Barbara Incerti

2.2k total citations · 1 hit paper
18 papers, 1.6k citations indexed

About

Barbara Incerti is a scholar working on Molecular Biology, Biochemistry and Clinical Biochemistry. According to data from OpenAlex, Barbara Incerti has authored 18 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Biochemistry and 5 papers in Clinical Biochemistry. Recurrent topics in Barbara Incerti's work include Amino Acid Enzymes and Metabolism (6 papers), Metabolism and Genetic Disorders (5 papers) and Hypothalamic control of reproductive hormones (5 papers). Barbara Incerti is often cited by papers focused on Amino Acid Enzymes and Metabolism (6 papers), Metabolism and Genetic Disorders (5 papers) and Hypothalamic control of reproductive hormones (5 papers). Barbara Incerti collaborates with scholars based in Italy, United States and Norway. Barbara Incerti's co-authors include Andrea Ballabio, Brunella Franco, Antonella Pragliola, Giovanna Camerino, Barbara Bardoni, Silvana Guioli, Rossana Tonlorenzi, Elena Maestrini, Patricia Taillon‐Miller and Huntington F. Willard and has published in prestigious journals such as Nature, New England Journal of Medicine and Nature Genetics.

In The Last Decade

Barbara Incerti

18 papers receiving 1.5k 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.

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1991 638 citations Brunella Franco, Silvana Guioli et al. Nature profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Barbara Incerti Italy	16	830	577	570	267	207	18	1.6k
Salome Gluecksohn‐Waelsch United States	24	1.1k 1.3×	55 0.1×	537 0.9×	135 0.5×	146 0.7×	72	1.8k
Eugene M. Rinchik United States	32	1.9k 2.3×	65 0.1×	1.1k 1.9×	51 0.2×	60 0.3×	82	2.6k
Claire Redin France	10	888 1.1×	123 0.2×	482 0.8×	73 0.3×	97 0.5×	18	1.3k
Johannes Wilbertz Sweden	19	1.3k 1.6×	310 0.5×	511 0.9×	32 0.1×	33 0.2×	24	2.2k
Joyce C. Wu United States	16	905 1.1×	210 0.4×	242 0.4×	24 0.1×	44 0.2×	20	1.5k
Véronique Paquis‐Flucklinger France	27	2.0k 2.4×	118 0.2×	413 0.7×	42 0.2×	633 3.1×	88	2.5k
Brigitte Anliker Germany	13	1.3k 1.6×	138 0.2×	361 0.6×	95 0.4×	14 0.1×	18	2.3k
Chaim Jalas United States	23	724 0.9×	72 0.1×	375 0.7×	92 0.3×	87 0.4×	60	1.7k
A Zanini Italy	19	787 0.9×	149 0.3×	96 0.2×	19 0.1×	17 0.1×	27	1.4k
Sandra Meulemans Belgium	19	470 0.6×	17 0.0×	201 0.4×	46 0.2×	45 0.2×	29	1.0k

Countries citing papers authored by Barbara Incerti

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Incerti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Incerti

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

All Works

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18 of 18 papers shown

Palmisano, Ilaria, Paola Bagnato, Giulio Innamorati, et al.. (2008). The ocular albinism type 1 protein, an intracellular G protein-coupled receptor, regulates melanosome transport in pigment cells. Human Molecular Genetics. 17(22). 3487–3501. 67 indexed citations

Banfi, Sandro, et al.. (2000). Identification and Characterization of YME1L1, a Novel Paraplegin-Related Gene. Genomics. 66(1). 48–54. 75 indexed citations

Sperandeo, Maria Pia, Maria Teresa Bassi, Mirko Riboni, et al.. (2000). Structure of the SLC7A7 Gene and Mutational Analysis of Patients Affected by Lysinuric Protein Intolerance. The American Journal of Human Genetics. 66(1). 92–99. 56 indexed citations

Incerti, Barbara. (2000). Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1. Human Molecular Genetics. 9(19). 2781–2788. 75 indexed citations

Bassi, Maria Teresa, Maria Pia Sperandeo, Barbara Incerti, et al.. (1999). SLC7A8, a Gene Mapping within the Lysinuric Protein Intolerance Critical Region, Encodes a New Member of the Glycoprotein-Associated Amino Acid Transporter Family. Genomics. 62(2). 297–303. 16 indexed citations

Borsani, Giuseppe, Maria Teresa Bassi, Maria Pia Sperandeo, et al.. (1999). SLC7A7, encoding a putative permease-related protein, is mutated in patients with lysinuric protein intolerance. Nature Genetics. 21(3). 297–301. 185 indexed citations

Buanne, Pasquale, et al.. (1998). Cloning of the Human Interferon-Related Developmental Regulator (IFRD1) Gene Coding for the PC4 Protein, a Member of a Novel Family of Developmentally Regulated Genes. Genomics. 51(2). 233–242. 30 indexed citations

Sperandeo, Maria Pia, Giuseppe Borsani, Barbara Incerti, et al.. (1998). The Gene Encoding a Cationic Amino Acid Transporter (SLC7A4) Maps to the Region Deleted in the Velocardiofacial Syndrome. Genomics. 49(2). 230–236. 41 indexed citations

Parenti, Giancarlo, Gianfranco Sebastio, Pietro Strisciuglio, et al.. (1995). Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course. The Journal of Pediatrics. 126(2). 246–251. 44 indexed citations

10.

Parenti, Giancarlo, Salvatore Di Maio, Maria Pia Sperandeo, et al.. (1995). Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL gene. American Journal of Medical Genetics. 57(3). 476–478. 45 indexed citations

11.

Incerti, Barbara, Gianfranco Sebastio, & Giancarlo Parenti. (1994). The structure of the gene ATRC1 coding for a cationic amino acid transport system in man: Molecular studies in lysinuric protein intolerance. The American Journal of Human Genetics. 55. 1 indexed citations

12.

Incerti, Barbara, et al.. (1994). Structure of the mouse growth/differentiation factor 9 gene. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1222(1). 125–128. 24 indexed citations

13.

Guioli, Silvana, Barbara Incerti, Elena Zanaria, et al.. (1992). Kallmann syndrome due to a translocation resulting in an X/Y fusion gene. Nature Genetics. 1(5). 337–340. 45 indexed citations

14.

Incerti, Barbara, Silvana Guioli, Antonella Pragliola, et al.. (1992). Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomes. Nature Genetics. 2(4). 311–314. 40 indexed citations

15.

Bick, David, Brunella Franco, Richard J. Sherins, et al.. (1992). Intragenic Deletion of theKALIG-1Gene in Kallmann's Syndrome. New England Journal of Medicine. 326(26). 1752–1755. 141 indexed citations

16.

Bick, David, Brunella Franco, Richard J. Sherins, et al.. (1992). Brief Report. Obstetrical & Gynecological Survey. 47(11). 795–796. 58 indexed citations

17.

Franco, Brunella, Silvana Guioli, Antonella Pragliola, et al.. (1991). A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature. 353(6344). 529–536. 638 indexed citations breakdown →

18.

Sebastio, Gianfranco, et al.. (1990). The ΔF508 mutation in cystic fibrosis patients of Southern Italy. Human Genetics. 85(4). 430–431. 2 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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