Skip to Main Content

Author Details

Fereydoun Hormozdiari
University of California davis
2007
53
30
PMIDPaper TitleJournal TitlePublished Year
36550274SVDSS: structural variation discovery in hard-to-call genomic regions using sample-specific strings from accurate long reads.Nat Methods2023
35596027Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation.J Autism Dev Disord2023
36625266Dr.Nod: computational framework for discovery of regulatory non-coding drivers in tissue-matched distal regulatory elements.Nucleic Acids Res2023
36699383MAGI-MS: multiple seed-centric module discovery.Bioinform Adv2022
33503255Nebula: ultra-efficient mapping-free structural variant genotyper.Nucleic Acids Res2021
36700094Comparative genome analysis using sample-specific string detection in accurate long reads.Bioinform Adv2021
31584621Meltos: multi-sample tumor phylogeny reconstruction for structural variants.Bioinformatics2020
30559488Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.Nat Genet2019
31653223Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.Genome Med2019
31492842Functional disease architectures reveal unique biological role of transposable elements.Nat Commun2019
31377530Kevlar: A Mapping-Free Framework for Accurate Discovery of De Novo Variants.iScience2019
30898144TAD fusion score: discovery and ranking the contribution of deletions to genome structure.Genome Biol2019
30833765How bioinformatics and open data can boost basic science in countries and universities with limited resources.Nat Biotechnol2019
30937433Discovery of tandem and interspersed segmental duplications using high-throughput sequencing.Bioinformatics2019
29618373Genetic variation associated with increased insecticide resistance in the malaria mosquito, Anopheles coluzzii.Parasit Vectors2018
29880660High-resolution comparative analysis of great ape genomes.Science2018
30297454Combinatorial Approach for Complex Disorder Prediction: Case Study of Neurodevelopmental Disorders.Genetics2018
28583483Toolkit for automated and rapid discovery of structural variants.Methods2017
28191889Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.Nat Genet2017
28965761Genomic Patterns of De Novo Mutation in Simplex Autism.Cell2017
26749308Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.Am J Hum Genet2016
27708267A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.Nat Commun2016
25378250The discovery of integrated gene networks for autism and related disorders.Genome Res2015
26249230Global diversity, population stratification, and selection of human copy-number variation.Science2015
26432246An integrated map of structural variation in 2,504 human genomes.Nature2015
25883321Characteristics of de novo structural changes in the human genome.Genome Res2015
25383537Resolving the complexity of the human genome using single-molecule sequencing.Nature2015
25116239Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma.PLoS One2014
23721540The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild.BMC Genomics2013
23884656Rates and patterns of great ape retrotransposition.Proc Natl Acad Sci U S A2013
23823723Great ape genetic diversity and population history.Nature2013
22294438Integrated genome and transcriptome sequencing identifies a novel form of hybrid and aggressive prostate cancer.J Pathol2012
22553170From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.J Pathol2012
21131385Alu repeat discovery and characterization within human genomes.Genome Res2011
22048523Simultaneous structural variation discovery among multiple paired-end sequenced genomes.Genome Res2011
21625565deFuse: an algorithm for gene fusion discovery in tumor RNA-Seq data.PLoS Comput Biol2011
21685127Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee.Genome Res2011
21293372Mapping copy number variation by population-scale genome sequencing.Nature2011
21478487Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.Bioinformatics2011
20078394Towards improved assessment of functional similarity in large-scale screens: a study on indel length.J Comput Biol2010
20500021Protein-protein interaction network evaluation for identifying potential drug targets.J Comput Biol2010
20529927Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery.Bioinformatics2010
20676076mrsFAST: a cache-oblivious algorithm for short-read mapping.Nat Methods2010
20385726Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.Bioinformatics2010
19213135Dense graphlet statistics of protein interaction and random networks.Pac Symp Biocomput2009
19718026Personalized copy number and segmental duplication maps using next-generation sequencing.Nat Genet2009
19483690MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions.Nat Methods2009
19447966Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes.Genome Res2009
19193143The effect of insertions and deletions on wirings in protein-protein interaction networks: a large-scale study.J Comput Biol2009
18586721Biomolecular network motif counting and discovery by color coding.Bioinformatics2008
  • 1 - 50 of 53

Recommended Authors

Baylor College of Medicine
Career Start Year 2012
Number of shared co-authors 29
Broad Institute of MIT and Harvard
Career Start Year 2012
Number of shared co-authors 7
Boulder and BioFrontiers Institute, University of Colorado Boulder
Career Start Year 2011
Number of shared co-authors 2
Berlin Institute of Health
Career Start Year 2011
Number of shared co-authors 0
Berlin Institute of Health of Health at Charite - Universitatsmedizin Berlin
Career Start Year 2010
Number of shared co-authors 2
Stanford School of Medicine
Career Start Year 2010
Number of shared co-authors 29
The Hospital for Sick Children
Career Start Year 2010
Number of shared co-authors 10
Charite Universitatsmedizin Berlin
Career Start Year 2010
Number of shared co-authors 0
Radboud University Medical Center
Career Start Year 2009
Number of shared co-authors 11
Center for Public Health Genomics, University of Virginia
Career Start Year 2008
Number of shared co-authors 24
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year 2008
Number of shared co-authors 14
Institute of Computer Science, Warsaw University of Technology
Career Start Year 2007
Number of shared co-authors 14
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 12
University of Utah
Career Start Year 2007
Number of shared co-authors 9
Institute of Medical Genetics and Applied Genomics, University of Tubingen
Career Start Year 2006
Number of shared co-authors 8
Stanley Institute for Cognitive Genomics
Career Start Year 2005
Number of shared co-authors 8
European Bioinformatics Institute
Career Start Year 2005
Number of shared co-authors 13
Institute for Genomic Medicine, Nationwide Children's Hospital
Career Start Year 2005
Number of shared co-authors 36
University of California San Diego
Career Start Year 2004
Number of shared co-authors 4
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 30
The Peter Doherty Institute for Infection and Immunity, The University of Melbourne
Career Start Year 2003
Number of shared co-authors 17
Columbia University
Career Start Year 2002
Number of shared co-authors 17
Center for Molecular Medicine, University Medical Center Utrecht
Career Start Year 2001
Number of shared co-authors 4
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 11
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2000
Number of shared co-authors 40
Broad Institute of MIT and Harvard
Career Start Year 1999
Number of shared co-authors 16
Harvard Medical School
Career Start Year 1997
Number of shared co-authors 40
University of Utah
Career Start Year 1994
Number of shared co-authors 20
Rutgers University-New Brunswick, Rutgers University
Career Start Year 1989
Number of shared co-authors 1
University of Cambridge
Career Start Year 1964
Number of shared co-authors 45

Collaborators

University of Washington
Co-authored papers 24
National Cancer Institute, National Institutes of Health
Co-authored papers 18
Bilkent University
Co-authored papers 15
Institute for Computational Biomedicine
Co-authored papers 11
University of Washington School of Medicine
Co-authored papers 7
University of Michigan Medical School ann arbor
Co-authored papers 6
University of British Columbia
Co-authored papers 6
University of California san francisco
Co-authored papers 5
Memorial Sloan Kettering Cancer Center
Co-authored papers 5
Co-authored papers 4
Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University
Co-authored papers 3
The Ohio State University
Co-authored papers 3
University of Southern California
Co-authored papers 3
University of Washington
Co-authored papers 3
Clemson University
Co-authored papers 3
Co-authored papers 3
Barcelonabeta Brain Research Center (BBRC), Pasqual Maragall Foundation
Co-authored papers 3
Louisiana State University
Co-authored papers 3
University of British Columbia
Co-authored papers 3
University of British Columbia
Co-authored papers 3
University of British Columbia
Co-authored papers 3
Contextual Genomics Inc.
Co-authored papers 3
Co-authored papers 3
University of British Columbia
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
University of Texas MD Anderson Cancer Center
Co-authored papers 2
University of Michigan Medical School ann arbor
Co-authored papers 2
Yale University
Co-authored papers 2