From case studies to community knowledge base: MSeqDR provides a platform for the curation and genomic analysis of mitochondrial diseases

Por Falk, Marni J., Shen, Lishuang, Gai, Xiaowu
Publicado no Cold Spring Harb Mol Case Stud (2016)

Gene discovery using the maize genome database ZmDB

Por Gai, Xiaowu, Lal, Shailesh, Xing, Liqun, Brendel, Volker, Walbot, Virginia
Publicado em 2000

Ty5 gag Mutations Increase Retrotransposition and Suggest a Role for Hydrogen Bonding in the Function of the Nucleocapsid Zinc Finger

Por Gao, Xiang, Rowley, Daniel J., Gai, Xiaowu, Voytas, Daniel F.
Publicado em 2002

Innovative genomic collaboration using the GENESIS (GEM.app) platform

Por Gonzalez, Michael, Falk, Marni, Gai, Xiaowu, Schüle, Rebecca, Zuchner, Stephan
Publicado no Hum Mutat (2015)

Clinical utility of the low-density Infinium QC genotyping Array in a genomics-based diagnostics laboratory

Por Ponomarenko, Petr, Ryutov, Alex, Maglinte, Dennis T., Baranova, Ancha, Tatarinova, Tatiana V., Gai, Xiaowu
Publicado no BMC Med Genomics (2017)

Comprehensive Genome Analysis of 6,000 USA SARS-CoV-2 Isolates Reveals Haplotype Signatures and Localized Transmission Patterns by State and by Country

Por Shen, Lishuang, Dien Bard, Jennifer, Biegel, Jaclyn A., Judkins, Alexander R., Gai, Xiaowu
Publicado no Front Microbiol (2020)

Targeting of the Yeast Ty5 Retrotransposon to Silent Chromatin Is Mediated by Interactions between Integrase and Sir4p

Por Xie, Weiwu, Gai, Xiaowu, Zhu, Yunxia, Zappulla, David C., Sternglanz, Rolf, Voytas, Daniel F.
Publicado em 2001

Clinical Bioinformatics in Precise Diagnosis of Mitochondrial Disease

Por Shen, Lishuang, McCormick, Elizabeth M., Muraresk, Colleen C, Falk, Marni J., Gai, Xiaowu
Publicado no Clin Lab Med (2020)

MSeqDR mvTool: a Mitochondrial DNA Web and API Resource for Comprehensive Variant Annotation, Universal Nomenclature Collation, and Reference Genome Conversion

Por Shen, Lishuang, Attimonelli, Marcella, Bai, Renkui, Lott, Marie T., Wallace, Douglas C., Falk, Marni J., Gai, Xiaowu
Publicado no Hum Mutat (2018)

Emerging variants of concern in SARS-CoV-2 membrane protein: a highly conserved target with potential pathological and therapeutic implications

Por Shen, Lishuang, Bard, Jennifer Dien, Triche, Timothy J., Judkins, Alexander R., Biegel, Jaclyn A., Gai, Xiaowu
Publicado no Emerg Microbes Infect (2021)

Rapidly emerging SARS-CoV-2 B.1.1.7 sub-lineage in the United States of America with spike protein D178H and membrane protein V70L mutations

Por Shen, Lishuang, Bard, Jennifer Dien, Triche, Timothy J., Judkins, Alexander R., Biegel, Jaclyn A., Gai, Xiaowu
Publicado no Emerg Microbes Infect (2021)

Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies

Por Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
Publicado no Congenit Heart Dis (2011)

On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness

Por Bryant, Laura, Lozynska, Olga, Han, Grace, Morgan, Jessica I.W., Gai, Xiaowu, Maguire, Albert M., Aleman, Tomas, Bennett, Jean
Publicado no Ophthalmic Genet (2017)

Landscape of germline and somatic mitochondrial DNA mutations in pediatric malignancies

Por Triska, Petr, Kaneva, Kristiyana, Merkurjev, Daria, Sohail, Noor, Falk, Marni J., Triche, Timothy J., Biegel, Jaclyn A., Gai, Xiaowu
Publicado no Cancer Res (2019)

Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods

Por Kaneva, Kristiyana, Merkurjev, Daria, Ostrow, Dejerianne, Ryutov, Alex, Triska, Petr, Stachelek, Kevin, Cobrinik, David, Biegel, Jaclyn A., Gai, Xiaowu
Publicado no Mitochondrion (2020)

TBIO-12. THE SPECTRUM OF MITOCHONDRIAl DNA (mtDNA) MUTATIONS IN PEDIATRIC CENTRAL NERVOUS SYSTEM (CNS) TUMORS

Por Kaneva, Kristiyana, Triska, Petr, Merkurjev, Daria, Bootwalla, Moiz, Cotter, Jennifer, Ostrow, Dejerianne, O’Halloran, Katrina, Biegel, Jaclyn, Gai, Xiaowu
Publicado no Neuro Oncol (2020)

Utility of viral whole-genome sequencing for institutional infection surveillance during the coronavirus disease 2019 (COVID-19) pandemic

Por Ryutov, Alex, Gai, Xiaowu, Ostrow, Dejerianne, Maglinte, Dennis T., Flores, Jessica, Salas, Edahrline J., Glucoft, Marisa, Smit, Michael, Dien Bard, Jennifer
Publicado no Infect Control Hosp Epidemiol (2021)

Comparison of RNA Expression Profiles Based on Maize Expressed Sequence Tag Frequency Analysis and Micro-Array Hybridization

Por Fernandes, John, Brendel, Volker, Gai, Xiaowu, Lal, Shailesh, Chandler, Vicki L., Elumalai, Rangasamy P., Galbraith, David W., Pierson, Elizabeth A., Walbot, Virginia
Publicado em 2002

RARE-57. PEDIATRIC CHORDOMA: WHOLE EXOME SEQUENCING OF 11 PEDIATRIC CHORDOMA SAMPLES

Por O’Halloran, Katrina, Bootwalla, Moiz, Merkurjev, Daria, Kaneva, Kristiyana, Ryutov, Alex, Cotter, Jennifer, Ji, Jianling, Ostrow, Dejerianne, Biegel, Jaclyn A, Gai, Xiaowu
Publicado no Neuro Oncol (2020)

A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants

Por Ji, Jianling, Shen, Lishuang, Bootwalla, Moiz, Quindipan, Catherine, Tatarinova, Tatiana, Maglinte, Dennis T., Buckley, Jonathan, Raca, Gordana, Saitta, Sulagna C., Biegel, Jaclyn A., Gai, Xiaowu
Publicado no Cold Spring Harb Mol Case Stud (2019)