The perovskite-like transition-metal oxide Gd1−xSrxTiO3 is investigated by measurements of resistivity, specific-heat, and electron paramagnetic resonance (EPR). Approaching the metal-toinsulator transition from the metallic regime (x ≥ 0.2), the Sommerfeld coefficient γ of the specific heat becomes strongly enhanced and the resistivity increases quadratically at low temperatures, which both are fingerprints of strong electronic correlations. The temperature dependence of the dynamic susceptibility, as determined from the Gd 3+ -EPR linewidth, signals the importance of strong spin fluctuations, as observed in heavy-fermion compounds. PACS: 71.30, 71.27, 76.30 The transition-metal oxides RTiO 3 (where R denotes Y 3+ , La 3+ , or some trivalent rare-earth ion) are known as typical Mott-Hubbard insulators with Ti 3+ in a 3d 1 electronic configuration [1]. Doping R 1−x A x TiO 3 with divalent alkali-earth ions A like Ca 2+ or Sr 2+ partially changes the Ti valence to Ti 4+ (3d 0 ) and induces metallic behavior at a certain doping concentration x. The metal-to-insulator transition of La 1−x Sr x TiO 3 and Y 1−x Ca x TiO 3 has been investigated in detail [2,3]. A critical increase of the Sommerfeld coefficient γ of the specific heat approaching the metal-to-insulator transition has been observed in both compounds with γ ≈ 25 mJ/(mole K 2 ) in Y 0.6 Ca 0.4 TiO 3 , indicating an enhancement of the effective electron mass. Heavy-fermion formation has been observed in a number of transitionmetal oxides, with Sr 1−x Ca x RuO 3 [4] and LiV 2 O 4 [5] being the most prominent examples. In the latter two compounds the temperature dependence of the dynamic susceptibility, as probed by the spin-lattice relaxation time in NMR experiments, played a key role in identifying the heavy-fermion behavior. In this letter we investigate the dynamic susceptibility utilizing Gd EPR and provide experimental evidence of heavy-fermion behavior in Gd 1−x Sr x TiO 3 .Ceramic samples of Gd 1−x Sr x TiO 3 have been calcinated from TiO 2 , SrCO 3 , Gd 2 O 3 and Ti 2 O 3 powders of high purity (better than 3N) and pressed into pellets. These pellets have been annealed at 1473 K under N 2 atmosphere for 15 hours and finally arc-melted under argon atmosphere. For Sr concentrations x ≤ 0.7 X-ray powder diffraction revealed the proper orthorhombically distorted GdFeO 3 perovskite structure [6]. For x > 0.7 the system attains the cubic perovskite structure like pure SrTiO 3 . The volume of the unit cell remains nearly constant at about 235Å 3 in the whole concentration range. Susceptibility measurements were performed with a commercial SQUID magnetometer (Quantum Design) in a temperature range 4.2 ≤ T ≤ 400 K. Pure GdTiO 3 shows a ferrimagnetic susceptibility, which follows a Curie-Weiss law χ ∝ (T + Θ) −1 with Θ = 10 K at high temperatures T > 100 K, and exhibits an ordering temperature T C ≈ 28 K. This fits reasonably to the value of 34 K given in literature [7], where the ordered state is reported to show an antiparallel alignment of the ferromagne...