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

di HALL, MEGAN P., HO, C. KIONG
Pubblicazione 2006

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

di Hall, Megan P., Ho, C. Kiong
Pubblicazione 2006

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

di Hall, Megan P., Huang, Sui, Black, Douglas L.
Pubblicazione 2004

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

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

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

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

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

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

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

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

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

di 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
Pubblicazione 2010

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

di 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
Pubblicazione 2014

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

di 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.
Pubblicato in Nat Med (2019)