Gd 2 Sn 2 O 7 and Gd 2 Ti 2 O 7 have been regarded as good experimental realizations of the classical Heisenberg pyrochlore antiferromagnet with dipolar interaction. The former was found to adopt the Palmer-Chalker state via a single, first-order transition at T N ≈ 1 K, while the latter enters a distinct, partially ordered state through two successive transitions at T N1 ≈ 1 K and T N2 = 0.75 K, respectively. To shed more light on their distinct magnetic ground states, we have synthesized two more gadolinium-based pyrochlore oxides, Gd 2 Ge 2 O 7 and Gd 2 Pt 2 O 7 , under high-pressure conditions, and performed detailed characterizations via X-ray powder diffraction, dc and ac magnetic susceptibility, and specific heat measurements down to 100 mK. We found that both compounds enter a long-range antiferromagnetically ordered state through a single, first-order transition at T N = 1.4 K for Gd 2 Ge 2 O 7 and T N = 1.56 K for Gd 2 Pt 2 O 7 , respectively, with the specific-heat anomaly similar to that of Gd 2 Sn 2 O 7 rather than Gd 2 Ti 2 O 7 . Interestingly, the lowtemperature magnetic specific heat of both Gd 2 Ge 2 O 7 and Gd 2 Pt 2 O 7 was found to follow nicely the T 3 -dependence as expected for a three-dimensional antiferromagnet with gapless spin-wave excitations. We have rationalized the enhancement of T N in terms of the reduced Gd-Gd distances for the chemically pressurized Gd 2 Ge 2 O 7 and the addition of extra superexchange pathways through the empty Pt-e g orbitals for Gd 2 Pt 2 O 7 , respectively. Our current study has expanded the family of gadolinium-based pyrochlores, and permits us to achieve a better understanding on their distinct magnetic properties in a more comprehensive perspective.