D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 55 Citations 8,622 340 World Ranking 2804 National Ranking 118

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Internal medicine
  • Enzyme

Naomi Kondo mostly deals with Genetics, Molecular biology, Immunology, Peroxisomal disorder and Peroxisome. The study incorporates disciplines such as Point mutation, Gene mutation, Complementary DNA, Green fluorescent protein and Nuclear localization sequence in addition to Molecular biology. The Immunology study combines topics in areas such as Peripheral blood mononuclear cell and Pneumonia.

Her research integrates issues of Zellweger syndrome and PEX6 in her study of Peroxisomal disorder. Her biological study spans a wide range of topics, including Complementation and Exon. Her research in Peroxisome intersects with topics in Complementation group, DNA ligase and Chinese hamster ovary cell.

Her most cited work include:

  • Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity (546 citations)
  • Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly (197 citations)
  • Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. (143 citations)

What are the main themes of her work throughout her whole career to date?

Her main research concerns Immunology, Molecular biology, Genetics, Internal medicine and Gene. As part of her studies on Immunology, Naomi Kondo frequently links adjacent subjects like Peripheral blood mononuclear cell. Her Molecular biology research is multidisciplinary, relying on both Mutation, Mutant, Point mutation, Biochemistry and Complementary DNA.

Her studies in Exon, Allele, Zellweger syndrome, Peroxisomal disorder and Missense mutation are all subfields of Genetics research. Her study looks at the relationship between Internal medicine and fields such as Endocrinology, as well as how they intersect with chemical problems. Her Peroxisome research includes themes of Complementation, Biogenesis and Chinese hamster ovary cell.

She most often published in these fields:

  • Immunology (28.67%)
  • Molecular biology (23.86%)
  • Genetics (20.24%)

What were the highlights of her more recent work (between 2008-2020)?

  • Immunology (28.67%)
  • Asthma (7.23%)
  • Internal medicine (13.73%)

In recent papers she was focusing on the following fields of study:

Her scientific interests lie mostly in Immunology, Asthma, Internal medicine, Genetics and Molecular biology. Her study in Immunology is interdisciplinary in nature, drawing from both Casein, Complication, Mutation and Desensitization. She has researched Asthma in several fields, including Immunoglobulin E, Pharmacokinetics and Intensive care medicine.

As a part of the same scientific study, she usually deals with the Internal medicine, concentrating on Endocrinology and frequently concerns with Compound heterozygosity and Mutation. Her study in Thiolase and Haploinsufficiency is done as part of Genetics. Her Molecular biology research incorporates themes from Gene, Mutant, Homologous recombination and Exon.

Between 2008 and 2020, her most popular works were:

  • STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern (113 citations)
  • Japanese Guideline for Food Allergy 2014. (84 citations)
  • Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency (66 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Enzyme

Genetics, Molecular biology, Mutant, Mutation and Guideline are her primary areas of study. Many of her studies involve connections with topics such as Agenesis of the corpus callosum and Genetics. Within one scientific family, Naomi Kondo focuses on topics pertaining to RNA splicing under Molecular biology, and may sometimes address concerns connected to Mutation testing.

She interconnects IRAK4, Blot, HEK 293 cells, Reporter gene and Single-nucleotide polymorphism in the investigation of issues within Mutant. Her Compound heterozygosity research focuses on Enzyme assay and how it connects with Internal medicine. Her Internal medicine study integrates concerns from other disciplines, such as Endocrinology and Pathology.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity

Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe.
Immunity (2006)

711 Citations

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

Yuji Matsuzono;Naohiko Kinoshita;Shigehiko Tamura;Nobuyuki Shimozawa.
Proceedings of the National Academy of Sciences of the United States of America (1999)

277 Citations

Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.

Kenji E. Orii;Youngsoo Lee;Naomi Kondo;Peter J. McKinnon.
Proceedings of the National Academy of Sciences of the United States of America (2006)

228 Citations

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Masanori Honsho;Shigehiko Tamura;Nobuyuki Shimozawa;Yasuyuki Suzuki.
American Journal of Human Genetics (1998)

218 Citations

MOLECULAR CLONING OF CDNA ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE

Atsushi Uchiyama;Toshifumi Aoyama;Keiju Kamijo;Yasushi Uchida.
Journal of Biological Chemistry (1996)

209 Citations

Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.

Fukao T;Song Xq;Mitchell Ga;Yamaguchi S.
Pediatric Research (1997)

182 Citations

Cord blood lymphocyte responses to food antigens for the prediction of allergic disorders.

N Kondo;Y Kobayashi;S Shinoda;K Kasahara.
Archives of Disease in Childhood (1992)

180 Citations

d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder

Yasuyuki Suzuki;Ling Ling Jiang;Masayoshi Souri;Shoko Miyazawa.
American Journal of Human Genetics (1997)

146 Citations

STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern

Hirotomo Saitsu;Mitsuhiro Kato;Ippei Okada;Kenji E. Orii.
Epilepsia (2010)

144 Citations

PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

Kanji Okumoto;Nobuyuki Shimozawa;Atsusi Kawai;Shigehiko Tamura.
Molecular and Cellular Biology (1998)

140 Citations

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