Vincent M. Aita

2.4k citations

16 papers · 1.3k indexed · 1 hit paper · h-index 13

Molecular Biology top 10%
Epidemiology top 5%
Cell Biology top 5%
Urology top 1%
Genetics top 10%

Co-authors: T. Conrad Gilliam Angela M. Christiano Weiping Yu David L. Pincus V.V.V.S. Murty Xiao Liang Eftìhia Cayanis Beth Levine
Topics: Hair Growth and Disorders (8 papers)RNA regulation and disease (6 papers)Wnt/β-catenin signaling in development and cancer (5 papers)
Cited by: Urology Cell Biology Epidemiology
Journals: Science Journal of Cell Science The American Journal of Human Genetics
Partner nations: United States Germany Israel

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

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

#	Work	Indexed citations
1	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. 2002 ·Journal of Investigative Dermatology ·Abraham Zlotogorski,Andrey A. Panteleyev,Vincent M. Aita,Angela M. Christiano	48
2	Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene 2002 ·Laboratory Animals ·Wasim Ahmad,Marion S. Ratterree,Andrey A. Panteleyev,Vincent M. Aita,John P. Sundberg,Angela M. Christiano	16
3	Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members 2001 ·Experimental Dermatology ·Peter B. Cserhalmi‐Friedman,Jorge Frank,Wasim Ahmad,Andrey A. Panteleyev,Vincent M. Aita,Angela M. Christiano	3
4	Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile 2001 ·Human Heredity ·Jorge Frank,Vincent M. Aita,Wasim Ahmad,(unknown),C Wolff,Angela M. Christiano	18
5	Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions 2001 ·Journal of Investigative Dermatology ·Andrey A. Panteleyev,Vincent M. Aita,Angela M. Christiano,Abraham Zlotogorski	57
6	Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12 2001 ·Experimental Dermatology ·Jorge Frank,Peter B. Cserhalmi‐Friedman,Wasim Ahmad,Andrey A. Panteleyev,Vincent M. Aita,Angela M. Christiano	16
7	The genetics of alopecia areata 2001 ·Dermatologic Therapy ·Vincent M. Aita,Angela M. Christiano	17
8	Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix 2001 ·Journal of Cell Science ·Karima Djabali,Vincent M. Aita,Angela M. Christiano	35
9	A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions 2000 ·Experimental Dermatology ·Vincent M. Aita,Wasim Ahmad,Andrey A. Panteleyev,(unknown),Aleksandra Kozłowska,T. Conrad Gilliam,Stefania Jabłońska,Angela M. Christiano	39
10	A Comprehensive Linkage Analysis of Chromosome 21q22 Supports Prior Evidence for a Putative Bipolar Affective Disorder Locus 1999 ·The American Journal of Human Genetics ·Vincent M. Aita,(unknown),James A. Knowles,Joseph D. Terwilliger,Romulo Baltazar,Adina Grunn,J E Loth,Kyra Kanyas,Bernard Lerer,Jean Endicott,(unknown),Graciela K. Penchaszadeh,T. Conrad Gilliam,(unknown)	87
11	Cloning and Genomic Organization of Beclin 1, a Candidate Tumor Suppressor Gene on Chromosome 17q21breakdown → 1999 ·Genomics ·Vincent M. Aita,Xiao Liang,V.V.V.S. Murty,David L. Pincus,Weiping Yu,Eftìhia Cayanis,(unknown),T. Conrad Gilliam,Beth Levine	646
12	Mapping complex traits in diseases of the hair and skin 1999 ·Experimental Dermatology ·Vincent M. Aita,Angela M. Christiano,T. Conrad Gilliam	15
13	Chromosome 21 workshop 1999 ·American Journal of Medical Genetics ·David Curtis,Vincent M. Aita,Maayan Baron,Philip C. Bennett,S D Detera-Wadleigh,Andrew McQuillin,Daniela S. Gerhard,John R. Kelsoe,Tatiana Foroud	12
14	C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria 1998 ·Annals of Human Genetics ·Joachim Frank,Xiaofeng Wang,(unknown),Vincent M. Aita,Frank K. Jugert,G. Goerz,Hans F. Merk,Maureen B. Poh‐Fitzpatrick,Angela M. Christiano	18
15	Alopecia Universalis Associated with a Mutation in the Human hairless Gene 1998 ·Science ·Wasim Ahmad,Muhammad Faiyaz ul Haque,Valeria Brancolini,Hui C. Tsou,(unknown),HaMut Lam,Vincent M. Aita,Jason E. Owen,(unknown),Jorge Frank,Peter B. Cserhalmi‐Friedman,Andrew Leask,John A. McGrath,Monica Peacocke,Mahmud Ahmad,Jürg Ott,Angela M. Christiano	287
16	A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3. 1996 ·PubMed ·Ricardo Fujita,Eve L. Bingham,Paul Forsythe,Christina L. McHenry,Vincent M. Aita,(unknown),Katherine L. Dry,(unknown),Marcella Devoto,G.A.P. Bruns,(unknown),Jürg Ott,Paul A. Sieving,Anand Swaroop	11

About Vincent M. Aita

Vincent M. Aita is a scholar working on Urology, Cell Biology and Molecular Biology, having authored 16 papers that have together received 1.3k indexed citations. Recurring topics across this 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). The work is most often cited by research in Urology (408 citations), Cell Biology (431 citations) and Epidemiology (561 citations). Vincent M. Aita has collaborated with scholars based in United States, Germany and Israel. Frequent 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. Their work appears in journals such as Science, Journal of Cell Science and The American Journal of Human 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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