OKAMOTO NANA 岡本奈那

Researcher Number	60645216
Affiliation (based on the past Project Information) *help	2019: 神戸大学, 医学研究科, 医学研究員 2016: 神戸大学, 医学部附属病院, 医員 2014 – 2015: 神戸大学, 医学部附属病院, その他
Review Section/Research Field	Principal Investigator Basic Section 57070:Developmental dentistry-related / Orthodontics/Pediatric dentistry
Keywords	Principal Investigator 顎顔面 / 奇形 / 先天異常 / 遺伝子 / 先天異常疾患 / 歯科 / 変異 / 顎顔面形態 / ゲノム

Morphological evaluation system of maxillofacial region based on genePrincipal Investigator
- Principal Investigator
  
  岡本奈那
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 57070:Developmental dentistry-related
- Research Institution
  Kobe University
Search for causative genes for birth defects expressed in maxillofacial areaPrincipal Investigator
- Principal Investigator
  
  OKAMOTO NANA
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Orthodontics/Pediatric dentistry
- Research Institution
  Kobe University

All 2017 2016 2015 2014

All Journal Article Presentation

[Journal Article] A 590 kb deletion caused by non-allelic homologous recombination between two LINE-1 elements in a patient with mesomelia-synostosis syndrome.2017
- Author(s)
  Kohmoto T, Naruto T, Watanabe M, Fujita Y, Ujiro S, Okamoto N, Horikawa H, Masuda K, Imoto I.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 173 Issue: 4 Pages: 1082-1086
- DOI
  10.1002/ajmg.a.38122
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26293304, KAKENHI-PROJECT-26861783, KAKENHI-PROJECT-15K08949, KAKENHI-PROJECT-16K15618
[Journal Article] A FRMD7 variant in a Japanese family causes congenital nystagmus.2015
- Author(s)
  Kohmoto T, Okamoto N, Satomura S, Naruto T, Komori T, Hashimoto T, Imoto I.
- Journal Title
  
  Hum Genome Variation
  
  Volume: 2 Issue: 1 Pages: 15002-15002
- DOI
  10.1038/hgv.2015.2
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26293304, KAKENHI-PROJECT-26861783
[Journal Article] A novel COL11A1 mutation affecting splicing in a apatient with Stickler syndrome2015
- Author(s)
  Tomohiko Kohmoto,Takuya Naruto, Haruka Kobayashi, Miki Watanabe, Nana Okamoto, Kiyoshi Masuda, Issei Imoto, Nobuhiko Okamoto
- Journal Title
  
  Human Genome Variation
  
  Volume: 2 Issue: 1 Pages: 15043-15043
- DOI
  10.1038/hgv.2015.43
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26861783, KAKENHI-PROJECT-26293304
[Journal Article] A novel PTCH1 mutation in a patient with Gorlin syndrome.2014
- Author(s)
  Okamoto N, Naruto T, Kohmoto T, Komori T, Imoto I
- Journal Title
  
  Hum Genome Variation
  
  Volume: 1 Issue: 1
- DOI
  10.1038/hgv.2014.22
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26293304, KAKENHI-PROJECT-26861783
[Presentation] A novel COL11A1 mutation affecting splicing in a Japanese patient with Stickler syndrome2016
- Author(s)
  Takuya Naruto, Tohomiro Kohmoto, Haruka Kobayashi, Miki Watanabe, Nana Okamoto, Kiyoshi Masuda, Nobuhiko Okamoto, Issei Imoto
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26861783
[Presentation] A novel COL11A1 mutation affecting splicing in a Japanese patient with Stickler syndrome2016
- Author(s)
  Takuya Naruto,Tomohiro Kohmoto, Haruka Kobayashi, Miki Watanabe, Nana Okamoto, Kiyoshi Masuda, Nobuhiko Okamoto, Issei Imoto
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26861783
[Presentation] 連続する1q42.12-q42.2のduplication,1q42.2-q43のtriplicationと1q43-qterの片親性アイソダイソミーを認めた症例2015
- Author(s)
  岡本奈那,、村田知慧、増田清士、河本知大、里村茂子、岡本伸彦、堀川秀昌、古森孝秀、井本逸勢
- Organizer
  日本人類遺伝学会第60回大会
- Place of Presentation
  京王プラザホテル、東京
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-26861783
[Presentation] 大理石骨病患者に対し矯正治療を行った1例2015
- Author(s)
  北山美登里、岡本奈那、西村珠美、木本明、古森孝秀
- Organizer
  第32回日本障害者歯科学会
- Place of Presentation
  名古屋国際会議場、愛知
- Year and Date
  2015-11-06
- Data Source
  KAKENHI-PROJECT-26861783

1. 橘逸勢

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
2. 増田清士

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

OKAMOTO NANA 岡本 奈那

Research Projects

Research Products

Co-Researchers

Morphological evaluation system of maxillofacial region based on genePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Search for causative genes for birth defects expressed in maxillofacial areaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A 590 kb deletion caused by non-allelic homologous recombination between two LINE-1 elements in a patient with mesomelia-synostosis syndrome.2017

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A FRMD7 variant in a Japanese family causes congenital nystagmus.2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A novel COL11A1 mutation affecting splicing in a apatient with Stickler syndrome2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A novel PTCH1 mutation in a patient with Gorlin syndrome.2014

Author(s)

Journal Title

DOI

Data Source

[Presentation] A novel COL11A1 mutation affecting splicing in a Japanese patient with Stickler syndrome2016

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] A novel COL11A1 mutation affecting splicing in a Japanese patient with Stickler syndrome2016

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] 連続する1q42.12-q42.2のduplication,1q42.2-q43のtriplicationと1q43-qterの片親性アイソダイソミーを認めた症例2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] 大理石骨病患者に対し矯正治療を行った1例2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

OKAMOTO NANA 岡本奈那