Ordered catenation of sequence-tagged sites and multiplexed SNP genotyping by sequencing

par Higasa, Koichiro, Hayashi, Kenshi
Publié 2002

Periodicity of SNP distribution around transcription start sites

par Higasa, Koichiro, Hayashi, Kenshi
Publié 2006

D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples

par Higasa, Koichiro, Miyatake, Katsuyuki, Kukita, Yoji, Tahira, Tomoko, Hayashi, Kenshi
Publié 2007

Evaluation of Haplotype Inference Using Definitive Haplotype Data Obtained from Complete Hydatidiform Moles, and Its Significance for the Analyses of Positively Selected Regions

par Higasa, Koichiro, Kukita, Yoji, Kato, Kiyoko, Wake, Norio, Tahira, Tomoko, Hayashi, Kenshi
Publié 2009

Precise Estimation of Allele Frequencies of Single-Nucleotide Polymorphisms by a Quantitative SSCP Analysis of Pooled DNA

par Sasaki, Tomonari, Tahira, Tomoko, Suzuki, Akari, Higasa, Koichiro, Kukita, Yoji, Baba, Shingo, Hayashi, Kenshi
Publié 2001

A definitive haplotype map of structural variations determined by microarray analysis of duplicated haploid genomes

par Tahira, Tomoko, Yahara, Koji, Kukita, Yoji, Higasa, Koichiro, Kato, Kiyoko, Wake, Norio, Hayashi, Kenshi
Publié dans Genom Data (2014)

Combined Single Nucleotide Variants of ORAI1 and BLK in a Child with Refractory Kawasaki Disease

par Kanda, Saki, Fujii, Yoshimitsu, Hori, Shin-ichiro, Ohmachi, Taichi, Yoshimura, Ken, Higasa, Koichiro, Kaneko, Kazunari
Publié dans Children (Basel) (2021)

Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data

par Okada, Daigo, Nakamura, Naotoshi, Setoh, Kazuya, Kawaguchi, Takahisa, Higasa, Koichiro, Tabara, Yasuharu, Matsuda, Fumihiko, Yamada, Ryo
Publié dans J Hum Genet (2020)

A Definitive Haplotype Map as Determined by Genotyping Duplicated Haploid Genomes Finds a Predominant Haplotype Preference at Copy-Number Variation Events

par Kukita, Yoji, Yahara, Koji, Tahira, Tomoko, Higasa, Koichiro, Sonoda, Miki, Yamamoto, Ken, Kato, Kiyoko, Wake, Norio, Hayashi, Kenshi
Publié 2010

Large-Scale East-Asian eQTL Mapping Reveals Novel Candidate Genes for LD Mapping and the Genomic Landscape of Transcriptional Effects of Sequence Variants

par Narahara, Maiko, Higasa, Koichiro, Nakamura, Seiji, Tabara, Yasuharu, Kawaguchi, Takahisa, Ishii, Miho, Matsubara, Kenichi, Matsuda, Fumihiko, Yamada, Ryo
Publié 2014

A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension

par Higasa, Koichiro, Ogawa, Aiko, Terao, Chikashi, Shimizu, Masakazu, Kosugi, Shinji, Yamada, Ryo, Date, Hiroshi, Matsubara, Hiromi, Matsuda, Fumihiko
Publié dans BMC Pulm Med (2017)

Next-generation sequencing-based comprehensive molecular analysis of 43 Japanese patients with cone and cone-rod dystrophies

par Oishi, Maho, Oishi, Akio, Gotoh, Norimoto, Ogino, Ken, Higasa, Koichiro, Iida, Kei, Makiyama, Yukiko, Morooka, Satoshi, Matsuda, Fumihiko, Yoshimura, Nagahisa
Publié dans Mol Vis (2016)

EYS is a major gene involved in retinitis pigmentosa in Japan: genetic landscapes revealed by stepwise genetic screening

par Numa, Shogo, Oishi, Akio, Higasa, Koichiro, Oishi, Maho, Miyata, Manabu, Hasegawa, Tomoko, Ikeda, Hanako Ohashi, Otsuka, Yuki, Matsuda, Fumihiko, Tsujikawa, Akitaka
Publié dans Sci Rep (2020)

Accurate diagnosis of mismatch repair deficiency in colorectal cancer using high-quality DNA samples from cultured stem cells

par Yamaura, Tadayoshi, Miyoshi, Hiroyuki, Maekawa, Hisatsugu, Morimoto, Tomonori, Yamamoto, Takehito, Kakizaki, Fumihiko, Higasa, Koichiro, Kawada, Kenji, Matsuda, Fumihiko, Sakai, Yoshiharu, Taketo, M. Mark
Publié dans Oncotarget (2018)

Positive renal familial history in IgA nephropathy is associated with worse renal outcomes: a single-center longitudinal study

par Sato, Yoshinori, Tsukaguchi, Hiroyasu, Higasa, Koichiro, Kawata, Naoto, Inui, Kiyoko, Linh, Tran Nguyen Truc, Quynh, Tran Thuy Huong, Yoshihiko, Inoue, Koiwa, Fumihiko, Yoshimura, Ashio
Publié dans BMC Nephrol (2021)

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles

par Kukita, Yoji, Miyatake, Katsuyuki, Stokowski, Renee, Hinds, David, Higasa, Koichiro, Wake, Norio, Hirakawa, Toshio, Kato, Hidenori, Matsuda, Takao, Pant, Krishna, Cox, David, Tahira, Tomoko, Hayashi, Kenshi
Publié 2005

Population dynamics in the Japanese Archipelago since the Pleistocene revealed by the complete mitochondrial genome sequences

par Mizuno, Fuzuki, Gojobori, Jun, Kumagai, Masahiko, Baba, Hisao, Taniguchi, Yasuhiro, Kondo, Osamu, Matsushita, Masami, Matsushita, Takayuki, Matsuda, Fumihiko, Higasa, Koichiro, Hayashi, Michiko, Wang, Li, Kurosaki, Kunihiko, Ueda, Shintaroh
Publié dans Sci Rep (2021)

Novel Germline Mutation in the Transmembrane Domain of HER2 in Familial Lung Adenocarcinomas

par Yamamoto, Hiromasa, Higasa, Koichiro, Sakaguchi, Masakiyo, Shien, Kazuhiko, Soh, Junichi, Ichimura, Koichi, Furukawa, Masashi, Hashida, Shinsuke, Tsukuda, Kazunori, Takigawa, Nagio, Matsuo, Keitaro, Kiura, Katsuyuki, Miyoshi, Shinichiro, Matsuda, Fumihiko, Toyooka, Shinichi
Publié 2013

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN

par Mizobuchi, Kei, Hayashi, Takaaki, Oishi, Noriko, Kubota, Daiki, Kameya, Shuhei, Higasa, Koichiro, Futami, Takuma, Kondo, Hiroyuki, Hosono, Katsuhiro, Kurata, Kentaro, Hotta, Yoshihiro, Yoshitake, Kazutoshi, Iwata, Takeshi, Matsuura, Tomokazu, Nakano, Tadashi
Publié dans J Clin Med (2021)

Comprehensive assessment of the expression of the SWI/SNF complex defines two distinct prognostic subtypes of ovarian clear cell carcinoma

par Abou-Taleb, Hisham, Yamaguchi, Ken, Matsumura, Noriomi, Murakami, Ryusuke, Nakai, Hidekatsu, Higasa, Koichiro, Amano, Yasuaki, Abiko, Kaoru, Yoshioka, Yumiko, Hamanishi, Junzo, Koshiyama, Masafumi, Baba, Tsukasa, Yamada, Ryo, Matsuda, Fumihiko, Konishi, Ikuo, Mandai, Masaki
Publié dans Oncotarget (2016)