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Xiaowu Gai
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Urine is not sterile: use of enhanced urine culture techniques to detect resident bacterial flora in the adult female bladder
EE Hilt, K McKinley, MM Pearce, AB Rosenfeld, MJ Zilliox, ER Mueller, ...
Journal of clinical microbiology 52 (3), 871-876, 2014
8752014
The female urinary microbiome: a comparison of women with and without urgency urinary incontinence
MM Pearce, EE Hilt, AB Rosenfeld, MJ Zilliox, K Thomas-White, C Fok, ...
MBio 5 (4), 10.1128/mbio. 01283-14, 2014
6602014
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
J Elia, X Gai, HM Xie, JC Perin, E Geiger, JT Glessner, M D'arcy, ...
Molecular psychiatry 15 (6), 637-646, 2010
6432010
Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report
JF Arboleda-Velasquez, F Lopera, M O’Hare, S Delgado-Tirado, C Marino, ...
Nature medicine 25 (11), 1680-1683, 2019
4972019
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies
BJ Keating, S Tischfield, SS Murray, T Bhangale, TS Price, JT Glessner, ...
PloS one 3 (10), e3583, 2008
4542008
High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications
TH Shaikh, X Gai, JC Perin, JT Glessner, H Xie, K Murphy, R O'Hara, ...
Genome research 19 (9), 1682-1690, 2009
4372009
A GATA-1-regulated microRNA locus essential for erythropoiesis
LC Dore, JD Amigo, CO Dos Santos, Z Zhang, X Gai, JW Tobias, D Yu, ...
Proceedings of the National Academy of Sciences 105 (9), 3333-3338, 2008
4272008
The female urinary microbiome in urgency urinary incontinence
MM Pearce, MJ Zilliox, AB Rosenfeld, KJ Thomas-White, HE Richter, ...
American journal of obstetrics and gynecology 213 (3), 347. e1-347. e11, 2015
3002015
Incontinence medication response relates to the female urinary microbiota
KJ Thomas-White, EE Hilt, C Fok, MM Pearce, ER Mueller, S Kliethermes, ...
International urogynecology journal 27, 723-733, 2016
2832016
Duplication of 7q34 in pediatric low‐grade astrocytomas detected by high‐density single‐nucleotide polymorphism‐based genotype arrays results in a novel BRAF fusion gene
AJ Sievert, EM Jackson, X Gai, H Hakonarson, AR Judkins, AC Resnick, ...
Brain pathology 19 (3), 449-458, 2009
2772009
Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing
MB Consugar, D Navarro-Gomez, EM Place, KM Bujakowska, ME Sousa, ...
Genetics in Medicine 17 (4), 253-261, 2015
2572015
NMNAT1 mutations cause Leber congenital amaurosis
MJ Falk, Q Zhang, E Nakamaru-Ogiso, C Kannabiran, Z Fonseca-Kelly, ...
Nature genetics 44 (9), 1040-1045, 2012
2222012
Rare structural variation of synapse and neurotransmission genes in autism
X Gai, HM Xie, JC Perin, N Takahashi, K Murphy, AS Wenocur, M D'arcy, ...
Molecular psychiatry 17 (4), 402-411, 2012
2122012
Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive …
EM Jackson, AJ Sievert, X Gai, H Hakonarson, AR Judkins, L Tooke, ...
Clinical cancer research 15 (6), 1923-1930, 2009
2122009
Acute and chronic ophthalmic involvement in Stevens-Johnson syndrome/toxic epidermal necrolysis–a comprehensive review and guide to therapy. II. Ophthalmic disease
S Kohanim, S Palioura, HN Saeed, EK Akpek, G Amescua, S Basu, ...
The ocular surface 14 (2), 168-188, 2016
2032016
Targeting of the yeast Ty5 retrotransposon to silent chromatin is mediated by interactions between integrase and Sir4p
W Xie, X Gai, Y Zhu, DC Zappulla, R Sternglanz, DF Voytas
Molecular and cellular biology 21 (19), 6606-6614, 2001
1932001
Next-generation sequencing: the solution for high-resolution, unambiguous human leukocyte antigen typing
C Lind, D Ferriola, K Mackiewicz, S Heron, M Rogers, L Slavich, R Walker, ...
Human immunology 71 (10), 1033-1042, 2010
1832010
Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
KM Bujakowska, Q Zhang, AM Siemiatkowska, Q Liu, E Place, MJ Falk, ...
Human molecular genetics 24 (1), 230-242, 2015
1752015
A compilation of soybean ESTs: generation and analysis
R Shoemaker, P Keim, L Vodkin, E Retzel, SW Clifton, R Waterston, ...
Genome 45 (2), 329-338, 2002
1702002
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy
X Gai, D Ghezzi, MA Johnson, CA Biagosch, HE Shamseldin, TB Haack, ...
The American Journal of Human Genetics 93 (3), 482-495, 2013
1652013
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