Isabella Fogh

5.0k total citations
17 papers, 345 citations indexed

About

Isabella Fogh is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Isabella Fogh has authored 17 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 8 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Isabella Fogh's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Isabella Fogh is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Isabella Fogh collaborates with scholars based in Italy, United Kingdom and Netherlands. Isabella Fogh's co-authors include Ammar Al‐Chalabi, Antonia Ratti, Christopher E. Shaw, Stephen Newhouse, Ashley Jones, Vincenzo Silani, John Powell, Pamela J. Shaw, Karen Morrison and Lidia Cova and has published in prestigious journals such as Neurology, International Journal of Molecular Sciences and PLoS Medicine.

In The Last Decade

Isabella Fogh

17 papers receiving 341 citations

Peers

Isabella Fogh

NEURO

GENET

PHYSI

Francisca Ballesta Spain

Samira Ait-El-Mkadem France

Sali M.K. Farhan Canada

Chengyuan Song China

Mathieu Gravel Canada

Bert M. Verheijen Netherlands

Courtney Ackeifi United States

Janel O. Johnson United States

Maria Guarnaccia Italy

Stéphanie Efthymiou United Kingdom

Francisca Ballesta Spain

Isabella Fogh

98 ×0.6

NEURO

169 ×1.1

80 ×0.8

GENET

168 ×2.2

GENET

114 ×1.9

PHYSI

Citations per year, relative to Isabella Fogh Isabella Fogh (= 1×) peers Francisca Ballesta

Countries citing papers authored by Isabella Fogh

Since Specialization

Citations

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

Fields of papers citing papers by Isabella Fogh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabella Fogh

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

All Works

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17 of 17 papers shown

Manini, Arianna, Alessio Maranzano, Francesco Gentile, et al.. (2023). Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis. Frontiers in Aging Neuroscience. 15. 1067954–1067954. 9 indexed citations

Manini, Arianna, Antonia Ratti, Alessio Maranzano, et al.. (2022). TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 23(16). 9276–9276. 5 indexed citations

Iacoangeli, Alfredo, Ahmad Al Khleifat, Ashley Jones, et al.. (2019). C9orf72 intermediate expansions of 24–30 repeats are associated with ALS. Acta Neuropathologica Communications. 7(1). 115–115. 68 indexed citations

Verde, Federico, Cinzia Tiloca, Claudia Morelli, et al.. (2019). PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival. Neurological Sciences. 40(7). 1469–1473. 13 indexed citations

Iacoangeli, Alfredo, Ahmad Al Khleifat, William Sproviero, et al.. (2019). ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 20(3-4). 207–215. 7 indexed citations

Rooney, James, Isabella Fogh, Henk-Jan Westeneng, et al.. (2016). C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 88(4). 281.1–281. 30 indexed citations

Rooney, James, Russell L. McLaughlin, Alice Vajda, et al.. (2016). Novel Gender Selective Survival Effect of C9orf72 in European ALS Cohorts (P5.093). Neurology. 86(16_supplement). 2 indexed citations

Gaastra, Ben, Aleksey Shatunov, Sara L. Pulit, et al.. (2016). Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(7-8). 593–599. 14 indexed citations

Proitsi, Petroula, Michelle K. Lupton, Latha Velayudhan, et al.. (2014). Genetic Predisposition to Increased Blood Cholesterol and Triglyceride Lipid Levels and Risk of Alzheimer Disease: A Mendelian Randomization Analysis. PLoS Medicine. 11(9). e1001713–e1001713. 66 indexed citations

10.

Fogh, Isabella, Sandra D’Alfonso, Cinzia Gellera, et al.. (2009). No association of DPP6 with amyotrophic lateral sclerosis in an Italian population. Neurobiology of Aging. 32(5). 966–967. 18 indexed citations

11.

Giessen, Elsmarieke van de, Isabella Fogh, Bradley Smith, et al.. (2008). Association study on glutathione S‐transferase omega 1 and 2 and familial ALS. Amyotrophic Lateral Sclerosis. 9(2). 81–84. 18 indexed citations

12.

Cova, Lidia, Antonia Ratti, Manuela Volta, et al.. (2004). Stem Cell Therapy for Neurodegenerative Diseases: The Issue of Transdifferentiation. Stem Cells and Development. 13(1). 121–131. 20 indexed citations

13.

Silani, Vincenzo, Isabella Fogh, Antonia Ratti, et al.. (2002). Stem cells in the treatment of amyotrophic lateral sclerosis (ALS). Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders. 3(4). 173–181. 16 indexed citations

14.

Lucchiari, Sabrina, Isabella Fogh, A. Prelle, et al.. (2002). Clinical and genetic variability of glycogen storage disease type IIIa: Seven novel AGL gene mutations in the mediterranean area. American Journal of Medical Genetics. 109(3). 183–190. 25 indexed citations

15.

Stuppia, Liborio, Valentina Gatta, Isabella Fogh, et al.. (2001). Genomic Organization, Physical Mapping, and Involvement in Yq Microdeletions of the VCY2 (BPY 2) Gene. Genomics. 72(2). 153–157. 14 indexed citations

16.

Ratti, Antonia, Liborio Stuppia, Valentina Gatta, et al.. (2000). Characterization of a new TSPY gene family member in Yq (TSPYq1). Cytogenetic and Genome Research. 88(1-2). 159–162. 14 indexed citations

17.

Stuppia, Liborio, Valentina Gatta, Isabella Fogh, et al.. (2000). Characterization of novel genes in AZF regions. Journal of Endocrinological Investigation. 23(10). 659–663. 6 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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