Eriko Nishi

676 citations

32 papers · 252 indexed · h-index 9

Developmental Biology
Genetics
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 4
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3
Aging
Genetics
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 5
- Genetic Syndromes and Imprinting 4
Molecular Biology
- RNA modifications and cancer 6
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 3
Surgery
- Congenital Anomalies and Fetal Surgery 3

Co-authors: Tomoki Kosho Tomohiko Nakamura Takehiko Hiroma Hiroshi Kawame Seiji Mizuno Satoshi Takamizawa Yoshimitsu Fukushima Nobuhiko Okamoto
Cited by: Developmental Biology Genetics Pediatrics, Perinatology and Child Health
Journals: Brain and Development (2 papers)American Journal of Medical Genetics Part A (15 papers)PLoS Genetics (1 paper)
Partner nations: Japan United States Hong Kong

In The Last Decade

Eriko Nishi

28 papers receiving 245 citations

Peers

Countries citing papers authored by Eriko Nishi

Since Specialization

Citations

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

Fields of papers citing papers by Eriko Nishi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	A Clinical Study of Nine Patients With ReNU Syndrome American Journal of Medical Genetics Part A ·Nobuhiko Okamoto,Eriko Nishi,Annie Delienne,Shinji Higuchi,Ichiro Kuki,Kumiko Yanagi,Tadashi Kaname,Yuri Uchiyama,Naomichi Matsumoto	2025	1
2	Intrarenal pressure during the flexible and navigable suction ureteral access sheath-assisted retrograde intrarenal surgery: a two-center study International Urology and Nephrology ·Lan Nguyen Tran,Takafumi Yanagisawa,浦野雅史,Eriko Nishi,Zewang Yu,Gelsomino Nl,Frédéric Allemand,Yuka Yasuda,Xiaoyun Fan,Laysa Franca Colares,Carolyn M. Norgate,Шахназаров Карэн Юрьевич,Motohashi Ken	2025	0
3	Impact of ureteral access sheath size on intrarenal pressure evaluated by LithoVue™ elite single use ureteroscope International Urology and Nephrology ·Lan Nguyen Tran,Takafumi Yanagisawa,Lingru Li,Zewang Yu,Eriko Nishi,Augustin Guibaud,Gelsomino Nl,Carolyn M. Norgate,Motohashi Ken	2025	2
4	Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome Clinical Pediatric Endocrinology ·Yasuko Shoji,Aboudramane Camara,박부용,Barrie Thomas Dickie,Annie Delienne,Eriko Nishi,Shinobu Ida,Yuri Etani,Tetsuya Niihori,Yoko Aoki,Nobuhiko Okamoto,Masanobu Kawai	2024	1
5	Clinical details of individuals with Rauch–Steindl syndrome due to NSD2 truncating variants Molecular Genetics & Genomic Medicine ·Eriko Nishi,Kumiko Yanagi,Tadashi Kaname,Nobuhiko Okamoto	2024	0
6	Craniosynostosis in molecularly diagnosed Kabuki syndrome: Prevalence and clinical implications American Journal of Medical Genetics Part A ·Eriko Nishi,Noriko Miyake,Rie Kawamura,Kana Hosoki,Annie Delienne,Naomichi Matsumoto,Nobuhiko Okamoto	2023	0
7	Identification of small-sized intrachromosomal segments at the ends of INV–DUP–DEL patterns Journal of Human Genetics ·В. І. Марчик,Ghulam Rasul,Nobuhiko Okamoto,Eriko Nishi,Atsuko Noguchi,Ikuko Takahashi,Yukio Sawaishi,Masaki Shimizu,Hitoshi Kanno,Yohei Minakuchi,Atsushi Toyoda,Toshiyuki Yamamoto	2023	1
8	CDKN1C hyperexpression in two patients with severe growth failure and microdeletions affecting the paternally inherited KCNQ1OT1:TSS-DMR Journal of Medical Genetics ·Ardina Malika,Kazuki Yamazawa,Satsuki Tanaka,Eriko Nishi,Maki Fukami,Masayo Kagami	2022	1
9	Chiasmata and the kinetochore component Dam1 are crucial for elimination of erroneous chromosome attachments and centromere oscillation at meiosis I Open Biology ·Mariangela J. Alfeo,Eriko Nishi,Shinnosuke Kawai,Amanda Skierkiewicz,Mark K. Gino Galang,Hsu Ming Vicky Chan,Ade Harry Situmorang,Ayumu Yamamoto	2021	5
10	Blended phenotype of combination of HERC2 and AP3B2 deficiency and Angelman syndrome caused by paternal isodisomy of chromosome 15 American Journal of Medical Genetics Part A ·Kimiko Ueda,Satoru Ogawa,K. Matsuda,Annie Delienne,Eriko Nishi,Kumiko Yanagi,Tadashi Kaname,Toshiyuki Yamamoto,Nobuhiko Okamoto	2021	4
11	Clinical spectrum of individuals with de novo EBF3 variants or deletions American Journal of Medical Genetics Part A ·Eriko Nishi,Tomoko Uehara,Kumiko Yanagi,Annie Delienne,Kimiko Ueda,Tadashi Kaname,Toshiyuki Yamamoto,Kenjiro Kosaki,Nobuhiko Okamoto	2021	8
12	Trimodal therapy with high-dose-rate brachytherapy and hypofractionated external beam radiation combined with long-term androgen deprivation for unfavorable-risk prostate cancer Strahlentherapie und Onkologie ·Keiichiro Mori,Hiroshi Sasaki,N. A. Verzbinskaja,Shun Sato,陈灿斯,Gita Nur Ayni,Eriko Nishi,W. H. Christie,Toshihiro Yamamoto,Yusuke Koike,Jun Miki,Tatsuya Shimomura,Takahiro Kimura,Kenta Miki,Shahrokh F. Shariat,Hiroyuki Takahashi,Manabu Aoki,Shin Egawa	2021	5
13	Position matters: multiple functions of LINC-dependent chromosome positioning during meiosis Current Genetics ·Mark K. Gino Galang,Eriko Nishi,Sadia Afrin,Andreu Taberner Palau,Ayumu Yamamoto	2017	4
14	Loss-of-function mutations and global rearrangements in GPC3 in patients with Simpson–Golabi–Behmel syndrome Human Genome Variation ·Keiko Shimojima,Yumiko Ondo,Eriko Nishi,Seiji Mizuno,Sabine Lamprecht,Sevgi Gouml,H. Hajnajari,Maho Sato,Masami Inoue,Nobuhiko Okamoto,Toshiyuki Yamamoto	2016	10
15	A Taz1- and Microtubule-Dependent Regulatory Relationship between Telomere and Centromere Positions in Bouquet Formation Secures Proper Meiotic Divisions PLoS Genetics ·Mark K. Gino Galang,Hsu Ming Vicky Chan,C.B. Ramesha,Eriko Nishi,Yan Gao,علي حسين مهدي عزيز الأسدي,Lu Zhang,Lian Ma,Ayumu Yamamoto	2016	8
16	Dissecting the phenotype of supernumerary marker chromosome 20 in a patient with syndromic pierre robin sequence: Combinatorial effect of gene dosage and uniparental disomy American Journal of Medical Genetics Part A ·Kosuke Izumi,Noriko Kubota,Aysenur Gullu,Kristina Araminaitė,Antonius Wella,Tomohiko Nakamura,Eriko Nishi,Eiko Hidaka	2015	4
17	Exome Sequencing Identification of <b><i>EP300</i></b> Mutation in a Proband with Coloboma and Imperforate Anus: Possible Expansion of the Phenotypic Spectrum of Rubinstein-Taybi Syndrome Molecular Syndromology ·Koji Masuda,覃寿伟,Aysenur Gullu,Eriko Nishi,Danielle D. Rogers,Tsukasa Higuchi,Yuki Katou,Katsuhiko Shirahige,Kosuke Izumi	2015	7
18	A novel heterozygous MAP2K1 mutation in a patient with Noonan syndrome with multiple lentigines American Journal of Medical Genetics Part A ·Eriko Nishi,Seiji Mizuno,Kotropoulos,Tetsuya Niihori,Yoshimitsu Fukushima,Yoichi Matsubara,Yoko Aoki,Tomoki Kosho	2014	17
19	Surgical intervention for esophageal atresia in patients with trisomy 18 American Journal of Medical Genetics Part A ·Eriko Nishi,Satoshi Takamizawa,MMsc Sagar Acharya,Yasumasa Yamada,Dr.D Kirubha,Lys Ann Taylor Shore,Takehiko Hiroma,Seiji Mizuno,Hiroshi Kawame,Yoshimitsu Fukushima,Tomohiko Nakamura,Tomoki Kosho	2013	36
20	Various types of LRP5 mutations in four patients with osteoporosis‐pseudoglioma syndrome: Identification of a 7.2‐kb microdeletion using oligonucleotide tiling microarray American Journal of Medical Genetics Part A ·Satoshi Narumi,Chikahiko Numakura,Takashi Shiihara,Rebekah Holbrook,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	2009	30

About Eriko Nishi

Eriko Nishi is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 32 papers that have together received 252 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), RNA modifications and cancer (6 papers), Genomics and Rare Diseases (5 papers), Genetic Syndromes and Imprinting (4 papers), DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). The work is most often cited by research in Developmental Biology (9 citations), Genetics (84 citations) and Pediatrics, Perinatology and Child Health (47 citations). Eriko Nishi has collaborated with scholars based in Japan, United States and Hong Kong. Frequent co-authors include Tomoki Kosho, Tomohiko Nakamura, Takehiko Hiroma, Hiroshi Kawame, Seiji Mizuno, Satoshi Takamizawa, Yoshimitsu Fukushima, Nobuhiko Okamoto, Kosuke Izumi and Eiko Hidaka. Their work appears in journals such as Brain and Development, American Journal of Medical Genetics Part A, PLoS Genetics, Human Genetics and Journal of Medical Genetics.

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