Keiko Wakui

5.2k citations

89 papers · 2.3k indexed · h-index 28

Genetics top 1%
- Genomic variations and chromosomal abnormalities 25
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 7
- Connective tissue disorders research 6
Molecular Biology top 5%
- Congenital heart defects research 11
- Epigenetics and DNA Methylation 7
Sensory Systems top 5%
Developmental Biology top 5%
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 9
Plant Science
- Chromosomal and Genetic Variations 12

Co-authors: Yoshimitsu Fukushima Norio Niikawa Tomoki Kosho Lisa G. Shaffer Hirofumi Ohashi Takeo Kubota James R. Lupski Paweł Stankiewicz
Cited by: Genetics Molecular Biology Sensory Systems
Journals: Journal of Biological Chemistry (1 paper)SHILAP Revista de lepidopterología (1 paper)The Journal of Clinical Endocrinology & Metabolism (3 papers)
Partner nations: Japan United States Australia

In The Last Decade

Keiko Wakui

88 papers receiving 2.2k citations

Peers

Countries citing papers authored by Keiko Wakui

Since Specialization

Citations

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

Fields of papers citing papers by Keiko Wakui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Neuropsychological and neurophysiological features of WAGR syndrome: Detailed comprehensive evaluation of a patient with severe intellectual disability and autism spectrum disorder Brain and Development ·Hitomi Nishizawa,Mitsuo Motobayashi,Miwa Akahane,Keiko Wakui,Noritaka Kitazawa,Yuji Inaba,Yoshimitsu Fukushima,Tomoki Kosho	2021	0
2	Frequency and clinical features of hearing loss caused by STRC deletions Scientific Reports ·Yoh Yokota,Hideaki Moteki,Shin‐ya Nishio,Tomomi Yamaguchi,Keiko Wakui,Yumiko Kobayashi,Kenji Ohyama,Hiromitsu Miyazaki,Rina Matsuoka,Satoko Abe,Kozo Kumakawa,Masahiro Takahashi,Hirofumi Sakaguchi,Natsumi Uehara,Takashi Ishino,Tomoki Kosho,Yoshimitsu Fukushima,Shin‐ichi Usami	2019	51
3	A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8 Human Genome Variation ·Tsuneaki Yoshinaga,Katsuya Nakamura,Masumi Ishikawa,Tomomi Yamaguchi,Kyoko Takano,Keiko Wakui,Tomoki Kosho,Kunihiro Yoshida,Yoshimitsu Fukushima,Yoshiki Sekijima	2017	12
4	Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: A clinical report and review of literature American Journal of Medical Genetics Part A ·Yoko Narumi,Sachiko Nishina,Motoharu Tokimitsu,Yoko Aoki,Rika Kosaki,Keiko Wakui,Noriyuki Azuma,Toshinori Murata,Fumio Takada,Yoshimitsu Fukushima,Tomoki Kosho	2014	28
5	Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan Journal of Human Genetics ·Keiko Tanaka,Yoshiki Sekijima,Kunihiro Yoshida,Mariko Tamai,Tomoki Kosho,Akihiro Sakurai,Keiko Wakui,Shu‐ichi Ikeda,Yoshimitsu Fukushima	2013	8
6	Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization Chromosome Research ·Rie Kawamura,Hideyuki Tanabe,Takahito Wada,Shinji Saitoh,Yoshimitsu Fukushima,Keiko Wakui	2012	11
7	Linkage analysis and mapping of scar markers linked to CMV-B2 resistance gene in melon. SABRAO Journal of Breeding and Genetics ·Budi Setiadi Daryono,Keiko Wakui,Keiko T. Natsuaki	2010	5
8	One Third of Japanese Patients with Multiple Osteochondromas May Have Mutations in Genes Other Than EXT1 or EXT2 Genetic Testing ·Hirofumi Kojima,Takahito Wada,Hiroshi Seki,Takeo Kubota,Keiko Wakui,Yoshimitsu Fukushima	2008	5
9	Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5–11.1 Mb terminal deletion of 1p36 American Journal of Medical Genetics Part A ·Shoji Saito,Rie Kawamura,Tomoki Kosho,Takashi Shimizu,Koki Aoyama,Kenichi Koike,Takahito Wada,Naomichi Matsumoto,Mitsuhiro Kato,Keiko Wakui,Yoshimitsu Fukushima	2008	18
10	Molecular characterization of a novel translocation t(5;14)(q21;q32) in a patient with congenital abnormalities Journal of Human Genetics ·Shawkat Haider,Rie Matsumoto,Nobuyuki Kurosawa,Keiko Wakui,Yoshimitsu Fukushima,Masaharu Isobe	2006	5
11	A genome wide search for Kawasaki disease susceptibility genes The American Journal of Human Genetics ·Yoshihiro Onouchi,S. Onoue,Mayumi Tamari,Keiko Wakui,Yasuto Fukushima,M. Yashiro,Hiroshi Yanagawa,Tomisaku Kawasaki,Yoshimasa Nakamura,Akira Hata	2003	1
12	Genome Architecture Catalyzes Nonrecurrent Chromosomal Rearrangements The American Journal of Human Genetics ·Paweł Stankiewicz,Christine J. Shaw,Jason Dapper,Keiko Wakui,Lisa G. Shaffer,Marjorie Withers,Leah I. Elizondo,Sung Sup Park,James R. Lupski	2003	144
13	The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females Cytogenetic and Genome Research ·Takeo Kubota,Keiko Wakui,Takamitsu Nakamura,Haruhiko Ohashi,Yoriko Watanabe,Makoto Yoshino,Tomonobu KIDA,Nobuhiko Okamoto,Masayuki MATSUMURA,Koji Muroya,Tsutomu Ogata,Y. Goto,Y. Fukushima	2002	27
14	Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus–Merzbacher disease Prenatal Diagnosis ·Ken Inoue,Makoto Kanai,Yuzo Tanabe,Takeo Kubota,Catherine D. Kashork,Keiko Wakui,Yoshimitsu Fukushima,James R. Lupski,Lisa G. Shaffer	2001	21
15	Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern Human Genetics ·Tsutomu Ogata,Keiko Wakui,Koji Muroya,Hirofumi Ohashi,Nobutake Matsuo,Donna M. Brown,Takashi Ishii,Yoshimitsu Fukushima	1998	27
16	Tetramelic mirror-image like polydactyly and de novo balanced autosomal translocation, 46,XY,t(2;14)(p23.2;q13) : The 35th Annual Meeting of the Japanese Teratology Society Congenital Anomalies ·Hirofumi Ohashi,M. Iwamura,Tamio Ohno,Mihoko Sato,S. Maizumi,Toshinori Aihara,Akira Yamagishi,Keiko Wakui,Yoshitora Kin,Y. Fukushima	1995	1
17	A rapid method for starting a culture for the establishment of Epstein-Barr virus-transformed human lymphoblastoid cell lines The Japanese Journal of Human Genetics ·Yoshimitsu Fukushima,Hirofumi Ohashi,Keiko Wakui,Toshiro Nishida,Tsutomu Oh‐ishi	1992	22
18	ARE THE GENES FOR AICARDI SYNDROME AND GOLTZ-SYNDROME CONTIGUOUS - A CASE OF BOTH SYNDROMES WITH XP22.3 DELETION The American Journal of Human Genetics ·Norio Niikawa,H Ohashi,Toshifumi Nara,Kimiaki Ogawa,Yasuo Ueoka,Takeo Nishida,Keiko Wakui,Y Fukushima	1991	1
19	De novo interstitial deletion of 4q[46,XX,del(4)(q27q28.2)] with intact blood group-MN locus, confining its locus to 4q28.2–4q31.1 The Japanese Journal of Human Genetics ·Keiko Wakui,Toshiro Nishida,Jun-ichiro Masuda,Takeshi Itoh,Daisuke Katsumata,Tsutomu Ohno,Yoshimitsu Fukushima	1991	3
20	Craniosynostosis in an infant with an interstitial deletion of 15q [46, XY,del(15)(q15q22.1)] American Journal of Medical Genetics ·Yoshimitsu Fukushima,Keiko Wakui,Toshiro Nishida,Hiroshi Nishimoto	1990	19

About Keiko Wakui

Keiko Wakui is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 89 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Chromosomal and Genetic Variations (12 papers), Congenital heart defects research (11 papers), Prenatal Screening and Diagnostics (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Epigenetics and DNA Methylation (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Connective tissue disorders research (6 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (1.3k citations) and Sensory Systems (92 citations). Keiko Wakui has collaborated with scholars based in Japan, United States and Australia. Frequent co-authors include Yoshimitsu Fukushima, Norio Niikawa, Tomoki Kosho, Lisa G. Shaffer, Hirofumi Ohashi, Takeo Kubota, James R. Lupski, Paweł Stankiewicz, Tsutomu Ogata and Toshiro Nishida. Their work appears in journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

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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