Vincent M. Aita

2.4k total citations · 1 hit paper
16 papers, 1.3k citations indexed

About

Vincent M. Aita is a scholar working on Molecular Biology, Urology and Cell Biology. According to data from OpenAlex, Vincent M. Aita has authored 16 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Urology and 5 papers in Cell Biology. Recurrent topics in Vincent M. Aita's work include Hair Growth and Disorders (8 papers), RNA regulation and disease (6 papers) and Wnt/β-catenin signaling in development and cancer (5 papers). Vincent M. Aita is often cited by papers focused on Hair Growth and Disorders (8 papers), RNA regulation and disease (6 papers) and Wnt/β-catenin signaling in development and cancer (5 papers). Vincent M. Aita collaborates with scholars based in United States, Germany and Israel. Vincent M. Aita's co-authors include T. Conrad Gilliam, Angela M. Christiano, Weiping Yu, David L. Pincus, V.V.V.S. Murty, Xiao Liang, Eftìhia Cayanis, Beth Levine, Andrey A. Panteleyev and Wasim Ahmad and has published in prestigious journals such as Science, Journal of Cell Science and The American Journal of Human Genetics.

In The Last Decade

Vincent M. Aita

16 papers receiving 1.3k 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.

Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21

1999 646 citations Vincent M. Aita, Xiao Liang et al. Genomics profile →

Peers

Vincent M. Aita

EPIDE

UROLO

GENET

Efrat Wertheimer Israel

Angustias Page Spain

Xueli Fan China

Masato Matsuki Japan

María D. Mayán Spain

Kumi Shirai Japan

Martin Wolkersdorfer Austria

Tammy‐Claire Troy Canada

Hidetoshi Takahashi Japan

Bing Zhu China

Efrat Wertheimer Israel

Vincent M. Aita

736 ×0.9

51 ×0.1

EPIDE

164 ×0.4

32 ×0.1

UROLO

136 ×0.8

GENET

Citations per year, relative to Vincent M. Aita Vincent M. Aita (= 1×) peers Efrat Wertheimer

Countries citing papers authored by Vincent M. Aita

Since Specialization

Citations

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

Fields of papers citing papers by Vincent M. Aita

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent M. Aita

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent M. Aita. A scholar is included among the top collaborators of Vincent M. Aita 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 M. Aita. Vincent M. Aita is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Zlotogorski, Abraham, Andrey A. Panteleyev, Vincent M. Aita, & Angela M. Christiano. (2002). Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.. Journal of Investigative Dermatology. 118(5). 887–890. 48 indexed citations

Ahmad, Wasim, Marion S. Ratterree, Andrey A. Panteleyev, et al.. (2002). Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene. Laboratory Animals. 36(1). 61–67. 16 indexed citations

Cserhalmi‐Friedman, Peter B., Jorge Frank, Wasim Ahmad, et al.. (2001). Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members. Experimental Dermatology. 10(2). 95–99. 3 indexed citations

Frank, Jorge, et al.. (2001). Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile. Human Heredity. 51(3). 160–168. 18 indexed citations

Panteleyev, Andrey A., Vincent M. Aita, Angela M. Christiano, & Abraham Zlotogorski. (2001). Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions. Journal of Investigative Dermatology. 117(6). 1662–1665. 57 indexed citations

Frank, Jorge, Peter B. Cserhalmi‐Friedman, Wasim Ahmad, et al.. (2001). Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12. Experimental Dermatology. 10(2). 90–94. 16 indexed citations

Aita, Vincent M. & Angela M. Christiano. (2001). The genetics of alopecia areata. Dermatologic Therapy. 14(4). 329–339. 17 indexed citations

Djabali, Karima, Vincent M. Aita, & Angela M. Christiano. (2001). Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix. Journal of Cell Science. 114(2). 367–376. 35 indexed citations

Aita, Vincent M., Wasim Ahmad, Andrey A. Panteleyev, et al.. (2000). A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Experimental Dermatology. 9(2). 157–162. 39 indexed citations

10.

Aita, Vincent M., James A. Knowles, Joseph D. Terwilliger, et al.. (1999). A Comprehensive Linkage Analysis of Chromosome 21q22 Supports Prior Evidence for a Putative Bipolar Affective Disorder Locus. The American Journal of Human Genetics. 64(1). 210–217. 87 indexed citations

11.

Aita, Vincent M., Xiao Liang, V.V.V.S. Murty, et al.. (1999). Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21. Genomics. 59(1). 59–65. 646 indexed citations breakdown →

12.

Aita, Vincent M., Angela M. Christiano, & T. Conrad Gilliam. (1999). Mapping complex traits in diseases of the hair and skin. Experimental Dermatology. 8(6). 439–452. 15 indexed citations

13.

Curtis, David, Vincent M. Aita, Maayan Baron, et al.. (1999). Chromosome 21 workshop. American Journal of Medical Genetics. 88(3). 272–275. 12 indexed citations

14.

Frank, Joachim, Xiaofeng Wang, Vincent M. Aita, et al.. (1998). C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria. Annals of Human Genetics. 62(3). 225–230. 18 indexed citations

15.

Ahmad, Wasim, Muhammad Faiyaz ul Haque, Valeria Brancolini, et al.. (1998). Alopecia Universalis Associated with a Mutation in the Human hairless Gene. Science. 279(5351). 720–724. 287 indexed citations

16.

Fujita, Ricardo, Eve L. Bingham, Paul Forsythe, et al.. (1996). A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.. PubMed. 59(1). 152–8. 11 indexed citations

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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