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Yulia Mostovoy
Yulia Mostovoy
Staff Scientist, Mass General Hospital and Broad Institute
Verified email at broadinstitute.org
Title
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Cited by
Year
A hybrid approach for de novo human genome sequence assembly and phasing
Y Mostovoy, M Levy-Sakin, J Lam, ET Lam, AR Hastie, P Marks, J Lee, ...
Nature methods 13 (7), 587-590, 2016
2512016
Genome maps across 26 human populations reveal population-specific patterns of structural variation
M Levy-Sakin, S Pastor, Y Mostovoy, L Li, AKY Leung, J McCaffrey, ...
Nature communications 10 (1), 1025, 2019
1502019
Genome-wide structural variation detection by genome mapping on nanochannel arrays
ACY Mak, YYY Lai, ET Lam, TP Kwok, AKY Leung, A Poon, Y Mostovoy, ...
Genetics 202 (1), 351-362, 2016
1482016
Polygenic and directional regulatory evolution across pathways in Saccharomyces
JH Bullard, Y Mostovoy, S Dudoit, RB Brem
Proceedings of the National Academy of Sciences 107 (11), 5058-5063, 2010
1122010
Comparative genome analysis of programmed DNA elimination in nematodes
J Wang, S Gao, Y Mostovoy, Y Kang, M Zagoskin, Y Sun, B Zhang, ...
Genome research 27 (12), 2001-2014, 2017
1042017
Genome of the Komodo dragon reveals adaptations in the cardiovascular and chemosensory systems of monitor lizards
AL Lind, YYY Lai, Y Mostovoy, AK Holloway, A Iannucci, ACY Mak, ...
Nature ecology & evolution 3 (8), 1241-1252, 2019
672019
Mutant neuropeptide S receptor reduces sleep duration with preserved memory consolidation
L Xing, G Shi, Y Mostovoy, NW Gentry, Z Fan, TB McMahon, PY Kwok, ...
Science translational medicine 11 (514), eaax2014, 2019
562019
Evaluating the quality of the 1000 genomes project data
S Belsare, M Levy-Sakin, Y Mostovoy, S Durinck, S Chaudhuri, M Xiao, ...
BMC genomics 20, 1-14, 2019
542019
The 22q11 low copy repeats are characterized by unprecedented size and structural variability
W Demaerel, Y Mostovoy, F Yilmaz, L Vervoort, S Pastor, MS Hestand, ...
Genome research 29 (9), 1389-1401, 2019
492019
Inferring evolutionary histories of pathway regulation from transcriptional profiling data
JG Schraiber, Y Mostovoy, TY Hsu, RB Brem
PLoS computational biology 9 (10), e1003255, 2013
412013
Mutations in metabotropic glutamate receptor 1 contribute to natural short sleep trait
G Shi, C Yin, Z Fan, L Xing, Y Mostovoy, PY Kwok, LH Ashbrook, ...
Current Biology 31 (1), 13-24. e4, 2021
312021
Divergence of iron metabolism in wild Malaysian yeast
HN Lee, Y Mostovoy, TY Hsu, AH Chang, RB Brem
G3: Genes, Genomes, Genetics 3 (12), 2187-2194, 2013
182013
Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation
Y Mostovoy, F Yilmaz, SK Chow, C Chu, C Lin, EA Geiger, NJL Meeks, ...
Genetics 217 (2), iyaa038, 2021
172021
The driver of extreme human-specific Olduvai repeat expansion remains highly active in the human genome
IE Heft, Y Mostovoy, M Levy-Sakin, W Ma, AJ Stevens, S Pastor, ...
Genetics 214 (1), 179-191, 2020
162020
A high-resolution, chromosome-assigned Komodo dragon genome reveals adaptations in the cardiovascular, muscular, and chemosensory systems of monitor lizards
AL Lind, YYY Lai, Y Mostovoy, AK Holloway, A Iannucci, ACY Mak, ...
bioRxiv, 551978, 2019
62019
The role of transcription factors at antisense-expressing gene pairs in yeast
Y Mostovoy, A Thiemicke, TY Hsu, RB Brem
Genome biology and evolution 8 (6), 1748-1761, 2016
62016
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing
F Yilmaz, U Gurusamy, TJ Mosley, P Hallast, K Kim, Y Mostovoy, ...
Genome medicine 15 (1), 35, 2023
32023
Multi-modal investigation of the schizophrenia-associated 3q29 genomic interval reveals global genetic diversity with unique haplotypes and segments that increase the risk for …
F Yilmaz, U Gurusamy, TJ Mosley, Y Mostovoy, TH Shaikh, ME Zwick, ...
medRxiv, 2021.11. 10.21266197, 2021
32021
Regulation and function of antisense transcription in Saccharomyces yeast
Y Mostovoy
University of California, Berkeley, 2014
32014
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease
G Lemire, A Sanchis-Juan, K Russell, S Baxter, KR Chao, M Singer-Berk, ...
medRxiv, 2023
12023
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