Ferid Fathalli

1.4k total citations
11 papers, 410 citations indexed

About

Ferid Fathalli is a scholar working on Psychiatry and Mental health, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ferid Fathalli has authored 11 papers receiving a total of 410 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Psychiatry and Mental health, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ferid Fathalli's work include Schizophrenia research and treatment (5 papers), Bipolar Disorder and Treatment (3 papers) and Genetic Associations and Epidemiology (2 papers). Ferid Fathalli is often cited by papers focused on Schizophrenia research and treatment (5 papers), Bipolar Disorder and Treatment (3 papers) and Genetic Associations and Epidemiology (2 papers). Ferid Fathalli collaborates with scholars based in Canada, Tunisia and France. Ferid Fathalli's co-authors include Ridha Joober, Norbert Schmitz, Guy A. Rouleau, Sarojini M. Sengupta, Nicole Pawliuk, Suzanne King, Antonio Ciampi, Ashok Malla, Martín Lepage and Cecilia Flores and has published in prestigious journals such as Neuropsychopharmacology, Schizophrenia Research and Molecular Brain Research.

In The Last Decade

Ferid Fathalli

11 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ferid Fathalli Canada 10 231 93 86 73 68 11 410
Douglas Blackwood United Kingdom 8 155 0.7× 94 1.0× 85 1.0× 81 1.1× 136 2.0× 11 425
Ivanor Meira‐Lima Brazil 9 182 0.8× 130 1.4× 74 0.9× 113 1.5× 139 2.0× 13 432
Emile D. Risby United States 12 194 0.8× 42 0.5× 56 0.7× 110 1.5× 115 1.7× 25 455
Renata B. Cupertino Brazil 12 118 0.5× 49 0.5× 97 1.1× 64 0.9× 63 0.9× 32 309
Agnieszka Słopień Poland 14 170 0.7× 118 1.3× 127 1.5× 128 1.8× 149 2.2× 25 520
Urs Heilbronner Germany 12 164 0.7× 63 0.7× 142 1.7× 45 0.6× 77 1.1× 39 447
Raya Lapidus Israel 5 144 0.6× 45 0.5× 44 0.5× 104 1.4× 100 1.5× 7 412
Céline Goldberger France 9 145 0.6× 99 1.1× 70 0.8× 59 0.8× 74 1.1× 19 335
Vadim D. Khait United States 7 149 0.6× 81 0.9× 143 1.7× 86 1.2× 139 2.0× 8 485
Carla Morganti Italy 10 284 1.2× 133 1.4× 150 1.7× 57 0.8× 50 0.7× 17 477

Countries citing papers authored by Ferid Fathalli

Since Specialization
Citations

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

Fields of papers citing papers by Ferid Fathalli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ferid Fathalli

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

All Works

11 of 11 papers shown
1.
Sengupta, Sarojini M., Kathleen MacDonald, Ferid Fathalli, et al.. (2016). Polygenic Risk Score associated with specific symptom dimensions in first-episode psychosis. Schizophrenia Research. 184. 116–121. 27 indexed citations
2.
Cassidy, Clifford, Lisa Buchy, Michael Bodnar, et al.. (2014). Association of a risk allele of ANK3 with cognitive performance and cortical thickness in patients with first-episode psychosis. Journal of Psychiatry and Neuroscience. 39(1). 31–39. 32 indexed citations
3.
Albanna, Ammar, Zia Choudhry, Philippe‐Olivier Harvey, et al.. (2013). TCF4 gene polymorphism and cognitive performance in patients with first episode psychosis. Schizophrenia Research. 152(1). 124–129. 20 indexed citations
4.
Grant, Alanna, Ferid Fathalli, Guy A. Rouleau, Ridha Joober, & Cecilia Flores. (2012). Association between schizophrenia and genetic variation in DCC: A case–control study. Schizophrenia Research. 137(1-3). 26–31. 46 indexed citations
5.
Bodnar, Michael, Ashok Malla, Yvonne Czechowska, et al.. (2010). Neural markers of remission in first-episode schizophrenia: A volumetric neuroimaging study of the hippocampus and amygdala. Schizophrenia Research. 122(1-3). 72–80. 30 indexed citations
6.
Klink, Ruby, Ferid Fathalli, Émmanuel Stip, et al.. (2008). Are metabolic indices different between drug-naïve first-episode psychosis patients and healthy controls?. Schizophrenia Research. 102(1-3). 329–336. 84 indexed citations
7.
Fathalli, Ferid, Guy A. Rouleau, Lan Xiong, et al.. (2007). No association between the DRD3 Ser9Gly polymorphism and schizophrenia. Schizophrenia Research. 98(1-3). 98–104. 20 indexed citations
8.
Schmitz, Norbert, Nicole Pawliuk, Ferid Fathalli, et al.. (2007). Validation of the English and French versions of the Community Assessment of Psychic Experiences (CAPE) with a Montreal community sample. Schizophrenia Research. 95(1-3). 86–95. 82 indexed citations
9.
Joober, Ridha, Natalie Grizenko, Sarojini M. Sengupta, et al.. (2006). Dopamine Transporter 3′-UTR VNTR Genotype and ADHD: a Pharmaco-Behavioural Genetic Study with Methylphenidate. Neuropsychopharmacology. 32(6). 1370–1376. 51 indexed citations
10.
Sengupta, Sarojini M., Lan Xiong, Ferid Fathalli, et al.. (2006). Association study of the trinucleotide repeat polymorphism within SMARCA2 and schizophrenia. BMC Genetics. 7(1). 34–34. 8 indexed citations
11.
Xiong, Lan, Guy A. Rouleau, Lynn E. DeLisi, et al.. (2004). CAA insertion polymorphism in the 3′UTR of Nogo gene on 2p14 is not associated with schizophrenia. Molecular Brain Research. 133(1). 153–156. 10 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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