Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 116

1.

3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome.

Tadaka S, Katsuoka F, Ueki M, Kojima K, Makino S, Saito S, Otsuki A, Gocho C, Sakurai-Yageta M, Danjoh I, Motoike IN, Yamaguchi-Kabata Y, Shirota M, Koshiba S, Nagasaki M, Minegishi N, Hozawa A, Kuriyama S, Shimizu A, Yasuda J, Fuse N; Tohoku Medical Megabank Project Study Group, Tamiya G, Yamamoto M, Kinoshita K.

Hum Genome Var. 2019 Jun 18;6:28. doi: 10.1038/s41439-019-0059-5. eCollection 2019.

2.

Construction of JRG (Japanese reference genome) with single-molecule real-time sequencing.

Nagasaki M, Kuroki Y, Shibata TF, Katsuoka F, Mimori T, Kawai Y, Minegishi N, Hozawa A, Kuriyama S, Suzuki Y, Kawame H, Nagami F, Takai-Igarashi T, Ogishima S, Kojima K, Misawa K, Tanabe O, Fuse N, Tanaka H, Yaegashi N, Kinoshita K, Kure S, Yasuda J, Yamamoto M.

Hum Genome Var. 2019 Jun 7;6:27. doi: 10.1038/s41439-019-0057-7. eCollection 2019.

3.

Identification of genetic alterations in extramammary Paget disease using whole exome analysis.

Kiniwa Y, Yasuda J, Saito S, Saito R, Motoike IN, Danjoh I, Kinoshita K, Fuse N, Yamamoto M, Okuyama R.

J Dermatol Sci. 2019 Apr;94(1):229-235. doi: 10.1016/j.jdermsci.2019.03.006. Epub 2019 Apr 11.

4.

Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals.

Yamaguchi-Kabata Y, Yasuda J, Uruno A, Shimokawa K, Koshiba S, Suzuki Y, Fuse N, Kawame H, Tadaka S, Nagasaki M, Kojima K, Katsuoka F, Kumada K, Tanabe O, Tamiya G, Yaegashi N, Kinoshita K, Yamamoto M, Kure S; Tohoku Medical Megabank Project Study Group.

Hum Genet. 2019 Apr;138(4):389-409. doi: 10.1007/s00439-019-01998-7. Epub 2019 Mar 18.

PMID:
30887117
5.

Outlier detection for questionnaire data in biobanks.

Sakurai R, Ueki M, Makino S, Hozawa A, Kuriyama S, Takai-Igarashi T, Kinoshita K, Yamamoto M, Tamiya G.

Int J Epidemiol. 2019 Mar 8. pii: dyz012. doi: 10.1093/ije/dyz012. [Epub ahead of print]

PMID:
30848787
6.

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.

Mori M, Hira A, Yoshida K, Muramatsu H, Okuno Y, Shiraishi Y, Anmae M, Yasuda J, Tadaka S, Kinoshita K, Osumi T, Noguchi Y, Adachi S, Kobayashi R, Kawabata H, Imai K, Morio T, Tamura K, Takaori-Kondo A, Yamamoto M, Miyano S, Kojima S, Ito E, Ogawa S, Matsuo K, Yabe H, Yabe M, Takata M.

Haematologica. 2019 Feb 21. pii: haematol.2018.207241. doi: 10.3324/haematol.2018.207241. [Epub ahead of print]

7.

Maternity Log study: a longitudinal lifelog monitoring and multiomics analysis for the early prediction of complicated pregnancy.

Sugawara J, Ochi D, Yamashita R, Yamauchi T, Saigusa D, Wagata M, Obara T, Ishikuro M, Tsunemoto Y, Harada Y, Shibata T, Mimori T, Kawashima J, Katsuoka F, Igarashi-Takai T, Ogishima S, Metoki H, Hashizume H, Fuse N, Minegishi N, Koshiba S, Tanabe O, Kuriyama S, Kinoshita K, Kure S, Yaegashi N, Yamamoto M, Hiyama S, Nagasaki M.

BMJ Open. 2019 Feb 19;9(2):e025939. doi: 10.1136/bmjopen-2018-025939.

8.

A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing.

Mizuguchi T, Suzuki T, Abe C, Umemura A, Tokunaga K, Kawai Y, Nakamura M, Nagasaki M, Kinoshita K, Okamura Y, Miyatake S, Miyake N, Matsumoto N.

J Hum Genet. 2019 May;64(5):359-368. doi: 10.1038/s10038-019-0569-5. Epub 2019 Feb 13.

PMID:
30760880
9.

Value of global metabolomics in association with diagnosis and clinicopathological factors of renal cell carcinoma.

Sato T, Kawasaki Y, Maekawa M, Takasaki S, Saigusa D, Ota H, Shimada S, Yamashita S, Mitsuzuka K, Yamaguchi H, Ito A, Kinoshita K, Koshiba S, Mano N, Arai Y.

Int J Cancer. 2019 Jul 15;145(2):484-493. doi: 10.1002/ijc.32115. Epub 2019 Jan 24.

PMID:
30628065
10.

COXPRESdb v7: a gene coexpression database for 11 animal species supported by 23 coexpression platforms for technical evaluation and evolutionary inference.

Obayashi T, Kagaya Y, Aoki Y, Tadaka S, Kinoshita K.

Nucleic Acids Res. 2019 Jan 8;47(D1):D55-D62. doi: 10.1093/nar/gky1155.

11.

Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare.

Yasuda J, Kinoshita K, Katsuoka F, Danjoh I, Sakurai-Yageta M, Motoike IN, Kuroki Y, Saito S, Kojima K, Shirota M, Saigusa D, Otsuki A, Kawashima J, Yamaguchi-Kabata Y, Tadaka S, Aoki Y, Mimori T, Kumada K, Inoue J, Makino S, Kuriki M, Fuse N, Koshiba S, Tanabe O, Nagasaki M, Tamiya G, Shimizu R, Takai-Igarashi T, Ogishima S, Hozawa A, Kuriyama S, Sugawara J, Tsuboi A, Kiyomoto H, Ishii T, Tomita H, Minegishi N, Suzuki Y, Suzuki K, Kawame H, Tanaka H, Taki Y, Yaegashi N, Kure S, Nagami F; Tohoku Medical Megabank Project Study Group, Kosaki K, Sutoh Y, Hachiya T, Shimizu A, Sasaki M, Yamamoto M.

J Biochem. 2019 Feb 1;165(2):139-158. doi: 10.1093/jb/mvy096.

PMID:
30452759
12.

Molecular Mechanism of Depolarization-Dependent Inactivation in W366F Mutant of Kv1.2.

Kondo HX, Yoshida N, Shirota M, Kinoshita K.

J Phys Chem B. 2018 Dec 6;122(48):10825-10833. doi: 10.1021/acs.jpcb.8b09446. Epub 2018 Nov 26.

PMID:
30395463
13.

Zn2+-Binding to the Voltage-Gated Proton Channel Hv1/VSOP.

Iwaki M, Takeshita K, Kondo HX, Kinoshita K, Okamura Y, Takano Y, Nakagawa A, Kandori H.

J Phys Chem B. 2018 Oct 4;122(39):9076-9080. doi: 10.1021/acs.jpcb.8b04890. Epub 2018 Sep 25.

PMID:
30204443
14.

Regional genetic differences among Japanese populations and performance of genotype imputation using whole-genome reference panel of the Tohoku Medical Megabank Project.

Yasuda J, Katsuoka F, Danjoh I, Kawai Y, Kojima K, Nagasaki M, Saito S, Yamaguchi-Kabata Y, Tadaka S, Motoike IN, Kumada K, Sakurai-Yageta M, Tanabe O, Fuse N, Tamiya G, Higasa K, Matsuda F, Yasuda N, Iwasaki M, Sasaki M, Shimizu A, Kinoshita K, Yamamoto M.

BMC Genomics. 2018 Jul 24;19(1):551. doi: 10.1186/s12864-018-4942-0.

15.

De novo profile generation based on sequence context specificity with the long short-term memory network.

Yamada KD, Kinoshita K.

BMC Bioinformatics. 2018 Jul 18;19(1):272. doi: 10.1186/s12859-018-2284-1.

16.

Matataki: an ultrafast mRNA quantification method for large-scale reanalysis of RNA-Seq data.

Okamura Y, Kinoshita K.

BMC Bioinformatics. 2018 Jul 16;19(1):266. doi: 10.1186/s12859-018-2279-y.

17.

Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project.

Koshiba S, Motoike I, Saigusa D, Inoue J, Shirota M, Katoh Y, Katsuoka F, Danjoh I, Hozawa A, Kuriyama S, Minegishi N, Nagasaki M, Takai-Igarashi T, Ogishima S, Fuse N, Kure S, Tamiya G, Tanabe O, Yasuda J, Kinoshita K, Yamamoto M.

Genes Cells. 2018 Jun;23(6):406-417. doi: 10.1111/gtc.12588. Epub 2018 Apr 27. Review.

18.

Zinc finger-IRF composite elements bound by Ikaros/IRF4 complexes function as gene repression in plasma cell.

Ochiai K, Kondo H, Okamura Y, Shima H, Kurokochi Y, Kimura K, Funayama R, Nagashima T, Nakayama K, Yui K, Kinoshita K, Igarashi K.

Blood Adv. 2018 Apr 24;2(8):883-894. doi: 10.1182/bloodadvances.2017010413.

19.

Construction of full-length Japanese reference panel of class I HLA genes with single-molecule, real-time sequencing.

Mimori T, Yasuda J, Kuroki Y, Shibata TF, Katsuoka F, Saito S, Nariai N, Ono A, Nakai-Inagaki N, Misawa K, Tateno K, Kawai Y, Fuse N, Hozawa A, Kuriyama S, Sugawara J, Minegishi N, Suzuki K, Kinoshita K, Nagasaki M, Yamamoto M.

Pharmacogenomics J. 2019 Apr;19(2):136-146. doi: 10.1038/s41397-017-0010-4. Epub 2018 Jan 19.

20.

ATTED-II in 2018: A Plant Coexpression Database Based on Investigation of the Statistical Property of the Mutual Rank Index.

Obayashi T, Aoki Y, Tadaka S, Kagaya Y, Kinoshita K.

Plant Cell Physiol. 2018 Feb 1;59(2):440. doi: 10.1093/pcp/pcx209. No abstract available.

Supplemental Content

Loading ...
Support Center