuroscience, Neurology, ACS - Amsterdam Cardiovascular Sciences, Graduate School, Human genetics, Anatomy and neurosciences, NCA - Neurodegeneration, Pollak, Pierre, Neuroscience Campus Amsterdam - Neurodegeneration

المصدر: The lancet 377(9766), 641-649 (2011). doi:10.1016/S0140-6736(10)62345-8
Nalls, M A, Plagnol, V, Hernandez, D G, Sharma, M, Sheerin, U M, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Arepalli, S, Barker, R, Ben-Shlomo, Y, Berendse, H W, Berg, D, Bhatia, K, de Bie, R M A, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Bras, J M, Brockmann, K, Brooks, J, Burn, D J, Charlesworth, G, Chen, H L, Chinnery, P F, Chong, S, Clarke, C E, Cookson, M R, Cooper, J M, Corvol, J C, Counsell, C, Damier, P, Dartigues, J F, Deloukas, P, Deuschl, G, Dexter, D T, van Dijk, K D, Dillman, A, Durif, F, Durr, A, Edkins, S, Evans, J R, Foltynie, T, Gao, J J, Gardner, M, Gibbs, J R, Goate, A, Gray, E, Guerreiro, R, Gustafsson, O, Harris, C, van Hilten, J J, Hofman, A, Hollenbeck, A, Holton, J, Hu, M, Huang, X M, Huber, H, Hudson, G, Hunt, S E, Huttenlocher, J, Illig, T, Jonsson, P V, Lambert, J C, Langford, C, Lees, A, Lichtner, P, Limousin, P, Lopez, G, Lorenz, D, McNeill, A, Moorby, C, Moore, M, Morris, H R, Morrison, K E, Mudanohwo, E, O'Sullivan, S S, Pearson, J, Perlmutter, J S, Petursson, H, Pollak, P, Post, B, Potter, S, Ravina, B, Revesz, T, Riess, O, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Schapira, A, Scheffer, H, Shaw, K, Shoulson, I, Sidransky, E, Smith, C, Heutink, P, Singleton, A B & Wood, N W 2011, ' Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies ', Lancet, vol. 377, no. 9766, pp. 641-649 . https://doi.org/10.1016/S0140-6736Test(10)62345-8
Lancet, 377(9766), 641-649
Nalls, M A, Plagnol, V, Hernandez, D G, Sharma, M, Sheerin, U-M, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Arepalli, S, Barker, R, Ben-Shlomo, Y, Berendse, H W, Berg, D, Bhatia, K, de Bie, R M A, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Bras, J M, Brockmann, K, Brooks, J, Burn, D J, Charlesworth, G, Chen, H, Chinnery, P F, Chong, S, Clarke, C E, Cookson, M R, Cooper, J M, Corvol, J C, Counsell, C, Damier, P, Dartigues, J-F, Deloukas, P, Deuschl, G, Dexter, D T, van Dijk, K D, Dillman, A, Durif, F, Duerr, A, Edkins, S, Evans, J R, Foltynie, T, Gao, J, Gardner, M & Gibbs, J R & Smith, C 2011, ' Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies ', The Lancet, vol. 377, no. 9766, pp. 641-649 . https://doi.org/10.1016/S0140-6736Test(10)62345-8
Lancet, 377(9766), 641-649. Elsevier Limited
The Lancet, Vol. 377, No 9766 (2011) pp. 641-9
The Lancet (London), 377, 641-9
The Lancet (London), 377, 9766, pp. 641-9

مصطلحات موضوعية: Male, Genome-wide association study, Genomic disorders and inherited multi-system disorders Functional Neurogenomics [IGMD 3], 0302 clinical medicine, genetics [Parkinson Disease], Parkinson Disease/genetics, Age of Onset, genetics [Genetic Predisposition to Disease], Genetics, 0303 health sciences, Genetic Predisposition to Disease/genetics, Parkinson Disease, General Medicine, Middle Aged, Polymorphism, Single Nucleotide/genetics, LRRK2, genetics [Genetic Variation], 3. Good health, Genetic Variation/genetics, Meta-analysis, Genetic Loci/genetics, genetics [Polymorphism, Single Nucleotide], Female, Functional Neurogenomics [DCN 2], Sequence Analysis, Adult, Genotype, Single-nucleotide polymorphism, genetics [Genetic Loci], Biology, Polymorphism, Single Nucleotide, Risk Assessment, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Genetic variation, Humans, Genetic Predisposition to Disease, ddc:610, Alleles, 030304 developmental biology, Aged, Genetic Variation, Odds ratio, nervous system diseases, ddc:616.8, Genetic Loci, Age of onset, 030217 neurology & neurosurgery, Imputation (genetics), Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30302ee533afcdd040276757682befa9Test
http://ora.ox.ac.uk/objects/uuid:e314ae57-18ba-411e-abb0-e758bce2c949Test

المؤلفون: Consortium, International Parkinson's Disease Genomics, 2, Wellcome Trust Case Control Consortium, Schulte, Claudia, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, de Silva, Rohan, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Lesage, Suzanne, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Su, Zhan, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Sveinbjörnsdóttir, Sigurlaug, Uitterlinden, André G, Vandrovcova, Jana, Velseboer, Daan, Vidailhet, Marie, Vukcevic, Damjan, Walker, Robert, van de Warrenburg, Bart, Weale, Michael E, Williams, Nigel, Williams-Gray, Caroline H, Amouyel, Philippe, Wickremaratchi, Mirdhu, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Donnelly, Peter, Singleton, Andrew B, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Arepalli, Sampath, Wood, Nicholas W, Band, Gavin, Barker, Roger A, Bellinguez, Céline, Ben-Shlomo, Yoav, Berendse, Henk W, Plagnol, Vincent, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Nalls, Michael A, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Bras, Jose M, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Hernandez, Dena G, Foltynie, Thomas, Freeman, Colin, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, Sharma, Manu, Hellenthal, Garrett, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Sheerin, Una-Marie, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Saad, Mohamad, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Pearson, Richard, Perlmutter, Joel S, Pétursson, Hjörvar, Simón-Sánchez, Javier, Pirinen, Matti, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina

المساهمون: Neuroscience Campus Amsterdam - Neurodegeneration, Pollak, Pierre, Human genetics, Neurology, Anatomy and neurosciences, NCA - Neurodegeneration, ANS - Amsterdam Neuroscience, ACS - Amsterdam Cardiovascular Sciences, Graduate School

المصدر: PLoS Genetics, 7(6):e1002142. Public Library of Science
2011, ' A two-stage meta-analysis identifies several new loci for Parkinson's disease ', PLoS Genetics, vol. 7, no. 6, pp. e1002142 . https://doi.org/10.1371/journal.pgen.1002142Test
PLoS Genetics, Vol 7, Iss 6, p e1002142 (2011)
PLoS Genetics, 7(6)
PLOS Genetics, Vol. 7, No 6 (2011) P. e1002142
Plagnol, V, Nalls, M A, Bras, J M, Hernandez, D G, Sharma, M, Sheerin, U M, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Amouyel, P, Arepalli, S, Band, G, Barker, R A, Bellinguez, C, Ben-Shlomo, Y, Berendse, H W, Berg, D, Bhatia, K, de Bie, R M A, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Brockmann, K, Brooks, J, Burn, D J, Charlesworth, G, Chen, H L, Chinnery, P F, Chong, S, Clarke, C E, Cookson, M R, Cooper, J M, Corvol, J C, Counsell, C, Damier, P, Dartigues, J F, Deloukas, P, Deuschl, G, Dexter, D T, van Dijk, K D, Dillman, A, Durif, F, Durr, A, Edkins, S, Evans, J R, Foltynie, T, Freeman, C, Gao, J J, Gardner, M, Gibbs, J R, Goate, A, Gray, E, Guerreiro, R, Gustafsson, O, Harris, C, Hellenthal, G, van Hilten, J J, Hofman, A, Hollenbeck, A, Holton, J, Hu, M, Huang, X M, Huber, H, Hudson, G, Hunt, S E, Huttenlocher, J, Illig, T, Jonsson, P V, Langford, C, Lees, A, Lichtner, P, Limousin, P, Lopez, G, Lorenz, D, McNeill, A, Moorby, C, Moore, M, Morris, H, Morrison, K E, Mudanohwo, E, O'Sullivan, S S, Pearson, J, Pearson, R, Perlmutter, J S, Petursson, H, Pirinen, M, Pollak, P, Post, B, Potter, S, Ravina, B, Revesz, T, Riess, O, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Heutink, P & Wood, N W 2011, ' A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease ', PLoS Genetics, vol. 7, no. 6, e1002142 . https://doi.org/10.1371/journal.pgen.1002142Test
PLoS Genetics
PLoS Genetics 7(6), e1002142 (2011). doi:10.1371/journal.pgen.1002142
PLoS genetics, 7(6). Public Library of Science

مصطلحات موضوعية: Cancer Research, Candidate gene, Genome-wide association study, QH426-470, 0302 clinical medicine, genetics [Parkinson Disease], Parkinson Disease/genetics, Genetics (clinical), Genetics, 0303 health sciences, education.field_of_study, Brain, Parkinson Disease, Polymorphism, Single Nucleotide/genetics, Genetic Loci/genetics, genetics [Polymorphism, Single Nucleotide], Research Article, Population, Single-nucleotide polymorphism, genetics [Genetic Loci], Biology, Polymorphism, Single Nucleotide, Risk Assessment, 03 medical and health sciences, Genome-Wide Association Studies, Brain/metabolism, Humans, Genetic Predisposition to Disease, ddc:610, education, Molecular Biology, Genotyping, QH426, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Genetic association, GPNMB, Gene Expression Profiling, Haplotype, DNA Methylation, ddc:616.8, Gene Expression Regulation, metabolism [Brain], Genetic Loci, Genetics of Disease, RC0321, 030217 neurology & neurosurgery, Neuroscience, Genome-Wide Association Study

وصف الملف: application/pdf; application/octet-stream

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48bbf6f6447606cdef45c8b79f0c6b4cTest
https://research.vu.nl/en/publications/6dd02677-9daa-478c-9dfc-977fa803d9e6Test