المؤلفون: Glessner, Joseph T, Ningappa, Mylarappa B, Ngo, Kim A, Zahid, Maliha, So, Juhoon, Higgs, Brandon W, Sleiman, Patrick MA, Narayanan, Tejaswini, Ranganathan, Sarangarajan, March, Michael, Prasadan, Krishna, Vaccaro, Courtney, Reyes-Mugica, Miguel, Velazquez, Jeremy, Salgado, Claudia M, Ebrahimkhani, Mo R, Schmitt, Lori, Rajasundaram, Dhivyaa, Paul, Morgan, Pellegrino, Renata, Gittes, George K, Li, Dong, Wang, Xiang, Billings, Jonathan, Squires, Robert, Ashokkumar, Chethan, Sharif, Khalid, Kelly, Deirdre, Dhawan, Anil, Horslen, Simon, Lo, Cecilia W, Shin, Donghun, Subramaniam, Shankar, Hakonarson, Hakon, Sindhi, Rakesh

المصدر: Journal of Hepatology. 79(6)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Liver Disease, Organ Transplantation, Chronic Liver Disease and Cirrhosis, Congenital Structural Anomalies, Perinatal Period - Conditions Originating in Perinatal Period, Genetics, Digestive Diseases, Transplantation, Prevention, Human Genome, Rare Diseases, Pediatric, 2.1 Biological and endogenous factors, Oral and gastrointestinal, Child, Animals, Mice, Humans, Biliary Atresia, Genome-Wide Association Study, Genetic Predisposition to Disease, Zebrafish, Canada, Polygenic Susceptibility, Ciliogenesis, Portal Vein, Vascular Development, Tube Morphogenesis, Public Health and Health Services, Gastroenterology & Hepatology, Clinical sciences

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URL الوصول: https://escholarship.org/uc/item/5rj4d8tv
https://escholarship.org/content/qt5rj4d8tv/qt5rj4d8tv.pdf

المؤلفون: Tylee, Daniel S, Sun, Jiayin, Hess, Jonathan L, Tahir, Muhammad A, Sharma, Esha, Malik, Rainer, Worrall, Bradford B, Levine, Andrew J, Martinson, Jeremy J, Nejentsev, Sergey, Speed, Doug, Fischer, Annegret, Mick, Eric, Walker, Brian R, Crawford, Andrew, Grant, Struan FA, Polychronakos, Constantin, Bradfield, Jonathan P, Sleiman, Patrick MA, Hakonarson, Hakon, Ellinghaus, Eva, Elder, James T, Tsoi, Lam C, Trembath, Richard C, Barker, Jonathan N, Franke, Andre, Dehghan, Abbas, Team, The 23 and Me Research, Consortium, The Inflammation Working Group of the CHARGE, Consortium, The METASTROKE Consortium of the International Stroke Genetics, Registry, The Netherlands Twin, Group, The neuroCHARGE Working, Consortium, The Obsessive Compulsive and Tourette Syndrome Working Group of the Psychiatric Genomics, Faraone, Stephen V, Glatt, Stephen J

المصدر: American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(7)

مصطلحات موضوعية: Pharmacology and Pharmaceutical Sciences, Biological Sciences, Biomedical and Clinical Sciences, Genetics, Human Genome, Brain Disorders, Serious Mental Illness, Behavioral and Social Science, Mental Illness, Autoimmune Disease, Pediatric, Schizophrenia, Mental Health, 2.1 Biological and endogenous factors, Inflammatory and immune system, Mental health, Autoimmune Diseases, Comorbidity, Databases, Factual, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Linkage Disequilibrium, Male, Mental Disorders, Multifactorial Inheritance, Polymorphism, Single Nucleotide, White People, allergy, anorexia nervosa, attention deficit-hyperactivity disorder, autoimmune disorder, bipolar disorder, celiac disease, childhood ear infection, C-reactive protein, Crohn's disease, genetic correlation, genome-wide association, hypothyroidism, major depression, neuroticism, obsessive schizophrenia, primary biliary cirrhosis, rheumatoid arthritis, smoking, systemic lupus erythematosus, Tourette syndrome, tuberculosis susceptibility, type 1 diabetes, ulcerative colitis, and Me Research Team, Inflammation Working Group of the CHARGE Consortium, METASTROKE Consortium of the International Stroke Genetics Consortium, Netherlands Twin Registry, neuroCHARGE Working Group, Obsessive Compulsive and Tourette Syndrome Working Group of the Psychiatric Genomics Consortium, Clinical Sciences, Neurosciences, Clinical sciences

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URL الوصول: https://escholarship.org/uc/item/8jp583mj
https://escholarship.org/content/qt8jp583mj/qt8jp583mj.pdf

المؤلفون: Chen, Zhao, Tang, Hua, Qayyum, Rehan, Schick, Ursula M, Nalls, Michael A, Handsaker, Robert, Li, Jin, Lu, Yingchang, Yanek, Lisa R, Keating, Brendan, Meng, Yan, van Rooij, Frank JA, Okada, Yukinori, Kubo, Michiaki, Rasmussen-Torvik, Laura, Keller, Margaux F, Lange, Leslie, Evans, Michele, Bottinger, Erwin P, Linderman, Michael D, Ruderfer, Douglas M, Hakonarson, Hakon, Papanicolaou, George, Zonderman, Alan B, Gottesman, Omri, Project, CHARGE Consortium BioBank Japan, Thomson, Cynthia, Ziv, Elad, Singleton, Andrew B, Loos, Ruth JF, Sleiman, Patrick MA, Ganesh, Santhi, McCarroll, Steven, Becker, Diane M, Wilson, James G, Lettre, Guillaume, Reiner, Alexander P

المصدر: Human Molecular Genetics. 22(12)

مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Minority Health, Hematology, Health Disparities, 2.1 Biological and endogenous factors, Blood, Adolescent, Adult, Black or African American, Child, Chromosomes, Human, Pair 16, Cohort Studies, Erythrocyte Count, Erythrocyte Indices, Erythrocytes, Female, Genome-Wide Association Study, Hemoglobins, Humans, Male, Polymorphism, Single Nucleotide, White People, Young Adult, alpha-Globins, BioBank Japan Project, CHARGE Consortium, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/44x5s24k
https://escholarship.org/content/qt44x5s24k/qt44x5s24k.pdf

المؤلفون: Bradfield, Jonathan P, Taal, H Rob, Timpson, Nicholas J, Scherag, Andre, Lecoeur, Cecile, Warrington, Nicole M, Hypponen, Elina, Holst, Claus, Valcarcel, Beatriz, Thiering, Elisabeth, Salem, Rany M, Schumacher, Fredrick R, Cousminer, Diana L, Sleiman, Patrick MA, Zhao, Jianhua, Berkowitz, Robert I, Vimaleswaran, Karani S, Jarick, Ivonne, Pennell, Craig E, Evans, David M, St Pourcain, Beate, Berry, Diane J, Mook-Kanamori, Dennis O, Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G, van Duijn, Cornelia M, van der Valk, Ralf JP, de Jongste, Johan C, Postma, Dirkje S, Boomsma, Dorret I, Gauderman, W James, Hassanein, Mohamed T, Lindgren, Cecilia M, Magi, Reedik, Boreham, Colin AG, Neville, Charlotte E, Moreno, Luis A, Elliott, Paul, Pouta, Anneli, Hartikainen, Anna-Liisa, Li, Mingyao, Raitakari, Olli, Lehtimaki, Terho, Eriksson, Johan G, Palotie, Aarno, Dallongeville, Jean, Das, Shikta, Deloukas, Panos, McMahon, George, Ring, Susan M, Kemp, John P, Buxton, Jessica L, Blakemore, Alexandra IF, Bustamante, Mariona, Guxens, Monica, Hirschhorn, Joel N, Gillman, Matthew W, Kreiner-Moller, Eskil, Bisgaard, Hans, Gilliland, Frank D, Heinrich, Joachim, Wheeler, Eleanor, Barroso, Ines, O'Rahilly, Stephen, Meirhaeghe, Aline, Sorensen, Thorkild IA, Power, Chris, Palmer, Lyle J, Hinney, Anke, Widen, Elisabeth, Farooqi, I Sadaf, McCarthy, Mark I, Froguel, Philippe, Meyre, David, Hebebrand, Johannes, Jarvelin, Marjo-Riitta, Jaddoe, Vincent WV, Smith, George Davey, Hakonarson, Hakon, Grant, Struan FA

المصدر: Nature Genetics. 44(5)

مصطلحات موضوعية: Biological Sciences, Genetics, Pediatric, Nutrition, Obesity, Human Genome, Metabolic and endocrine, Oral and gastrointestinal, Stroke, Cancer, Cardiovascular, Adolescent, Adult, Body Mass Index, Case-Control Studies, Genetic Loci, Genetic Markers, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Young Adult, Early Growth Genetics Consortium, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9r69s4pk

المؤلفون: Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Nguyen, Kenny, Qu, Jingchun, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick MA, Hakonarson, Hakon

المساهمون: The Children’s Hospital of Philadelphia Endowed Chair in Genomic Research, Institutional Development Funds from the Children’s Hospital of Philadelphia

المصدر: Experimental Biology and Medicine ; volume 246, issue 21, page 2317-2323 ; ISSN 1535-3702 1535-3699

الاتاحة: http://dx.doi.org/10.1177/15353702211018970
http://journals.sagepub.com/doi/pdf/10.1177/15353702211018970
http://journals.sagepub.com/doi/full-xml/10.1177/15353702211018970

المؤلفون: Höglinger, Günter U, Melhem, Nadine M, Dickson, Dennis W, Sleiman, Patrick MA, Wang, Li-San, Klei, Lambertus, Rademakers, Rosa, de Silva, Rohan, Litvan, Irene, Riley, David E, van Swieten, John C, Heutink, Peter, Wszolek, Zbigniew K, Uitti, Ryan J, Vandrovcova, Jana, Hurtig, Howard I, Gross, Rachel G, Maetzler, Walter, Goldwurm, Stefano, Tolosa, Eduardo, Borroni, Barbara, Pastor, Pau, Cantwell, Laura B, Han, Mi Ryung, Dillman, Allissa, van der Brug, Marcel P, Gibbs, J Raphael, Cookson, Mark R, Hernandez, Dena G, Singleton, Andrew B, Farrer, Matthew J, Yu, Chang-En, Golbe, Lawrence I, Revesz, Tamas, Hardy, John, Lees, Andrew J, Devlin, Bernie, Hakonarson, Hakon, Müller, Ulrich, Schellenberg, Gerard D

المصدر: Nature Genetics. 43(7)

مصطلحات موضوعية: Biological Sciences, Genetics, Pediatric, Prevention, Cerebral Palsy, Rare Diseases, Neurodegenerative, Brain Disorders, Acquired Cognitive Impairment, Human Genome, Perinatal Period - Conditions Originating in Perinatal Period, Frontotemporal Dementia (FTD), Dementia, Neurosciences, Aetiology, 2.1 Biological and endogenous factors, Neurological, Case-Control Studies, Chromosomes, Human, Cohort Studies, Genetic Loci, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Prognosis, Risk Factors, Supranuclear Palsy, Progressive, Tauopathies, tau Proteins, PSP Genetics Study Group, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3z78h0m8

المؤلفون: Van Deerlin, Vivianna M, Sleiman, Patrick MA, Martinez-Lage, Maria, Chen-Plotkin, Alice, Wang, Li-San, Graff-Radford, Neill R, Dickson, Dennis W, Rademakers, Rosa, Boeve, Bradley F, Grossman, Murray, Arnold, Steven E, Mann, David MA, Pickering-Brown, Stuart M, Seelaar, Harro, Heutink, Peter, van Swieten, John C, Murrell, Jill R, Ghetti, Bernardino, Spina, Salvatore, Grafman, Jordan, Hodges, John, Spillantini, Maria Grazia, Gilman, Sid, Lieberman, Andrew P, Kaye, Jeffrey A, Woltjer, Randall L, Bigio, Eileen H, Mesulam, Marsel, al-Sarraj, Safa, Troakes, Claire, Rosenberg, Roger N, White, Charles L, Ferrer, Isidro, Lladó, Albert, Neumann, Manuela, Kretzschmar, Hans A, Hulette, Christine Marie, Welsh-Bohmer, Kathleen A, Miller, Bruce L, Alzualde, Ainhoa, de Munain, Adolfo Lopez, McKee, Ann C, Gearing, Marla, Levey, Allan I, Lah, James J, Hardy, John, Rohrer, Jonathan D, Lashley, Tammaryn, Mackenzie, Ian RA, Feldman, Howard H, Hamilton, Ronald L, Dekosky, Steven T, van der Zee, Julie, Kumar-Singh, Samir, Van Broeckhoven, Christine, Mayeux, Richard, Vonsattel, Jean Paul G, Troncoso, Juan C, Kril, Jillian J, Kwok, John BJ, Halliday, Glenda M, Bird, Thomas D, Ince, Paul G, Shaw, Pamela J, Cairns, Nigel J, Morris, John C, McLean, Catriona Ann, DeCarli, Charles, Ellis, William G, Freeman, Stefanie H, Frosch, Matthew P, Growdon, John H, Perl, Daniel P, Sano, Mary, Bennett, David A, Schneider, Julie A, Beach, Thomas G, Reiman, Eric M, Woodruff, Bryan K, Cummings, Jeffrey, Vinters, Harry V, Miller, Carol A, Chui, Helena C, Alafuzoff, Irina, Hartikainen, Päivi, Seilhean, Danielle, Galasko, Douglas, Masliah, Eliezer, Cotman, Carl W, Tuñón, M Teresa, Martínez, M Cristina Caballero, Munoz, David G, Carroll, Steven L, Marson, Daniel, Riederer, Peter F, Bogdanovic, Nenad, Schellenberg, Gerard D, Hakonarson, Hakon, Trojanowski, John Q, Lee, Virginia M-Y

المصدر: Nature Genetics. 42(3)

مصطلحات موضوعية: Biological Sciences, Genetics, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Frontotemporal Dementia (FTD), Dementia, Aging, Brain Disorders, Neurodegenerative, Acquired Cognitive Impairment, Alzheimer's Disease Related Dementias (ADRD), Neurosciences, 2.1 Biological and endogenous factors, Case-Control Studies, Chromosomes, Human, Pair 7, DNA-Binding Proteins, Frontotemporal Lobar Degeneration, Gene Frequency, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Inclusion Bodies, Intercellular Signaling Peptides and Proteins, Linkage Disequilibrium, Membrane Proteins, Polymorphism, Single Nucleotide, Progranulins, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/6dm6028c
https://escholarship.org/content/qt6dm6028c/qt6dm6028c.pdf

المؤلفون: Fahey, Lisa M., Chandramouleeswaran, Prasanna M., Guan, Shaobo, Benitez, Alain J., Furuta, Glenn T., Aceves, Seema S., Wang, Mei-Lun, Liacouras, Chris A., Muir, Amanda B., Sleiman, Patrick MA, Hakonarson, Hakon, Spergel, Jonathan M., Cianferoni, Antonella

المصدر: Clinical and Translational Gastroenterology ; volume 9, issue 3, page e139 ; ISSN 2155-384X

الاتاحة: http://dx.doi.org/10.1038/s41424-018-0003-x
http://www.nature.com/articles/s41424-018-0003-x
http://www.nature.com/articles/s41424-018-0003-x.pdf
https://journals.lww.com/01720094-201803000-00005

المؤلفون: International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Céline, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Martinelli Boneschi, Filippo, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Françoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Bénédicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica, Fontenille, Claire, Foote, Simon, Franke, Andre, Galimberti, Daniela, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan FA, Guerini, Franca Rosa, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N, Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G, Kilpatrick, Trevor J, Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S, Leone, Maurizio A, Leppä, Virpi, Liljedahl, Ulrika, Bomfim, Izaura Lima, Lincoln, Robin R, Link, Jenny, Liu, Jianjun, Lorentzen, Aslaug R, Lupoli, Sara, Macciardi, Fabio, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L, Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L, Ramsay, Patricia P, Reunanen, Mauri, Reynolds, Richard, Rioux, John D, Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P, Rückert, Ina-Maria, Salvetti, Marco, Salvi, Erika, Santaniello, Adam, Schaefer, Catherine A, Schreiber, Stefan, Schulze, Christian, Scott, Rodney J, Sellebjerg, Finn, Selmaj, Krzysztof W, Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick MA, Smestad, Cathrine, Sørensen, Per Soelberg, Søndergaard, Helle Bach, Stankovich, Jim, Strange, Richard C, Sulonen, Anna-Maija, Sundqvist, Emilie, Syvänen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M, Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A, Tronczynska, Ewa, Casas, Juan P, Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S, Wang, Kai, Mathew, Christopher G, Wason, James, Palmer, Colin NA, Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C, Yaouanq, Jacqueline, Viswanathan, Ananth C, Zhang, Haitao, Wood, Nicholas W, Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R, Pericak-Vance, Margaret A, Haines, Jonathan L, Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J, De Jager, Philip L, Peltonen, Leena, Stewart, Graeme J, Hafler, David A, Hauser, Stephen L, McVean, Gil, Donnelly, Peter, Compston, Alastair

وصف الملف: text

Relation: https://researchonline.lshtm.ac.uk/id/eprint/153/1/ukmss-36028.pdf; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium 2; Sawcer, Stephen; Hellenthal, Garrett; Pirinen, Matti; Spencer, Chris CA; Patsopoulos, Nikolaos A; Moutsianas, Loukas; Dilthey, Alexander; Su, Zhan; +234 more. Freeman, Colin; Hunt, Sarah E; Edkins, Sarah; Gray, Emma; Booth, David R; Potter, Simon C; Goris, An; Band, Gavin; Oturai, Annette Bang; Strange, Amy; Saarela, Janna; Bellenguez, Céline; Fontaine, Bertrand; Gillman, Matthew; Hemmer, Bernhard; Gwilliam, Rhian; Zipp, Frauke; Jayakumar, Alagurevathi; Martin, Roland; Leslie, Stephen; Hawkins, Stanley; Giannoulatou, Eleni; D'alfonso, Sandra; Blackburn, Hannah; Martinelli Boneschi, Filippo; Liddle, Jennifer; Harbo, Hanne F; Perez, Marc L; Spurkland, Anne; Waller, Matthew J; Mycko, Marcin P; Ricketts, Michelle; Comabella, Manuel; Hammond, Naomi; Kockum, Ingrid; McCann, Owen T; Ban, Maria; Whittaker, Pamela; Kemppinen, Anu; Weston, Paul; Hawkins, Clive; Widaa, Sara; Zajicek, John; Dronov, Serge; Robertson, Neil; Bumpstead, Suzannah J; Barcellos, Lisa F; Ravindrarajah, Rathi; Abraham, Roby; Alfredsson, Lars; Ardlie, Kristin; Aubin, Cristin; Baker, Amie; Baker, Katharine; Baranzini, Sergio E; Bergamaschi, Laura; Bergamaschi, Roberto; Bernstein, Allan; Berthele, Achim; Boggild, Mike; Bradfield, Jonathan P; Brassat, David; Broadley, Simon A; Buck, Dorothea; Butzkueven, Helmut; Capra, Ruggero; Carroll, William M; Cavalla, Paola; Celius, Elisabeth G; Cepok, Sabine; Chiavacci, Rosetta; Clerget-Darpoux, Françoise; Clysters, Katleen; Comi, Giancarlo; Cossburn, Mark; Cournu-Rebeix, Isabelle; Cox, Mathew B; Cozen, Wendy; Cree, Bruce AC; Cross, Anne H; Cusi, Daniele; Daly, Mark J; Davis, Emma; de Bakker, Paul IW; Debouverie, Marc; D'hooghe, Marie Beatrice; Dixon, Katherine; Dobosi, Rita; Dubois, Bénédicte; Ellinghaus, David; Elovaara, Irina; Esposito, Federica; Fontenille, Claire; Foote, Simon; Franke, Andre; Galimberti, Daniela; Ghezzi, Angelo; Glessner, Joseph; Gomez, Refujia; Gout, Olivier; Graham, Colin; Grant, Struan FA; Guerini, Franca Rosa; Hakonarson, Hakon; Hall, Per; Hamsten, Anders; Hartung, Hans-Peter; Heard, Rob N; Heath, Simon; Hobart, Jeremy; Hoshi, Muna; Infante-Duarte, Carmen; Ingram, Gillian; Ingram, Wendy; Islam, Talat; Jagodic, Maja; Kabesch, Michael; Kermode, Allan G; Kilpatrick, Trevor J; Kim, Cecilia; Klopp, Norman; Koivisto, Keijo; Larsson, Malin; Lathrop, Mark; Lechner-Scott, Jeannette S; Leone, Maurizio A; Leppä, Virpi; Liljedahl, Ulrika; Bomfim, Izaura Lima; Lincoln, Robin R; Link, Jenny; Liu, Jianjun; Lorentzen, Aslaug R; Lupoli, Sara; Macciardi, Fabio; Mack, Thomas; Marriott, Mark; Martinelli, Vittorio; Mason, Deborah; McCauley, Jacob L; Mentch, Frank; Mero, Inger-Lise; Mihalova, Tania; Montalban, Xavier; Mottershead, John; Myhr, Kjell-Morten; Naldi, Paola; Ollier, William; Page, Alison; Palotie, Aarno; Pelletier, Jean; Piccio, Laura; Pickersgill, Trevor; Piehl, Fredrik; Pobywajlo, Susan; Quach, Hong L; Ramsay, Patricia P; Reunanen, Mauri; Reynolds, Richard; Rioux, John D; Rodegher, Mariaemma; Roesner, Sabine; Rubio, Justin P; Rückert, Ina-Maria; Salvetti, Marco; Salvi, Erika; Santaniello, Adam; Schaefer, Catherine A; Schreiber, Stefan; Schulze, Christian; Scott, Rodney J; Sellebjerg, Finn; Selmaj, Krzysztof W; Sexton, David; Shen, Ling; Simms-Acuna, Brigid; Skidmore, Sheila; Sleiman, Patrick MA; Smestad, Cathrine; Sørensen, Per Soelberg; Søndergaard, Helle Bach; Stankovich, Jim; Strange, Richard C; Sulonen, Anna-Maija; Sundqvist, Emilie; Syvänen, Ann-Christine; Taddeo, Francesca; Taylor, Bruce; Blackwell, Jenefer M; Tienari, Pentti; Bramon, Elvira; Tourbah, Ayman; Brown, Matthew A; Tronczynska, Ewa; Casas, Juan P ; Tubridy, Niall; Corvin, Aiden; Vickery, Jane; Jankowski, Janusz; Villoslada, Pablo; Markus, Hugh S; Wang, Kai; Mathew, Christopher G; Wason, James; Palmer, Colin NA; Wichmann, H-Erich; Plomin, Robert; Willoughby, Ernest; Rautanen, Anna; Winkelmann, Juliane; Wittig, Michael; Trembath, Richard C; Yaouanq, Jacqueline; Viswanathan, Ananth C; Zhang, Haitao; Wood, Nicholas W; Zuvich, Rebecca; Deloukas, Panos; Langford, Cordelia; Duncanson, Audrey; Oksenberg, Jorge R; Pericak-Vance, Margaret A; Haines, Jonathan L; Olsson, Tomas; Hillert, Jan; Ivinson, Adrian J; De Jager, Philip L; Peltonen, Leena; Stewart, Graeme J; Hafler, David A; Hauser, Stephen L; McVean, Gil; Donnelly, Peter; Compston, Alastair; (2011) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature, 476 (7359). pp. 214-219. ISSN 0028-0836 DOI: https://doi.org/10.1038/nature10251

الاتاحة: https://researchonline.lshtm.ac.uk/id/eprint/153/
https://researchonline.lshtm.ac.uk/id/eprint/153/1/ukmss-36028.pdf

المؤلفون: Sleiman, Patrick MA, Grant, Struan FA

المصدر: Clinical Chemistry ; volume 56, issue 5, page 723-728 ; ISSN 0009-9147 1530-8561

الاتاحة: http://dx.doi.org/10.1373/clinchem.2009.141564
http://academic.oup.com/clinchem/article-pdf/56/5/723/32653659/clinchem0723.pdf

المؤلفون: Li, Yun Rose, Glessner, Joseph T, Coe, Bradley P, Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan FA, Sleiman, Patrick MA, Li, Mingyao, Eichler, Evan E, Hakonarson, Hakon

وصف الملف: application/pdf; text/plain

Relation: http://d-scholarship.pitt.edu/43667/1/Rare%20copy%20number%20variants%20in%20over%20100,000%20European%20ancestry%20subjects%20reveal%20multiple%20disease%20associations.pdf; http://d-scholarship.pitt.edu/43667/9/licenseagreement_dscholarship.txt; Li, Yun Rose and Glessner, Joseph T and Coe, Bradley P and Li, Jin and Mohebnasab, Maede and Chang, Xiao and Connolly, John and Kao, Charlly and Wei, Zhi and Bradfield, Jonathan and Kim, Cecilia and Hou, Cuiping and Khan, Munir and Mentch, Frank and Qiu, Haijun and Bakay, Marina and Cardinale, Christopher and Lemma, Maria and Abrams, Debra and Bridglall-Jhingoor, Andrew and Behr, Meckenzie and Harrison, Shanell and Otieno, George and Thomas, Alexandria and Wang, Fengxiang and Chiavacci, Rosetta and Wu, Lawrence and Hadley, Dexter and Goldmuntz, Elizabeth and Elia, Josephine and Maris, John and Grundmeier, Robert and Devoto, Marcella and Keating, Brendan and March, Michael and Pellagrino, Renata and Grant, Struan FA and Sleiman, Patrick MA and Li, Mingyao and Eichler, Evan E and Hakonarson, Hakon (2019) Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations. Nat Commun, 11 (1). 255 - ?.

الاتاحة: http://d-scholarship.pitt.edu/43667/
http://d-scholarship.pitt.edu/43667/1/Rare%20copy%20number%20variants%20in%20over%20100,000%20European%20ancestry%20subjects%20reveal%20multiple%20disease%20associations.pdf
http://d-scholarship.pitt.edu/43667/9/licenseagreement_dscholarship.txt

المؤلفون: Li, Yun R, Zhao, Sihai D, Li, Jin, Bradfield, Jonathan P, Mohebnasab, Maede, Steel, Laura, Kobie, Julie, Abrams, Debra J, Mentch, Frank D, Glessner, Joseph T, Guo, Yiran, Wei, Zhi, Connolly, John J, Cardinale, Christopher J, Bakay, Marina, Li, Dong, Maggadottir, S Melkorka, Thomas, Kelly A, Qui, Haijun, Chiavacci, Rosetta M, Kim, Cecilia E, Wang, Fengxiang, Snyder, James, Flatø, Berit, Førre, Øystein, Denson, Lee A, Thompson, Susan D, Becker, Mara L, Guthery, Stephen L, Latiano, Anna, Perez, Elena, Resnick, Elena, Strisciuglio, Caterina, Staiano, Annamaria, Miele, Erasmo, Silverberg, Mark S, Lie, Benedicte A, Punaro, Marilynn, Russell, Richard K, Wilson, David C, Dubinsky, Marla C, Monos, Dimitri S, Annese, Vito, Munro, Jane E, Wise, Carol, Chapel, Helen, Cunningham-Rundles, Charlotte, Orange, Jordan S, Behrens, Edward M, Sullivan, Kathleen E, Kugathasan, Subra, Griffiths, Anne M, Satsangi, Jack, Grant, Struan FA, Sleiman, Patrick MA, Finkel, Terri H, Polychronakos, Constantin, Baldassano, Robert N, Luning Prak, Eline T, Ellis, Justine A, Li, Hongzhe, Keating, Brendan J, Hakonarson, Hakon

وصف الملف: application/pdf; text/plain

Relation: http://d-scholarship.pitt.edu/43677/1/Genetic%20sharing%20and%20heritability%20of%20paediatric%20age%20of%20onset%20autoimmune%20diseases.pdf; http://d-scholarship.pitt.edu/43677/7/licenseagreement_dscholarship.txt; Li, Yun R and Zhao, Sihai D and Li, Jin and Bradfield, Jonathan P and Mohebnasab, Maede and Steel, Laura and Kobie, Julie and Abrams, Debra J and Mentch, Frank D and Glessner, Joseph T and Guo, Yiran and Wei, Zhi and Connolly, John J and Cardinale, Christopher J and Bakay, Marina and Li, Dong and Maggadottir, S Melkorka and Thomas, Kelly A and Qui, Haijun and Chiavacci, Rosetta M and Kim, Cecilia E and Wang, Fengxiang and Snyder, James and Flatø, Berit and Førre, Øystein and Denson, Lee A and Thompson, Susan D and Becker, Mara L and Guthery, Stephen L and Latiano, Anna and Perez, Elena and Resnick, Elena and Strisciuglio, Caterina and Staiano, Annamaria and Miele, Erasmo and Silverberg, Mark S and Lie, Benedicte A and Punaro, Marilynn and Russell, Richard K and Wilson, David C and Dubinsky, Marla C and Monos, Dimitri S and Annese, Vito and Munro, Jane E and Wise, Carol and Chapel, Helen and Cunningham-Rundles, Charlotte and Orange, Jordan S and Behrens, Edward M and Sullivan, Kathleen E and Kugathasan, Subra and Griffiths, Anne M and Satsangi, Jack and Grant, Struan FA and Sleiman, Patrick MA and Finkel, Terri H and Polychronakos, Constantin and Baldassano, Robert N and Luning Prak, Eline T and Ellis, Justine A and Li, Hongzhe and Keating, Brendan J and Hakonarson, Hakon (2015) Genetic sharing and heritability of paediatric age of onset autoimmune diseases. Nat Commun, 6. 8442 - ?.

الاتاحة: http://d-scholarship.pitt.edu/43677/
http://d-scholarship.pitt.edu/43677/1/Genetic%20sharing%20and%20heritability%20of%20paediatric%20age%20of%20onset%20autoimmune%20diseases.pdf
http://d-scholarship.pitt.edu/43677/7/licenseagreement_dscholarship.txt

المؤلفون: Paternoster, Lavinia, Standl, Marie, Waage, Johannes, Baurecht, Hansjörg, Hotze, Melanie, Strachan, David P, Curtin, John A, Bønnelykke, Klaus, Tian, Chao, Takahashi, Atsushi, Esparza-Gordillo, Jorge, Alves, Alexessander Couto, Thyssen, Jacob P, den Dekker, Herman T, Ferreira, Manuel A, Altmaier, Elisabeth, Sleiman, Patrick MA, Xiao, Feng Li, Gonzalez, Juan R, Marenholz, Ingo, Kalb, Birgit, Yanes, Maria Pino, Xu, Cheng-Jian, Carstensen, Lisbeth, Groen-Blokhuis, Maria M, Venturini, Cristina, Pennell, Craig E, Barton, Sheila J, Levin, Albert M, Curjuric, Ivan, Bustamante, Mariona, Kreiner-Møller, Eskil, Lockett, Gabrielle A, Bacelis, Jonas, Bunyavanich, Supinda, Myers, Rachel A, Matanovic, Anja, Kumar, Ashish, Tung, Joyce Y, Hirota, Tomomitsu, Kubo, Michiaki, McArdle, Wendy L, Henderson, A J, Kemp, John P, Zheng, Jie, Smith, George Davey, Rüschendorf, Franz, Bauerfeind, Anja, Lee-Kirsch, Min Ae, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O, Mangold, Elisabeth, Cichon, Sven, Keil, Thomas, Rodríguez, Elke, Peters, Annette, Franke, Andre, Lieb, Wolfgang, Novak, Natalija, Fölster-Holst, Regina, Horikoshi, Momoko, Pekkanen, Juha, Sebert, Sylvain, Husemoen, Lise L, Grarup, Niels, de Jongste, Johan C, Rivadeneira, Fernando, Hofman, Albert, Jaddoe, Vincent WV, Pasmans, Suzanne GMA, Elbert, Niels J, Uitterlinden, André G, Marks, Guy B, Thompson, Philip J, Matheson, Melanie C, Robertson, Colin F, Ried, Janina S, Li, Jin, Zuo, Xian Bo, Zheng, Xiao Dong, Yin, Xian Yong, Sun, Liang Dan, McAleer, Maeve A, O'Regan, Grainne M, Fahy, Caoimhe MR, Campbell, Linda E, Macek, Milan, Kurek, Michael, Hu, Donglei, Eng, Celeste, Postma, Dirkje S, Feenstra, Bjarke, Geller, Frank, Hottenga, Jouke Jan, Middeldorp, Christel M, Hysi, Pirro, Bataille, Veronique, Spector, Tim, Tiesler, Carla MT, Thiering, Elisabeth, Pahukasahasram, Badri, Yang, James J, Imboden, Medea, Huntsman, Scott, Vilor-Tejedor, Natàlia, Relton, Caroline L, Myhre, Ronny, Nystad, Wenche, Custovic, Adnan, Weiss, Scott T, Meyers, Deborah A, Söderhäll, Cilla, Melén, Erik, Ober, Carole, Raby, Benjamin A, Simpson, Angela, Jacobsson, Bo, Holloway, John W, Bisgaard, Hans, Sunyer, Jordi, Hensch, Nicole M Probst, Williams, L Keoki, Godfrey, Keith M, Wang, Carol A, Boomsma, Dorret I, Melbye, Mads, Koppelman, Gerard H, Jarvis, Deborah, McLean, WH Irwin, Irvine, Alan D, Zhang, Xue Jun, Hakonarson, Hakon, Gieger, Christian, Burchard, Esteban G, Martin, Nicholas G, Duijts, Liesbeth, Linneberg, Allan, Jarvelin, Marjo-Riitta, Noethen, Markus M, Lau, Susanne, Hübner, Norbert, Lee, Young-Ae, Tamari, Mayumi, Hinds, David A, Glass, Daniel, Brown, Sara J, Heinrich, Joachim, Evans, David M, Weidinger, Stephan

وصف الملف: application/pdf

Relation: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753676/pdf/; Nature genetics; Paternoster, L., M. Standl, J. Waage, H. Baurecht, M. Hotze, D. P. Strachan, J. A. Curtin, et al. 2015. “Multi-ethnic genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.” Nature genetics 47 (12): 1449-1456. doi:10.1038/ng.3424. http://dx.doi.org/10.1038/ng.3424.; http://nrs.harvard.edu/urn-3:HUL.InstRepos:27320465

الاتاحة: http://nrs.harvard.edu/urn-3:HUL.InstRepos:27320465
https://doi.org/10.1038/ng.3424

المؤلفون: Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick MA, Zhang, HaitaoT, Kim, Cecilia E, Robison, Reid, Lyon, Gholson J, Flory, James H, Bradfield, Jonathan P, Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C, Chiavacci, Rosetta M, Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A, Thomas, Kelly A, Garris, Maria, Mentch, Frank, Freitag, Christine M, Steinhausen, Hans-Christoph, Todorov, Alexandre A, Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O, Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P, Mulas, Fernando, Oades, Robert D, Sergeant, Joseph, Barke, Edmund, Renner, Tobias J, Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K, Smalley, Susan L, Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard JL, Gaynor, J William, Shaw, Philip, Devoto, Marcella, White, Peter S, Grant, Struan FA, Buxbaum, Joseph D, Rapoport, Judith L, Williams, Nigel M, Nelson, Stanley F, Faraone, Stephen V, Hakonarson, Hakon

المصدر: NATURE GENETICS ; ISSN: 1061-4036

مصطلحات موضوعية: Biology and Life Sciences, ADHD, REPLICATION, CHILDREN, DEFICIT/HYPERACTIVITY-DISORDER, MICE LACKING, SNP GENOTYPING DATA, SPONTANEOUSLY HYPERTENSIVE-RAT, HIDDEN-MARKOV MODEL, AUTISM SPECTRUM DISORDERS, LINKAGE

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/3022195; http://hdl.handle.net/1854/LU-3022195; http://dx.doi.org/10.1038/ng.1013; https://biblio.ugent.be/publication/3022195/file/6779533

الاتاحة: https://biblio.ugent.be/publication/3022195
http://hdl.handle.net/1854/LU-3022195
https://doi.org/10.1038/ng.1013
https://biblio.ugent.be/publication/3022195/file/6779533

المؤلفون: Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris CA, Patsopoulos, Nikolaos A, Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E, Edkins, Sarah, Gray, Emma, Booth, David R, Potter, Simon C, Goris, An, Band, Gavin, Oturai, Annette Bang, Strange, Amy, Saarela, Janna, Bellenguez, Celine, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Boneschi, Filippo Martinelli, Liddle, Jennifer, Harbo, Hanne F, Perez, Marc L, Spurkland, Anne, Waller, Matthew J, Mycko, Marcin P, Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T, Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, Paul, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J, Barcellos, Lisa F, Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E, Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, Jonathan P, Brassat, David, Broadley, Simon A, Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M, Cavalla, Paola, Celius, Elisabeth G, Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Francoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Mathew B, Cozen, Wendy, Cree, Bruce AC, Cross, Anne H, Cusi, Daniele, Daly, Mark J, Davis, Emma, de Bakker, Paul IW, Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Benedicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica, Fontenille, Claire, Foote, Simon, Franke, Andre, Galimberti, Daniela, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan FA, Guerini, Franca Rosa, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N, Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G, Kilpatrick, Trevor J, Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S, Leone, Maurizio A, Leppa, Virpi, Liljedahl, Ulrika, Bomfim, Izaura Lima, Lincoln, Robin R, Link, Jenny, Liu, Jianjun, Lorentzen, Aslaug R, Lupoli, Sara, Macciardi, Fabio, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L, Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L, Ramsay, Patricia P, Reunanen, Mauri, Reynolds, Richard, Rioux, Johnd, Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P, Rueckert, Ina-Maria, Salvetti, Marco, Salvi, Erika, Santaniello, Adam, Schaefer, Catherine A, Schreiber, Stefan, Schulze, Christian, Scott, Rodney J, Sellebjerg, Finn, Selmaj, Krzysztof W, Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick MA, Smestad, Cathrine, Sorensen, Per Soelberg, Sondergaard, Helle Bach, Stankovich, Jim, Strange, Richard C, Sulonen, Anna-Maija, Sundqvist, Emilie, Syvaenen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M, Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A, Tronczynska, Ewa, Casas, Juan P, Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S, Wang, Kai, Mathew, Christopher G, Wason, James, Palmer, Colin NA, Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C, Yaouanq, Jacqueline, Viswanathan, Ananth C, Zhang, Haitao, Wood, Nicholas W, Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R, Pericak-Vance, Margaret A, Haines, Jonathan L, Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J, De Jager, Philip L, Peltonen, Leena, Stewart, Graeme J, Hafler, David A, Hauser, Stephen L, McVean, Gil, Donnelly, Peter, Compston, Alastair

مصطلحات موضوعية: Medical and Health Sciences not elsewhere classified

Relation: Nature; http://hdl.handle.net/10072/44111

الاتاحة: http://hdl.handle.net/10072/44111
https://doi.org/10.1038/nature10251

المؤلفون: Sleiman, Patrick MA, Hakonarson, Hakon

المصدر: Current Opinion in Pediatrics ; volume 22, issue 3, page 307-312 ; ISSN 1040-8703

الاتاحة: http://dx.doi.org/10.1097/mop.0b013e328339553d
https://journals.lww.com/10.1097/MOP.0b013e328339553d

المؤلفون: Sleiman, Patrick MA, Hakonarson, Hakon

المصدر: Personalized Medicine ; volume 6, issue 4, page 409-416 ; ISSN 1741-0541 1744-828X

الاتاحة: http://dx.doi.org/10.2217/pme.09.30
https://www.tandfonline.com/doi/pdf/10.2217/pme.09.30

المؤلفون: March,Michael E, Sleiman,Patrick MA, Hakonarson,Hakon

مصطلحات موضوعية: International Journal of General Medicine

وصف الملف: text/html

Relation: https://www.dovepress.com/genetic-polymorphisms-and-associated-susceptibility-to-asthma-peer-reviewed-fulltext-article-IJGM

الاتاحة: https://www.dovepress.com/genetic-polymorphisms-and-associated-susceptibility-to-asthma-peer-reviewed-fulltext-article-IJGM