Darryl Nishimura

9.6k citations

74 papers · 6.7k indexed · 1 hit paper · h-index 37

Ophthalmology top 0.2%
- Glaucoma and retinal disorders 11
- Retinal Diseases and Treatments 4
Genetics top 0.5%
- Genetic and Kidney Cyst Diseases 29
- Genetic Syndromes and Imprinting 25
Molecular Biology top 1%
- Hedgehog Signaling Pathway Studies 20
- Retinal Development and Disorders 6
- Congenital heart defects research 5
Cell Biology top 1%
Radiology, Nuclear Medicine and Imaging top 2%
- Corneal surgery and disorders 5

Co-authors: Val C. Sheffield Edwin M. Stone Charles Searby Ruth E. Swiderski Wallace L.M. Alward David A. Mackey Abbot F. Clark Rivka Carmi
Cited by: Ophthalmology Genetics Molecular Biology
Journals: The American Journal of Human Genetics (6 papers)Proceedings of the National Academy of Sciences (5 papers)Genomics (4 papers)
Partner nations: United States Israel United Kingdom

In The Last Decade

Darryl Nishimura

72 papers receiving 6.5k citations

Hit Papers

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Peers

Countries citing papers authored by Darryl Nishimura

Since Specialization

Citations

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

Fields of papers citing papers by Darryl Nishimura

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Metabolic and proteomic indications of diabetes progression in human aqueous humor PLoS ONE ·久実上居,Jessica M. Skeie,Eun Duc Na,A. Tim Johnson,Thomas A. Oetting,Prest,Christopher S. Sáles,Darryl Nishimura,Eric B. Taylor,Gregory A. Schmidt,Mark A. Greiner	2023	7
2	Gene Therapeutic Reversal of Peripheral Olfactory Impairment in Bardet-Biedl Syndrome Molecular Therapy ·Corey Williams,Cedric R. Uytingco,Warren W. Green,Jeremy C. McIntyre,Kirill Ukhanov,Arthur D. Zimmerman,Marcel G.G. Verheij,Lian Zhang,Darryl Nishimura,Val C. Sheffield,Jeffrey R. Martens	2017	36
3	Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma Journal of Clinical Investigation ·Gulab Zode,Markus H. Kuehn,Darryl Nishimura,Charles Searby,Kabhilan Mohan,Siniša D. Grozdanić,Kevin Bugge,Michael G. Anderson,Abbot F. Clark,Edwin M. Stone,Val C. Sheffield	2011	212
4	Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity Genetics in Medicine ·Julie C. Sapp,Darryl Nishimura,Jennifer J. Johnston,Edwin M. Stone,Elise Héon,Val C. Sheffield,Leslie G. Biesecker	2010	11
5	Bardet-Biedl syndrome in Denmark-report of 13 novel sequence variations in six genes Human Mutation ·Tina Duelund Hjortshøj,Karen Grønskov,Alisdair R. Philp,Darryl Nishimura,Ruth Riise,Val C. Sheffield,Thomas Rosenberg,Karen Brøndum‐Nielsen	2010	60
6	Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3) The American Journal of Human Genetics ·Annie Chiang,Darryl Nishimura,Charles Searby,Khalil Elbedour,Rivka Carmi,Jiandong Hong,Tony Ku,Terry A. Braun,Thomas L. Casavant,Edwin M. Stone,Val C. Sheffield	2004	175
7	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome Nature Genetics ·Kirk Mykytyn,Darryl Nishimura,Charles Searby,林炯,Amarílis Maria Farias da Silva,John S. Beck,Terry A. Braun,Luan M. Streb,Alberto S. Cornier,Gerald F. Cox,Anne B. Fulton,Rivka Carmi,Güven Lüleci,Settara C. Chandrasekharappa,Francis S. Collins,Samuel G. Jacobson,John R. Heckenlively,Richard G. Weleber,Edwin M. Stone,Val C. Sheffield	2002	258
8	Optimal procedure for extracting RNA from human ocular tissues and expression profiling of the congenital glaucoma gene FOXC1 using quantitative RT-PCR. PubMed ·马汉钦,Loretta G. McNatt,Allan R. Shepard,Nasreen Jacobson,Darryl Nishimura,Edwin M. Stone,Val C. Sheffield,Abbot F. Clark	2001	38
9	BioCarta Darryl Nishimura	2001	392
10	GeneCards Darryl Nishimura	2001	1
11	A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye The American Journal of Human Genetics ·Darryl Nishimura,Charles Searby,Wallace L.M. Alward,David S. Walton,Jamie E. Craig,David A. Mackey,Kazuhide Kawase,Adam B. Kanis,Shivanand R. Patil,Edwin M. Stone,Val C. Sheffield	2001	172
12	Generation of a High-Density Rat EST Map Genome Research ·Todd E. Scheetz,I. E. Yesaulenko,Darryl Nishimura,Steve Chelminski,Floris van Rooij,Andrea Buhala,Jack M. Gardiner,Jie Zhang,Tahir Bicakci,Christine Sun,Anne E. Kwitek,Howard J. Jacob,Thomas L. Casavant,Marcelo B. Soares,Val C. Sheffield	2001	24
13	RepeatMasker Darryl Nishimura	2000	34
14	Editor’s Page Darryl Nishimura	2000	1
15	Sequencher 3.1.1 Darryl Nishimura	2000	12
16	ChromaTool 1.0 Darryl Nishimura	2000	0
17	The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25 Nature Genetics ·Darryl Nishimura,Ruth E. Swiderski,Wallace L.M. Alward,Charles Searby,Shivanand R. Patil,E Referowska,Adam B. Kanis,Julie M. Gastier,Edwin M. Stone,Val C. Sheffield	1998	359
18	CEPH(ヒト多形性研究センター)共同製作ヒト1番染色体連鎖地図 Genomics ·Rodrigo Lr,P. O’Connell,Kenneth H. Buetow,Darryl Nishimura,Carl W. Helms,Fry A T,Jonathan Wood,N.E. Morton,A. Bale	1991	54
19	A detailed multipoint gene map of chromosome 1q Genomics ·Kenneth H. Buetow,Darryl Nishimura,Phil Green,Yusuke Nakamura,Ou Jiang,J.C. Murray	1990	15
20	Assignment of the gene for the small nuclear ribonucleoprotein E (SNRPE) to human chromosome 1q25–q43 Genomics ·Katherine Neiswanger,David R. Stanford,R S Sparkes,Darryl Nishimura,T. Mohandas,Ivana Klisak,Camilla Heinzmann,Eric D. Wieben	1990	6

About Darryl Nishimura

Darryl Nishimura is a scholar working on Ophthalmology, Genetics, Molecular Biology, Radiology, Nuclear Medicine and Imaging and Endocrine and Autonomic Systems, having authored 74 papers that have together received 6.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (29 papers), Genetic Syndromes and Imprinting (25 papers), Hedgehog Signaling Pathway Studies (20 papers), Glaucoma and retinal disorders (11 papers), Retinal Development and Disorders (6 papers), Congenital heart defects research (5 papers), Corneal surgery and disorders (5 papers) and Retinal Diseases and Treatments (4 papers). The work is most often cited by research in Ophthalmology (1.8k citations), Genetics (3.1k citations), Molecular Biology (4.4k citations), Cell Biology (827 citations) and Radiology, Nuclear Medicine and Imaging (714 citations). Darryl Nishimura has collaborated with scholars based in United States, Israel and United Kingdom. Frequent co-authors include Val C. Sheffield, Edwin M. Stone, Charles Searby, Ruth E. Swiderski, Wallace L.M. Alward, David A. Mackey, Abbot F. Clark, Rivka Carmi, Jeffrey W. Kalenak and Brian E. Nichols. Their work appears in journals such as The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, Genomics, Nature Genetics and Human Molecular Genetics.

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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