R. Yoshida

Protein-tyrosine phosphatase, nonreceptor type 11 mutation analysis and clinical assessment in 45 patients with Noonan syndrome.

H. Kanegane, T. Ogata, Toshiaki Tanaka, 2004, The Journal of clinical endocrinology and metabolism.

KRAS Analysis in 34 Noonan Syndrome Patients without PTPN11 Mutation

T. Ogata, R. Yoshida, Kaoru Yamamoto, 2007, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Malignant melanoma in a woman with LEOPARD syndrome: identification of a germline PTPN11 mutation and a somatic BRAF mutation

T. Ogata, M. Seishima, R. Yoshida, 2007, The British journal of dermatology.

PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.

T. Ogata, R. Yoshida, 2005, Pediatric endocrinology reviews : PER.

Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation

T. Ogata, N. Masawa, T. Nagai, 2008, Pediatric blood & cancer.

Familial cases of atypical clinical features genetically diagnosed as LEOPARD syndrome (multiple lentigines syndrome)

T. Ogata, K. Yoshimura, R. Yoshida, 2010, International journal of dermatology.

Acute myeloid leukemia in an adult Noonan syndrome patient with PTPN11 mutation

T. Ogata, R. Yoshida, T. Fukaya, 2005, American journal of hematology.

Two novel and one recurrent PTPN11 mutations in LEOPARD syndrome

T. Ogata, Toshiaki Tanaka, T. Hasegawa, 2004, American journal of medical genetics. Part A.

A 3‐bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia

T. Ogata, T. Nagai, R. Yoshida, 2004, American journal of medical genetics. Part A.

Haplotype analysis of the estrogen receptor 1 gene in male genital and reproductive abnormalities.

T. Ogata, N. Kamatani, I. Sasagawa, 2007, Human reproduction.

Association of cryptorchidism with a specific haplotype of the estrogen receptor alpha gene: implication for the susceptibility to estrogenic environmental endocrine disruptors.

T. Ogata, N. Kamatani, I. Sasagawa, 2005, The Journal of clinical endocrinology and metabolism.

Association of Primary Ovarian Insufficiency with a Specific Human Leukocyte Antigen Haplotype (A*24:02-C*03:03-B*35:01) in Japanese Women

T. Ogata, R. Yoshida, Y. Yoshimura, 2011, Sexual Development.

Haplotype analysis of ESR2 in Japanese patients with spermatogenic failure

T. Ogata, R. Yoshida, Y. Yoshimura, 2012, Journal of Human Genetics.

Abstracts from the 9th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society (APPES) and the 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology (JSPE)

T. Ogata, N. Kamatani, I. Yokota, 2017, International Journal of Pediatric Endocrinology.