Shinsuke Ninomiya - Concepedia

Author

Shinsuke Ninomiya

Also Known As

Hiroshi Suzumura, Ninomiya, S., S Ninomiya, S. Ninomiya, SHINSUKE NINOMIYA, Shinsuke NINOMIYA, Shinsuke Ninomiya, Shinsuke Ninomiya,

Publications

668

Citations

H-Index

Concepts

All Affiliations

Okayama University Helsinki University Hospital Kurashiki Central Hospital University of Helsinki National Center For Child Health and Development

About

Shinsuke Ninomiya is an author at Okayama University specializing in medicine, genetics, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	194
2	Cell Biology	3	3	60
3	Natural Sciences	2	2	48
4	Biochemistry	2	2	48
5	Engineering	1	1	18

Shinsuke Ninomiya

Publications

524

Citations

H-Index

Page 1

	Year	Citations
Isolation of a Testis-Specific cDNA on Chromosome 17q from a Region Adjacent to the Breakpoint of t(12, 17) Observed in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal Shinsuke Ninomiya, Minoru Isomura, Kouji Narahara, Human Molecular Genetics	1996	50
Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji, Human Genetics Ocular DiseaseFamilial TOphthalmologyPediatric OphthalmologyGlaucoma	1992	45
Growth hormone deficiency and empty sella syndrome in a boy with dup(x)(q13.3→q21.2) Yuji Yokoyama, Kouji Narahara, Kazushiro Tsuji, American Journal of Medical Genetics	1992	44
Renal and skin involvement in a patient with complete Kearns‐Sayre syndrome Kazuhiro Mori, Kouji Narahara, Shinsuke Ninomiya, American Journal of Medical Genetics	1991	40
Two novel mutations of SURF1 in Leigh syndrome with cytochrome c oxidase deficiency Michio Teraoka, Yuji Yokoyama, Shinsuke Ninomiya, Human Genetics Mendelian DisorderBiochemistryGenetic DisorderNatural SciencesGenetics	1999	37
Update of the genotype and phenotype of<scp><i>KMT2D</i></scp>and<scp><i>KDM6A</i></scp>by genetic screening of 100 patients with clinically suspected Kabuki syndrome Hiroaki Murakami, Yoshinori Tsurusaki, Keisuke Enomoto, American Journal of Medical Genetics Part A	2020	34
Array comparative genomic hybridization identifies a distinct DNA copy number profile in renal cell cancer associated with hereditary leiomyomatosis and renal cell cancer Taru A. Koski, Heli Lehtonen, Kowan Ja Jee, Genes Chromosomes and Cancer	2009	31
Focal 9p instability in hematologic neoplasias revealed by comparative genomic hybridization and single‐nucleotide polymorphism microarray analyses Anu Usvasalo, Shinsuke Ninomiya, Riikka Räty, Genes Chromosomes and Cancer	2009	29
Array comparative genomic hybridization reveals frequent alterations of G1/S checkpoint genes in undifferentiated pleomorphic sarcoma of bone Tarja Niini, Leo Lahti, Francesca Michelacci, Genes Chromosomes and Cancer BioinformaticsTumor BiologyArray CghSomatic VariantG1/s Checkpoint Genes	2011	28
Novel TRPV6 mutations in the spectrum of transient neonatal hyperparathyroidism Yoshiro Suzuki, Hirotake Sawada, Tomoko Tokumasu, The Journal of Physiological Sciences	2020	28

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