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Iman Hajirasouliha
Iman Hajirasouliha
Associate Professor, Weill Cornell Medicine of Cornell University, New York City
Verified email at med.cornell.edu - Homepage
Title
Cited by
Cited by
Year
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
80542010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
25222012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
11682011
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
6332011
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
3962013
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 1-9, 2014
3572014
Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery
F Hormozdiari, I Hajirasouliha, P Dao, F Hach, D Yorukoglu, C Alkan, ...
Bioinformatics 26 (12), i350-i357, 2010
2632010
Deep convolutional neural networks enable discrimination of heterogeneous digital pathology images
P Khosravi, E Kazemi, M Imielinski, O Elemento, I Hajirasouliha
EBioMedicine 27, 317-328, 2018
2212018
Biomolecular network motif counting and discovery by color coding
N Alon, P Dao, I Hajirasouliha, F Hormozdiari, SC Sahinalp
Bioinformatics 24 (13), i241-i249, 2008
2032008
Fast and scalable inference of multi-sample cancer lineages
V Popic, R Salari, I Hajirasouliha, D Kashef-Haghighi, RB West, ...
Genome biology 16 (1), 1-17, 2015
1902015
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer
AV Lapuk, C Wu, AW Wyatt, A McPherson, BJ McConeghy, S Brahmbhatt, ...
The Journal of pathology 227 (3), 286-297, 2012
1852012
A robust benchmark for detection of germline large deletions and insertions
JM Zook, NF Hansen, ND Olson, L Chapman, JC Mullikin, C Xiao, ...
Nature biotechnology 38 (11), 1347-1355, 2020
180*2020
Deep learning enables robust assessment and selection of human blastocysts after in vitro fertilization
P Khosravi, E Kazemi, Q Zhan, JE Malmsten, M Toschi, P Zisimopoulos, ...
NPJ digital medicine 2 (1), 1-9, 2019
1792019
Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions
D Butler, C Mozsary, C Meydan, J Foox, J Rosiene, A Shaiber, D Danko, ...
Nature communications 12 (1), 1-17, 2021
163*2021
Detection and characterization of novel sequence insertions using paired-end next-generation sequencing
I Hajirasouliha, F Hormozdiari, C Alkan, JM Kidd, I Birol, EE Eichler, ...
Bioinformatics 26 (10), 1277-1283, 2010
1522010
A combinatorial approach for analyzing intra-tumor heterogeneity from high-throughput sequencing data
I Hajirasouliha, A Mahmoody, BJ Raphael
Bioinformatics 30 (12), i78-i86, 2014
1182014
Alu repeat discovery and characterization within human genomes
F Hormozdiari, C Alkan, M Ventura, I Hajirasouliha, M Malig, F Hach, ...
Genome Research 21 (6), 840-849, 2011
1132011
Simultaneous structural variation discovery among multiple paired-end sequenced genomes
F Hormozdiari, I Hajirasouliha, A McPherson, EE Eichler, SC Sahinalp
Genome research 21 (12), 2203-2212, 2011
1022011
Breast cancer histopathological image classification: a deep learning approach
M Jannesari, M Habibzadeh, HR Aboulkheyr, P Khosravi, O Elemento, ...
2018 IEEE International Conference on Bioinformatics and Biomedicine (BIBM …, 2018
100*2018
Characterization of structural variants with single molecule and hybrid sequencing approaches
A Ritz, A Bashir, S Sindi, D Hsu, I Hajirasouliha, BJ Raphael
Bioinformatics 30 (24), 3458-3466, 2014
842014
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