Genotyping of Bacillus cereus Strains by Microarray-Based Resequencing

por Zwick, Michael E., Kiley, Maureen P., Stewart, Andrew C., Mateczun, Alfred, Read, Timothy D.
Publicado 2008

Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale

por Kotlar, Alex V., Trevino, Cristina E., Zwick, Michael E., Cutler, David J., Wingo, Thomas S.
Publicado 2018

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry

por Glassford, Megan R., Rosenfeld, Jill A., Freedman, Alexa A., Zwick, Michael E., Mulle, Jennifer G.
Publicado 2016

Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders

por Mosley, Trenell J., Johnston, H. Richard, Cutler, David J., Zwick, Michael E., Mulle, Jennifer G.
Publicado 2021

Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays

por Mulle, Jennifer G., Patel, Viren C., Warren, Stephen T., Hegde, Madhuri R., Cutler, David J., Zwick, Michael E.
Publicado 2010

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

por Steinberg, Karyn Meltz, Ramachandran, Dhanya, Patel, Viren C, Shetty, Amol C, Cutler, David J, Zwick, Michael E
Publicado 2012

Omicseq: a web-based search engine for exploring omics datasets

por Sun, Xiaobo, Pittard, William S., Xu, Tianlei, Chen, Li, Zwick, Michael E., Jiang, Xiaoqian, Wang, Fusheng, Qin, Zhaohui S.
Publicado 2017

Genetic variation and linkage disequilibrium in Bacillus anthracis

por Zwick, Michael E., Thomason, Maureen Kiley, Chen, Peter E., Johnson, Henry R., Sozhamannan, Shanmuga, Mateczun, Alfred, Read, Timothy D.
Publicado 2011

Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants

por Venkateswaran, Suresh, Denson, Lee A., Jurickova, Ingrid, Dodd, Anne, Zwick, Michael E., Cutler, David J., Kugathasan, Subra, Okou, David T.
Publicado 2019

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse

por Sun, Miao, Mondal, Kajari, Patel, Viren, Horner, Vanessa L., Long, Alyssa B., Cutler, David J., Caspary, Tamara, Zwick, Michael E.
Publicado 2012

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry

por Pollak, Rebecca M., Murphy, Melissa M., Epstein, Michael P., Zwick, Michael E., Klaiman, Cheryl, Saulnier, Celine A., Mulle, Jennifer G.
Publicado 2019

Microarray-based resequencing of multiple Bacillus anthracis isolates

por Zwick, Michael E, Mcafee, Farrell, Cutler, David J, Read, Timothy D, Ravel, Jacques, Bowman, Gregory R, Galloway, Darrell R, Mateczun, Alfred
Publicado 2005

SeqAnt: A web service to rapidly identify and annotate DNA sequence variations

por Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Publicado 2010

Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome–Like Phenotype

por Collins, Stephen C., Coffee, Brad, Benke, Paul J., Berry-Kravis, Elizabeth, Gilbert, Fred, Oostra, Ben, Halley, Dicky, Zwick, Michael E., Cutler, David J., Warren, Stephen T.
Publicado 2010

High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing

por Yilmaz, Feyza, Gurusamy, Umamaheswaran, Mosley, Trenell J., Hallast, Pille, Kim, Kwondo, Mostovoy, Yulia, Purcell, Ryan H., Shaikh, Tamim H., Zwick, Michael E., Kwok, Pui-Yan, Lee, Charles, Mulle, Jennifer G.
Publicado 2023

Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior

por Badshah, Noor, Mattison, Kari A., Ahmad, Sohail, Chopra, Pankaj, Johnston, H. Richard, Ahmad, Shakoor, Khan, Sher Hayat, Sarwar, Muhammad Tahir, Cutler, David J., Taylor, Micheal, Vadlamani, Gayatri, Zwick, Michael E., Escayg, Andrew
Publicado 2022

Induced pluripotent stem cells from subjects with Lesch-Nyhan disease

por Sutcliffe, Diane J., Dinasarapu, Ashok R., Visser, Jasper E., Hoed, Joery den, Seifar, Fatemeh, Joshi, Piyush, Ceballos-Picot, Irene, Sardar, Tejas, Hess, Ellen J., Sun, Yan V., Wen, Zhexing, Zwick, Michael E., Jinnah, H. A.
Publicado 2021

Dysbiosis, inflammation, and response to treatment: a longitudinal study of pediatric subjects with newly diagnosed inflammatory bowel disease

por Shaw, Kelly A., Bertha, Madeline, Hofmekler, Tatyana, Chopra, Pankaj, Vatanen, Tommi, Srivatsa, Abhiram, Prince, Jarod, Kumar, Archana, Sauer, Cary, Zwick, Michael E., Satten, Glen A., Kostic, Aleksandar D., Mulle, Jennifer G., Xavier, Ramnik J., Kugathasan, Subra
Publicado 2016

Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects

por Rambo-Martin, Benjamin L., Mulle, Jennifer G., Cutler, David J., Bean, Lora J. H., Rosser, Tracie C., Dooley, Kenneth J., Cua, Clifford, Capone, George, Maslen, Cheryl L., Reeves, Roger H., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2017

Genomic characterization of the Bacillus cereus sensu lato species: Backdrop to the evolution of Bacillus anthracis

por Zwick, Michael E., Joseph, Sandeep J., Didelot, Xavier, Chen, Peter E., Bishop-Lilly, Kimberly A., Stewart, Andrew C., Willner, Kristin, Nolan, Nichole, Lentz, Shannon, Thomason, Maureen K., Sozhamannan, Shanmuga, Mateczun, Alfred J., Du, Lei, Read, Timothy D.
Publicado 2012