Tatsuro Kondoh

3.6k citations

59 papers · 1.2k indexed · h-index 19

Genetics top 5%
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 7
- Genetics and Neurodevelopmental Disorders 7
- Craniofacial Disorders and Treatments 5
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 8
Immunology and Allergy top 10%
Molecular Biology
- Epigenetics and DNA Methylation 7
Immunology
Clinical Biochemistry
- Metabolism and Genetic Disorders 5
Public Health, Environmental and Occupational Health
- Down syndrome and intellectual disability research 5

Co-authors: Hiroyuki Moriuchi Tadashi Matsumoto Norio Niikawa Naoki Harada Koh-ichiro Yoshiura Kenji Kurosawa Ian D. Krantz Laird G. Jackson
Cited by: Genetics Pediatrics, Perinatology and Child Health Immunology and Allergy
Journals: The Journal of Immunology (2 papers)PLoS ONE (1 paper)Scientific Reports (1 paper)
Partner nations: Japan United States Hong Kong

In The Last Decade

Tatsuro Kondoh

58 papers receiving 1.2k citations

Peers

Countries citing papers authored by Tatsuro Kondoh

Since Specialization

Citations

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

Fields of papers citing papers by Tatsuro Kondoh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Brothers with novel compound heterozygous mutations in COL27A1 causing dental and genital abnormalities European Journal of Medical Genetics ·Chisei Satoh,Tatsuro Kondoh,Hitomi Shimizu,Akira Kinoshita,Hiroyuki Mishima,Gen Nishimura,M Miyazaki,Kunihiko Okano,Yoshihiko Kumai,Koh-ichiro Yoshiura	2020	3
2	Evaluation of Face2Gene using facial images of patients with congenital dysmorphic syndromes recruited in Japan Journal of Human Genetics ·Hiroyuki Mishima,Hisato Suzuki,Michiko Doi,M Miyazaki,Satoshi Watanabe,Tadashi Matsumoto,Kanako Morifuji,Hiroyuki Moriuchi,Koh-ichiro Yoshiura,Tatsuro Kondoh,Kenjiro Kosaki	2019	58
3	Three brothers with a nonsense mutation in KAT6A caused by parental germline mosaicism Human Genome Variation ·Chisei Satoh,Ryuta Maekawa,Akira Kinoshita,Hiroyuki Mishima,Michiko Doi,M Miyazaki,Masafumi Fukuda,Haruo Takahashi,Tatsuro Kondoh,Koh-ichiro Yoshiura	2017	11
4	Familial brain arteriovenous malformation maps to 5p13–q14, 15q11–q13 or 18p11: Linkage analysis with clipped fingernail DNA on high-density SNP array European Journal of Medical Genetics ·Masahiro Oikawa,Hideo Kuniba,Tatsuro Kondoh,Akira Kinoshita,Takeshi Nagayasu,Norio Niikawa,Koh-ichiro Yoshiura	2010	7
5	Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome Journal of Human Genetics ·Hideo Kuniba,Koh-ichiro Yoshiura,Tatsuro Kondoh,Hirofumi Ohashi,Kenji Kurosawa,Hidefumi Tonoki,Toshiro Nagai,Nobuhiko Okamoto,Mitsuhiro Kato,Yoshimitsu Fukushima,Tadashi Kaname,Kenji Naritomi,Tadashi Matsumoto,Hiroyuki Moriuchi,Tatsuya Kishino,Akira Kinoshita,Noriko Miyake,Naomichi Matsumoto,Norio Niikawa	2009	27
6	Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2–H19 domain in bodies and placentas Journal of Molecular Medicine ·Kazuki Yamazawa,Masayo Kagami,Toshiro Nagai,Tatsuro Kondoh,Kazumichi Onigata,Katsuhiro Maeyama,Tomonobu Hasegawa,Yukihiro Hasegawa,Toshio Yamazaki,Seiji Mizuno,Yoko Miyoshi,Shinichiro Miyagawa,Reiko Horikawa,Kentaro Matsuoka,Tsutomu Ogata	2008	43
7	Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause American Journal of Medical Genetics Part A ·Kiyonori Miura,Koh‐ichiro Yoshiura,Shoko Miura,Tatsuro Kondoh,Naoki Harada,Kentaro Yamasaki,Yoko Fujimoto,Yoko Yamasaki,Terumi Tanigawa,Yuriko Kitajima,Takako Shimada,Atsushi Yoshida,Daisuke Nakayama,Masato Tagawa,Shuichiro Yoshimura,Joseph Wagstaff,Yoshihiro Jinno,Tadayuki Ishimaru,Norio Niikawa,Hideaki Masuzaki	2006	23
8	Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency Genetics in Medicine ·Naohiro Kurotaki,Joseph Shen,Mayumi Touyama,Tatsuro Kondoh,Remco Visser,Takao Ozaki,Junji Nishimoto,Takashi Shiihara,Kimiaki Uetake,Yoshio Makita,Naoki Harada,Salmo Raskin,Chester Brown,Pia Höglund,Nobuhiko Okamoto,James R. Lupski	2005	33
9	Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia Journal of Human Genetics ·Tetsuya Niihori,Yoko Aoki,Hirofumi Ohashi,Kenji Kurosawa,Tatsuro Kondoh,Satoshi Ishikiriyama,Hiroshi Kawame,Hotaka Kamasaki,Tsutomu Yamanaka,Fumio Takada,Kimio Nishio,Masahiro Sakurai,Hiroshi Tamai,Tatsuro Nagashima,Yoichi Suzuki,Shigeo Kure,Kunihiro Fujii,Masue Imaizumi,Yoichi Matsubara	2005	87
10	ABNORMAL FOLIC ACID HOMOCYSTEINE METABOLISM AS MATERNAL RISK FACTORS FOR DOWN SYNDROME IN JAPAN Health and Ecology Issues ·Noboru Takamura,Tatsuro Kondoh,Syohei Ohgi,Kokichi Arisawa,Mariko Mine,Shunichi Yamashita,Kiyoshi Aoyagi	2004	4
11	Molecular characterization of inv dup del(8p): Analysis of five cases American Journal of Medical Genetics Part A ·Osamu Shimokawa,Kenji Kurosawa,Tomoko Ida,Naoki Harada,Tatsuro Kondoh,Noriko Miyake,Koh-ichiro Yoshiura,Tatsuya Kishino,Tohru Ohta,Norio Niikawa,Naomichi Matsumoto	2004	61
12	Genotype-phenotype correlation of 5p- syndrome: pitfall of diagnosis Journal of Human Genetics ·Tatsuro Kondoh,Osamu Shimokawa,Naoki Harada,Tomoki Doi,Chyuns Yun,Yuji Gohda,Fumiko Kinoshita,Tadashi Matsumoto,Hiroyuki Moriuchi	2004	17
13	Abnormal folic acid-homocysteine metabolism as maternal risk factors for Down syndrome in Japan European Journal of Nutrition ·Noboru Takamura,Tatsuro Kondoh,Syohei Ohgi,Kokichi Arisawa,Mariko Mine,Shunichi Yamashita,Kiyoshi Aoyagi	2004	29
14	Hearing impairment, undescended testis, circumferential skin creases, and mental handicap (HITCH) syndrome: A case report American Journal of Medical Genetics Part A ·Tatsuro Kondoh,Jiro Eguchi,Yoichiro Hamasaki,Tomoki Doi,Eiichi Kinoshita,Tadashi Matsumoto,Kuniko Abe,Yoshinobu Ohtani,Hiroyuki Moriuchi	2003	8
15	Spontaneous In Vivo Reversion of an Inherited Mutation in the Wiskott-Aldrich Syndrome The Journal of Immunology ·Tadashi Ariga,Tatsuro Kondoh,Koji Yamaguchi,Masafumi Yamada,Satoshi Sasaki,David L. Nelson,Hisami Ikeda,Kunihiko Kobayashi,Hiroyuki Moriuchi,Yukio Sakiyama	2001	84
16	A case of Schinzel–Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy Pediatrics International ·Tatsuro Kondoh,Naohisa Kamimura,Akira Tsuru,Tadashi Matsumoto,Tetsuo Matsuzaka,Hiroyuki Moriuchi	2001	17
17	Improvement of C-Reactive Protein Levels and Body Temperature of an Elderly Patient Infected with Pseudomonas aeruginosa on Treatment with Mao-Bushi-Saishin-To The Journal of Alternative and Complementary Medicine ·Tsutomu Kamei,Tatsuro Kondoh,Satoshi Nagura,Yoshitaka Toriumi,Hiroaki Kumano,Haruaki Tomioka	2000	15
18	Determination of Carrier Status for the Wiskott-Aldrich Syndrome by Flow Cytometric Analysis of Wiskott-Aldrich Syndrome Protein Expression in Peripheral Blood Mononuclear Cells The Journal of Immunology ·Masafumi Yamada,Tadashi Ariga,Nobuaki Kawamura,Koji Yamaguchi,Makoto Ohtsu,David L. Nelson,Tatsuro Kondoh,Ichiro Kobayashi,Motohiko Okano,Kunihiko Kobayashi,Yukio Sakiyama	2000	34
19	A point mutation at ATP-binding region of the ALD gene in a family with X-linked adrenoleukodystrophy The Japanese Journal of Human Genetics ·Tadashi Matsumoto,Tatsuro Kondoh,Hideaki Masuzaki,Naoki Harada,Tetsuo Matsusaka,Eiichi Kinoshita,Goh Takeo,Mitsuhiro Tsujihata,Yasuyuki Suzuki,Yoshiro Tsuji	1994	10
20	5′ Structure and Expression of Human Glucose-6-Phosphate Dehydrogenase mRNA DNA and Cell Biology ·Hitoshi Kanno,Tatsuro Kondoh,Akira Yoshida	1993	6

About Tatsuro Kondoh

Tatsuro Kondoh is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 59 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (8 papers), Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Metabolism and Genetic Disorders (5 papers), Down syndrome and intellectual disability research (5 papers) and Craniofacial Disorders and Treatments (5 papers). The work is most often cited by research in Genetics (534 citations), Pediatrics, Perinatology and Child Health (252 citations) and Immunology and Allergy (64 citations). Tatsuro Kondoh has collaborated with scholars based in Japan, United States and Hong Kong. Frequent co-authors include Hiroyuki Moriuchi, Tadashi Matsumoto, Norio Niikawa, Naoki Harada, Koh-ichiro Yoshiura, Kenji Kurosawa, Ian D. Krantz, Laird G. Jackson, Nancy B. Spinner and Zhe Zhang. Their work appears in journals such as The Journal of Immunology, PLoS ONE and Scientific Reports.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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