Maki Fukami
Toho University(JP)Tokai University(JP)Tohoku University(JP)Hokkaido University(JP)National Center For Child Health and Development(JP)
Publications by Year
Research Areas
Genetic Syndromes and Imprinting, Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Sexual Differentiation and Disorders, Prenatal Screening and Diagnostics, Epigenetics and DNA Methylation
Most-Cited Works
- → Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome(1997)947 cited
- → SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7(2016)325 cited
- → Endometrial preparation methods for frozen-thawed embryo transfer are associated with altered risks of hypertensive disorders of pregnancy, placenta accreta, and gestational diabetes mellitus(2019)228 cited
- → Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system(2014)224 cited
- → Deletions of the Homeobox GeneSHOX(Short Stature Homeobox) Are an Important Cause of Growth Failure in Children with Short Stature(2002)208 cited
- → The IG-DMR and the MEG3-DMR at Human Chromosome 14q32.2: Hierarchical Interaction and Distinct Functional Properties as Imprinting Control Centers(2010)