Hiroshi Yoshihashi

1.0k citations

44 papers · 609 indexed · h-index 13

Genetics top 10%
- Genetic Syndromes and Imprinting 9
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
- Congenital Ear and Nasal Anomalies 4
- Genomics and Rare Diseases 3
Genetics top 10%
- Genetic Syndromes and Imprinting 9
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
- Congenital Ear and Nasal Anomalies 4
- Genomics and Rare Diseases 3
Molecular Biology
- Hedgehog Signaling Pathway Studies 5
- Epigenetics and DNA Methylation 5
Sensory Systems
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 6

Co-authors: Kenjiro Kosaki Rika Kosaki Nobutake Matsuo Tomonobu Hasegawa Tsutomu Ogata Toshiki Takenouchi Takao Takahashi Tomoko Uehara
Cited by: Genetics Molecular Biology
Journals: The Journal of Clinical Endocrinology & Metabolism (1 paper)Scientific Reports (1 paper)The American Journal of Human Genetics (2 papers)
Partner nations: Japan United States Germany

In The Last Decade

Hiroshi Yoshihashi

40 papers receiving 599 citations

Peers

Countries citing papers authored by Hiroshi Yoshihashi

Since Specialization

Citations

This map shows the geographic impact of Hiroshi Yoshihashi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Hiroshi Yoshihashi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hiroshi Yoshihashi more than expected).

Fields of papers citing papers by Hiroshi Yoshihashi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hiroshi Yoshihashi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Hiroshi Yoshihashi. The network helps show where Hiroshi Yoshihashi may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hiroshi Yoshihashi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hiroshi Yoshihashi Line = papers co-authored together Hiroshi Yoshihashi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B Parkinsonism & Related Disorders ·Naoto Sugeno,Satoko Kumada,Hirofumi Kashii,Jun Ikezawa,Toshitaka Kawarai,Takaaki Nakamura,Ako Miyata,Shun Ishiyama,Kazuki Sato,Shun Yoshida,Hutoshi Sekiguchi,Kohei Hamanaka,Satoko Miyatake,Noriko Miyake,Naomichi Matsumoto,Hiroyuki Akagawa,Kenjiro Kosaki,Hiroshi Yoshihashi,Takafumi Hasegawa,Masashi Aoki	2024	1
2	Long‐term clinical course of Heyn‐Sproul‐Jackson syndrome Congenital Anomalies ·Hiroshi Futagawa,Shiho Ito,Kenjiro Kosaki,Hiroshi Yoshihashi	2023	1
3	Recurrent NFIA K125E substitution represents a loss‐of‐function allele: Sensitive in vitro and in vivo assays for nontruncating alleles American Journal of Medical Genetics Part A ·Tomoko Uehara,Rikako Sanuki,Yurie Ogura,Atsushi Yokoyama,Takeshi Yoshida,Hiroshi Futagawa,Hiroshi Yoshihashi,Mamiko Yamada,Hisato Suzuki,Toshiki Takenouchi,Kohei Matsubara,Hiromi Hirata,Kenjiro Kosaki,Toshiyuki Takano‐Shimizu	2021	8
4	Status Epilepticus due to Asfotase Alfa Interruption in Perinatal Severe Hypophosphatasia Pediatric Neurology ·Eri Ogawa,Kazuhiro Shimura,Hiroshi Yoshihashi,Sahoko Miyama	2021	3
5	White matter abnormality in Jacobsen syndrome assessed by serial MRI Brain and Development ·Shuhei Fujino,Hiroshi Yoshihashi,Ryojun Takeda,Satoshi Ihara,Sahoko Miyama	2020	0
6	IGF2 Mutations The Journal of Clinical Endocrinology & Metabolism ·Yohei Masunaga,Takanobu Inoue,Kaori Yamoto,Yasuko Fujisawa,Yasuhiro Sato,Yuki Kawashima-Sonoyama,Naoya Morisada,Kazumoto Iijima,Yasuhisa Ohata,Noriyuki Namba,Hiroshi Suzumura,Ryota Kuribayashi,Yu Yamaguchi,Hiroshi Yoshihashi,Maki Fukami,Hirotomo Saitsu,Masayo Kagami,Tsutomu Ogata	2019	32
7	Novel compound heterozygous mutations identified by whole exome sequencing in a Japanese patient with geroderma osteodysplastica European Journal of Medical Genetics ·Ryojun Takeda,Masaki Takagi,Hiroyuki Shinohara,Hiroshi Futagawa,Satoshi Narumi,Tomonobu Hasegawa,Gen Nishimura,Hiroshi Yoshihashi	2017	6
8	A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of sotos syndrome American Journal of Medical Genetics Part A ·Yoshie Nakamura,Masaki Takagi,Hiroshi Yoshihashi,Masaru Miura,Satoshi Narumi,Tomonobu Hasegawa,Yoshishige Miyake,Yukihiro Hasegawa	2015	10
9	Microduplication of Xq24 and Hartsfield syndrome with holoprosencephaly, ectrodactyly, and clefting American Journal of Medical Genetics Part A ·Toshiki Takenouchi,Hironobu Okuno,Rika Kosaki,Daisuke Ariyasu,Chiharu Torii,Suketaka Momoshima,Naoki Harada,Hiroshi Yoshihashi,Takao Takahashi,Midori Awazu,Kenjiro Kosaki	2012	8
10	Congenital corneal staphyloma as a complication of Kabuki syndrome American Journal of Medical Genetics Part A ·Ryuma Tanaka,Toshiki Takenouchi,Keiko Uchida,Takeshi Sato,Hiroyuki Fukushima,Hiroshi Yoshihashi,Takao Takahashi,Kazuo Tsubota,Kenjiro Kosaki	2012	11
11	Hypomyelination with atrophy of the basal ganglia and cerebellum in an infant with Down syndrome Clinical Dysmorphology ·Yoko Narumi,Takashi Shiihara,Hiroshi Yoshihashi,Satoru Sakazume,Marjo S. van der Knaap,Akira Nishimura‐Tadaki,Naomichi Matsumoto,Yoshimitsu Fukushima	2011	2
12	1p36 deletion syndrome associated with Prader–Willi‐like phenotype Pediatrics International ·Yu Tsuyusaki,Hiroshi Yoshihashi,Noritaka Furuya,Masanori Adachi,Hitoshi Osaka,Kayono Yamamoto,Kenji Kurosawa	2010	25
13	Survival of a Male Mosaic for PORCN Mutation with Mild Focal Dermal Hypoplasia Phenotype Pediatric Dermatology ·Hiroshi Yoshihashi,Hirotaka Ohki,Chiharu Torii,Akira Ishiko,Kenjiro Kosaki	2010	7
14	Screening for Alagille Syndrome Mutations in the JAG1 and NOTCH2 Genes Using Denaturing High-Performance Liquid Chromatography Genetic Testing ·Hazuki Samejima,Chiharu Torii,Rika Kosaki,Kenji Kurosawa,Hiroshi Yoshihashi,Koji Muroya,Nobuhiko Okamoto,Yoriko Watanabe,Tomoki Kosho,Michiru Kubota,Osamu Matsuda,M. Goto,Kosuke Izumi,Takao Takahashi,Kenjiro Kosaki	2007	7
15	Phenotypic spectrum of CHARGE syndrome with CHD7 mutations The Journal of Pediatrics ·Michihiko Aramaki,Toru Udaka,Rika Kosaki,Yoshio Makita,Nobuhiko Okamoto,Hiroshi Yoshihashi,Hirotaka Oki,Kenji Nanao,Nobuko Moriyama,Shozo Oku,Tomonobu Hasegawa,Takao Takahashi,Yoshimitsu Fukushima,Hiroshi Kawame,Kenjiro Kosaki	2006	118
16	Jun Shindo,Masaki Ito,Masahisa Shiraishi,Kyoko Takamura,Hiroshi Yoshihashi,Chikako Nakajima,Seiichi Hirobe,Shoichiro Kamagata,Yukihiko Morikawa,Tetsuo Yokoyama	2005	4
17	Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis Teratology ·Hideki Fujita,Rika Kosaki,Hiroshi Yoshihashi,Tsutomu Ogata,Masaru Tomita,Tomonobu Hasegawa,Takao Takahashi,Nobutake Matsuo,Kenjiro Kosaki	2002	41
18	Reply to Mergenthaler et al. The American Journal of Human Genetics ·Hiroshi Yoshihashi,Katsuhiro Maeyama,Rika Kosaki,Tsutomu Ogata,Masato Tsukahara,Yu‐ichi Goto,Junichi Hata,Nobutake Matsuo,Robert J. Smith,Kenjiro Kosaki	2001	4
19	Fluorescence-based DHPLC for allelic quantification by single-nucleotide primer extension Journal of Biochemical and Biophysical Methods ·Kenjiro Kosaki,Hiroshi Yoshihashi,Yuko Ohashi,Rika Kosaki,Taichi A. Suzuki,Nobutake Matsuo	2001	9
20	Imprinting of Human GRB10 and Its Mutations in Two Patients with Russell-Silver Syndrome The American Journal of Human Genetics ·Hiroshi Yoshihashi,Katsuhiro Maeyama,Rika Kosaki,Tsutomu Ogata,Masato Tsukahara,Yu-ichi Goto,Jun-ichi Hata,Nobutake Matsuo,Robert J. Smith,Kenjiro Kosaki	2000	69

About Hiroshi Yoshihashi

Hiroshi Yoshihashi is a scholar working on Genetics, Business and International Management and Genetics, having authored 44 papers that have together received 609 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Prenatal Screening and Diagnostics (6 papers), Hedgehog Signaling Pathway Studies (5 papers), Epigenetics and DNA Methylation (5 papers), Congenital Ear and Nasal Anomalies (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (111 citations), Genetics (280 citations) and Molecular Biology (341 citations). Hiroshi Yoshihashi has collaborated with scholars based in Japan, United States and Germany. Frequent co-authors include Kenjiro Kosaki, Rika Kosaki, Nobutake Matsuo, Tomonobu Hasegawa, Tsutomu Ogata, Toshiki Takenouchi, Takao Takahashi, Tomoko Uehara, Yoshimitsu Fukushima and Kenji Kurosawa. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Scientific Reports and The American Journal of Human Genetics.

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