Yasuhiro Indo

2.9k citations

55 papers · 2.2k indexed · h-index 25

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 25
- Metabolism and Genetic Disorders 25
Cellular and Molecular Neuroscience 21
- Hereditary Neurological Disorders 17

Co-authors: Kay Tanaka Ichiro Matsuda Hiroshi Mitsubuchi Yutaka Awaya F. Endo Kohji Ohta Tomoyasu Kawano Paul M. Coates
Journals: Journal of Clinical Investigation (6 papers)Journal of Inherited Metabolic Disease (5 papers)Human Genetics (5 papers)Pediatric Research (5 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2 papers)
Partner nations: Japan United States Italy

In The Last Decade

Yasuhiro Indo

55 papers receiving 2.1k 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-authorship network

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

#	Work
1	NGF-dependent neurons and neurobiology of emotions and feelings: Lessons from congenital insensitivity to pain with anhidrosis Neuroscience & Biobehavioral Reviews ·Yasuhiro Indo	2018	54
2	Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis Clinical Genetics ·Yasuhiro Indo	2012	60
3	Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis Expert Review of Neurotherapeutics ·Yasuhiro Indo	2010	53
4	Nerve growth factor, interoception, and sympathetic neuron: Lesson from congenital insensitivity to pain with anhidrosis Autonomic Neuroscience ·Yasuhiro Indo	2009	20
5	No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V Annals of Neurology ·R Stnik, Alessandro Simonati, Yasuhiro Indo, Generoso Andria	2002	13
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	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, R Stnik, Generoso Andria, Vito Pavone, Deborah Brown, Tanuwat Larptansuphaphol, Fumio Endo, Ichiro Matsuda	2001	51
8	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	135
9	Multisystem Involvement in Congenital Insensitivity to Pain with Anhidrosis (CIPA), a Nerve Growth Factor Receptor(Trk A)-Related Disorder Neuropediatrics ·Evelina Toscano, Roberto Della Casa, Sek Mardy, Lucia Gaetaniello, Francesco Sadile, Yasuhiro Indo, Claudio Pignata, Generoso Andria	2000	33
10	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 ·Alice Frisinghelli, Makoto Hiura, Katsumi Torigoe, Osamu Numata, GE Xiao-xia, Masamichi Matsunaga, Satoshi Hasegawa, Arini Hidayati Jamil, Ichiro Matsuda, Hasan Yilmaz, Yasuhiro Indo, Sek Mardy, Fumio Endo	2000	49
11	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, A.N. SOKOLOV, Yasuhiro Indo	2000	79
12	Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain α-keto acid dehydrogenase complex Journal of Human Genetics ·Tomohiro Seki, Hiroshi Mitsubuchi, Sek Mardy, Yuichi Miura, Zheng-Bin Gu, Akihiko Kinugasa, Takateru Ishitsu, Ichiro Matsuda, Yasuhiro Indo	1998	24
13	Human ESP1/CRP2, a Member of the LIM Domain Protein Family: Characterization of the cDNA and Assignment of the Gene Locus to Chromosome 14q32.3 Genomics ·Mohammad A. Karim, Kohji Ohta, Marcos Wílian da Silva, Yoshihiro Jinno, Norio Niikawa, Ichiro Matsuda, Yasuhiro Indo	1996	27
14	Deficiency of the E1β subunit in the branched-chain α-keto acid dehydrogenase complex due to a single base substitution to the intron 5, resulting in two alternatively spliced mRNAs in patient with maple syrup urine disease Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Zheng-Bin Gu, Hiroshi Mitsubuchi, Yasuhiro Indo, Kohji Ohta, Fumio Endo, Yoshiro Wada, Ichiro Matsuda	1994	16
15	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	96
16	Immunochemical Characterization of Variant Medium-Chain Acyl-CoA Dehydrogenase in Fibroblasts from Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency Pediatric Research ·Paul M. Coates, Yasuhiro Indo, D S Young, Daniel E. Hale, Kay Tanaka	1992	23
17	Maple syrup urine disease caused by a partial deletion in the inner E2 core domain of the branched chain alpha-keto acid dehydrogenase complex due to aberrant splicing. A single base deletion at a 5'-splice donor site of an intron of the E2 gene disrupts the consensus sequence in this region. Journal of Clinical Investigation ·Hiroshi Mitsubuchi, Yoshitaka Nobukuni, Izumi Akaboshi, Yasuhiro Indo, F. Endo, Iwao Matsuda	1991	23
18	Immunochemical Characterization of Variant Long-Chain Acyl-CoA Dehydrogenase in Cultured Fibroblasts from Nine Patients with Long-Chain Acyl-CoA Dehydrogenase Deficiency Pediatric Research ·Yasuhiro Indo, Paul M. Coates, Daniel E. Hale, Kay Tanaka	1991	20
19	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	64
20	Immunochemical Studies of Human Prolidase with Monoclonal and Polyclonal Antibodies:Absence of the Subunit of Prolidase in Erythrocytes from a Patient with Prolidase Deficiency Pediatric Research ·Fumio Endo, Kunihiko Motohara, Yasuhiro Indo, Ichiro Matsuda	1987	27

About Yasuhiro Indo

Yasuhiro Indo is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience, Biochemistry, Rheumatology and Cell Biology, having authored 55 papers that have together received 2.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (25 papers), Hereditary Neurological Disorders (17 papers), Biochemical and Molecular Research (12 papers), Peroxisome Proliferator-Activated Receptors (8 papers), Toxin Mechanisms and Immunotoxins (8 papers), Urticaria and Related Conditions (7 papers), Amino Acid Enzymes and Metabolism (4 papers) and Pain Mechanisms and Treatments (4 papers). The work is most often cited by research in Clinical Biochemistry (616 citations), Cellular and Molecular Neuroscience (853 citations), Physiology (523 citations), Molecular Biology (1.1k citations) and Biochemistry (109 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, F. Endo, Kohji Ohta, Tomoyasu Kawano, Paul M. Coates, Mohammad A. Karim and Etsuo Naito. Their work appears in journals such as Journal of Clinical Investigation, Journal of Inherited Metabolic Disease, Human Genetics, Pediatric Research and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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