Hiroshi Kawame

6.1k citations

66 papers · 2.1k indexed · h-index 23

Molecular Biology top 10%
Genetics top 5%
Immunology top 10%
Surgery
Pediatrics, Perinatology and Child Health top 5%

Co-authors: Kenji Kurosawa Hirofumi Ohashi Shigeo Kure Yoichi Matsubara Tetsuya Niihori Yoko Aoki Yoichi Suzuki Yukichi Tanaka
Topics: Genomic variations and chromosomal abnormalities (13 papers)Genomics and Rare Diseases (10 papers)Lysosomal Storage Disorders Research (10 papers)
Cited by: Genetics Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Japan United States United Kingdom

In The Last Decade

Hiroshi Kawame

62 papers receiving 2.0k citations

Peers

Countries citing papers authored by Hiroshi Kawame

Since Specialization

Citations

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

Fields of papers citing papers by Hiroshi Kawame

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiroshi Kawame

This figure shows the co-authorship network connecting the top 25 collaborators of Hiroshi Kawame. A scholar is included among the top collaborators of Hiroshi Kawame based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Hiroshi Kawame. Hiroshi Kawame is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Association of Quinolone Exposure in the First‐Trimester of Pregnancy and the Risk of Major Congenital Malformations: A Health Administrative Database Study in Japan 2025 ·Pharmacoepidemiology and Drug Safety ·(unknown),Taku Obara,Tomofumi Ishikawa,(unknown),(unknown),Noriyuki Iwama,(unknown),Aoi Noda,Masatsugu Orui,Mami Ishikuro,Hiroshi Kawame,Nariyasu Mano,Shinichi Kuriyama	0
2	Risk of Major Congenital Malformations Associated with the Use of Japanese Traditional (Kampo) Medicine Containing Ephedra During the First Trimester of Pregnancy 2024 ·Drugs - Real World Outcomes ·Aoi Noda,Taku Obara,(unknown),Satoko Suzuki,Ryutaro Arita,Minoru Ohsawa,(unknown),(unknown),Fumihiko Ueno,(unknown),Masatsugu Orui,Keiko Murakami,Mami Ishikuro,Akiko Kikuchi,Shin Takayama,Tadashi Ishii,Hiroshi Kawame,Shigeo Kure,Shinichi Kuriyama	3
3	Difficulties in disclosing secondary findings by facilities performing comprehensive germline genetic testing for rare diseases in Japan 2024 ·Congenital Anomalies ·(unknown),Takahiro Yamada,(unknown),Hiroshi Kawame,Eiji Nanba,Yu‐ichi Goto,Shinji Kosugi	0
4	The Health History of First-Degree Relatives’ Dyslipidemia Can Affect Preferences and Intentions following the Return of Genomic Results for Monogenic Familial Hypercholesterolemia 2024 ·Genes ·(unknown),(unknown),Akimune Fukushima,(unknown),Yasushi Ishigaki,Hiroshi Kawame,Nobuo Fuse,Fuji Nagami,Yoichi Suzuki,Mika Sakurai‐Yageta,Akira Uruno,Kichiya Suzuki,Kozo Tanno,Hideki Ohmomo,Atsushi Shimizu,Masayuki Yamamoto,Makoto Sasaki	0
5	Real‐world prevalence, time of diagnosis, and co‐occurrence patterns of birth defects in live‐born infants, 2014–2020: A health administrative database study in Japan 2023 ·Birth Defects Research ·Tomofumi Ishikawa,Hiroshi Kawame,Nariyasu Mano,Taku Obara	4
6	Risk of major congenital malformations associated with first-trimester antihypertensives, including amlodipine and methyldopa: A large claims database study 2010–2019 2023 ·Pregnancy Hypertension ·Tomofumi Ishikawa,Hidekazu Nishigori,Manabu Akazawa,Keiko Miyakoda,Aoi Noda,Mami Ishikuro,Hirohito Metoki,Noriyuki Iwama,Masatoshi Saito,Junichi Sugawara,Hiroshi Kawame,Nobuo Yaegashi,Shinichi Kuriyama,Nariyasu Mano,Taku Obara	14
7	Challenges of secondary finding disclosure in genomic medicine in rare diseases: A nation-wide survey of Japanese facilities outsourcing comprehensive genetic testing 2022 ·Journal of Human Genetics ·(unknown),Takahiro Yamada,(unknown),Hiroshi Kawame,Eiji Nanba,Yu‐ichi Goto,Shinji Kosugi	3
8	Novel missense COL2A1 variant in a fetus with achondrogenesis type II 2022 ·Human Genome Variation ·(unknown),(unknown),(unknown),Kana Harada,(unknown),(unknown),Ken Takahashi,Hiroshi Kawame,Kenichiro Hata,Osamu Samura,Aikou Okamoto	2
9	Risk of major congenital malformations associated with first‐trimester exposure to propulsives: A health administrative database study in Japan 2021 ·Pharmacoepidemiology and Drug Safety ·Tomofumi Ishikawa,Taku Obara,Manabu Akazawa,Aoi Noda,(unknown),(unknown),Keiko Miyakoda,Hidekazu Nishigori,Hiroshi Kawame,Nobuo Yaegashi,Shinichi Kuriyama,Nariyasu Mano	11
10	Validity of congenital malformation diagnoses in healthcare claims from a university hospital in Japan 2021 ·Pharmacoepidemiology and Drug Safety ·Tomofumi Ishikawa,(unknown),Taku Obara,Aoi Noda,(unknown),(unknown),Ryusuke Inoue,Hiroshi Kawame,Nariyasu Mano	14
11	Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individuals 2019 ·Human Genetics ·Yumi Yamaguchi‐Kabata,Jun Yasuda,Akira Uruno,Kazuro Shimokawa,S. Koshiba,Yoichi Suzuki,Nobuo Fuse,Hiroshi Kawame,Shu Tadaka,Masao Nagasaki,Kaname Kojima,Fumiki Katsuoka,Kazuki Kumada,Osamu Tanabe,Gen Tamiya,Nobuo Yaegashi,Kengo Kinoshita,Masayuki Yamamoto,Shigeo Kure	6
12	Surgical intervention for esophageal atresia in patients with trisomy 18 2013 ·American Journal of Medical Genetics Part A ·Eriko Nishi,Satoshi Takamizawa,(unknown),Yasumasa Yamada,(unknown),(unknown),Takehiko Hiroma,Seiji Mizuno,Hiroshi Kawame,Yoshimitsu Fukushima,Tomohiko Nakamura,Tomoki Kosho	36
13	Attitudes toward non‐invasive prenatal diagnosis among pregnant women and health professionals in Japan 2012 ·Prenatal Diagnosis ·Junko Yotsumoto,Akihiko Sekizawa,Keiko Koide,Yuditiya Purwosunu,Kiyotake Ichizuka,Ryu Matsuoka,Hiroshi Kawame,Takashi Okai	40
14	Prevalence and clinical features of Costello syndrome and cardio‐facio‐cutaneous syndrome in Japan: Findings from a nationwide epidemiological survey 2012 ·American Journal of Medical Genetics Part A ·Yu Abe,Yoko Aoki,Shinichi Kuriyama,Hiroshi Kawame,Nobuhiko Okamoto,Kenji Kurosawa,Hirofumi Ohashi,Seiji Mizuno,Tsutomu Ogata,Shigeo Kure,Tetsuya Niihori,Yoichi Matsubara,(unknown)	63
15	Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies 2010 ·Journal of Human Genetics ·Shoko Komatsuzaki,Yoko Aoki,Tetsuya Niihori,Nobuhiko Okamoto,Raoul C. M. Hennekam,Saskia Hopman,Hirofumi Ohashi,Seiji Mizuno,Yoriko Watanabe,Hotaka Kamasaki,Ikuko Kondo,Nobuko Moriyama,Kenji Kurosawa,Hiroshi Kawame,Ryuhei Okuyama,Masue Imaizumi,Takeshi Rikiishi,Shigeru Tsuchiya,Shigeo Kure,Yoichi Matsubara	35
16	Various types of LRP5 mutations in four patients with osteoporosis‐pseudoglioma syndrome: Identification of a 7.2‐kb microdeletion using oligonucleotide tiling microarray 2009 ·American Journal of Medical Genetics Part A ·Satoshi Narumi,Chikahiko Numakura,Takashi Shiihara,(unknown),Yasuyuki Nozaki,Takanori Yamagata,Mariko Y. Momoi,Yoriko Watanabe,Makoto Yoshino,Toyojiro Matsuishi,Eriko Nishi,Hiroshi Kawame,Tsutomu Akahane,Gen Nishimura,Mitsuru Emi,Tomonobu Hasegawa	30
17	Phenotypic spectrum of CHARGE syndrome with CHD7 mutations 2006 ·The Journal of Pediatrics ·Michihiko Aramaki,Toru Udaka,Rika Kosaki,Yoshio Makita,Nobuhiko Okamoto,Hiroshi Yoshihashi,(unknown),Kenji Nanao,Nobuko Moriyama,Shozo Oku,Tomonobu Hasegawa,Takao Takahashi,Yoshimitsu Fukushima,Hiroshi Kawame,Kenjiro Kosaki	118
18	Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia 2005 ·Journal of Human Genetics ·Tetsuya Niihori,Yoko Aoki,Hirofumi Ohashi,Kenji Kurosawa,Tatsuro Kondoh,Satoshi Ishikiriyama,Hiroshi Kawame,Hotaka Kamasaki,Tsutomu Yamanaka,Fumio Takada,(unknown),Masahiro Sakurai,Hiroshi Tamai,(unknown),Yoichi Suzuki,Shigeo Kure,Kunihiro Fujii,Masue Imaizumi,Yoichi Matsubara	87
19	Phenotypic spectrum and management issues in Kabuki syndrome 1999 ·The Journal of Pediatrics ·Hiroshi Kawame,Mark Hannibal,Louanne Hudgins,Roberta A Pagon	123
20	Mutations in the Arylsulfatase A Gene of Japanese Patients with Metachromatic Leukodystrophy 1993 ·DNA and Cell Biology ·(unknown),Hiroshi Kawame,Yoshikatsu Eto	14

About Hiroshi Kawame

Hiroshi Kawame is a scholar working on Genetics, Rheumatology and Cell Biology, having authored 66 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (10 papers) and Lysosomal Storage Disorders Research (10 papers). The work is most often cited by research in Genetics (634 citations), Genetics (194 citations) and Molecular Biology (1.1k citations). Hiroshi Kawame has collaborated with scholars based in Japan, United States and United Kingdom. Frequent co-authors include Kenji Kurosawa, Hirofumi Ohashi, Shigeo Kure, Yoichi Matsubara, Tetsuya Niihori, Yoko Aoki, Yoichi Suzuki, Yukichi Tanaka, Mirella Filocamo and Yoshimitsu Fukushima. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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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