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Haematologica
|
April 3, 2020
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients
Minako Mori, Asuka Hira, Kenichi Yoshida, et al.
Haematologica
|
February 23, 2019
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients
Minako Mori, Asuka Hira, Kenichi Yoshida, et al.
Journal of Human Genetics
|
January 17, 2025
Returning genetic risk information for hereditary cancers to participants in a population-based cohort study in Japan
Kinuko Ohneda, Yoichi Suzuki, Yohei Hamanaka, et al.
Frontiers in Neuroscience
|
August 15, 2024
Functional evaluation of novel variants of <i>B4GALNT1</i> in a patient with hereditary spastic paraplegia and the general population
Kei-Ichiro Inamori, Katsuya Nakamura, Fumi Shishido, et al.
JMA Journal
|
May 25, 2022
A Pilot Study for Return of Individual Pharmacogenomic Results to Population-Based Cohort Study Participants
Kinuko Ohneda, Masahiro Hiratsuka, Hiroshi Kawame, et al.
Psychiatry and Clinical Neurosciences
|
October 15, 2024
Copy number variations in RNF216 and postsynaptic membrane-associated genes are associated with bipolar disorder: a case-control study in the Japanese population
Masahiro Nakatochi, Itaru Kushima, Branko Aleksic, et al.
Journal of Biochemistry
|
November 20, 2018
Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare
Jun Yasuda, Kengo Kinoshita, Fumiki Katsuoka, et al.
Human Genome Variation
|
December 10, 2021
dbTMM: an integrated database of large-scale cohort, genome and clinical data for the Tohoku Medical Megabank Project
Soichi Ogishima, Satoshi Nagaie, Satoshi Mizuno, et al.
Journal of Biomedical Semantics
|
February 6, 2014
BioHackathon series in 2011 and 2012: penetration of ontology and linked data in life science domains
Toshiaki Katayama, Mark D Wilkinson, Kiyoko F Aoki-Kinoshita, et al.
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of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Haematologica
|
April 3, 2020
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients
Minako Mori, Asuka Hira, Kenichi Yoshida, et al.
Haematologica
|
February 23, 2019
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients
Minako Mori, Asuka Hira, Kenichi Yoshida, et al.
Journal of Human Genetics
|
January 17, 2025
Returning genetic risk information for hereditary cancers to participants in a population-based cohort study in Japan
Kinuko Ohneda, Yoichi Suzuki, Yohei Hamanaka, et al.
Frontiers in Neuroscience
|
August 15, 2024
Functional evaluation of novel variants of <i>B4GALNT1</i> in a patient with hereditary spastic paraplegia and the general population
Kei-Ichiro Inamori, Katsuya Nakamura, Fumi Shishido, et al.
JMA Journal
|
May 25, 2022
A Pilot Study for Return of Individual Pharmacogenomic Results to Population-Based Cohort Study Participants
Kinuko Ohneda, Masahiro Hiratsuka, Hiroshi Kawame, et al.
Psychiatry and Clinical Neurosciences
|
October 15, 2024
Copy number variations in RNF216 and postsynaptic membrane-associated genes are associated with bipolar disorder: a case-control study in the Japanese population
Masahiro Nakatochi, Itaru Kushima, Branko Aleksic, et al.
Journal of Biochemistry
|
November 20, 2018
Genome analyses for the Tohoku Medical Megabank Project towards establishment of personalized healthcare
Jun Yasuda, Kengo Kinoshita, Fumiki Katsuoka, et al.
Human Genome Variation
|
December 10, 2021
dbTMM: an integrated database of large-scale cohort, genome and clinical data for the Tohoku Medical Megabank Project
Soichi Ogishima, Satoshi Nagaie, Satoshi Mizuno, et al.
Journal of Biomedical Semantics
|
February 6, 2014
BioHackathon series in 2011 and 2012: penetration of ontology and linked data in life science domains
Toshiaki Katayama, Mark D Wilkinson, Kiyoko F Aoki-Kinoshita, et al.
Page
of 5