VKORC1 Common Variation and Bone Mineral Density in the Third National Health and Nutrition Examination Survey

Por Crawford, Dana C., Brown-Gentry, Kristin, Rieder, Mark J.
Publicado em 2010

Identifying the genotype behind the phenotype: a role model found in VKORC1 and its association with warfarin dosing

Por Crawford, Dana C., Ritchie, Marylyn D., Rieder, Mark J.
Publicado em 2007

MEASURES OF EXPOSURE IMPACT GENETIC ASSOCIATION STUDIES: AN EXAMPLE IN VITAMIN K LEVELS AND VKORC1

Por CRAWFORD, DANA C., BROWN-GENTRY, KRISTIN, RIEDER, MARK J.
Publicado no Pac Symp Biocomput (2015)

Allele Frequency Matching Between SNPs Reveals an Excess of Linkage Disequilibrium in Genic Regions of the Human Genome

Por Eberle, Michael A, Rieder, Mark J, Kruglyak, Leonid, Nickerson, Deborah A
Publicado em 2006

Novel CYP2C9 Promoter Variants and Assessment of Their Impact on Gene Expression

Por Kramer, Melissa A., Rettie, Allan E., Rieder, Mark J., Cabacungan, Erwin T., Hines, Ronald N.
Publicado em 2008

Selecting a Maximally Informative Set of Single-Nucleotide Polymorphisms for Association Analyses Using Linkage Disequilibrium

Por Carlson, Christopher S., Eberle, Michael A., Rieder, Mark J., Yi, Qian, Kruglyak, Leonid, Nickerson, Deborah A.
Publicado em 2004

CYP4F2 Is a Vitamin K(1) Oxidase: An Explanation for Altered Warfarin Dose in Carriers of the V433M Variant

Por McDonald, Matthew G., Rieder, Mark J., Nakano, Mariko, Hsia, Clara K., Rettie, Allan E.
Publicado em 2009

New genetic variant that might improve warfarin dose prediction in African Americans

Por Schelleman, Hedi, Brensinger, Colleen M, Chen, Jinbo, Finkelman, Brian S, Rieder, Mark J, Kimmel, Stephen E
Publicado em 2010

Annotation of pseudogenic gene segments by massively parallel sequencing of rearranged lymphocyte receptor loci

Por Dean, Jared, Emerson, Ryan O., Vignali, Marissa, Sherwood, Anna M., Rieder, Mark J., Carlson, Christopher S., Robins, Harlan S.
Publicado no Genome Med (2015)

Sequence-Based Linkage Analysis

Por Furman, Itay, Rieder, Mark J., da Ponte, Suzanne, Carrington, Dana P., Nickerson, Deborah A., Kruglyak, Leonid, Markianos, Kyriacos
Publicado em 2004

A case study of acenocoumarol sensitivity and genotype-phenotype discordancy explained by combinations of polymorphisms in VKORC1 and CYP2C9

Por Rettie, Allan E, Farin, Frederico M, Beri, Nitasha G, Srinouanprachanh, Sengkeo L, Rieder, Mark J, Thijssen, Henk H
Publicado em 2006

Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes

Por Akey, Joshua M, Eberle, Michael A, Rieder, Mark J, Carlson, Christopher S, Shriver, Mark D, Nickerson, Deborah A, Kruglyak, Leonid
Publicado em 2004

Genomic regions exhibiting positive selection identified from dense genotype data

Por Carlson, Christopher S., Thomas, Daryl J., Eberle, Michael A., Swanson, Johanna E., Livingston, Robert J., Rieder, Mark J., Nickerson, Deborah A.
Publicado em 2005

Human Liver Expression of CYP2C8: Gender, Age, and Genotype Effects

Por Naraharisetti, Suresh Babu, Lin, Yvonne S., Rieder, Mark J., Marciante, Kristin D., Psaty, Bruce M., Thummel, Kenneth E., Totah, Rheem A.
Publicado em 2010

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome

Por Heike, Carrie L., Starr, Jacqueline R., Rieder, Mark J., Cunningham, Michael L., Edwards, Karen L., Stanaway, Ian, Crawford, Dana C.
Publicado no Birth Defects Res A Clin Mol Teratol (2010)

An excess of rare genetic variation in ABCE1 among Yorubans and African-American individuals with HIV-1

Por Crawford, Dana C., Zheng, Natalie, Speelmon, Emily C, Stanaway, Ian, Rieder, Mark J., Nickerson, Deborah A., McElrath, M. Juliana, Lingappa, Jairam
Publicado em 2009

IGF1R Variants Associated with Isolated Single Suture Craniosynostosis

Por Cunningham, Michael L., Horst, Jeremy A., Rieder, Mark J., Hing, Anne V., Stanaway, Ian B., Park, Sarah S., Samudrala, Ram, Speltz, Matthew L.
Publicado em 2011

Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

Por Norton, Nadine, Robertson, Peggy D., Rieder, Mark J., Zuchner, Stephan, Rampersaud, Evadnie, Martin, Eden, Li, Duanxiang, Nickerson, Deborah A., Hershberger, Ray E.
Publicado em 2012

“Mandibulofacial Dysostosis with Microcephaly” Caused by EFTUD2 Mutations: Expanding the Phenotype

Por Luquetti, Daniela V, Hing, Anne V, Rieder, Mark J, Nickerson, Deborah A, Turner, Emily H, Smith, Joshua, Park, Sarah, Cunningham, Michael L
Publicado em 2012

Allelic spectrum of the natural variation in CRP

Por Crawford, Dana C., Yi, Qian, Smith, Joshua D., Shephard, Cynthia, Wong, Michelle, Witrak, Laura, Livingston, Robert J., Rieder, Mark J., Nickerson, Deborah A.
Publicado em 2006