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I. Iossifov · SciRah

Researcher profile · Semantic Scholar

I. Iossifov

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I. Iossifov — researcher profile on SciRah

h-index: 29
Works: 63
Citations: 9,447

Most-cited papers

The contribution of de novo coding mutations to autism spectrum disorder
I. Iossifov, B. O'Roak, Stephan J Sanders, M. Ronemus +43 more
2014Nature2,511 citations Open access
Semantic Scholar
De Novo Gene Disruptions in Children on the Autistic Spectrum
I. Iossifov, M. Ronemus, D. Levy, Zi-Hua Wang +31 more
2012Neuron1,468 citations Open access
Semantic Scholar
Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
D. Levy, M. Ronemus, B. Yamrom, Yoon-ha Lee +13 more
2011Neuron750 citations Open access
Semantic Scholar
De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects
Jason G. Homsy, S. Zaidi, Yu-Feng Shen, J. Ware +37 more
2015Science741 citations Open access
Semantic Scholar
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
S. R. Gilman, I. Iossifov, D. Levy, M. Ronemus +2 more
2011Neuron701 citations Open access
Semantic Scholar
The role of de novo mutations in the genetics of autism spectrum disorders
M. Ronemus, I. Iossifov, D. Levy, M. Wigler
2014Nature reviews genetics391 citations
Semantic Scholar
GeneWays: a system for extracting, analyzing, visualizing, and integrating molecular pathway data
A. Rzhetsky, I. Iossifov, T. Koike, M. Krauthammer +8 more
2004Journal of Biomedical Informatics292 citations Open access
Semantic Scholar
Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.
Tychele N. Turner, F. Hormozdiari, Michael H. Duyzend, S. Mcclymont +20 more
2016American Journal of Human Genetics274 citations Open access
Semantic Scholar
Increased Frequency of De Novo Copy Number Variations in Congenital Heart Disease by Integrative Analysis of SNP Array and Exome Sequence Data
J. Glessner, Alexander G. Bick, K. Ito, Jason G. Homsy +26 more
2014Circulation Research245 citations Open access
Semantic Scholar
Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk
S. Castel, Alejandra Cervera, P. Mohammadi, F. Aguet +6 more
2018Nature Genetics197 citations Open access
Semantic Scholar
Accurate detection of de novo and transmitted indels within exome-capture data using micro-assembly
Giuseppe Narzisi, Jason A. O'Rawe, I. Iossifov, Han Fang +6 more
2014Nature Methods187 citations Open access
Semantic Scholar
Reducing INDEL calling errors in whole genome and exome sequencing data
Han Fang, Yi-Yang Wu, Giuseppe Narzisi, Jason O'Rawe +6 more
2014Genome Medicine185 citations Open access
Semantic Scholar
Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder
R. Cheng, S. Juo, J. Loth, J. Nee +11 more
2006Molecular Psychiatry159 citations Open access
Semantic Scholar
Low load for disruptive mutations in autism genes and their biased transmission
I. Iossifov, D. Levy, Jeremy Allen, Kenny Q. Ye +4 more
2015Proceedings of the National Academy of Sciences of the United States of America157 citations Open access
Semantic Scholar
A comparative analysis of exome capture
Jennifer S. Parla, I. Iossifov, Ian Grabill, M. Spector +2 more
2011Genome Biology141 citations Open access
Semantic Scholar
Analysis of Drosophila Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer
Jiang Liu, M. Ghanim, Lei Xue, Christopher D. Brown +14 more
2009Science129 citations Open access
Semantic Scholar
Indel variant analysis of short-read sequencing data with Scalpel
Han Fang, Ewa A. Bergmann, K. Arora, V. Vacic +15 more
2015Nature Protocols124 citations Open access
Semantic Scholar
How many scientific papers should be retracted?
Murat Cokol, I. Iossifov, Raul Rodriguez-Esteban, A. Rzhetsky
2007EMBO Reports89 citations Open access
Semantic Scholar
Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network.
I. Iossifov, T. Zheng, M. Baron, T. Gilliam +1 more
2008Genome Research74 citations Open access
Semantic Scholar
Damaging de novo mutations diminish motor skills in children on the autism spectrum
A. Buja, N. Volfovsky, A. Krieger, C. Lord +3 more
2018Proceedings of the National Academy of Sciences of the United States of America63 citations Open access
Semantic Scholar
Emergent behavior of growing knowledge about molecular interactions
Murat Cokol, I. Iossifov, C. Weinreb, A. Rzhetsky
2005Nature Biotechnology63 citations
Semantic Scholar
Of truth and pathways: chasing bits of information through myriads of articles
M. Krauthammer, Pauline Kra, I. Iossifov, Shawn M. Gomez +4 more
2002Intelligent Systems in Molecular Biology61 citations Open access
Semantic Scholar
Microparadigms: chains of collective reasoning in publications about molecular interactions.
A. Rzhetsky, I. Iossifov, J. Loh, K. White
2006Proceedings of the National Academy of Sciences of the United States of America53 citations Open access
Semantic Scholar
Rates of contributory de novo mutation in high and low-risk autism families
Seungtai Yoon, Adriana Muñoz, B. Yamrom, Yoon-ha Lee +13 more
2021Communications Biology38 citations Open access
Semantic Scholar
Probabilistic inference of molecular networks from noisy data sources
I. Iossifov, M. Krauthammer, Carol Friedman, V. Hatzivassiloglou +3 more
2004Bioinform.38 citations
Semantic Scholar
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms
S. Jansen, I. M. van der Werf, A. Innes, A. Afenjar +47 more
2019European Journal of Human Genetics34 citations Open access
Semantic Scholar
Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction.
Xi Shi, Cong-Yi Lu, Alba Corman, Alexandria Nikish +6 more
2023American Journal of Human Genetics32 citations Open access
Semantic Scholar
Target-Independent Prediction of Drug Synergies Using Only Drug Lipophilicity
K. Yılancıoğlu, Zohar B. Weinstein, Cem Meydan, Azat Akhmetov +6 more
2014Journal of Chemical Information and Modeling31 citations Open access
Semantic Scholar
Imitating Manual Curation of Text-Mined Facts in Biomedicine
Raul Rodriguez-Esteban, I. Iossifov, A. Rzhetsky
2006PLoS Comput. Biol.30 citations Open access
Semantic Scholar
Mast-cell leukemia exome sequencing reveals a mutation in the IgE mast-cell receptor β chain and KIT V654A
M. Spector, I. Iossifov, A. Kritharis, C. He +3 more
2012Leukemia29 citations Open access
Semantic Scholar
Large-Scale Identification and Analysis of Suppressive Drug Interactions
Murat Cokol, Zohar B. Weinstein, K. Yılancıoğlu, M. Taşan +14 more
2014Chemistry and Biology28 citations Open access
Semantic Scholar
Figure mining for biomedical research
Raul Rodriguez-Esteban, I. Iossifov
2009Bioinform.21 citations Open access
Semantic Scholar
Looking at Cerebellar Malformations through Text-Mined Interactomes of Mice and Humans
I. Iossifov, Raul Rodriguez-Esteban, I. Mayzus, K. Millen +1 more
2009PLoS Comput. Biol.20 citations Open access
Semantic Scholar
MUMdex: MUM-based structural variation detection
Peter A. Andrews, I. Iossifov, J. Kendall, S. Marks +4 more
2016bioRxiv9 citations Open access
Semantic Scholar
Modified penetrance of coding variants by cis-regulatory variation shapes human traits
S. Castel, Alejandra Cervera, P. Mohammadi, F. Aguet +6 more
2017bioRxiv8 citations Open access
Semantic Scholar
De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects
Jason G. Homsy, S. Zaidi, Yu-Feng Shen, J. Ware +42 more
20168 citations
Semantic Scholar
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Jonah Einson, Dafni A. Glinos, E. Boerwinkle, P. Castaldi +29 more
2023Genetics7 citations Open access
Semantic Scholar
Measuring shared variants in cohorts of discordant siblings with applications to autism
Kenny Q. Ye, I. Iossifov, D. Levy, B. Yamrom +3 more
2017Proceedings of the National Academy of Sciences of the United States of America7 citations Open access
Semantic Scholar
Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline
Laura T. Jiménez-Barrón, Jason O'Rawe, Yi-Yang Wu, Margaret Yoon +3 more
2015bioRxiv6 citations Open access
Semantic Scholar
A race model for singular olfactory receptor expression
B. Kolterman, I. Iossifov, A. Koulakov
20126 citations
Semantic Scholar
Sharing parental genomes by siblings concordant or discordant for autism
Mathew Wroten, Seungtai Yoon, P. Andrews, B. Yamrom +7 more
2023Cell Genomics5 citations Open access
Semantic Scholar
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants
Jonah Einson, Dafni A. Glinos, E. Boerwinkle, P. Castaldi +29 more
2023bioRxiv5 citations Open access
Semantic Scholar
Reducing INDEL errors in whole-genome and exome sequencing
Han Fang, Giuseppe Narzisi, Jason O'Rawe, Yi-Yang Wu +5 more
20145 citations
Semantic Scholar
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
J. Glessner, Alexander G. Bick, K. Ito, Jason G. Homsy +26 more
5 citations
Semantic Scholar
A rule-based approach for automatically identifying gene and protein names in MEDLINE abstracts
Hong Yu, V. Hatzivassiloglou, Carol Friedman, I. Iossifov +1 more
20024 citations
Semantic Scholar
De novo indels within introns contribute to ASD incidence
Adriana Muñoz, B. Yamrom, Yoon-ha Lee, P. Andrews +7 more
2017bioRxiv3 citations Open access
Semantic Scholar
Most girls in my village are married before 18. Report on obstacles to education for girls North Shewa Amhara Ethiopia.
I. Iossifov, A. Wassie
20163 citations
Semantic Scholar
The Dutch press policy: A model to follow or a model to change.
I. Iossifov
20013 citations
Semantic Scholar
Analyzing the large and complex SFARI autism cohort data using the Genotypes and Phenotypes in Families (GPF) platform
Liubomir Chorbadjiev, Murat Cokol, Zohar Weinstein, Kevin Shi +14 more
2025Genome Research2 citations Open access
Semantic Scholar
N-terminal variant Asp14 Asn of the human p70 S6 Kinase 1 enhances translational signaling causing different effects in developing and mature neuronal cells.
Janani Priya Venkatasubramani, Prakash Subramanyam, Rakhi Pal, B. Reddy +5 more
2020Neurobiology of Learning and Memory2 citations
Semantic Scholar

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