Characterization of a Trypanosoma brucei RNA cap (guanine N-7) methyltransferase

Tekijä HALL, MEGAN P., HO, C. KIONG
Julkaistu 2006

Functional characterization of a 48 kDa Trypanosoma brucei cap 2 RNA methyltransferase

Tekijä Hall, Megan P., Ho, C. Kiong
Julkaistu 2006

Differentiation-induced Colocalization of the KH-type Splicing Regulatory Protein with Polypyrimidine Tract Binding Protein and the c-src Pre-mRNA

Tekijä Hall, Megan P., Huang, Sui, Black, Douglas L.
Julkaistu 2004

Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach

Tekijä Hall, Megan P., Hill, Matthew, Zimmermann, Bernhard, Sigurjonsson, Styrmir, Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Julkaistu 2014

Quaking and PTB control overlapping splicing regulatory networks during muscle cell differentiation

Tekijä Hall, Megan P., Nagel, Roland J., Fagg, W. Samuel, Shiue, Lily, Cline, Melissa S., Perriman, Rhonda J., Donohue, John Paul, Ares, Manuel
Julkaistu 2013

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

Tekijä Samango-Sprouse, Carole, Kırkızlar, Eser, Hall, Megan P., Lawson, Patrick, Demko, Zachary, Zneimer, Susan M., Curnow, Kirsten J., Gross, Susan, Gropman, Andrea
Julkaisussa PLoS One (2016)

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy

Tekijä Samango-Sprouse, Carole, Banjevic, Milena, Ryan, Allison, Sigurjonsson, Styrmir, Zimmermann, Bernhard, Hill, Matthew, Hall, Megan P., Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Julkaistu 2013

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

Tekijä Du, Hongqing, Cline, Melissa S., Osborne, Robert J., Tuttle, Daniel L., Clark, Tyson A., Donohue, John Paul, Hall, Megan P., Shiue, Lily, Swanson, Maurice S., Thornton, Charles A., Ares, Manuel
Julkaistu 2010

Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort

Tekijä Pergament, Eugene, Cuckle, Howard, Zimmermann, Bernhard, Banjevic, Milena, Sigurjonsson, Styrmir, Ryan, Allison, Hall, Megan P., Dodd, Michael, Lacroute, Phil, Stosic, Melissa, Chopra, Nikhil, Hunkapiller, Nathan, Prosen, Dennis E., McAdoo, Sallie, Demko, Zachary, Siddiqui, Asim, Hill, Matthew, Rabinowitz, Matthew
Julkaistu 2014

High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants

Tekijä Razavi, Pedram, Li, Bob T., Brown, David N., Jung, Byoungsok, Hubbell, Earl, Shen, Ronglai, Abida, Wassim, Juluru, Krishna, De Bruijn, Ino, Hou, Chenlu, Venn, Oliver, Lim, Raymond, Anand, Aseem, Maddala, Tara, Gnerre, Sante, Satya, Ravi Vijaya, Liu, Qinwen, Shen, Ling, Eattock, Nicholas, Yue, Jeanne, Blocker, Alexander W., Lee, Mark, Sehnert, Amy, Xu, Hui, Hall, Megan P., Santiago-Zayas, Angie, Novotny, William F., Isbell, James M., Rusch, Valerie W., Plitas, George, Heerdt, Alexandra S., Ladanyi, Marc, Hyman, David M., Jones, David R., Morrow, Monica, Riely, Gregory J., Scher, Howard I., Rudin, Charles M., Robson, Mark E., Diaz, Luis A., Solit, David B., Aravanis, Alexander M., Reis-Filho, Jorge S.
Julkaisussa Nat Med (2019)