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

von HALL, MEGAN P., HO, C. KIONG
Veröffentlicht 2006

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

von Hall, Megan P., Ho, C. Kiong
Veröffentlicht 2006

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

von Hall, Megan P., Huang, Sui, Black, Douglas L.
Veröffentlicht 2004

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

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

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

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

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

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

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

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

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

von 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
Veröffentlicht 2010

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

von 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
Veröffentlicht 2014

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

von 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.
Veröffentlicht in Nat Med (2019)