검색어 : 통합검색[Lathrop Daniel]
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161
- Effects of Lightning on the House of Capt. Daniel Merry, and Several Other Houses in the Vicinity, on the Evening of the 11th of May, 1805
- Lathrop, John; ; (Memoirs of the American Academy of Arts and Sciences, v.3, 1809, pp.86)
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162
- Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits
- Billings, Liana K.; Hsu, Yi-Hsiang; Ackerman, Rachel J.; Dupuis, José e; Voight, Benjamin F.; Rasmussen-Torvik, Laura J.; Hercberg, Serge; Lathrop, Mark; Barnes, Daniel; Langenberg, Claudia; Hui, Jennie; Fu, Mao; Bouatia-Naji, Nabila; Lecoeur, Cecile; An, Ping; Magnusson, Patrik K.; Surakka, Ida; Ripatti, Samuli; Christiansen, Lene; Dalgå rd, Christine; Folkersen, Lasse; Grundberg, Elin; Eriksson, Per; Kaprio, Jaakko; Ohm Kyvik, Kirsten; Pedersen, Nancy L.; Borecki, Ingrid B.; Province, Michael A.; Balkau, Beverley; Froguel, Philippe; Shuldiner, Alan R.; Palmer, Lyle J.; Wareham, Nick; Meneton, Pierre; Johnson, Toby; Pankow, James S.; Karasik, David; Meigs, James B.; Kiel, Douglas P.; Florez, Jose C.; Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts; Hebrew SeniorLife Institute for Aging Research and Harvard Medical School, Boston, Massachusetts; Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts; Framingham Heart Study, Framingham, Massachusetts; Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois; INSERM, National Institute of Agronomic Research, University of Paris, Bobigny, France; National Genotyping Center, Atomic Energy Commission, Institute of Genomics, Evry, France; Medical Research Council Epidemiology Unit, Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge, U.K.; Medical Research Council Epidemiology Unit, Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge, U.K.; Molecular Genetics, PathWest Laboratory Medicin; (Diabetes, v.61, 2012, pp.2176-2186)
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163
- Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.
- Sofat, Reecha; Casas, Juan P; Webster, Andrew R; Bird, Alan C; Mann, Samantha S; Yates, John R W; Moore, Anthony T; Sepp, Tiina; Cipriani, Valentina; Bunce, Catey; Khan, Jane C; Shahid, Humma; Swaroop, Anand; Abecasis, Gon?alo; Branham, Kari E H; Zareparsi, Sepideh; Bergen, Arthur A; Klaver, Caroline C W; Baas, Dominique C; Zhang, Kang; Chen, Yuhong; Gibbs, Daniel; Weber, Bernhard H F; Keilhauer, Claudia N; Fritsche, Lars G; Lotery, Andrew; Cree, Angela J; Griffiths, Helen L; Bhattacharya, Shomi S; Chen, Li L; Jenkins, Sharon A; Peto, Tunde; Lathrop, Mark; Leveillard, Thierry; Gorin, Michael B; Weeks, Daniel E; Ortube, Maria Carolina; Ferrell, Robert E; Jakobsdottir, Johanna; Conley, Yvette P; Rahu, Mati; Seland, Johan H; Soubrane, Gisele; Topouzis, Fotis; Vioque, Jesus; Tomazzoli, Laura; Young, Ian; Whittaker, John; Chakravarthy, Usha; de Jong, Paulus T V M; Smeeth, Liam; Fletcher, Astrid; Hingorani, Aroon D; ; (International journal of epidemiology, v.41, 2012, pp.250-262)
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164
- A Genome‐Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
- Tang, Weihong; Teichert, Martina; Chasman, Daniel I.; Heit, John A.; Morange, Pierre‐ Emmanuel; Li, Guo; Pankratz, Nathan; Leebeek, Frank W.; Paré , Guillaume; de Andrade, Mariza; Tzourio, Christophe; Psaty, Bruce M.; Basu, Saonli; Ruiter, Rikje; Rose, Lynda; Armasu, Sebastian M.; Lumley, Thomas; Heckbert, Susan R.; Uitterlinden, André G.; Lathrop, Mark; Rice, Kenneth M.; Cushman, Mary; Hofman, Albert; Lambert, Jean‐ Charles; Glazer, Nicole L.; Pankow, James S.; Witteman, Jacqueline C.; Amouyel, Philippe; Bis, Joshua C.; Bovill, Edwin G.; Kong, Xiaoxiao; ; (Genetic epidemiology, v.37, 2013, pp.512-521)
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165
- Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
- Bis, Joshua C.; Jian, Xueqiu; Kunkle, Brian W.; Chen, Yuning; Hamilton-Nelson, Kara L.; Bush, William S.; Salerno, William J.; Lancour, Daniel; Ma, Yiyi; Renton, Alan E.; Marcora, Edoardo; Farrell, John J.; Zhao, Yi; Qu, Liming; Ahmad, Shahzad; Amin, Najaf; Amouyel, Philippe; Beecham, Gary W.; Below, Jennifer E.; Campion, Dominique; Cantwell, Laura; Charbonnier, Camille; Chung, Jaeyoon; Crane, Paul K.; Cruchaga, Carlos; Cupples, L. Adrienne; Dartigues, Jean-Franç ois; Debette, Sté phanie; Deleuze, Jean-Franç ois; Fulton, Lucinda; Gabriel, Stacey B.; Genin, Emmanuelle; Gibbs, Richard A.; Goate, Alison; Grenier-Boley, Benjamin; Gupta, Namrata; Haines, Jonathan L.; Havulinna, Aki S.; Helisalmi, Seppo; Hiltunen, Mikko; Howrigan, Daniel P.; Ikram, M. Arfan; Kaprio, Jaakko; Konrad, Jan; Kuzma, Amanda; Lander, Eric S.; Lathrop, Mark; Lehtimä ki, Terho; Lin, Honghuang; Mattila, Kari; Mayeux, Richard; Muzny, Donna M.; Nas; Department of Medicine (General Internal Medicine), University of Washington, Seattle, WA USA; Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX USA; John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL USA; Departments of Biostatistics, Boston University School of Public Health, Boston, MA USA; John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL USA; Case Western Reserve University, Cleveland Heights, OH USA; Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX USA; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, MA USA; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, MA USA; Department of Neuroscience and Ronald M Loeb Center for Alzheimer’s Diseas; (Molecular psychiatry, v.25, 2020, pp.1859-1875)
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166
- Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
- Bis, Joshua C.; Jian, Xueqiu; Kunkle, Brian W.; Chen, Yuning; Hamilton-Nelson, Kara L.; Bush, William S.; Salerno, William J.; Lancour, Daniel; Ma, Yiyi; Renton, Alan E.; Marcora, Edoardo; Farrell, John J.; Zhao, Yi; Qu, Liming; Ahmad, Shahzad; Amin, Najaf; Amouyel, Philippe; Beecham, Gary W.; Below, Jennifer E.; Campion, Dominique; Cantwell, Laura; Charbonnier, Camille; Chung, Jaeyoon; Crane, Paul K.; Cruchaga, Carlos; Cupples, L. Adrienne; Dartigues, Jean-Franç ois; Debette, Sté phanie; Deleuze, Jean-Franç ois; Fulton, Lucinda; Gabriel, Stacey B.; Genin, Emmanuelle; Gibbs, Richard A.; Goate, Alison; Grenier-Boley, Benjamin; Gupta, Namrata; Haines, Jonathan L.; Havulinna, Aki S.; Helisalmi, Seppo; Hiltunen, Mikko; Howrigan, Daniel P.; Ikram, M. Arfan; Kaprio, Jaakko; Konrad, Jan; Kuzma, Amanda; Lander, Eric S.; Lathrop, Mark; Lehtimä ki, Terho; Lin, Honghuang; Mattila, Kari; Mayeux, Richard; Muzny, Donna M.; Nas; Department of Medicine (General Internal Medicine), University of Washington, Seattle, WA USA; Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX USA; John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL USA; Departments of Biostatistics, Boston University School of Public Health, Boston, MA USA; John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, FL USA; Case Western Reserve University, Cleveland Heights, OH USA; Human Genome Sequencing Center and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX USA; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, MA USA; Department of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, MA USA; Department of Neuroscience and Ronald M Loeb Center for Alzheimer’s Diseas; (Molecular psychiatry, v.25, 2020, pp.1901-1903)
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167
- Clinical characteristics, racial inequities, and outcomes in patients with breast cancer and COVID-19: A COVID-19 and cancer consortium (CCC19) cohort study
- Nagaraj, Gayathri; Vinayak, Shaveta; Khaki, Ali Raza; Sun, Tianyi; Kuderer, Nicole M; Aboulafia, David M; Acoba, Jared D; Awosika, Joy; Bakouny, Ziad; Balmaceda, Nicole B; Bao, Ting; Bashir, Babar; Berg, Stephanie; Bilen, Mehmet A; Bindal, Poorva; Blau, Sibel; Bodin, Brianne E; Borno, Hala T; Castellano, Cecilia; Choi, Horyun; Deeken, John; Desai, Aakash; Edwin, Natasha; Feldman, Lawrence E; Flora, Daniel B; Friese, Christopher R; Galsky, Matthew D; Gonzalez, Cyndi J; Grivas, Petros; Gupta, Shilpa; Haynam, Marcy; Heilman, Hannah; Hershman, Dawn L; Hwang, Clara; Jani, Chinmay; Jhawar, Sachin R; Joshi, Monika; Kaklamani, Virginia; Klein, Elizabeth J; Knox, Natalie; Koshkin, Vadim S; Kulkarni, Amit A; Kwon, Daniel H; Labaki, Chris; Lammers, Philip E; Lathrop, Kate I; Lewis, Mark A; Li, Xuanyi; Lopes, Gilbert de Lima; Lyman, Gary H; Makower, Della F; Mansoor, Abdul-Hai; Markham, Merry-Jennifer; Mashru, Sandeep H; McKay, Rana R; Messing; Loma Linda University Cancer Center; Fred Hutchinson Cancer Research Center; Stanford University; Vanderbilt University Medical Center; University of Washington; Virginia Mason Cancer Institute; University of Hawaii Cancer Center; University of Cincinnati Cancer Center; Dana-Farber Cancer Institute; The University of Kansas Cancer Center; Memorial Sloan Kettering Cancer Center; Sidney Kimmel Comprehensive Cancer Center, Thomas Jefferson University; Loyola University Medical Center; Winship Cancer Institute, Emory University; Beth Israel Deaconess Medical Center; Northwest Medical Specialties; Herbert Irving Comprehensive Cancer Center, Columbia University; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco; Winship Cancer Institute, Emory University; University of Hawaii Cancer Center; Inova Schar Cancer Institute; Mayo Clinic; ThedaCare Cancer Care; University of Illinois Hospital & Health Sciences System; St. Elizabeth Hea; (eLife, v.12, 2023, pp.e82618)
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168
- Skipper-CCD sensors for the Oscura experiment: requirements and preliminary tests
- Cervantes-Vergara, Brenda A.; Perez, Santiago; Estrada, Juan; Botti, Ana; Chavez, Claudio R.; Chierchie, Fernando; Saffold, Nathan; Aguilar-Arevalo, Alexis; Alcalde-Bessia, Fabricio; Avalos, Nicolá s; Baez, Oscar; Baxter, Daniel; Bertou, Xavier; Bonifazi, Carla; Cancelo, Gustavo; Castelló -Mor, Nuria; Chavarria, Alvaro E.; De Egea, Juan Manuel; D'Olivo, Juan Carlos; Dreyer, Cyrus; Drlica-Wagner, Alex; Essig, Rouven; Estrada, Ezequiel; Etzion, Erez; Grylls, Paul; Fernandez-Moroni, Guillermo; Ferná ndez-Serra, Marivi; Ferreyra, Santiago; Holland, Stephen; Lantero Barreda, Agustí n; Lathrop, Andrew; Lawson, Ian; Loer, Ben; Luoma, Steffon; Marrufo Villalpando, Edgar; Martinez Montero, Mauricio; McGuire, Kellie; Molina, Jorge; Munagavalasa, Sravan; Norcini, Danielle; Piers, Alexander; Privitera, Paolo; Rodrigues, Dario; Saldanha, Richard; Singal, Aman; Smida, Radomir; Sofo-Haro, Miguel; Stalder, Diego; Stefanazzi, Leand; ; (Journal of instrumentation an IOP and SISSA journal, v.18, 2023, pp.P08016)
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169
- Combined sequence-based and genetic mapping analysis of complex traits in outbred rats
- Baud, Amelie; Hermsen, Roel; Guryev, Victor; Stridh, Pernilla; Graham, Delyth; McBride, Martin W; Foroud, Tatiana; Calderari, Sophie; Diez, Margarita; Ockinger, Johan; Beyeen, Amennai D; Gillett, Alan; Abdelmagid, Nada; Guerreiro-Cacais, Andre Ortlieb; Jagodic, Maja; Tuncel, Jonatan; Norin, Ulrika; Beattie, Elisabeth; Huynh, Ngan; Miller, William H; Koller, Daniel L; Alam, Imranul; Falak, Samreen; Osborne-Pellegrin, Mary; Martinez-Membrives, Esther; Canete, Toni; Blazquez, Gloria; Vicens-Costa, Elia; Mont-Cardona, Carme; Diaz-Moran, Sira; Tobena, Adolf; Hummel, Oliver; Zelenika, Diana; Saar, Kathrin; Patone, Giannino; Bauerfeind, Anja; Bihoreau, Marie-Therese; Heinig, Matthias; Lee, Young-Ae; Rintisch, Carola; Schulz, Herbert; Wheeler, David A; Worley, Kim C; Muzny, Donna M; Gibbs, Richard A; Lathrop, Mark; Lansu, Nico; Toonen, Pim; Ruzius, Frans Paul; de Bruijn, Ewart; Wellcome Trust Centre for Human Genetics, Oxford, UK.; Hubrecht Institute, Koninklijke Nederlandse Akademie van Wetenschappen and University Medical Center Utrecht, Utrecht, The Netherlands.; 1] Hubrecht Institute, Koninklijke Nederlandse Akademie van Wetenschappen and University Medical Center Utrecht, Utrecht, The Netherlands. [2] European Research Institute for the Biology of Ageing, Rijksuniversiteit Groningen, Universitair Medisch Centrum Groningen, Groningen, The Netherlands.; Neuroimmunology Unit, Department of Clinical Neuroscience, Centre for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; British Heart Foundation (BHF) Glasgow Cardiovascular Research Centre, Institute of Cardiovascular & Medical Sciences, Glasgow University, Glasgow, UK.; British Heart Foundation (BHF) Glasgow Cardiovascular Research Centre, Institute of Cardiovascular & Medical Sciences, Glasgow University, Glasgow, UK.; Department of Medical and Molecular Genetics, Indiana University Sc; (Nature genetics, v.45, 2013, pp.767-775)
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170
- Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
- Nicolas, Gaë l; Wallon, David; Charbonnier, Camille; Quenez, Olivier; Rousseau, Sté phane; Richard, Anne-Claire; Rovelet-Lecrux, Anne; Coutant, Sophie; Le Guennec, Kilan; Bacq, Delphine; Garnier, Jean-Guillaume; Olaso, Robert; Boland, Anne; Meyer, Vincent; Deleuze, Jean-Franç ois; Munter, Hans Markus; Bourque, Guillaume; Auld, Daniel; Montpetit, Alexandre; Lathrop, Mark; Guyant-Maré chal, Lucie; Martinaud, Olivier; Pariente, Jé ré mie; Rollin-Sillaire, Adeline; Pasquier, Florence; Le Ber, Isabelle; Sarazin, Marie; Croisile, Bernard; Boutoleau-Bretonniè re, Claire; Thomas-Anté rion, Catherine; Paquet, Claire; Sauvé e, Mathilde; Moreaud, Olivier; Gabelle, Audrey; Sellal, Franç ois; Ceccaldi, Mathieu; Chamard, Ludivine; Blanc, Fré dé ric; Frebourg, Thierry; Campion, Dominique; Hannequin, Didier; Department of Genetics, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Department of Neurology, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; Department of Genetics, Rouen University Hospital, Rouen, France; Inserm U1079, Rouen University, IRIB, Normandy University, Rouen, France; Inserm U1079, Rouen University, IRIB; (European journal of human genetics : EJHG, v.24, 2016, pp.710-716)
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