Publications

All publications, Patents

Select publications

Fang W, Bell CM, Sapirstein A, Asami S, Leeper K, Zack DJ, Ji H†, Kalhor R† (2022). Quantitative fate mapping: A general framework for analyzing progenitor state dynamics via retrospective lineage barcoding. Cell. 185(24):4604-4620.e32 (bioRxiv, PubMed, PDF)

Leeper K, Kalhor K, Vernet A, Graveline A, Church GM, Mali P, Kalhor R† (2021). Lineage barcoding in mice with homing CRISPR. Nature Protocols. 16(4):2088-2108 (PubMed, PDF)

Lee HH＊, Kalhor R＊, Goela N＊, Bolot J, Church GM (2019). Terminator-free template-independent enzymatic DNA synthesis for digital information storage. Nature Communications. 10(1):2383 (bioRxiv, PubMed, PDF)

Kalhor R†, Kalhor K, Mejia L, Leeper K, Graveline A, Mali P, Church GM (2018). Developmental barcoding of whole mouse via homing CRISPR. Science. 361(6405):eaat9804 (bioRxiv, PubMed, PDF)

Kalhor R, Mali P, Church, GM (2017). Rapidly evolving homing CRISPR barcodes. Nature Methods. 14(2):195-200 (bioRxiv, PubMed, PDF)

Kalhor R, Tjong H, Jayathilaka N, Alber F, Chen L (2012). Genome architectures revealed by tethered chromosome conformation capture and population-based modeling. Nature Biotechnology. 30(1):90-8 (PubMed, PDF, Cover Story)

All publications

Bold: Kalhor Lab members and associates ＊: Equal contribution †: Corresponding author

  1. Dekker J, Alber F, Aufmkolk S, Beliveau BJ, Bruneau BG, Belmont AS, Bintu L, Boettiger A, Calandrelli R, Disteche CM, Gilbert DM, Gregor T, Hansen AS, Huang B, Huangfu D, Kalhor R, Leslie CS, Li W, Li Y, Ma J, Noble WS, Park PJ, Phillips-Cremins JE, Pollard KS, Rafelski SM, Ren B, Ruan Y, Shav-Tal Y, Shen Y, Shendure J, Shu X, Strambio-De-Castillia C, Vertii A, Zhang H, Zhong S (2023). Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project. Molecular Cell. 3;83(15):2624-2640 (PubMed, PDF)
  2. Fang W, Bell CM, Sapirstein A, Asami S, Leeper K, Zack DJ, Ji H†, Kalhor R† (2022). Quantitative fate mapping: A general framework for analyzing progenitor state dynamics via retrospective lineage barcoding. Cell. 185(24):4604-4620.e32 (bioRxiv, PubMed, PDF)
  3. Zou RS＊, Marin-Gonzalez A＊, Liu Y, Liu HB, Shen L, Dveirin RK, Luo JXJ, Kalhor R, Ha T (2022). Massively parallel genomic perturbations with multi-target CRISPR interrogates Cas9 activity and DNA repair at endogenous sites. Nature Cell Biology. 24(9):1433-1444 (bioRxiv, PubMed, PDF)
  4. Leeper K, Kalhor K, Vernet A, Graveline A, Church GM, Mali P, Kalhor R† (2021). Lineage barcoding in mice with homing CRISPR. Nature Protocols. 16(4):2088-2108 (PubMed, PDF)
  5. Bhan N, Callisto A, Strutz J, Glaser J, Kalhor R, Boyden ES, Church G, Kording K, Tyo KEJ (2021). Recording Temporal Signals with Minutes Resolution Using Enzymatic DNA Synthesis. Journal of American Chemical Society. 143(40):16630-16640 (bioRxiv, PubMed, PDF)
  6. Lee HH＊, Kalhor R＊, Goela N＊, Bolot J, Church GM (2019). Terminator-free template-independent enzymatic DNA synthesis for digital information storage. Nature Communications. 10(1):2383 (bioRxiv, PubMed, PDF)
  7. Kalhor R†, Kalhor K, Mejia L, Leeper K, Graveline A, Mali P, Church GM (2018). Developmental barcoding of whole mouse via homing CRISPR. Science. 361(6405):eaat9804 (bioRxiv, PubMed, PDF)
  8. Ostrow AZ, Kalhor R, Gan Y, Villwock SK, Linke C, Barberis M, Chen L, Aparicio OM (2017). Conserved forkhead dimerization motif controls DNA replication timing and spatial organization of chromosomes in S. cerevisiae. Proc Natl Acad Sci U S A. 114(12):E2411-E2419 (PubMed, PDF)
  9. Kalhor R, Mali P, Church, GM (2017). Rapidly evolving homing CRISPR barcodes. Nature Methods. 14(2):195-200 (bioRxiv, PubMed, PDF)
  10. Tjong H, Li W, Kalhor R, Dai C, Hao S, Gong K, Zhou Y, Li H, Zhou XJ, Le Gros MA, Larabell CA, Chen L, Alber F (2016). Population-based 3D genome structure analysis reveals driving forces in spatial genome organization. Proc Natl Acad Sci U S A. 113(12):E1663-72 (PubMed, PDF)
  11. Lee JH, Daugharthy ER, Scheiman J, Kalhor R, Ferrante TC, Terry R, Turczyk BM, Yang JL, Lee HS, Aach J, Zhang K, Church GM (2015). Fluorescent in situ sequencing (FISSEQ) of RNA for gene expression profiling in intact cells and tissues. Nature Protocols. 10(3):442-58 (PubMed, PDF)
  12. Marblestone AH, Daugharthy ER, Kalhor R, Peikon ID, Kebschull JM, Shipman SL, Mishchenko Y, Lee JH, Kording KP, Boyden ES, Zador AM, Church GM (2014) Rosetta brains: A strategy for molecularly-annotated connectomics. arXiv:1404.5103 (PDF)
  13. Lee JH＊, Daugharthy ER＊, Scheiman J, Kalhor R, Yang JL, Ferrante TC, Terry R, Jeanty SS, Li C, Amamoto R, Peters DT, Turczyk BM, Marblestone AH, Inverso SA, Bernard A, Mali P, Rios X, Aach J, Church GM (2014). Highly multiplexed subcellular RNA sequencing in situ. Science. 343(6177):1360-3 (PubMed, PDF)
  14. Marblestone AH, Daugharthy ER, Kalhor R, Peikon ID, Kebschull JM, Shipman, SL, Mishchenko Y, Lee Jehyuk, Dalrymple DA, Zamft BM, Kording KP, Boyden ES, Zador AM, Church GM (2013). Conneconomics: The Economics of Large-Scale Neural Connectomics. bioRxiv, 001214 (PDF)
  15. Marblestone AH, Zamft BM, Maguire YG, Shapiro MG, Cybulski TR, Glaser JI, Amodei D, Stranges PB, Kalhor R, Dalrymple DA, Seo D, Alon E, Maharbiz MM, Carmena JM, Rabaey JM, Boyden ES, Church GM, Kording KP (2013). Physical principles for scalable neural recording. Frontiers in Computational Neuroscience. 7:137 (arXiv, PubMed, PDF)
  16. Kalhor R, Tjong H, Jayathilaka N, Alber F, Chen L (2012). Genome architectures revealed by tethered chromosome conformation capture and population-based modeling. Nature Biotechnology. 30(1):90-8 (PubMed, PDF, Cover Story)
  17. Suri F＊, Kalhor R＊, Zargar SJ, Nilforooshan N, Yazdani S, Nezari H, Paylakhi SH, Narooie-Nejhad M, Bayat B, Sedaghati T, Ahmadian A, Elahi E (2008). Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol. Molecular Vision. 14:2349-56 (PubMed, PDF)
  18. Shojaee S, Sina F, Banihosseini SS, Kazemi MH, Kalhor R, Shahidi GA, Fakhrai-Rad H, Ronaghi M, Elahi E (2008). Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays. American Journal of Human Genetics. 82(6):1375-84 (PubMed, PDF)
  19. Bates DL, Barthel KK, Wu Y, Kalhor R, Stroud JC, Giffin MJ, Chen L (2008). Crystal structure of NFAT bound to the HIV-1 LTR tandem kappaB enhancer element. Structure. 16(5):684-94 (PubMed, PDF)
  20. Alavi A, Elahi E, Tehrani MH, Amoli FA, Javadi MA, Rafati N, Chiani M, Banihosseini SS, Bayat B, Kalhor R, Amini SS (2007). Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients. Invest Ophthalmol Vis Sci. 48(10):4490-7 (PubMed, PDF)
  21. Elahi E, Kalhor R, Banihosseini SS, Torabi N, Pour-Jafari H, Houshmand M, Amini SS, Ramezani A, Loeys B (2006). Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype. J Invest Dermatol. 126(7):1506-9 (PubMed, PDF)

Patents

Inventors (priority date, publication date) Title (Assignee)

  1. Kalhor R, Lee HH, Church GM (2017, 2020) Enzymatic DNA synthesis using the terminal transferase activity of template-dependent DNA polymerases (Harvard University)
  2. Lee HH, Kalhor R, Church GM (2017, 2019) Methods of encoding and high-throughput decoding of information stored in DNA (Harvard University)
  3. Church GM, Kalhor R, Mali PG (2016, 2019) Engineered guide RNA sequences for in situ detection and sequencing (Harvard University)
  4. Kalhor R, Fernandez Juarez J, Lee HH, Church GM (2016, 2019) Frequency-based modulation of diverse species in a nucleic acid library (Harvard University)
  5. Church GM, Kalhor R, Mali PG (2016, 2019) Self-targeting guide RNAs in CRISPR system (Harvard University)
  6. Kalhor R, Lee HH, Church GM (2016, 2019). Enzymatic nucleic acid synthesis (Harvard University)
  7. Lee HH, Kalhor R, Church GM (2016, 2017) Method of secure communication via nucleotide polymers (Harvard University)
  8. Lee HH, Church GM, Kalhor R (2016, 2017) Enzymatic nucleic acid synthesis (Harvard University)
  9. Wu CT, Kalhor R (2013, 2014) Methods of hybridizing probes to genomic DNA (Harvard University)
  10. Steemers FJ, Gunderson K, Royce T, Pignatelli N, Goryshin IY, Caruccio N, Maffitt M, Jendrisak J, Amini S, Kaper F, Turk C, Kalhor R (2010, 2013) Linking sequence reads using paired code tags (Illumina Inc)
  11. Chen L, Kalhor R (2010, 2011) Tethered conformation capture (University of Southern California)
  12. Chen L, Kalhor R (2008, 2010) Genome-wide chromosome conformation capture (University of Southern California)