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APOE Modulates the Correlation Between Triglycerides, Cholesterol, and CHD Through Pleiotropy and Gene-by-Gene Interactions., Maxwell, Taylor J., Ballantyne Christie M., Cheverud James M., Guild Cameron S., Ndumele Chiadi E., and Boerwinkle Eric , Genetics, 2013 Oct 4, (2013) Abstract
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10., Matsuura, Tohru, Fang Ping, Lin Xi, Khajavi Mehrdad, Tsuji Kuniko, Rasmussen Astrid, Grewal Raji P., Achari Madhureeta, Alonso Maria E., Pulst Stefan M., et al. , American journal of human genetics, 2004 Jun, Volume 74, Issue 6, p.1216-24, (2004) Abstract
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10., Matsuura, T., Yamagata T., Burgess D. L., Rasmussen A., Grewal R. P., Watase K., Khajavi M., McCall A. E., Davis Caleb F., Zu L., et al. , Nature genetics, 2000 Oct, Volume 26, Issue 2, p.191-4, (2000) Abstract
Complete genome sequence of Treponema pallidum ssp. pallidum strain SS14 determined with oligonucleotide arrays., Matejková, Petra, Strouhal Michal, Smajs David, Norris Steven J., Palzkill Timothy, Petrosino Joseph F., Sodergren Erica, Norton Jason E., Singh Jaz, Richmond Todd A., et al. , BMC microbiology, 2008, Volume 8, p.76, (2008) Abstract
Pulmonary alveolar proteinosis caused by deletion of the GM-CSFRalpha gene in the X chromosome pseudoautosomal region 1., Martinez-Moczygemba, Margarita, Doan Minh L., Elidemir Okan, Fan Leland L., Cheung Sau Wai, Lei Jonathan T., Moore James P., Tavana Ghamartaj, Lewis Lora R., Zhu Yiming, et al. , The Journal of experimental medicine, 2008 Nov 24, Volume 205, Issue 12, p.2711-6, (2008) Abstract
An allylic/acyclic adenosine nucleoside triphosphate for termination of DNA synthesis by DNA template-dependent polymerases., Martinez, C. I., Thoresen L. H., Gibbs R. A., and Burgess K. , Nucleic acids research, 1999 Mar 1, Volume 27, Issue 5, p.1271-4, (1999) Abstract
Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion., Martinez, Diego, Challacombe Jean, Morgenstern Ingo, Hibbett David, Schmoll Monika, Kubicek Christian P., Ferreira Patricia, Ruiz-Duenas Francisco J., Martinez Angel T., Kersten Phil, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2009 Feb 10, Volume 106, Issue 6, p.1954-9, (2009) Abstract
Cyanobacterial signature genes., Martin, Kirt A., Siefert Janet L., Yerrapragada Sailaja, Lu Yue, McNeill Thomas Z., Moreno Pedro A., Weinstock George M., Widger William R., and Fox George E. , Photosynthesis research, 2003, Volume 75, Issue 3, p.211-21, (2003) Abstract
Conservation of virally encoded microRNAs in Kaposi sarcoma--associated herpesvirus in primary effusion lymphoma cell lines and in patients with Kaposi sarcoma or multicentric Castleman disease., Marshall, Vickie, Parks Thomas, Bagni Rachel, Wang Cheng Dian, Samols Mark A., Hu Jianhong, Wyvil Kathleen M., Aleman Karen, Little Richard F., Yarchoan Robert, et al. , The Journal of infectious diseases, 2007 Mar 1, Volume 195, Issue 5, p.645-59, (2007) Abstract
Mutations in KCTD1 cause scalp-ear-nipple syndrome., Marneros, Alexander G., Beck Anita E., Turner Emily H., McMillin Margaret J., Edwards Matthew J., Field Michael, de Macena Sobreira Nara Lygia, Perez Ana Beatriz A., Fortes Jose A. R., Lampe Anne K., et al. , American journal of human genetics, 2013 Apr 4, Volume 92, Issue 4, p.621-6, (2013) Abstract
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome., Margulies, Elliott H., Cooper Gregory M., Asimenos George, Thomas Daryl J., Dewey Colin N., Siepel Adam, Birney Ewan, Keefe Damian, Schwartz Ariel S., Hou Minmei, et al. , Genome research, 2007 Jun, Volume 17, Issue 6, p.760-74, (2007) Abstract
Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy., Majewski, Tadeusz, Lee Sangkyou, Jeong Joon, Yoon Dong-Sup, Kram Andrzej, Kim Mi-Sook, Tuziak Tomasz, Bondaruk Jolanta, Lee Sooyong, Park Weon-Seo, et al. , Laboratory investigation; a journal of technical methods and pathology, 2008 Jul, Volume 88, Issue 7, p.694-721, (2008) Abstract
A multilocus approach to the antihypertensive pharmacogenetics of hydrochlorothiazide., Maitland-van der Zee, Anke-Hilse, Turner Stephen T., Schwartz Gary L., Chapman Arlene B., Klungel Olaf H., and Boerwinkle Eric , Pharmacogenetics and genomics, 2005 May, Volume 15, Issue 5, p.287-93, (2005) Abstract
Absence of an interaction between the angiotensin-converting enzyme insertion-deletion polymorphism and pravastatin on cardiovascular disease in high-risk hypertensive patients: the Genetics of Hypertension-Associated Treatment (GenHAT) study., Maitland-van der Zee, Anke-Hilse, Boerwinkle Eric, Arnett Donna K., Davis Barry R., Leiendecker-Foster Catherine, Miller Michael B., Klungel Olaf H., Ford Charles E., and Eckfeldt John H. , American heart journal, 2007 Jan, Volume 153, Issue 1, p.54-8, (2007) Abstract
Pharmacogenetics of response to statins: where do we stand?, Maitland-van der Zee, Anke-Hilse, and Boerwinkle Eric , Current atherosclerosis reports, 2005 May, Volume 7, Issue 3, p.204-8, (2005) Abstract
Demographic, environmental, and genetic predictors of metabolic side effects of hydrochlorothiazide treatment in hypertensive subjects., Maitland-van der Zee, Anke-Hilse, Turner Stephen T., Schwartz Gary L., Chapman Arlene B., Klungel Olaf H., and Boerwinkle Eric , American journal of hypertension, 2005 Aug, Volume 18, Issue 8, p.1077-83, (2005) Abstract
PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13., Maheshwari, M., Belmont J., Fernbach S., Ho T., Molinari L., Yakub I., Yu F., Combes A., Towbin J., Craigen W. J., et al. , Human mutation, 2002 Oct, Volume 20, Issue 4, p.298-304, (2002) Abstract
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)., Maheshwari, Manjula, Christian S. L., Liu C., Badner J. A., Detera-Wadleigh S., Gershon E. S., and Gibbs Richard A. , BMC genomics, 2002 Oct 22, Volume 3, Issue 1, p.30, (2002) Abstract
Common and rare variants of DAOA in bipolar disorder., Maheshwari, Manjula, Shi Jiajun, Badner Judith A., Skol Andrew, Willour Virginia L., Muzny Donna M., Wheeler David A., Gerald Fowler R., Detera-Wadleigh Sevilla, McMahon Francis J., et al. , American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2009 Oct 5, Volume 150B, Issue 7, p.960-6, (2009) Abstract
Fosmid-based physical mapping of the Histoplasma capsulatum genome., Magrini, Vincent, Warren Wesley C., Wallis John, Goldman William E., Xu Jian, Mardis Elaine R., and McPherson John D. , Genome research, 2004 Aug, Volume 14, Issue 8, p.1603-9, (2004) Abstract
The Drosophila melanogaster Genetic Reference Panel., Mackay, Trudy F. C., Richards Stephen, Stone Eric A., Barbadilla Antonio, Ayroles Julien F., Zhu Dianhui, Casillas Sònia, Han Yi, Magwire Michael M., Cridland Julie M., et al. , Nature, 2012 Feb 9, Volume 482, Issue 7384, p.173-8, (2012) Abstract
A systematic survey of loss-of-function variants in human protein-coding genes., MacArthur, Daniel G., Balasubramanian Suganthi, Frankish Adam, Huang Ni, Morris James, Walter Klaudia, Jostins Luke, Habegger Lukas, Pickrell Joseph K., Montgomery Stephen B., et al. , Science (New York, N.Y.), 2012 Feb 17, Volume 335, Issue 6070, p.823-8, (2012) Abstract
Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia., Ma, Xiaotu, Edmonson Michael, Yergeau Donald, Muzny Donna M., Hampton Oliver A., Rusch Michael, Song Guangchun, Easton John, Harvey Richard C., Wheeler David A., et al. , Nature communications, 2015, Volume 6, p.6604, (2015) Abstract


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