Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Cathy Schaefer"'
Autor:
AK Hedström, Milena A. Gianfrancesco, Lars Alfredsson, Ellen M. Mowry, Cathy Schaefer, Xiaorong Shao, Ling Shen, Lisa F. Barcellos, Tomas Olsson
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry
Objective Previous studies on consumption of caffeine and risk of multiple sclerosis (MS) have yielded inconclusive results. We aimed to investigate whether consumption of coffee is associated with risk of MS. Methods Using two population-representat
Autor:
Fredrik Karpe, Graeme Stewart, Jan Hillert, Elisabetta Mascia, Matt J. Neville, Verena Grummel, Jonathan L. Haines, Kate Fitzgerald, Bernhard Hemmer, Julia Y Mescheriakova, Benedicte A. Lie, Efthimios Luessi, Federica Esposito, Andreas Ziegler, Ioanna Konidari, Cristin McCabe, Keith R. Edwards, Roland Martin, Daniele Cusi, Elisabeth Gulowsen Celius, Cristina Agliardi, Anne Spurkland, Georgios M. Hadjigeorgiou, Lena Guillot-Noel, Antonios Bayas, Uwe K. Zettl, Kjell-Morten Myhr, Maria Ban, Rogier Q. Hintzen, Frauke Zipp, Mireia Sospedra, Till F. M. Andlauer, Adrian J. Ivinson, Mary F. Davis, Mark Lathrop, Daniela Galimberti, Pierre-Antoine Gourraud, Genevieve Lachance, Bruce A.C. Cree, Robin Lemmens, Ashley Beecham, Steffan D. Bos, Bruce V. Taylor, Maurizio Leone, Manuel Comabella, Maja Jagodic, Helle Bach Søndergaard, David A. Hafler, Ingrid Kockum, Nadia Barizzone, Ralf Gold, Tania Kümpfel, Per Soelberg Sørensen, Seema Kalra, An Goris, Philip Van Damme, Marie B. D'hooghe, Cathy Schaefer, Efthimios Dardiotis, Alastair Compston, Lotti Tajoori, Sandra D'Alfonso, Ilijas Jelcic, Stephen Sawcer, Brigitte Wildemann, Friedemann Paul, Lise Wegner Thoerner, Silvia Delgado, Tomas Olsson, Mitja Mitrovic, Hayrettin Tumani, Henrik Ullum, Lisa F. Barcellos, Xavier Montalban, Ellen Lathi, Finn Sellebjerg, Thomas Werge, Christina M. Lill, Pernilla Stridh, Paul I.W. de Bakker, Cornelia M. van Duijn, Jyoti Khadake, Jac Charlesworth, Melissa Sorosina, Christiane Gasperi, Stephen L. Hauser, Anne H. Cross, Isabelle Cournu-Rebeix, Nikolaos A. Patsopoulos, Fredrik Piehl, Lars Alfredsson, Bertrand Fontaine, Marieme Dembele, Margaret A. Pericak-Vance, Janna Saarela, Ulf Ziemann, Annette Bang Oturai, Stacy J. Caillier, Jorge R. Oksenberg, Bénédicte Dubois, Björn Tackenberg, Christoph Heesen, Jacob L. McCauley, Florian Then Bergh, Clemens Warnke, Sergio E. Baranzini, Peter A. Calabresi, Chris Cotsapas, Clive Hawkins, Martin Stangel, Hakon Hakonarson, Sandra Vukusik, Christiane Graetz, Heinz Wiendl, Howard L. Weiner, Laura Piccio, Giancarlo Comi, Ralf A. Linker, Luisa Bernardinelli, Cristoforo Comi, Filippo Martinelli-Boneschi, Hanne F. Harbo, Dorothea Buck, Clara P. Manrique, David R. Booth, Benjamin Knier, Philip L. De Jager, Viola Pongratz, Laura Ferrè, Vincent Damotte, Adam Santaniello, Theresa Dankowski, Pirro G. Hysi
Multiple sclerosis is a common, complex neurological disease, where almost 20% of risk heritability can be attributed to common genetic variants, including >230 identified by genome-wide association studies (Patsopoulos et al., 2017). Multiple strand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca312b659a481d06422bdfe2f8ceb857
Autor:
Cathy Schaefer, Mark N. Kvale, Neil Risch, Stacey E. Alexeeff, Charles P. Quesenberry, Elizabeth H. Blackburn, Jun Shan, Stephen K. Van Den Eeden
Publikováno v:
ISEE Conference Abstracts. 2017
Autor:
Thomas J. Hoffmann, Neil Risch, Eric Jorgenson, Yambazi Banda, Cathy Schaefer, Khanh K. Thai, Mark N. Kvale
Publikováno v:
European Neuropsychopharmacology. 29:S899-S900
Background Large Genome-Wide Association Studies (GWAS) have identified common genetic variants that underlie Schizophrenia (SCZ) and Major Depressive Disorder (MDD), although Bipolar Disorder (BD) remains elusive. Cross disorder analysis has shown a
Autor:
Kathleen M. Giacomini, Wen Cc, Mark N. Kvale, Thomas J. Hoffmann, Cathy Schaefer, Sook Wah Yee, Eric Jorgenson, Neil Risch, Xiaomin Liang, Yambazi Banda
Publikováno v:
Clinical Pharmacology & Therapeutics. 97:518-525
The first-line treatment of hyperuricemia, which causes gout, is allopurinol. The allopurinol response is highly variable, with many users failing to achieve target serum uric acid (SUA) levels. No genome-wide association study (GWAS) has examined th
Autor:
Ashley Beecham, David A. Hafler, Colombe J, Ublick K, Stephen Sawcer, Marcus C. S. Lee, Adam Santaniello, An Goris, Frank Seibold, Xavier Montalban, G. Comi, Christiane Gasperi, Sandra D'Alfonso, Federica Esposito, Laurent Peyrin-Biroulet, Frauke Zipp, Ioanna Konidari, Elisabeth Gulowsen Celius, Achim Berthele, Amoroso A, Rogier Q. Hintzen, Johan Van Limbergen, Marieme Dembele, Fredrik Karpe, Zhang W, Robbins A, Moiola L, Annette Bang Oturai, Cristin McCabe, Filippo Martinelli-Boneschi, M Lindén, Keith R Edwards, Hanne F. Harbo, Zuccalà M, Marc Lémann, Felix Luessi, Noriko Isobe, Nadia Barizzone, Renata D'Incà, Croft A, Ioannis S. Vlachos, Frohlich I, Martinelli, Daniela Galimberti, Efthimios Dardiotis, Lisa F. Barcellos, Brendan T. Keenan, Maja Jagodic, Ferdinando Clarelli, Bénédicte Dubois, Nicholas A. Kennedy, Lohith Madireddy, Grant W. Montgomery, Tommy Olsson, Phil De Jager, Lo A, Peter A. Calabresi, Brandes A, Chris Cotsapas, Bakker Pd, Steffan D. Bos, Christina M. Lill, Karban A, Thoerner Lw, Tojo James, Wong G, Harald Peeters, M.-M. Hoshi, Roberts R, Fredrik Piehl, Lars Alfredsson, Giorgos M. Hadjigeorgiou, Bertrand Fontaine, Melissa Sorosina, Benedetti M, Maria Ban, Jorge R. Oksenberg, Howard L. Weiner, Ingrid Kockum, Mireia Sospedra, Taylor Km, Henrik Ullum, Izaura Lima Bomfim, Stronati L, Molyneux P, Replogle J, Stacy J. Caillier, Zhang H, Till F. M. Andlauer, Margaret A. Pericak-Vance, Jan Hillert, Luisa Bernardinelli, Taibo Li, Helle Bach Søndergaard, Ilijas Jelcic, Nikolaos A. Patsopoulos, Silvia Delgado, Cathy Schaefer, Thomas Korn, Laura Piccio, Mark Mühlau, Deborah D. Proctor, B. Hemmer, Elizabeth M. Bradshaw, Hysi P, Megan C Neville, Mary F. Davis, Dorlan J. Kimbrough, Jyoti Khadake, Jean-Pierre Hugot, David Gomez-Cabrero, Murray L. Barclay, Anne H. Cross, Kasper Lage, Stephen L. Hauser, A Compston, Zimmer A, Ivinson A, Anne Spurkland, Jonas Halfvarson, Charles C. White, Biberacher, Zarzycki O, Kathryn C. Fitzgerald, Finn Sellebjerg, Ellis Patrick, Andrea Zauli, Bruce V. Taylor, Maurizio Leone, Genevieve Lachance, Marta Olah, B. Cree, Manuel Comabella, Arie Levine, Domizia Vecchio, Mathias Chamaillard, Mark Lathrop, Clara Guaschino, Roland Martin, Hanigan K, Pierre-Antoine F. D. Gourraud, Maria Cimpean, Jonathan L. Haines, Dorothea Buck, Marco Salvetti, Per Soelberg Sørensen, Noel Lg, Mitja Mitrovic, Graeme J. Stewart, Benjamin Knier, Ellen Lathi, Cottone M, Laura Ferrè, Winn P, Duijn Cv, Monica Milla, Tune H. Pers, I. Oikonomou, An D, David R. Booth, Rebeix Ic, Clara P. Manrique, Massey D, Evelyn Ng Sm, Törkvist L, Daniele Cusi, Shoostari P, Vatn Mh, Paola Cavalla, Silvia Santoro, Gossum Av, Seema Kalra, Paul Rutgeerts, Clive Hawkins, Sandra Vukusik, Khan Ma, Hakon Hakonarson, Paul Henderson, Christiane Graetz, Julia Y Mescheriakova, Jean-François Rahier, Panteliadis I, Cristina Agliardi, Grummel, Jacob L. McCauley, Amie Baker, Janna Saarela, Sergio E. Baranzini, J W Thorpe, Damotte
We assembled and analyzed genetic data of 47,351 multiple sclerosis (MS) subjects and 68,284 control subjects and establish a reference map of the genetic architecture of MS that includes 200 autosomal susceptibility variants outside the major histoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3025a23da11c9c135923e48b9b008b4b
http://hdl.handle.net/2318/1771606
http://hdl.handle.net/2318/1771606
Autor:
Mark N. Kvale, Stephen K. Van Den Eeden, Cathy Schaefer, Stacey E. Alexeeff, Jun Shan, Elizabeth H. Blackburn, Neil Risch
Publikováno v:
ISEE Conference Abstracts. 2016
Autor:
Eric Jorgenson, Dilrini K. Ranatunga, Dana Ludwig, Cathy Schaefer, Stan Sciortino, Lawrence Walter, Julia Kay
Background/Aims The Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort has genotyped data on over 100,000 participants. In order to characterize many health conditions of interest found among respondents for sample-size estimation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf4c78d3d7b1acba3e8e05afa284b77
https://europepmc.org/articles/PMC3788526/
https://europepmc.org/articles/PMC3788526/
Autor:
Cathy Schaefer
Aims The Kaiser Permanente Research Program on Genes, Environment and Health (RPGEH) is designed as a resource for epidemiologic studies of genetic and environmental influences on health and disease. The resource links together clinical data from ele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35be829ae28cd2629c8f4d3a29290519
https://europepmc.org/articles/PMC3251456/
https://europepmc.org/articles/PMC3251456/
Autor:
Dilrini K. Ranatunga, Lawrence Walter, Yambazi Banda, Cathy Schaefer, Mark N. Kvale, Neil Risch, Stan Sciortino, Eric Jorgenson, Thomas J. Hoffmann, Ling Shen, Pui-Yan Kwok
Publikováno v:
Clinical Medicine & Research. 11:146-147
Background/Aims Age-related macular degeneration (AMD) is the most common cause of vision loss in individuals over the age of 50 in the United States. Genetic factors explain a large portion of the risk of developing AMD, and genetic variants at the