Ronemus, Michael
Cold Spring Harbor Laboratory
7 papers on CoChatORCID 0000-0003-0237-3540
Most cited papers
- Verified
The contribution of de novo coding mutations to autism spectrum disorder
Iossifov, I., O’Roak, B. J., Sanders, S. J., Ronemus, M., Krumm, N., Levy, D., Stessman, H. A., Witherspoon, K. T., Vives, L., Patterson, K. E., et al. (2014) · Nature
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,585
- Verified
De Novo Gene Disruptions in Children on the Autistic Spectrum
Iossifov, I., Ronemus, M., Levy, D., Wang, Z., Hakker, I., Rosenbaum, J., Yamrom, B., Lee, Y.-H., Narzisi, G., Leotta, A., et al. (2012) · Neuron
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research
Cited by 1,446
- Verified
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
Levy, D., Ronemus, M., Yamrom, B., Lee, Y.-H., Leotta, A., Kendall, J., Marks, S., Lakshmi, B., Pai, D., Ye, K., et al. (2011) · Neuron
Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research
Cited by 712
- Verified
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
Gilman, S. R., Iossifov, I., Levy, D., Ronemus, M., Wigler, M., & Vitkup, D. (2011) · Neuron
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 701
- Verified
The role of de novo mutations in the genetics of autism spectrum disorders
Ronemus, M., Iossifov, I., Levy, D., & Wigler, M. (2014) · Nature Reviews Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 390
- Verified
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data
Glessner, J. T., Bick, A. G., Ito, K., Homsy, J. G., Rodriguez-Murillo, L., Fromer, M., Mazaika, E., Vardarajan, B., Italia, M., Leipzig, J., et al. (2014) · Circulation Research
Genomic variations and chromosomal abnormalitiesCongenital heart defects research
Cited by 268
- Verified
Low load for disruptive mutations in autism genes and their biased transmission
Iossifov, I., Levy, D., Allen, J., Ye, K., Ronemus, M., Lee, Y.-H., Yamrom, B., & Wigler, M. (2015) · Proceedings of the National Academy of Sciences
Autism Spectrum Disorder ResearchGenomics and Rare Diseases
Cited by 156
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