Ngā hua rapu - Mark Daly
- E whakaatu ana i te 1 - 20 hua o te 26
- Haere ki te Whārangi Whai Ake
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1
Sugars, insulin sensitivity, and the postprandial state mā Mark Daly
I whakaputaina 2003Revisão -
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Haploview: analysis and visualization of LD and haplotype maps mā Jeffrey C. Barrett, Ben Fry, Julian Maller, Mark Daly
I whakaputaina 2004Artigo -
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Postprandial carbohydrate metabolism in healthy subjects and those with type 2 diabetes fed starches with slow and rapid hydrolysis rates determined <i>in vitro</i> mā Chris J. Seal, Mark Daly, Lois C. Thomas, Wendy Bal, Anne Birkett, Roger Jeffcoat, John C. Mathers
I whakaputaina 2003Artigo -
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Haplotype-based identification of a microsomal transfer protein marker associated with the human lifespan mā Bard J. Geesaman, Erica K. Benson, Stephanie Brewster, Louis M. Kunkel, Hélène Blanché, Gilles Thomas, Thomas T. Perls, Mark Daly, Annibale Alessandro Puca
I whakaputaina 2003Artigo -
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Genetic Control of Serum IgE Levels and Asthma: Linkage and Linkage Disequilibrium Studies in an Isolated Population mā Tarja Laitinen, Paula Kauppi, Jaakko Ignatius, Teemu Ruotsalainen, Mark Daly, H Kääriäinen, Leonid Kruglyak, H. Laitinen, Albert de la Chapelle, Eric S. Lander, L. A. Laitinen, Juha Kere
I whakaputaina 1997Artigo -
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Familial Eosinophilia Maps to the Cytokine Gene Cluster on Human Chromosomal Region 5q31-q33 mā John D. Rioux, Valerie Stone, Mark Daly, Michele Cargill, Todd Green, Huy Nguyen, Thomas B. Nutman, Peter A. Zimmerman, Margaret A. Tucker, Thomas J. Hudson, Alisa M. Goldstein, Eric S. Lander, Albert Y. Lin
I whakaputaina 1998Artigo -
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Support for involvement of neuregulin 1 in schizophrenia pathophysiology mā Tracey L. Petryshen, Frank A. Middleton, Andrew Kirby, Kimberly A. Aldinger, Shaun Purcell, A R Tahl, Christopher P. Morley, L McGann, Karen Gentile, Graham N. Rockwell, Helena Medeiros, Célia Barreto Carvalho, A. Macedo, A. Dourado, J. Valente, Carlos Paz Ferreira, Nick J. Patterson, Maria Helena Pinto de Azevedo, Mark Daly, Carlos N. Pato, Michele T. Pato, Pamela Sklar
I whakaputaina 2004Artigo -
11
Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis mā Eleonora A. Festen, Philippe Goyette, Rodney J. Scott, Vito Annese, Alexandra Zhernakova, Jingyao Lian, Christine Lefebvre, Steven R. Brant, J H Cho, Mark S. Silverberg, Kent D. Taylor, Dirk J. de Jong, P.C.F. Stokkers, Dermot McGovern, Orazio Palmieri, J-P Achkar, Ramnik J. Xavier, Mark Daly, Richard H. Duerr, Cisca Wijmenga, Rinse K. Weersma, John D. Rioux
I whakaputaina 2009Artigo -
12
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers mā Suna Önengüt-Gümüşcü, Wei‐Min Chen, Oliver S. Burren, Nick J. Cooper, Aaron R. Quinlan, Josyf C. Mychaleckyj, Emily Farber, Jessica Bonnie, Michał Szpak, Ellen Schofield, Premanand Achuthan, Hui Guo, Mary D Fortune, Helen Stevens, Neil Walker, Lucas D. Ward, Anshul Kundaje, M Kellis, Mark Daly, Jeffrey C. Barrett, Jason D. Cooper, Panos Deloukas, John A. Todd, Chris Wallace, Patrick Concannon, Stephen S. Rich
I whakaputaina 2015Artigo -
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Pervasive Sharing of Genetic Effects in Autoimmune Disease mā Chris Cotsapas, Benjamin F. Voight, Elizabeth J. Rossin, Kasper Lage, Benjamin M. Neale, Chris Wallace, Gonçalo R. Abecasis, Jeffrey C. Barrett, Timothy W. Behrens, Judy H. Cho, Philip L. De Jager, James T. Elder, Robert Graham, Peter K. Gregersen, Lars Klareskog, Katherine Siminovitch, David A. van Heel, Cisca Wijmenga, Jane Worthington, John A. Todd, David A. Hafler, Stephen S. Rich, Mark Daly
I whakaputaina 2011Revisão -
14
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC mā Paul I. W. de Bakker, Gil McVean, Pardis C. Sabeti, Marcos Miretti, Todd J. Green, Jonathan Marchini, Xiayi Ke, Alienke J. Monsuur, Pamela Whittaker, Marcos Delgado, Jonathan J. Morrison, Angela M. Richardson, Emily C. Walsh, Xiaojiang Gao, Luana Galver, John Hart, David A. Hafler, Margaret A. Pericak‐Vance, John A. Todd, Mark Daly, John Trowsdale, Cisca Wijmenga, Tim J. Vyse, Stephan Beck, Sarah S. Murray, Mary Carrington, Simon G. Gregory, Panos Deloukas, John D. Rioux
I whakaputaina 2006Artigo -
15
A High-Density Screen for Linkage in Multiple Sclerosis mā Stephen Sawcer, Maria Ban, Mel Maranian, Tai Wai Yeo, Alastair Compston, Andrew Kirby, Mark Daly, Philip L. De Jager, Emily Walsh, Eric S. Lander, John D. Rioux, David A. Hafler, Adrian J. Ivinson, Jacqueline Rimmler, Simon G. Gregory, Silke Schmidt, Margaret A Pericak‐Vance, Eva Åkesson, Jan Hillert, Pameli Datta, Annette Oturai, Lars P. Ryder, Hanne F. Harbo, Anne Spurkland, Kjell‐Morten Myhr, Mikko Laaksonen, David R. Booth, Robert Heard, Graeme J. Stewart, Robin Lincoln, Lisa F. Barcellos, Stephen L. Hauser, Jorge R. Oksenberg, S J Kenealy, Jonathan L. Haines
I whakaputaina 2005Artigo -
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Rare chromosomal deletions and duplications increase risk of schizophrenia mā Jennifer Stone, Michael O’Donovan, Hugh Gurling, George Kirov, Douglas H. R. Blackwood, Aiden Corvin, Nick Craddock, Michael Gill, Christina M. Hultman, Paul Lichtenstein, Andrew McQuillin, Carlos N. Pato, Douglas M. Ruderfer, Michael J. Owen, David St Clair, Patrick F. Sullivan, Pamela Sklar, Shaun Purcell, Joshua M. Korn, Stuart MacGregor, Derek W. Morris, Colm Ó'Dúshláine, Mark Daly, Peter M. Visscher, Peter Holmans, Edward M. Scolnick, Nigel Williams, L. Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Vihra Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, John L. Waddington, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, David Curtis, Caroline Crombie, Gillian Fraser, Soh Leh Kwan, Nicholas Walker, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, Maria Helena Pinto de Azevedo, Steve McCarroll, Mark Daly, Kimberly Chambert, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie
I whakaputaina 2008Artigo -
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Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations mā Jimmy Z. Liu, Suzanne van Sommeren, Hailiang Huang, Siew C. Ng, Rudi Alberts, Atsushi Takahashi, Stephan Ripke, James Lee, Luke Jostins-Dean, Tejas Shah, Shifteh Abedian, Jae Hee Cheon, Judy H. Cho, Naser Ebrahim Daryani, Lude Franke, Yuta Fuyuno, Ailsa Hart, Ramesh C. Juyal, Garima Juyal, Won Ho Kim, Andrew P. Morris, Hossein Poustchi, William G. Newman, Vandana Midha, Timothy R. Orchard, Homayon Vahedi, Ajit Sood, Joseph J.�Y. Sung, Reza Malekzadeh, Harm-Jan Westra, Keiko Yamazaki, Suk-Kyun Yang, Jeffrey C. Barrett, Andre Franke, Behrooz Z Alizadeh, Miles Parkes, B.K. Thelma, Mark Daly, Michiaki Kubo, Carl A. Anderson, Rinse K. Weersma
I whakaputaina 2015Revisão -
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Exome Sequencing in Suspected Monogenic Dyslipidemias mā Nathan O. Stitziel, Gina M. Peloso, Marianne Abifadel, Angelo B. Cefalù, Sigrid W. Fouchier, Mohammad Mahdi Motazacker, Hayato Tada, Daniel B. Larach, Zuhier Awan, Jorge F. Haller, Clive R. Pullinger, Mathilde Varret, Jean‐Pierre Rabès, Davide Noto, Patrizia Tarugi, Masa-aki Kawashiri, Atsushi Nohara, Masakazu Yamagishi, Marjorie Risman, Rahul C. Deo, Isabelle L. Ruel, Jay Shendure, Deborah A. Nickerson, James G. Wilson, Stephen S. Rich, Namrata Gupta, Deborah Farlow, Benjamin M. Neale, Mark Daly, John P. Kane, Mason W. Freeman, Jacques Genest, Daniel J. Rader, Hiroshi Mabuchi, John J.P. Kastelein, G. Kees Hovingh, Maurizio Averna, Stacey Gabriel, Cathérine Boileau, Sekar Kathiresan
I whakaputaina 2015Artigo -
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Association of Genetic Variants in <i>NUDT15</i> With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease mā G Walker, James Harrison, Graham Heap, Michiel Voskuil, Vibeke Andersen, Carl A. Anderson, Ashwin N. Ananthakrishnan, Jeffrey C. Barrett, Laurent Beaugerie, Claire Bewshea, Andy T. Cole, Fraser Cummings, Mark Daly, Pierre Ellul, Richard N. Fedorak, Eleonora A. Festen, Timothy H. Florin, Daniel R. Gaya, Jonas Halfvarson, Ailsa Hart, Neel Heerasing, Peter Hendy, Peter M. Irving, Samuel E. Jones, Jukka Koskela, James O. Lindsay, John Mansfield, Dermot McGovern, Miles Parkes, Richard Pollok, S. Ramakrishnan, David S. Rampton, Manuel A. Rivas, Richard K. Russell, Michael Schultz, Shaji Sebastian, Philippe Seksik, Abhey Singh, Kenji So, Harry Sokol, Kavitha Subramaniam, Anthony Todd, Vito Annese, Rinse K. Weersma, Ramnik J. Xavier, Rebecca Ward, Michael N. Weedon, James Goodhand, Nicholas A. Kennedy, Tariq Ahmad
I whakaputaina 2019Artigo -
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder mā Shaun Purcell, Naomi R. Wray, Jennifer Stone, Peter M. Visscher, Michael O’Donovan, Patrick F. Sullivan, Pamela Sklar, Douglas M. Ruderfer, Andrew McQuillin, Derek W. Morris, Colm O’Dushlaine, Aiden Corvin, Peter Holmans, Stuart MacGregor, Hugh Gurling, Douglas Blackwood, Nick Craddock, Michael Gill, Christina M. Hultman, George Kirov, Paul Lichtenstein, Walter Muir, Michael J. Owen, Carlos N. Pato, Edward M. Scolnick, David St Clair, Nigel Williams, Lyudmila Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Mariofanna Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, Emma M. Quinn, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, Caroline Crombie, Gillian Fraser, Soh Leh Kuan, Nicholas Walker, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, M.H. Azevedo, Andrew Kirby, Manuel A. R. Ferreira, Mark Daly, Kimberly Chambert, Finny G. Kuruvilla, Stacey B. Gabriel, Kristin Ardlie, Jennifer L. Moran
I whakaputaina 2009Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Medicine
Genotype
Internal medicine
Single-nucleotide polymorphism
Computational biology
Allele
Genetic association
Genome-wide association study
Haplotype
Disease
Genome
Linkage disequilibrium
Locus (genetics)
Psychiatry
Psychology
Pathology
Schizophrenia (object-oriented programming)
Endocrinology
Evolutionary biology
Genetic linkage
Inflammatory bowel disease
Obesity
Ulcerative colitis
1000 Genomes Project
Alternative medicine
Antibody
Biochemistry