Human Neural Tube Defects: Developmental Biology, Epidemiology, and Genetics

Por Detrait, Eric.R., George, Timothy. M., Etchevers, Heather.C., Gilbert, John.R., Vekemans, Michel., Speer, Marcy. C.
Publicado em 2005

Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

Por Deak, Kristen L., Siegel, Deborah G., George, Timothy M., Gregory, Simon, Ashley-Koch, Allison, Speer, Marcy C.
Publicado em 2008

Natural Food Folate and Late-Life Depression

Por Payne, Martha E., Jamerson, Brenda D., Potocky, Christopher F., Ashley-Koch, Allison E., Speer, Marcy C., Steffens, David C.
Publicado em 2009

Folate Metabolism Genes, Dietary Folate and Response to Antidepressant Medications in Late-Life Depression

Por Jamerson, Brenda D., Payne, Martha E., Garrett, Melanie E., Ashley-Koch, Allison E., Speer, Marcy C., Steffens, David C.
Publicado em 2012

Human neural crest cells display molecular and phenotypic hallmarks of stem cells

Por Thomas, Sophie, Thomas, Marie, Wincker, Patrick, Babarit, Candice, Xu, Puting, Speer, Marcy C., Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel, Etchevers, Heather C.
Publicado em 2008

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations

Por Markunas, Christina A., Tubbs, R. Shane, Moftakhar, Roham, Ashley-Koch, Allison E., Gregory, Simon G., Oakes, W. Jerry, Speer, Marcy C., Iskandar, Bermans J.
Publicado em 2012

myotilin Mutation Found in Second Pedigree with LGMD1A

Por Hauser, Michael A., Conde, Cecilia B., Kowaljow, Valeria, Zeppa, Guillermo, Taratuto, Ana L., Torian, Udana M., Vance, Jeffery, Pericak-Vance, Margaret A., Speer, Marcy C., Rosa, Alberto L.
Publicado em 2002

Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

Por Soldano, Karen L., Garrett, Melanie E., Cope, Heidi L., Rusnak, J. Michael, Ellis, Nathen J., Dunlap, Kaitlyn L., Speer, Marcy C., Gregory, Simon G., Ashley-Koch, Allison E.
Publicado em 2013

Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing

Por Boyles, Abee L., Scott, William K., Martin, Eden R., Schmidt, Silke, Li, Yi-Ju, Ashley-Koch, Allison, Bass, Meredyth P., Schmidt, Michael, Pericak-Vance, Margaret A., Speer, Marcy C., Hauser, Elizabeth R.
Publicado em 2005

High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35

Por Stamm, Demetra S., Rampersaud, Evadnie, Slifer, Susan H., Mehltretter, Lorraine, Siegel, Deborah G., Xie, Jianzhen, Hu-Lince, Diane, Craig, David W., Stephan, Dietrich A., George, Timothy M., Gilbert, John R., Speer, Marcy C.
Publicado em 2006

Gene Expression Profiling of Familial and Sporadic Interstitial Pneumonia

Por Yang, Ivana V., Burch, Lauranell H., Steele, Mark P., Savov, Jordan D., Hollingsworth, John W., McElvania-Tekippe, Erin, Berman, Katherine G., Speer, Marcy C., Sporn, Thomas A., Brown, Kevin K., Schwarz, Marvin I., Schwartz, David A.
Publicado em 2007

Genetic linkage mapping of chromosome 17 markers and neurofibromatosis type 1

Por Vance, Jeffery M., Pericak-Vance, Margaret A., Yamaoka, Larry H., Speer, Marcy C., Rosenwasser, George O. D., Small, Kent, Gaskell, P. C., Hung, Wu-Yen, Alberts, Mark J., Haynes, Carol S., Gilbert, John R., Aylsworth, Arthur S., Roses, Allen D.
Publicado em 1989

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal dominant form to chromosome 5q

Por Speer, Marcy C., Yamaoka, Larry H., Gilchrist, James H., Gaskell, C. P., Stajich, Jeffrey M., Vance, Jeffery M., Kazantsev, Alexey, Lastra, Anselmo A., Haynes, Carol S., Beckmann, Jacques S., Cohen, Daniel, Weber, James L., Roses, Allen D., Pericak-Vance, Margaret A.
Publicado em 1992

Clinical and Pathologic Features of Familial Interstitial Pneumonia

Por Steele, Mark P., Speer, Marcy C., Loyd, James E., Brown, Kevin K., Herron, Aretha, Slifer, Susan H., Burch, Lauranell H., Wahidi, Momen M., Phillips, John A., Sporn, Thomas A., McAdams, H. Page, Schwarz, Marvin I., Schwartz, David A.
Publicado em 2005

Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions

Por Boyles, Abee L., Billups, Ashley V., Deak, Kristen L., Siegel, Deborah G., Mehltretter, Lorraine, Slifer, Susan H., Bassuk, Alexander G., Kessler, John A., Reed, Michael C., Nijhout, H. Frederik, George, Timothy M., Enterline, David S., Gilbert, John R., Speer, Marcy C.
Publicado em 2006

Evidence for Locus Heterogeneity in Autosomal Dominant Limb-Girdle Muscular Dystrophy

Por Speer, Marcy C., Gilchrist, James M., Chutkow, Jerry G., McMichael, Robert, Westbrook, Carol A., Stajich, Jeffrey M., Jorgenson, Eric M., Gaskell, P. Craig, Rosi, Barbara L., Ramesar, Raj, Vance, Jeffery M., Yamaoka, Larry H., Roses, Allen D., Pericak-Vance, Margaret A.
Publicado em 1995

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

Por Deak, Kristen L., Boyles, Abee L., Etchevers, Heather C., Melvin, Elizabeth C., Siegel, Deborah G., Graham, Felicia L., Slifer, Susan H., Enterline, David S., George, Timothy M., Vekemans, Michel, McClay, David, Bassuk, Alexander G., Kessler, John A., Linney, Elwood, Gilbert, John R., Speer, Marcy C.
Publicado em 2005

Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy

Por Horstick, Eric J., Linsley, Jeremy W., Dowling, James J., Hauser, Michael A., McDonald, Kristin K., Ashley-Koch, Allison, Saint-Amant, Louis, Satish, Akhila, Cui, Wilson W., Zhou, Weibin, Sprague, Shawn M., Stamm, Demetra S., Powell, Cynthia M., Speer, Marcy C., Franzini-Armstrong, Clara, Hirata, Hiromi, Kuwada, John Y.
Publicado em 2013

A Common MUC5B Promoter Polymorphism and Pulmonary Fibrosis

Por Seibold, Max A., Wise, Anastasia L., Speer, Marcy C., Steele, Mark P., Brown, Kevin K., Loyd, James E., Fingerlin, Tasha E., Zhang, Weiming, Gudmundsson, Gunnar, Groshong, Steve D., Evans, Christopher M., Garantziotis, Stavros, Adler, Kenneth B., Dickey, Burton F., du Bois, Roland M., Yang, Ivana V., Herron, Aretha, Kervitsky, Dolly, Talbert, Janet L., Markin, Cheryl, Park, Joungjoa, Crews, Anne L., Slifer, Susan H., Auerbach, Scott, Roy, Michelle G., Lin, Jia, Hennessy, Corinne E., Schwarz, Marvin I., Schwartz, David A.
Publicado em 2011