Maki Fukami

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

Ercole Rao, Maki Fukami, Andreas Rump et al. · Nature Genetics · 1997 · 943 citations

Developmental Anomaly, Pseudoautosomal Deletions, Developmental Biology +9

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

Satoshi Narumi, Naoko Amano, Tomohiro Ishii et al. · Nature Genetics · 2016 · 321 citations

Mendelian Disorder, Genetic Disorder, Mirage Syndrome +9

Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system

Masafumi Inui, Mami Miyado, Maki Igarashi et al. · Scientific Reports · 2014 · 221 citations · Full text

Endometrial preparation methods for frozen-thawed embryo transfer are associated with altered risks of hypertensive disorders of pregnancy, placenta accreta, and gestational diabetes mellitus

Kazuki Saito, Akira Kuwahara, Tomonori Ishikawa et al. · Human Reproduction · 2019 · 221 citations

Deletions of the Homeobox Gene<i>SHOX</i>(Short Stature Homeobox) Are an Important Cause of Growth Failure in Children with Short Stature

Gudrun Rappold, Maki Fukami, Beate Niesler et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 208 citations

Short Stature, Human Growth, Complete Gene Deletions +17