Pe’er, Itsik
Columbia University
7 papers on CoChatORCID 0000-0002-6128-7231
Most cited papers
- Verified
De novo mutations in histone-modifying genes in congenital heart disease
Zaidi, S., Choi, M., Wakimoto, H., Ma, L., Jiang, J., Overton, J. D., Romano-Adesman, A., Bjornson, R. D., Breitbart, R. E., Brown, K. K., et al. (2013) · Nature
Congenital heart defects researchGenomics and Rare Diseases
Cited by 934
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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N.-Y., Chuang, L.-S., Carmi, S., Villaverde, N., Li, X., et al. (2018) · Science Translational Medicine
Parkinson's Disease Mechanisms and TreatmentsInflammatory Bowel Disease
Cited by 384
- Verified
Identity inference of genomic data using long-range familial searches
Erlich, Y., Shor, T., Pe’er, I., & Carmi, S. (2018) · Science
Forensic and Genetic ResearchGenetic Associations and Epidemiology
Cited by 367
- Verified
Length Distributions of Identity by Descent Reveal Fine-Scale Demographic History
Palamara, P. F., Lencz, T., Darvasi, A., & Pe’er, I. (2012) · The American Journal of Human Genetics
Forensic and Genetic ResearchGenetic diversity and population structure
Cited by 247
- Verified
SEACells infers transcriptional and epigenomic cellular states from single-cell genomics data
Persad, S., Choo, Z.-N., Dien, C., Sohail, N., Masilionis, I., Chaligné, R., Nawy, T., Brown, C. C., Sharma, R., Pe’er, I., et al. (2023) · Nature Biotechnology
Single-cell and spatial transcriptomicsGene Regulatory Network Analysis
Cited by 222
- Verified
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
Carmi, S., Hui, K. Y., Kochav, E., Liu, X., Xue, J., Grady, F., Guha, S., Upadhyay, K., Ben-Avraham, D., Mukherjee, S., et al. (2014) · Nature Communications
Forensic and Genetic ResearchGenetic Associations and Epidemiology
Cited by 188
- Verified
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder
Lencz, T., Guha, S., Liu, C., Rosenfeld, J., Mukherjee, S., DeRosse, P., John, M., Cheng, L., Zhang, C., Badner, J. A., et al. (2013) · Nature Communications
Schizophrenia research and treatmentGenetic Associations and Epidemiology
Cited by 111
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