Iman Hajirasouliha
Iman Hajirasouliha
Assistant Professor, Weill Cornell Medicine of Cornell University, New York City
Verified email at - Homepage
Cited by
Cited by
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
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
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
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), 2013
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini, GA McVean, P Donnelly, G Lunter, JL Marchini, ...
Nature communications 5, 3934, 2014
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
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
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
Fast and scalable inference of multi-sample cancer lineages
V Popic, R Salari, I Hajirasouliha, D Kashef-Haghighi, RB West, ...
Genome biology 16 (1), 91, 2015
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
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
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
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
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
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
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
Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer
C Wu, AW Wyatt, AV Lapuk, A McPherson, BJ McConeghy, RH Bell, ...
The Journal of Pathology, 2012
MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels
T Marschall, I Hajirasouliha, A Schönhuth
Bioinformatics 29 (24), 3143-3150, 2013
Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data
A McPherson, C Wu, I Hajirasouliha, F Hormozdiari, F Hach, A Lapuk, ...
Bioinformatics 27 (11), 1481, 2011
The system can't perform the operation now. Try again later.
Articles 1–20