Fadi F. Hamdan

1.3k total citations
13 papers, 458 citations indexed

About

Fadi F. Hamdan is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Fadi F. Hamdan has authored 13 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Fadi F. Hamdan's work include Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Cellular transport and secretion (3 papers). Fadi F. Hamdan is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Cellular transport and secretion (3 papers). Fadi F. Hamdan collaborates with scholars based in Canada, United States and Italy. Fadi F. Hamdan's co-authors include Paula Ribeiro, Mark Abramovitz, Mark Ungrin, Jacques L. Michaud, Guy A. Rouleau, Aisha Mousa, Jinling Xie, Yves Durocher, Alexandre Dionne‐Laporte and Dan Spiegelman and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of Medicinal Chemistry.

In The Last Decade

Fadi F. Hamdan

13 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fadi F. Hamdan Canada	12	181	133	121	76	69	13	458
Bowen Deng China	12	186 1.0×	124 0.9×	396 3.3×	58 0.8×	37 0.5×	33	678
Abdelhalim Azzi Switzerland	8	162 0.9×	45 0.3×	82 0.7×	59 0.8×	53 0.8×	19	523
Imilce A. Rodriguez‐Fernandez United States	10	296 1.6×	113 0.8×	107 0.9×	154 2.0×	11 0.2×	12	608
Yingcong Zheng China	5	910 5.0×	227 1.7×	358 3.0×	46 0.6×	43 0.6×	8	1.3k
Fangyuan Yin China	13	193 1.1×	28 0.2×	133 1.1×	82 1.1×	44 0.6×	36	522
Rodrigo Pacifico United States	9	130 0.7×	35 0.3×	344 2.8×	76 1.0×	53 0.8×	10	639
Estela M. Muñoz Argentina	15	173 1.0×	49 0.4×	150 1.2×	9 0.1×	32 0.5×	37	631
Heesun Kim South Korea	9	372 2.1×	96 0.7×	93 0.8×	10 0.1×	17 0.2×	18	510
Christopher S. Nelson United States	12	196 1.1×	48 0.4×	116 1.0×	13 0.2×	28 0.4×	21	560
Rebecca McWhirter United States	8	271 1.5×	42 0.3×	89 0.7×	12 0.2×	47 0.7×	11	595

Countries citing papers authored by Fadi F. Hamdan

Since Specialization

Citations

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

Fields of papers citing papers by Fadi F. Hamdan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fadi F. Hamdan. 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 Fadi F. Hamdan. The network helps show where Fadi F. Hamdan may publish in the future.

Co-authorship network of co-authors of Fadi F. Hamdan

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

All Works

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13 of 13 papers shown

Yam, Patricia T., Baoyu Chen, Alfonso Fasano, et al.. (2023). Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control. Science Advances. 9(19). eadd5501–eadd5501. 11 indexed citations

Moreau, Claudia, Stefan Wolking, Catherine Laprise, et al.. (2022). Assessment of burden and segregation profiles of CNVs in patients with epilepsy. Annals of Clinical and Translational Neurology. 9(7). 1050–1058. 2 indexed citations

Manti, Filippo, Francesca Nardecchia, Sabina Barresi, et al.. (2018). Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism. Parkinsonism & Related Disorders. 61. 207–210. 14 indexed citations

Monlong, Jean, Simon Girard, Caroline Meloche, et al.. (2018). Global characterization of copy number variants in epilepsy patients from whole genome sequencing. PLoS Genetics. 14(4). e1007285–e1007285. 35 indexed citations

Accogli, Andrea, Fadi F. Hamdan, Chantal Poulin, et al.. (2018). A novel homozygous AP4B1 mutation in two brothers with AP‐4 deficiency syndrome and ocular anomalies. American Journal of Medical Genetics Part A. 176(4). 985–991. 12 indexed citations

Berryer, Martin H., Bidisha Chattopadhyaya, Ilse Riebe, et al.. (2016). Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function. Nature Communications. 7(1). 13340–13340. 63 indexed citations

Ambalavanan, Amirthagowri, Simon Girard, Kwangmi Ahn, et al.. (2015). De novo variants in sporadic cases of childhood onset schizophrenia. European Journal of Human Genetics. 24(6). 944–948. 67 indexed citations

Tucker, Tracy, Farah Zahir, Malachi Griffith, et al.. (2013). Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes. European Journal of Human Genetics. 22(6). 792–800. 30 indexed citations

Boeglin, Damien, Fadi F. Hamdan, Rosa E. Meléndez, et al.. (2007). Calcitonin Gene-Related Peptide Analogues with Aza and Indolizidinone Amino Acid Residues Reveal Conformational Requirements for Antagonist Activity at the Human Calcitonin Gene-Related Peptide 1 Receptor. Journal of Medicinal Chemistry. 50(6). 1401–1408. 25 indexed citations

10.

Hamdan, Fadi F., Mark Abramovitz, Aisha Mousa, et al.. (2002). A novel Schistosoma mansoni G protein-coupled receptor is responsive to histamine. Molecular and Biochemical Parasitology. 119(1). 75–86. 52 indexed citations

11.

Hamdan, Fadi F. & Paula Ribeiro. (1999). Characterization of a Stable Form of Tryptophan Hydroxylase from the Human Parasite Schistosoma mansoni. Journal of Biological Chemistry. 274(31). 21746–21754. 39 indexed citations

12.

Hamdan, Fadi F., Mark Ungrin, Mark Abramovitz, & Paula Ribeiro. (1999). Characterization of a Novel Serotonin Receptor from Caenorhabditis elegans. Journal of Neurochemistry. 72(4). 1372–1383. 85 indexed citations

13.

Hamdan, Fadi F. & Paula Ribeiro. (1998). Cloning and Characterization of a Novel Form of Tyrosine Hydroxylase from the Human Parasite, Schistosoma mansoni. Journal of Neurochemistry. 71(4). 1369–1380. 23 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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