PICO Portalanswers from OpenAlex & ORCID
Michio Hirano
ResearcherPublications, citations & collaboration network
Michio Hirano is a researcher indexed in PICO Portal from OpenAlex & ORCID.
How many works does Michio Hirano have?
PICO Portalindexed works
Michio Hirano has 593 works in the PICO Portal index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Michio Hirano have?
PICO Portalcitation count
Michio Hirano has 32,807 citations in the OpenAlex counts PICO Portal stores.
What is the h-index of Michio Hirano?
PICO Portalh-index
Michio Hirano has an h-index of 101 in OpenAlex.
What is the i10-index of Michio Hirano?
PICO Portali10-index
Michio Hirano has an i10-index of 315 in OpenAlex.
What is the ORCID of Michio Hirano?
PICO Portalorcid
The ORCID for Michio Hirano is on the source record.
What is the OpenAlex record for Michio Hirano?
PICO Portalopenalex
The OpenAlex for Michio Hirano is on the source record.
What are the most-cited papers on Michio Hirano?
PICO Portalmost cited works
Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
Ichizo Nishino, Antonella Spinazzola, Alexandros Papadimitriou, Simon Hammans, Israel Steiner, Cecil D. Hahn, Anne M. Connolly, Alain Verloès, Jo�o Guimar�es, Ivan Maillard, H Hamano, Maria Alice Donati, Carol E. Semrad, James A. Russell, Antoni L. Andreu, Giorgos M. Hadjigeorgiou, Tuan Vu, S. Tadesse, Torbjoern G. Nygaard, Ikuya Nonaka, Ikuo Hirano, E. Bonilla, Lewis P. Rowland, S. DiMauro, Michio Hirano
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene
Klaus Gempel, Haluk Topaloğlu, Beril Talim, Peter Schneiderat, Benedikt Schoser, Volkmar Hans, Beatrix Pálmafy, Gülsev Kale, Ayşegül Tokatlı, Catarina M. Quinzii, Michio Hirano, Ali Naini, Salvatore DiMauro, Holger Prokisch, Hanns Lochmüller, Rita Horváth
Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants
Daniel Paull, Valentina Emmanuele, Keren A. Weiss, Nathan R. Treff, Latoya A. Stewart, Haiqing Hua, Matthew Zimmer, David J. Kahler, Robin Goland, Scott Noggle, Robert Prosser, Michio Hirano, Mark V. Sauer, Dieter Egli
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations
Antoine Muchir, Jacques Médioni, M. Laluc, Catherine Massart, Takuro Arimura, Anneke J. van der Kooi, Isabelle Desguerre, M. Mayer, Xavier Ferrer, Sylvain Briault, Michio Hirano, Howard J. Worman, Audrey Mallet, Manfred Wehnert, K Schwartz, Gisèle Bonne