Yasuhiro Indo

3.2k citations

59 papers · 2.4k · h-index 28

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Nerve injury and regeneration

Papers in

Clinical Biochemistry 26
- Metabolism and Genetic Disorders 26
Molecular Biology 25
- Biochemical and Molecular Research 12
- Peroxisome Proliferator-Activated Receptors 8

Co-authors: Kay Tanaka (11 shared papers)Ichiro Matsuda (14 shared papers)Hiroshi Mitsubuchi (11 shared papers)Yutaka Awaya (4 shared papers)Mohammad A. Karim (3 shared papers)F. Endo (12 shared papers)Kohji Ohta (4 shared papers)Tomoyasu Kawano (3 shared papers)
Journals: Journal of Clinical Investigation (6 papers)Pediatric Research (5 papers)Human Genetics (5 papers)Journal of Inherited Metabolic Disease (5 papers)Journal of Pediatric Gastroenterology and Nutrition (3 papers)
Partner nations: Japan United States Italy

In The Last Decade

Yasuhiro Indo

59 papers receiving 2.3k citations

Peers

Countries citing papers authored by Yasuhiro Indo

Since Specialization

Citations

This map shows the geographic impact of Yasuhiro Indo'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 Yasuhiro Indo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yasuhiro Indo more than expected).

Fields of papers citing papers by Yasuhiro Indo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yasuhiro Indo. 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 Yasuhiro Indo. The network helps show where Yasuhiro Indo may publish in the future.

Co-authors

The 25 scholars most cited alongside Yasuhiro Indo, 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 Yasuhiro Indo Line = papers co-authored together Yasuhiro Indo links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis Nature Genetics ·Yasuhiro Indo, Motoko Tsuruta, Yumi Hayashida, Mohammad A. Karim, Kohji Ohta, Tomoyasu Kawano, Hiroshi Mitsubuchi, Hidefumi Tonoki, Yutaka Awaya, Ichiro Matsuda	1996	462
2	Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): Mutations and polymorphisms inTRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor Human Mutation ·Yasuhiro Indo	2001	137
3	Molecular Cloning and Nucleotide Sequence of cDNAs Encoding the Precursors of Rat Long Chain Acyl-Coenzyme A, Short Chain Acyl-Coenzyme A, and Isovaleryl-Coenzyme A Dehydrogenases Journal of Biological Chemistry ·Yoichi Matsubara, Yasuhiro Indo, Etsuo Naito, H Ozasa, Robin Glassberg, Jerry Vockley, Yasuyuki Ikeda, Jan P. Kraus, Kay Tanaka	1989	137
4	Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA (NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor The American Journal of Human Genetics ·Sek Mardy, Yuichi Miura, Fumio Endo, Ichiro Matsuda, László Sztriha, Philippe Frossard, Allie Moosa, Essam A. R. Ismail, Alfons Macaya, Generoso Andria, Ennio Toscano, William T. Gibson, Gail E. Graham, Yasuhiro Indo	1999	121
5	Primary structure and gene localization of human prolidase Journal of Biological Chemistry ·F. Endo, Akito Tanoue, H. Nakai, Akira Hata, Yasuhiro Indo, Koiti Titani, Iwao Matsuda	1989	112
6	Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor. Clinical Autonomic Research ·Yasuhiro Indo	2002	98
7	Identification of Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Three Patients Previously Diagnosed with Long-Chain Acyl-CoA Dehydrogenase Deficiency Pediatric Research ·Seiji Yamaguchi, Yasuhiro Indo, Paul M. Coates, Takashi Hashimoto, Kay Tanaka	1993	95
8	Molecular basis of medium chain acyl-coenzyme A dehydrogenase deficiency. An A to G transition at position 985 that causes a lysine-304 to glutamate substitution in the mature protein is the single prevalent mutation. Journal of Clinical Investigation ·Ichiro Yokota, Yasuhiro Indo, Paul M. Coates, Kay Tanaka	1990	86
9	Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families Human Genetics ·Yoshiko Miura, Sek Mardy, Yutaka Awaya, Keiji Nihei, F. Endo, I. Matsuda, Yasuhiro Indo	2000	79
10	Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency. Journal of Clinical Investigation ·Etsuo Naito, Yasuhiro Indo, Kay Tanaka	1990	63
11	Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis Clinical Genetics ·Yasuhiro Indo	2012	61
12	NGF-dependent neurons and neurobiology of emotions and feelings: Lessons from congenital insensitivity to pain with anhidrosis Neuroscience & Biobehavioral Reviews ·Yasuhiro Indo	2018	54
13	Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis Expert Review of Neurotherapeutics ·Yasuhiro Indo	2010	53
14	Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of theTRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutantTRKA andPKLR genes in a family with CIPA and pyruvate kinase deficiency Human Mutation ·Yasuhiro Indo, Sek Mardy, Yuichi Miura, Allie Moosa, Essam A. R. Ismail, Ennio Toscano, Generoso Andria, Vito Pavone, Deborah Brown, Alice Brooks, Fumio Endo, Ichiro Matsuda	2001	51
15	Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis Human Genetics ·Yuichi Miura, Makoto Hiura, Katsumi Torigoe, Osamu Numata, Atsushi Kuwahara, Masamichi Matsunaga, Satoshi Hasegawa, Naoki Boku, Ichiro Matsuda, Haruyoshi Ino, Yasuhiro Indo, Sek Mardy, Fumio Endo	2000	49
16	Structure and organization of the humanTRKA gene encoding a high affinity receptor for nerve growth factor The Japanese Journal of Human Genetics ·Yasuhiro Indo, Sek Mardy, Motoko Tsuruta, Mohammad A. Karim, Ichiro Matsuda	1997	48
17	Altered kinetic properties of the branched-chain alpha-keto acid dehydrogenase complex due to mutation of the beta-subunit of the branched-chain alpha-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine disease. Journal of Clinical Investigation ·Yasuhiro Indo, Akito Kitano, F. Endo, Izumi Akaboshi, Iwao Matsuda	1987	47
18	Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2 Genomics ·Yasuhiro Indo, Teresa L. Yang‐Feng, Robin Glassberg, Kay Tanaka	1991	44
19	Medium Chain 3-Ketoacyl-Coenzyme A Thiolase Deficiency: A New Disorder of Mitochondrial Fatty Acid β-Oxidation Pediatric Research ·Takehiko Kamijo, Yasuhiro Indo, Masayoshi Souri, Toshifumi Aoyama, Tomokuni Hara, Shigenori Yamamoto, Seiichi Ushikubo, Piero Rinaldo, Ichiro Matsuda, Atsushi Komiyama, Takashi Hashimoto	1997	38
20	Oculocerebrorenal syndrome of Lowe: Three mutations in theOCRL1 gene derived from three patients with different phenotypes American Journal of Medical Genetics ·Tomoyasu Kawano, Yasuhiro Indo, Hitoshi Nakazato, Mitsunobu Shimadzu, Ichiro Matsuda	1998	34

About Yasuhiro Indo

Yasuhiro Indo is a scholar working on Clinical Biochemistry, Molecular Biology, Cellular and Molecular Neuroscience, Rheumatology and Immunology, having authored 59 papers that have together received 2.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (26 papers), Hereditary Neurological Disorders (18 papers), Biochemical and Molecular Research (12 papers), Toxin Mechanisms and Immunotoxins (9 papers), Peroxisome Proliferator-Activated Receptors (8 papers), Urticaria and Related Conditions (8 papers), Folate and B Vitamins Research (4 papers) and Amino Acid Enzymes and Metabolism (4 papers). The work is most often cited by research in Clinical Biochemistry (638 citations), Cellular and Molecular Neuroscience (935 citations), Physiology (519 citations), Biochemistry (119 citations) and Molecular Biology (1.1k citations). Yasuhiro Indo has collaborated with scholars based in Japan, United States and Italy. Frequent co-authors include Kay Tanaka, Ichiro Matsuda, Hiroshi Mitsubuchi, Yutaka Awaya, Mohammad A. Karim, F. Endo, Kohji Ohta, Tomoyasu Kawano, Paul M. Coates and Etsuo Naito. Their work appears in journals such as Journal of Clinical Investigation, Pediatric Research, Human Genetics, Journal of Inherited Metabolic Disease and Journal of Pediatric Gastroenterology and Nutrition.

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