A. Grifa

1.2k total citations
18 papers, 570 citations indexed

About

A. Grifa is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, A. Grifa has authored 18 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Hematology, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in A. Grifa's work include Iron Metabolism and Disorders (7 papers), Hemoglobinopathies and Related Disorders (3 papers) and Trace Elements in Health (2 papers). A. Grifa is often cited by papers focused on Iron Metabolism and Disorders (7 papers), Hemoglobinopathies and Related Disorders (3 papers) and Trace Elements in Health (2 papers). A. Grifa collaborates with scholars based in Italy, Canada and Switzerland. A. Grifa's co-authors include Paolo Gasparini, Antonella Roetto, Massimo Carella, Antonio Totaro, Clara Camaschella, Domenico Girelli, Luigi D’Ambrosio, Brunella Franco, Alberto Piperno and Leopoldo Zelante and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Genomics and Human Mutation.

In The Last Decade

A. Grifa

18 papers receiving 561 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Grifa Italy	12	410	352	351	81	52	18	570
Maria Regoni Italy	9	206 0.5×	114 0.3×	109 0.3×	152 1.9×	16 0.3×	16	467
Federica Perrone Italy	9	109 0.3×	52 0.1×	97 0.3×	100 1.2×	27 0.5×	15	254
Anagha Sawant United States	5	221 0.5×	192 0.5×	69 0.2×	80 1.0×	11 0.2×	7	341
Milena Cau Italy	10	89 0.2×	122 0.3×	57 0.2×	313 3.9×	14 0.3×	19	533
Ndona N. Nsumu United States	11	32 0.1×	72 0.2×	38 0.1×	440 5.4×	12 0.2×	12	585
L. Scot Bastian United States	9	127 0.3×	39 0.1×	41 0.1×	155 1.9×	8 0.2×	9	352
Adamantia Papachatzopoulou Greece	13	126 0.3×	172 0.5×	6 0.0×	190 2.3×	9 0.2×	28	364
Bird Td United States	6	21 0.1×	23 0.1×	11 0.0×	162 2.0×	28 0.5×	244	342
Mefford Hc	6	21 0.1×	21 0.1×	11 0.0×	163 2.0×	27 0.5×	239	337
Leïla Lazaro France	8	21 0.1×	68 0.2×	7 0.0×	254 3.1×	9 0.2×	9	411

Countries citing papers authored by A. Grifa

Since Specialization

Citations

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

Fields of papers citing papers by A. Grifa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Grifa

This figure shows the co-authorship network connecting the top 25 collaborators of A. Grifa. A scholar is included among the top collaborators of A. Grifa 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 A. Grifa. A. Grifa 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

Zelante, L., et al.. (2003). Interstitial “de novo” tandem duplication of 7(q31.1-q35): first reported case. Annales de Génétique. 46(1). 49–52. 5 indexed citations

López-Bigas, Núria, Salvatore Melchionda, Rafael de Cid, et al.. (2001). Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. Human Mutation. 18(6). 548–548. 23 indexed citations

Totaro, Antonio, Antonella Roetto, Johanna M. Rommens, et al.. (1998). Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22). European Journal of Human Genetics. 6(2). 105–113. 2 indexed citations

Grifa, A., Antonio Totaro, Johanna M. Rommens, et al.. (1998). GABA (γ-Amino-Butyric Acid) Neurotransmission: Identification and Fine Mapping of the Human GABABReceptor Gene. Biochemical and Biophysical Research Communications. 250(2). 240–245. 23 indexed citations

Totaro, Antonio, A. Grifa, Massimo Carella, et al.. (1998). Cloning of a New Gene (FB19) within HLA Class I Region. Biochemical and Biophysical Research Communications. 250(3). 555–557. 7 indexed citations

Camaschella, Clara, Antonella Roetto, M. Cicilano, et al.. (1998). Juvenile and adult hemochromatosis are distinct genetic disorders.. PubMed. 5(6). 371–5. 68 indexed citations

Totaro, Antonio, A. Grifa, Massimo Carella, et al.. (1997). Hereditary hemochromatosis: aHpal polymorphism within the HLA-H gene. Molecular and Cellular Probes. 11(3). 229–230. 14 indexed citations

Roetto, Antonella, Luca Sbaiz, S. Bosio, et al.. (1997). A recombination event close to HFE gene in hereditary hemochromatosis.. PubMed. 40(3). 150–3. 2 indexed citations

Camaschella, Clara, Antonella Roetto, M. Cicilano, et al.. (1997). Juvenile and Adult Hemochromatosis Are Distinct Genetic Disorders. European Journal of Human Genetics. 5(6). 371–375. 64 indexed citations

10.

Carella, Massimo, Luigi D’Ambrosio, Antonio Totaro, et al.. (1997). Mutation analysis of the HLA-H gene in Italian hemochromatosis patients.. PubMed. 60(4). 828–32. 262 indexed citations

11.

Totaro, Antonio, Johanna M. Rommens, A. Grifa, et al.. (1996). Hereditary Hemochromatosis: Generation of a Transcription Map within a Refined and Extended Map of the HLA Class I Region. Genomics. 31(3). 319–326. 20 indexed citations

12.

Giannattasio, Sergio, Luigi Bisceglia, Paolo Lattanzio, et al.. (1995). Molecular screening of genetic defects with RNA–SSCP analysis: the PKU and cystinuria model. Molecular and Cellular Probes. 9(3). 201–205. 3 indexed citations

13.

Totaro, Antonio, A. Grifa, Antonella Roetto, et al.. (1995). New polymorphisms and markers in the HLA class I region: relevance to hereditary hemochromatosis (HFE). Human Genetics. 95(4). 429–434. 13 indexed citations

14.

Grifa, A., Maria Rosaria Piemontese, Salvatore Melchionda, et al.. (1995). Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant. Clinical Genetics. 47(6). 281–284. 13 indexed citations

15.

Bisceglia, Luigi, A. Grifa, Leopoldo Zelante, & Paolo Gasparini. (1994). Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: Identification of two new mutations. Human Mutation. 4(2). 136–140. 19 indexed citations

16.

Totaro, Antonio, A. Grifa, Antonella Roetto, et al.. (1994). A new complex polymorphic repeat close to the HLA-A and HLA-E loci. Human Genetics. 94(5). 578–578. 2 indexed citations

17.

Gasparini, Paolo, A. Grifa, Salvatore Savasta, et al.. (1994). The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndrome. Human Genetics. 94(6). 671–4. 15 indexed citations

18.

Gasparini, Paolo, A. Grifa, Paola Origone, et al.. (1993). Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases. Molecular and Cellular Probes. 7(5). 415–418. 15 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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