Recent Work
Parent: Department of Mathematics
eScholarship stats: Breakdown by Item for April through July, 2026
| Item | Title | Total requests | Download | View-only | %Dnld |
|---|---|---|---|---|---|
| 9sg0d7mb | On Stable Khovanov Homology of Torus Knots | 408 | 242 | 166 | 59.3% |
| 34f3038j | On superintegral Kleinian sphere packings, bugs, and arithmetic groups | 353 | 309 | 44 | 87.5% |
| 992735rb | Hilbert schemes and y–ification of Khovanov–Rozansky homology | 288 | 60 | 228 | 20.8% |
| 88d39661 | Derived Traces of Soergel Categories | 250 | 102 | 148 | 40.8% |
| 0229d5mp | Unexpected Stein fillings, rational surface singularities and plane curve arrangements | 238 | 156 | 82 | 65.5% |
| 6997k34s | The equivariant Euler characteristic of moduli spaces of curves | 223 | 57 | 166 | 25.6% |
| 0zh8n5mh | Quadruply-graded colored homology of knots | 211 | 125 | 86 | 59.2% |
| 4sn2p0kg | A multiscale predictive digital twin for neurocardiac modulation | 205 | 82 | 123 | 40.0% |
| 2db2p1k7 | The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data | 200 | 63 | 137 | 31.5% |
| 2rp5d5q9 | Effective bounds for Vinberg’s algorithm for arithmetic hyperbolic lattices | 189 | 98 | 91 | 51.9% |
| 7961x6km | Surgery on links of linking number zero and the Heegaard Floer $d$-invariant | 188 | 82 | 106 | 43.6% |
| 9vq7313z | Hilbert schemes and $y$-ification of Khovanov-Rozansky homology | 188 | 85 | 103 | 45.2% |
| 5cp2c1bd | Common genetic variants influence human subcortical brain structures | 187 | 61 | 126 | 32.6% |
| 7bg31125 | Complexity of Finite Semigroups: History and Decidability | 186 | 126 | 60 | 67.7% |
| 4638g7zb | Derived traces of Soergel categories | 181 | 60 | 121 | 33.1% |
| 0481k543 | Use of machine-learning algorithms to aid in the early detection of leptospirosis in dogs | 180 | 84 | 96 | 46.7% |
| 7hf1p79d | Tree polynomials identify a link between co-transcriptional R-loops and nascent RNA folding | 180 | 99 | 81 | 55.0% |
| 4w18x7tz | Novel genetic loci associated with hippocampal volume | 175 | 51 | 124 | 29.1% |
| 5pg5p7j7 | Lipschitz decompositions of domains with bilaterally flat boundaries | 175 | 60 | 115 | 34.3% |
| 0vz4t8b4 | Interplay between DNA sequence and negative superhelicity drives R-loop structures | 173 | 91 | 82 | 52.6% |
| 01c0p4jn | Editor’s Note: Spontaneous SU2( C ) symmetry breaking in the ground states of quantum spin chain [J. Math. Phys. 59, 111701 (2018)] | 171 | 51 | 120 | 29.8% |
| 6zw6x3vt | Dynamics of adrenergic signaling in cardiac myocytes and implications for pharmacological treatment | 170 | 64 | 106 | 37.6% |
| 1f61q9zd | Flag Hilbert schemes, colored projectors and Khovanov-Rozansky homology | 169 | 63 | 106 | 37.3% |
| 1888k21h | A Note on Cumulant Technique in Random Matrix Theory | 167 | 94 | 73 | 56.3% |
| 4v83d64t | On Stable -Homology of Torus Knots | 167 | 80 | 87 | 47.9% |
| 74n254xw | Evaluations of annular Khovanov--Rozansky homology | 165 | 49 | 116 | 29.7% |
| 0nf7j6sq | Linear Algebra as an Introduction to Abstract Mathematics | 164 | 88 | 76 | 53.7% |
| 8240v1qf | A class of two-dimensional AKLT models with a gap | 164 | 69 | 95 | 42.1% |
| 57r3c1m9 | Affine Springer Fibers and Generalized Haiman Ideals (with an Appendix by Eugene Gorsky and Joshua P. Turner) | 160 | 62 | 98 | 38.8% |
| 17b7g47x | A Large-Scale Circuit Mechanism for Hierarchical Dynamical Processing in the Primate Cortex | 155 | 56 | 99 | 36.1% |
| 78d6r5wb | Helly numbers of algebraic subsets of ℝd and an extension of Doignon’s Theorem | 155 | 48 | 107 | 31.0% |
| 30d0p416 | Unified theory for finite Markov chains | 153 | 43 | 110 | 28.1% |
| 8x36h534 | A computational model predicts sex-specific responses to calcium channel blockers in mammalian mesenteric vascular smooth muscle | 150 | 59 | 91 | 39.3% |
| 9cb006k5 | Phase response properties of half-center oscillators | 150 | 72 | 78 | 48.0% |
| 9hs54474 | Triple linking numbers and Heegaard Floer homology | 148 | 90 | 58 | 60.8% |
| 3k9311pz | Patterson–Sullivan theory for Anosov subgroups | 145 | 72 | 73 | 49.7% |
| 3t23p33z | Synaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex | 145 | 88 | 57 | 60.7% |
| 4827g1tw | Weak orientability of matroids and polynomial equations | 145 | 46 | 99 | 31.7% |
| 6d41r9t3 | Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium | 143 | 54 | 89 | 37.8% |
| 29b5v2hp | Lieb-Robinson bounds, the spectral flow, and stability of the spectral gap for lattice fermion systems | 142 | 53 | 89 | 37.3% |
| 5hx005cj | Weinstein Handlebodies for Complements of Smoothed Toric Divisors | 141 | 68 | 73 | 48.2% |
| 7gf470j6 | Scalable smoothing strategies for a geometric multigrid method for the immersed boundary equations | 141 | 74 | 67 | 52.5% |
| 4xx713r9 | Self-organized mechano-chemical dynamics in amoeboid locomotion of Physarum fragments | 140 | 87 | 53 | 62.1% |
| 5m15t3g3 | Klein–Maskit combination theorem for Anosov subgroups: Amalgams | 140 | 46 | 94 | 32.9% |
| 2xq326p7 | Parabolic Hilbert schemes via the Dunkl-Opdam subalgebra | 137 | 45 | 92 | 32.8% |
| 98k4c5zk | Parameterization for In-Silico Modeling of Ion Channel Interactions with Drugs | 136 | 47 | 89 | 34.6% |
| 1tw883m1 | On quasihomomorphisms with noncommutative targets | 135 | 48 | 87 | 35.6% |
| 5qs3v0rs | Computing Fundamental Matrix Decompositions Accurately via the Matrix Sign Function in Two Iterations: The Power of Zolotarev's Functions | 135 | 43 | 92 | 31.9% |
| 6hv0g5jf | The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data | 135 | 66 | 69 | 48.9% |
| 91g365wv | An insertion algorithm on multiset partitions with applications to diagram algebras | 135 | 39 | 96 | 28.9% |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.