Vincent P. Stanton

6.0k total citations · 1 hit paper
38 papers, 2.7k citations indexed

About

Vincent P. Stanton is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Vincent P. Stanton has authored 38 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Vincent P. Stanton's work include Genomics and Chromatin Dynamics (6 papers), RNA Research and Splicing (6 papers) and RNA and protein synthesis mechanisms (5 papers). Vincent P. Stanton is often cited by papers focused on Genomics and Chromatin Dynamics (6 papers), RNA Research and Splicing (6 papers) and RNA and protein synthesis mechanisms (5 papers). Vincent P. Stanton collaborates with scholars based in United States, United Kingdom and Canada. Vincent P. Stanton's co-authors include Geoffrey M. Cooper, David E. Housman, James P. Basilion, Ling X. Shen, Andrew P. Laudano, Ian D. Dubé, R. Becher, Julian Borrow, Ezra S. Abrams and Frederick G. Behm and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Nature Genetics.

In The Last Decade

Vincent P. Stanton

38 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein

1996 603 citations Julian Borrow, Vincent P. Stanton et al. Nature Genetics profile →

Peers

Countries citing papers authored by Vincent P. Stanton

Since Specialization

Citations

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

Fields of papers citing papers by Vincent P. Stanton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent P. Stanton. 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 Vincent P. Stanton. The network helps show where Vincent P. Stanton may publish in the future.

Co-authorship network of co-authors of Vincent P. Stanton

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent P. Stanton. A scholar is included among the top collaborators of Vincent P. Stanton 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 Vincent P. Stanton. Vincent P. Stanton 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 analysis of adenosine A1 receptor gene (ADORA1) polymorphisms with schizophrenia in a Japanese population 2009 ·Psychiatric Genetics ·Leo Gotoh, Hiroshi Mitsuyasu, (unknown), Naoya Oribe, Atsushi Takata, Hideaki Ninomiya, Vincent P. Stanton, Gregory M. Springett, Hiroaki Kawasaki, Shigenobu Kanba	19
2	Genetic structure of the dopamine receptor D4 gene (DRD4) and lack of association with schizophrenia in Japanese patients 2006 ·Journal of Psychiatric Research ·Hiroshi Mitsuyasu, Hiroaki Kawasaki, Hideaki Ninomiya, Naoko Kinukawa, Takeharu Yamanaka, Tomoko Tahira, Vincent P. Stanton, Gregory M. Springett, Kenshi Hayashi, Nobutada Tashiro, Shigenobu Kanba	7
3	Dihydropyrimidine Dehydrogenase and Thymidylate Synthase Polymorphisms and Their Association with 5-Fluorouracil/Leucovorin Chemotherapy in Colorectal Cancer 2004 ·Clinical Colorectal Cancer ·Andrew X. Zhu, Thomas A. Puchalski, Vincent P. Stanton, David P. Ryan, Jeffrey W. Clark, (unknown), Olga Charlat, Patrick Kelly, (unknown), Bruce A. Chabner, Jeffrey G. Supko	18
4	Turbo-Decoder Implementation for the Deep Space Network 2001 ·K. Andrews, Vincent P. Stanton, S. Dolinar, (unknown), (unknown), F. Pollara	8
5	Molecular Genetic Characterisation of Frontotemporal Dementia on Chromosome 3 1999 ·Dementia and Geriatric Cognitive Disorders ·(unknown), S. J. Lloyd, Jeremy Brown, Susanne Gydesen, S. A. Sørensen, Arne Brun, Elisabet Englund, (unknown), David Housman, (unknown), Vincent P. Stanton, Kay Taylor, (unknown), David J. Munroe, (unknown), Martin N. Rossor, Elizabeth Fisher, John Collinge	44
6	Selective Killing of Cancer Cells Based on Loss of Heterozygosity and Normal Variation in the Human Genome: A New Paradigm for Anticancer Drug Therapy 1999 ·Molecular Pharmacology ·James P. Basilion, Andrea R. Schievella, (unknown), Patrice Rioux, (unknown), Brett P. Monia, Kristina M. Lemonidis, Vincent P. Stanton, David E. Housman	30
7	Single-nucleotide polymorphisms can cause different structural folds of mRNA 1999 ·Proceedings of the National Academy of Sciences ·Ling X. Shen, James P. Basilion, Vincent P. Stanton	264
8	The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9 1996 ·Nature Genetics ·Julian Borrow, Amanda M. Shearman, Vincent P. Stanton, R. Becher, Tucker Collins, Amy J. Williams, Ian D. Dubé, F Katz, Yok‐Lam Kwong, Christine M. Morris, Kazuma Ohyashiki, Keisuke Toyama, Janet D. Rowley, David E. Housman	372
9	The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein breakdown → 1996 ·Nature Genetics ·Julian Borrow, Vincent P. Stanton, J. Michael Andresen, R. Becher, Frederick G. Behm, R. S. K. Chaganti, Curt I. Civin, Christine M. Distèche, Ian D. Dubé, (unknown), Doug Horsman, Felix Mitelman, Stefano Volinia, A. E. Watmore, David E. Housman	603
10	Mapping 638 STSs to regions of human chromosome 3 1996 ·Cytogenetic and Genome Research ·Susan L. Naylor, Shanna L. Moore, Dawn Garcia, Xingjia Xiang, (unknown), (unknown), B.E. Reus, (unknown), Vincent P. Stanton, P. O’Connell, Robin J. Leach	16
11	Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach 1995 ·Genomics ·Jing Liu, Vincent P. Stanton, Takuya Fujiwara, (unknown), (unknown), M. JOYCE CRUMLEY, Kenneth Morgan, Philippe Gros, David E. Housman, Erwin Schurr	12
12	Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): Generation of a 5-cM, >5 megabase contig on mouse Chromosome 1 1994 ·Mammalian Genome ·Kent W. Hunter, (unknown), M. Watson, Vincent P. Stanton, Pablo Andrés Gutiérrez Sánchez, Deepti Bhat, Julie M. Rochelle, Sharon Graw, Martin Schalling, Hiroyuki Aburatani, S.D.M. Brown, Michael F. Seldin, David E. Housman	24
13	High-frequency DNA sequence polymorphisms in the insulin receptor gene detected by denaturing gradient gel blots 1992 ·Genomics ·Andrzej S. Królewski, Bozena Krolewski, Mark R. Gray, Vincent P. Stanton, James H. Warram, David Housman	10
14	[4] Use of denaturing gradient gel electrophoresis to study conformational transitions in nucleic acids 1992 ·Methods in enzymology on CD-ROM/Methods in enzymology ·Ezra S. Abrams, Vincent P. Stanton	107
15	Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3 1992 ·Genomics ·René Hubert, Vincent P. Stanton, Hiroyuki Aburatani, (unknown), Honghua Li, David E. Housman, Norman Arnheim	17
16	The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A 1992 ·Nature Genetics ·Linda J. Valentijn, Pieter A. Bolhuis, Ina Zorn, Jessica E. Hoogendijk, (unknown), Gerard W. Hensels, Vincent P. Stanton, David E. Housman, Kenneth H. Fischbeck, David A. Ross, Garth A. Nicholson, Eric J. Meershoek, Hans G. Dauwerse, G.J.B. van Ommen, Frank Baas	265
17	Ordering three DNA polymorphisms on human chromosome 3 by sperm typing 1991 ·Genomics ·Tushar M. Goradia, Vincent P. Stanton, Xiangfeng Cui, Hiroyuki Aburatani, Honghua Li, Kenneth Lange, David E. Housman, Norman Arnheim	32
18	Familial predisposition to wilms tumor does not segregate with the WT1 gene 1991 ·Genomics ·Charles E. Schwartz, Daniel A. Haber, Vincent P. Stanton, Louise C. Strong, Mark H. Skolnick, David E. Housman	54
19	Activation of Human raf Transforming Genes by Deletion of Normal Amino-Terminal Coding Sequences 1987 ·Molecular and Cellular Biology ·Vincent P. Stanton, Geoffrey M. Cooper	29
20	Free perforation of the jejunum in Crohn's disease. 1977 ·Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·Vincent P. Stanton	2

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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