Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kevin C. Cartier"'
Autor:
Catherine M Stein, Sarah Zalwango, LaShaunda L Malone, Sungho Won, Harriet Mayanja-Kizza, Roy D Mugerwa, Dmitry V Leontiev, Cheryl L Thompson, Kevin C Cartier, Robert C Elston, Sudha K Iyengar, W Henry Boom, Christopher C Whalen
Publikováno v:
PLoS ONE, Vol 3, Iss 12, p e4094 (2008)
Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), is an enduring public health problem globally, particularly in sub-Saharan Africa. Several studies have suggested a role for host genetic susceptibility in increased risk for TB but resul
Externí odkaz:
https://doaj.org/article/d2e4e435bac74916a4dac69ae6249f32
Autor:
Yuanjia Wang, N. Li, S. Waaijenborg, Joseph Beyene, J. S. Rao, A. T. Kraja, Catherine M. Stein, Kevin C. Cartier, Nora L. Nock, G. Jonasdottir, P. Wolkow, Shelley B. Bull, K. S. Wang, Elena Parkhomenko, David Tritchler, R. Sutradhar
Publikováno v:
Genetic epidemiology. 31
This paper summarizes contributions to group 12 of the 15th Genetic Analysis Workshop. The papers in this group focused on multivariate methods and applications for the analysis of molecular data including genotypic data as well as gene expression mi
Autor:
H. G. Taylor, Lisa Freebairn, Kevin C. Cartier, Christopher Millard, Lara Miscimarra, Sudha K. Iyengar, Barbara A. Lewis, Catherine M. Stein, Lawrence D. Shriberg, Amy J. Hansen, Amy Kluge
Publikováno v:
Human heredity. 63(1)
Background/Aims: Genetic studies have raised the possibility of common bases for cognitive linguistic disorders such as speech sound disorder (SSD), reading disorder (RD) and language impairment (LI). Thus, some of the same genes may jointly influenc
Autor:
Daniel Baechle, Kevin C. Cartier
Publikováno v:
BMC Genetics
BMC Genetics, Vol 6, Iss Suppl 1, p S129 (2005)
BMC Genetics, Vol 6, Iss Suppl 1, p S129 (2005)
The problem of estimating haplotype frequencies from population data has been considered by numerous investigators, resulting in a wide variety of possible algorithmic and statistical solutions. We propose a relatively unique approach that employs an
Autor:
L. Adrienne Cupples, Julia Bailey, Kevin C. Cartier, Catherine T. Falk, Kuang-Yu Liu, Yuanqing Ye, Robert Yu, Heping Zhang, Hongyu Zhao
Publikováno v:
Genetic epidemiology. 29
Group 14 used data-mining strategies to evaluate a number of issues, including appropriate diagnosis, haplotype estimation, genetic linkage and association studies, and type I error. Methods ranged from exploratory analyses, to machine learning strat
Publikováno v:
BMC Genetics, Vol 6, Iss Suppl 1, p S95 (2005)
BMC Genetics
BMC Genetics
Background In this analysis we applied a regression based transmission disequilibrium test to the binary trait presence or absence of Kofendred Personality Disorder in the Genetic Analysis Workshop 14 (GAW14) simulated dataset and determined the powe
Autor:
Barbara A. Lewis, Christopher Millard, Lara Miscimarra, Lawrence D. Shriberg, Amy Kluge, H. Gerry Taylor, Catherine M. Stein, Kevin C. Cartier, Lisa Freebairn, Sudha K. Iyengar, Amy J. Hansen
Publikováno v:
Behavior genetics. 36(6)
Despite a growing body of evidence indicating that speech sound disorder (SSD) has an underlying genetic etiology, researchers have not yet identified specific genes predisposing to this condition. The speech and language deficits associated with SSD
Autor:
John A. Hamley, Glen E. Bowers, Kevin C. Cartier, John R. Miller, Luis R. Pinero, Vincent K. Rawlin
Publikováno v:
31st Joint Propulsion Conference and Exhibit.
A 0.5-2.3 kW xenon ion propulsion system is presently being developed under the NASA Solar Electric Propulsion Technology Application Readiness (NSTAR) program. This propulsion system includes a 30 cm diameter xenon ion thruster, a Digital Control In
Autor:
Kevin C. Cartier, Sudha K. Iyengar, Yeunjoo E. Song, Lara Miscimarra, J. Sunil Rao, Jean-Eudes Dazard
Publikováno v:
BMC Proceedings
Standard genetic mapping techniques scan chromosomal segments for location of genetic linkage and association signals. The majority of these methods consider only correlations at single markers and/or phenotypes with explicit detailing of the genetic
Publikováno v:
BMC Genetics, Vol 4, Iss Suppl 1, p S82 (2003)
BMC Genetics
BMC Genetics
Only one genome scan to date has attempted to make use of the longitudinal data available in the Framingham Heart Study, and this attempt yielded evidence of linkage to a gene for mean systolic blood pressure. We show how the additional information a