1. Yonezawa Y, Guo L*, Kakinuma H, Otomo N, Yoshino S, Takeda K, Nakajima M, Shiraki T, Ogura Y, Takahashi Y, Koike Y, Minami S, Uno K, Kawakami N, Ito M, Yonezawa I,   Watanabe K, Kaito T, Yanagida H, Taneichi H, Harimaya K, Taniguchi Y, Shigematsu H, Iida T, Demura S, Sugawara R, Fujita N, Yagi M, Okada E, Hosogane N, Kono K, Chiba K, Kotani T, Sakuma T, Akazawa T, Suzuki T, Nishida K, Kakutani K, Tsuji T, Sudo H, Iwata A, Sato T, Inami S, Nakamura M, Matsumoto M, Terao C, Watanabe K*, Okamoto H, Ikegawa S. Identification of a Functional Susceptibility Variant for Adolescent Idiopathic Scoliosis that Upregulates Early Growth Response 1 (EGR1)-Mediated UNCX Expression. Journal of Bone and Mineral Research, 38(1):144-153, 2023.

2. Xue JY, Ikegawa S, Guo L*. SLC4A2, another gene involved in acid-base balancing machinery of osteoclasts, causes osteopetrosis. Bone, 167:116603, 2023.

3. Xue JY, Grigelioniene G, Wang Z, Nishimura G, Iida A, Matsumoto N, Tham E, Miyake N, Ikegawa S*, Guo L*. SLC4A2 Deficiency Causes a New Type of Osteopetrosis. Journal of Bone and Mineral Research, 37(2):226-235, 2022.

4. Guo L,* Iida A, Bhavani GS, Gowrishankar K, Wang Z, Xue JY, Wang J, Miyake N, Matsumoto N, Hasegawa T, Iizuka Y, Matsuda M, Nakashima T, Takechi M, Iseki S, Yambe S, Nishimura G, Koseki H, Shukunami C, Girisha KM,* Ikegawa S.* Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling. Nature Communications, 6;12(1):2046, 2021.

5. Xue JY*, Ikegawa S*, Guo L*. Genetic disorders associated with the RANKL/OPG/RANK pathway. Journal of Bone and Mineral Metabolism. 39:45-53, 2021.

6. Xue JY, Kiper POS, Utine GE, Yan L, Wang Z, Taskiran EZ, Karaosmanoglu B, Imren G, Gocmen R, Nishimura G, Matsumoto N, Miyake N, Ikegawa S*, Guo L*. Expanding the phenotypic spectrum of TNFRSF11A-associateddysosteosclerosis: a case with intracranial extramedullaryhematopoiesis. Journal of Human Genetics, 66(6):607-611, 2021.

7. Xue JY, Wang Z, Smithson SF, Burren CP, Matsumoto N, Nishimura G, Ikegawa S*, Guo L*. The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins. Journal of Human Genetics, 66(4):371-377, 2020.  

8. Xue JY, Wang Z, Shinagawa S, Ohashi H, Otomo N, Elcioglu N, Nakashima T, Nishimura G, Ikegawa S, Guo L*. TNFRSF11A-associated dysosteosclerosis: a report of the second case and characterization of the phenotypic spectrum. Journal of Bone and Mineral Research, 34(10): 1873-1879, 2019.

9. Guo L, Bertola DR*, Takanohashi A, Saito A, Segawa Y, Yokota T, Ishibashi S, Nishida Y, Yamamoto GL, da Silva Franco JF, Honjo RS, Kim CA, Musso CM, Timmons M, Pizzino A, Taft RJ, Lajoie B, Knight MA, Fischbeck FH, Singleton AB, Ferreira CR, Wang Z, Yan  L, Garbern JY, Kiper POS, Ohashi H, Robey PG, Boyde A, Matsumoto N, Miyake N, Spranger J, Schiffmann  R, Vanderver A, Nishimura G, Bueno MP, Simons C, Ishikawa K, Ikegawa S*. Bi-allelic CSF1R mutations cause a syndrome characterized by skeletal dysplasia of dysosteosclerosis-Pyle disease spectrum and degenerative encephalopathy with brain malformation. American Journal of Human Genetics, 104(5): 925-935, 2019.

10. Guo L, Yamashita H, Kou I, Takimoto A, Horike MM,  Horike SI, Sakuma T, Miura S, Adachi T, Yamamoto T, Ikegawa S, Hiraki Y, Shukunami C*. Functional investigation of a non-coding variant associated with adolescent idiopathic scoliosis in zebrafish: elevated expression of the ladybird homeobox gene causes body axis deformation. PLoS Genetics, 12: e1005802, 2016.

郭龙所有研究论文见PubMed(链接)。