# Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/deletions-and-epimutations-affecting-the-human-14q32-2-imprinted-region-in/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Masayo Kagami,Yoichi Sekita,Gen Nishimura,Masahito Irie,Fumiko Kato,Michiyo Okada,Shunji Yamamori,Hiroshi Kishimoto,Masahiro Nakayama,Yukichi Tanaka,Kentarou Matsuoka,Tsutomu Takahashi,Mika Noguchi,Yoko Tanaka,Kouji Masumoto,Takeshi Utsunomiya,Hiroko Kouzan,Yumiko Komatsu,Hirofumi Ohashi,Kenji Kurosawa,Kenjirou Kosaki,Anne C. Ferguson‐Smith,Fumitoshi Ishino,Tsutomu Ogata |
| Citations | 291 |
| DOI | 10.1038/ng.2007.56 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2038434389 |
| PMID | 18176563 |
| Type | article |
| Year | 2008 |

## Paper authors

- [Kouji Masumoto](https://scholariq.org/researchers/kouji-masumoto/)

## Paper primary topic

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Paper topics

- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Prenatal Screening and Diagnostics](https://scholariq.org/topics/prenatal-screening-and-diagnostics/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.
