Výsledky vyhledávání - Amy J. Swift

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  1. 1
    Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene

    Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene Autor Amanda J. DuBose, Stephen T. Lichtenstein, Narisu Narisu, Lori L. Bonnycastle, Amy J. Swift, Peter S. Chines, Francis S. Collins

    Vydáno 2013
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  2. 2
    Immunization of Humans with Recombinant Pneumococcal Surface Protein A (rPspA) Elicits Antibodies That Passively Protect Mice from Fatal Infection with<i>Streptococcus pneumoniae</i>Bearing Heterologous PspA

    Immunization of Humans with Recombinant Pneumococcal Surface Protein A (rPspA) Elicits Antibodies That Passively Protect Mice from Fatal Infection with<i>Streptococcus pneumoniae</... Autor David E. Briles, Susan K. Hollingshead, Janice King, Amy J. Swift, Patricia A. Braun, Moon K. Park, Laura M. Ferguson, Moon H. Nahm, Gary S. Nabors

    Vydáno 2000
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  3. 3
    Human pancreatic islet microRNAs implicated in diabetes and related traits by large-scale genetic analysis

    Human pancreatic islet microRNAs implicated in diabetes and related traits by large-scale genetic analysis Autor Henry J. Taylor, Yu-Han Hung, Narisu Narisu, Michael R. Erdos, Matthew Kanke, Tingfen Yan, Caleb M. Grenko, Amy J. Swift, Lori L. Bonnycastle, Praveen Sethupathy, Francis S. Collins, D. Leland Taylor

    Vydáno 2023
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  4. 4
    Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing

    Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing Autor Jamie K. Teer, Lori L. Bonnycastle, Peter S. Chines, Nancy F. Hansen, Natsuyo Aoyama, Amy J. Swift, Hatice Özel Abaan, Thomas J. Albert, Elliott H. Margulies, Eric D. Green, Francis S. Collins, James C. Mullikin, Leslie G. Biesecker

    Vydáno 2010
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  5. 5
    Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation

    Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation Autor Lori L. Bonnycastle, Peter S. Chines, Takashi Hara, Jeroen R. Huyghe, Amy J. Swift, Pirkko Heikinheimo, Jana Mahadevan, Sirkku Peltonen, Hanna Huopio, Pirjo Nuutila, Narisu Narisu, Rachel L. Goldfeder, Michael L. Stitzel, Simin Lu, Michael Boehnke, Fumihiko Urano, Francis S. Collins, Markku Laakso

    Vydáno 2013
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  6. 6
    Tissue-specific alternative splicing of TCF7L2

    Tissue-specific alternative splicing of TCF7L2 Autor Ludmila Prokunina‐Olsson, Cullan Welch, Ola Hansson, Neeta Adhikari, Laura J. Scott, N. Usher, Maurine Tong, Andrew G. Sprau, Amy J. Swift, Lori L. Bonnycastle, Michael R. Erdos, Zhi He, Richa Saxena, Brennan Harmon, Olga Kotova, Eric P. Hoffman, David Altshuler, Leif Groop, Michael Boehnke, Francis S. Collins, Jennifer L. Hall

    Vydáno 2009
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  7. 7
    Functional interrogation of twenty type 2 diabetes-associated genes using isogenic human embryonic stem cell-derived β-like cells

    Functional interrogation of twenty type 2 diabetes-associated genes using isogenic human embryonic stem cell-derived β-like cells Autor Dongxiang Xue, Narisu Narisu, D. Leland Taylor, Meili Zhang, Caleb M. Grenko, Henry J. Taylor, Tingfen Yan, Xuming Tang, Neelam Sinha, Jiajun Zhu, J. Jeya Vandana, Angie Chi Nok Chong, Angela Lee, Erin C. Mansell, Amy J. Swift, Michael R. Erdos, Aaron Zhong, Lori L. Bonnycastle, Ting Zhou, Shuibing Chen, Francis S. Collins

    Vydáno 2023
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  8. 8
    Hydroa vacciniforme–like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites

    Hydroa vacciniforme–like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites Autor Jeffrey I. Cohen, Irini Manoli, Kennichi Dowdell, Tammy Krogmann, Deborah Tamura, Pierce Radecki, Wei Bu, Siu-Ping Turk, Kelly Liepshutz, Ronald L. Hornung, Hiva Fassihi, Robert Sarkany, Lori L. Bonnycastle, Peter S. Chines, Amy J. Swift, Timothy G. Myers, Melissa A. Levoska, John J. DiGiovanna, Francis S. Collins, Kenneth H. Kraemer, Stefania Pittaluga, Elaine S. Jaffe

    Vydáno 2019
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  9. 9
    Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle

    Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle Autor D. Leland Taylor, Anne Jackson, Narisu Narisu, Gibran Hemani, Michael R. Erdos, Peter S. Chines, Amy J. Swift, Jackie Idol, John P. Didion, Ryan Welch, Leena Kinnunen, Jouko Saramies, Timo A. Lakka, Markku Laakso, Jaakko Tuomilehto, Stephen C. J. Parker, Heikki A. Koistinen, George Davey Smith, Michael Boehnke, Laura J. Scott, Ewan Birney, Francis S. Collins

    Vydáno 2019
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  10. 10
    Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns

    Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns Autor Lori L. Bonnycastle, Cristen J. Willer, Karen N. Conneely, Anne Jackson, Cecily P. Burrill, Richard M. Watanabe, Peter S. Chines, Narisu Narisu, Laura J. Scott, Sareena T. Enloe, Amy J. Swift, William L. Duren, Heather M. Stringham, Michael R. Erdos, Nancy L. Riebow, Thomas A. Buchanan, Timo T. Valle, Jaakko Tuomilehto, Richard N. Bergman, Karen L. Mohlke, Michael Boehnke, Francis S. Collins

    Vydáno 2006
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  11. 11
    Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes

    Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes Autor Cristen J. Willer, Lori L. Bonnycastle, Karen N. Conneely, William L. Duren, Anne Jackson, Laura J. Scott, Narisu Narisu, Peter S. Chines, Andrew D. Skol, Heather M. Stringham, John R. Petrie, Michael R. Erdos, Amy J. Swift, Sareena T. Enloe, Andrew G. Sprau, E. O’Brian Smith, Maurine Tong, Kimberly F. Doheny, Elizabeth Pugh, Richard M. Watanabe, Thomas A. Buchanan, Timo T. Valle, Richard N. Bergman, Jaakko Tuomilehto, Karen L. Mohlke, Francis S. Collins, Michael Boehnke

    Vydáno 2006
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  12. 12
    Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci

    Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci Autor Susan K. Service, Tanya M. Teslovich, Christian Fuchsberger, Vasily Ramensky, Pranav Yajnik, Daniel C. Koboldt, David E. Larson, Qunyuan Zhang, Lin Ling, Ryan Welch, Li Ding, Michael D. McLellan, Michele O’Laughlin, Catrina C. Fronick, Lucinda Fulton, Vincent Magrini, Amy J. Swift, Paul Elliott, Marjo‐Riitta Järvelin, Marika Kaakinen, Mark I. McCarthy, Leena Peltonen, Anneli Pouta, Lori L. Bonnycastle, Francis S. Collins, Narisu Narisu, Heather M. Stringham, Jaakko Tuomilehto, Samuli Ripatti, Robert S. Fulton, Chiara Sabatti, Richard K. Wilson, Michael Boehnke, Nelson B. Freimer

    Vydáno 2014
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  13. 13
    A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants

    A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants Autor Laura J. Scott, Karen L. Mohlke, Lori L. Bonnycastle, Cristen J. Willer, Yun Li, William L. Duren, Michael R. Erdos, Heather M. Stringham, Peter S. Chines, Anne Jackson, Ludmila Prokunina‐Olsson, Chia-Jen Ding, Amy J. Swift, Narisu Narisu, Tianle Hu, Randall Pruim, Rui Xiao, Xiaoyi Li, Karen N. Conneely, Nancy L. Riebow, Andrew G. Sprau, Maurine Tong, Peggy P. White, Kurt N. Hetrick, Michael W. Barnhart, Craig W. Bark, Janet L. Goldstein, Lee Watkins, Xiang Fang, Jouko Saramies, Thomas A. Buchanan, Richard M. Watanabe, Timo T. Valle, Leena Kinnunen, Gonçalo R. Abecasis, Elizabeth Pugh, Kimberly F. Doheny, Richard N. Bergman, Jaakko Tuomilehto, Francis S. Collins, Michael Boehnke

    Vydáno 2007
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  14. 14
    Newly identified loci that influence lipid concentrations and risk of coronary artery disease

    Newly identified loci that influence lipid concentrations and risk of coronary artery disease Autor Cristen J. Willer, Serena Sanna, Anne Jackson, Angelo Scuteri, Lori L. Bonnycastle, Robert Clarke, Simon Heath, Nicholas J. Timpson, Samer S. Najjar, Heather M. Stringham, James Strait, William L. Duren, Andrea Maschio, Fabio Busonero, Antonella Mulas, Giuseppe Albai, Amy J. Swift, Mario A. Morken, Narisu Narisu, Derrick Bennett, Sarah Parish, Haiqing Shen, Pilar Galán, Pierre Meneton, Serge Herçberg, Diana Zélénika, Wei‐Min Chen, Yun Li, Laura J. Scott, Paul Scheet, Jouko Sundvall, Richard M. Watanabe, Ramaiah Nagaraja, Shah Ebrahim, Debbie A. Lawlor, Yoav Ben‐Shlomo, George Davey Smith, Alan R. Shuldiner, Rory Collins, Richard N. Bergman, Manuela Uda, Jaakko Tuomilehto, Antonio Cao, Francis S. Collins, Edward G. Lakatta, G.M. Lathrop, Michael Boehnke, David Schlessinger, Karen L. Mohlke, Gonçalo R. Abecasis

    Vydáno 2008
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  15. 15
    Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels

    Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels Autor Wei‐Min Chen, Michael R. Erdos, Anne Jackson, Richa Saxena, Serena Sanna, Kristi D. Silver, Nicholas J. Timpson, Torben Hansen, Marco Orrù, Maria Grazia Piras, Lori L. Bonnycastle, Cristen J. Willer, Valeriya Lyssenko, Haiqing Shen, Johanna Kuusisto, Shah Ebrahim, Natascia Sestu, William L. Duren, Maria Cristina Spada, Heather M. Stringham, Laura J. Scott, Nazario Olla, Amy J. Swift, Samer S. Najjar, Braxton D. Mitchell, Debbie A. Lawlor, George Davey Smith, Yoav Ben‐Shlomo, Gary L. Andersen, Knut Borch‐Johnsen, Torben Jørgensen, Jouko Saramies, Timo T. Valle, Thomas A. Buchanan, Alan R. Shuldiner, Edward G. Lakatta, Richard N. Bergman, Manuela Uda, Jaakko Tuomilehto, Oluf Pedersen, Antonio Cao, Leif Groop, Karen L. Mohlke, Markku Laakso, David Schlessinger, Francis S. Collins, David Altshuler, Gonçalo R. Abecasis, Michael Boehnke, Angelo Scuteri, Richard M. Watanabe

    Vydáno 2008
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  16. 16
    Common variants at 30 loci contribute to polygenic dyslipidemia

    Common variants at 30 loci contribute to polygenic dyslipidemia Autor Sekar Kathiresan, Cristen J. Willer, Gina M. Peloso, Serkalem Demissie, Yan V. Sun, Eric E. Schadt, Lee M. Kaplan, Derrick Bennett, Yun Li, Toshiko Tanaka, Benjamin F. Voight, Lori L. Bonnycastle, Anne Jackson, Gabriel Crawford, Aarti Surti, Candace Guiducci, Noël P. Burtt, Sarah Parish, Robert Clarke, Diana Zélénika, Kari Kubalanza, Mario A. Morken, Laura J. Scott, Heather M. Stringham, Pilar Galán, Amy J. Swift, Johanna Kuusisto, Richard N. Bergman, Jouko Sundvall, Markku Laakso, Luigi Ferrucci, Paul Scheet, Serena Sanna, Manuela Uda, Qiong Yang, Kathryn L. Lunetta, Josée Dupuis, Paul I. W. de Bakker, Christopher J. O’Donnell, John C. Chambers, Jaspal S. Kooner, Serge Herçberg, Pierre Meneton, Edward G. Lakatta, Angelo Scuteri, David Schlessinger, Jaakko Tuomilehto, Francis S. Collins, Leif Groop, David Altshuler, Rory Collins, G.M. Lathrop, Olle Melander, Veikko Salomaa, Leena Peltonen, Marju Orho‐Melander, José M. Ordovás, Michael Boehnke, Gonçalo R. Abecasis, Karen L. Mohlke, L. Adrienne Cupples

    Vydáno 2008
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  17. 17
    Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity

    Impact of Type 2 Diabetes Susceptibility Variants on Quantitative Glycemic Traits Reveals Mechanistic Heterogeneity Autor Antigone S. Dimas, Vasiliki Lagou, Adam Barker, Joshua W. Knowles, Reedik Mägi, Marie‐France Hivert, Andrea Benazzo, Denis Rybin, Anne Jackson, Heather M. Stringham, Ci Song, Antje Fischer-Rosinský, Trine Welløv Boesgaard, Niels Grarup, Fahim Abbasi, Themistocles L. Assimes, Ke Hao, Xia Yang, Cécile Lecœur, Inês Barroso, Lori L. Bonnycastle, Yvonne Böttcher, Suzannah Bumpstead, Peter S. Chines, Michael R. Erdos, J. Graessler, Péter Kovács, Mario A. Morken, Narisu Narisu, Felicity Payne, Alena Stančáková, Amy J. Swift, Anke Tönjes, Stefan R. Bornstein, Stéphane Cauchi, Philippe Froguel, David Meyre, Peter E. H. Schwarz, Hans‐Ulrich Häring, Ulf Smith, Michael Boehnke, Richard N. Bergman, Francis S. Collins, Karen L. Mohlke, Jaakko Tuomilehto, Thomas Quertemous, Lars Lind, Torben Hansen, Oluf Pedersen, Mark Walker, A. Pfeiffer, Joachim Spranger, Michael Stümvoll, James B. Meigs, Nicholas J. Wareham, Johanna Kuusisto, Markku Laakso, Claudia Langenberg, Josée Dupuis, Richard M. Watanabe, José C. Florez, Erik Ingelsson, Mark I. McCarthy, Inga Prokopenko

    Vydáno 2013
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  18. 18
    Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans

    Detailed Physiologic Characterization Reveals Diverse Mechanisms for Novel Genetic Loci Regulating Glucose and Insulin Metabolism in Humans Autor Erik Ingelsson, Claudia Langenberg, Marie‐France Hivert, Inga Prokopenko, Valeriya Lyssenko, Josée Dupuis, Reedik Mägi, Stephen J. Sharp, Anne Jackson, Themistocles L. Assimes, Peter Shrader, Joshua W. Knowles, Björn Zethelius, Fahim Abbasi, Richard N. Bergman, Antje Bergmann, Christian Berne, Michael Boehnke, Lori L. Bonnycastle, Stefan R. Bornstein, Thomas A. Buchanan, Suzannah J. Bumpstead, Yvonne Böttcher, Peter S. Chines, Francis S. Collins, Cyrus Cooper, Elaine Dennison, Michael R. Erdos, Ele Ferrannini, Caroline S. Fox, J. Graessler, Ke Hao, Bo Isomaa, Anthony James, Péter Kovács, Johanna Kuusisto, Markku Laakso, Claes Ladenvall, Karen L. Mohlke, Mario A. Morken, Narisu Narisu, David M. Nathan, Laura Pascoe, Felicity Payne, John R. Petrie, Avan Aihie Sayer, Peter Schwarz, Laura J. Scott, Heather M. Stringham, Michael Stümvoll, Amy J. Swift, Ann‐Christine Syvänen, Jaakko Tuomilehto, Jaakko Tuomilehto, Anke Tönjes, Timo T. Valle, Gordon H. Williams, Lars Lind, Inês Barroso, Thomas Quertermous, Mark Walker, Nicholas J. Wareham, James B. Meigs, Mark I. McCarthy, Leif Groop, Richard M. Watanabe, José C. Florez

    Vydáno 2010
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  19. 19
    Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis

    Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis Autor Alan P. Tenney, Silvio Alessandro Di Gioia, Bryn D. Webb, Wai‐Man Chan, Elke de Boer, Sarah J. Garnai, Brenda J. Barry, Tammy Ray, Michael Kosicki, Caroline D. Robson, Zhongyang Zhang, Thomas E. Collins, Alon Gelber, Brandon M. Pratt, Yuko Fujiwara, Arushi Varshney, Monkol Lek, Peter E. Warburton, Carol Van Ryzin, Tanya Lehky, Christopher Zalewski, Kelly King, Carmen C. Brewer, Audrey Thurm, Joseph Snow, Flavia M. Facio, Narisu Narisu, Lori L. Bonnycastle, Amy J. Swift, Peter S. Chines, Jessica Bell, Suresh Mohan, Mary C. Whitman, Sandra E. Staffieri, James E. Elder, Joseph L. Demer, Alcy Torres, Elza Rachid, Christiane Al‐Haddad, Rose‐Mary Boustany, David A. Mackey, Angela F. Brady, María Fenollar‐Cortés, Mélanie Fradin, Tjitske Kleefstra, George W. Padberg, Salmo Raskin, Mário Teruo Sato, Stuart H. Orkin, Stephen C. J. Parker, Tessa A. Hadlock, Lisenka E.L.M. Vissers, Hans van Bokhoven, Ethylin Wang Jabs, Francis S. Collins, L Pennacchio, Irini Manoli, Elizabeth C. Engle

    Vydáno 2023
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  20. 20
    A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

    A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome Autor Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew F. Rose, Nicole M. Gilette, Pietro Artoni, Nara Sobreira, Wai‐Man Chan, Bryn D. Webb, Caroline D. Robson, Long Cheng, Carol Van Ryzin, Andres Ramirez-Martinez, Payam Mohassel, Mark Leppert, Mary Beth Scholand, Christopher Grunseich, Carlos R. Ferreira, Tyler Hartman, Ian Hayes, Tim Morgan, David Markie, Michela Fagiolini, Amy J. Swift, Peter S. Chines, Carlos E. Speck‐Martins, Francis S. Collins, Ethylin Wang Jabs, Carsten G. Bönnemann, Eric N. Olson, Caroline Andrews, Brenda J. Barry, David G. Hunter, Sarah MacKinnon, Sherin Shaaban, Mónica Erazo, Tamiesha Frempong, Ke Hao, Thomas P. Naidich, Janet C. Rucker, Zhongyang Zhang, Barbara B. Biesecker, Lori L. Bonnycastle, Carmen C. Brewer, Brian P. Brooks, John A. Butman, Wade W. Chien, Kathleen Farrell, Edmond J. FitzGibbon, Andrea Gropman, Elizabeth Hutchinson, Minal S. Jain, Kelly King, Tanya Lehky, Janice Lee, Denise K. Liberton, Narisu Narisu, Scott M. Paul, Neda Sadeghi, Joseph Snow, Beth Solomon, Angela C. Summers, Camilo Toro, Audrey Thurm, Christopher Zalewski, John C. Carey, Stephen P. Robertson, Irini Manoli, Elizabeth C. Engle

    Vydáno 2017
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