Fadi F. Hamdan

9.1k total citations
57 papers, 3.4k citations indexed

About

Fadi F. Hamdan is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Fadi F. Hamdan has authored 57 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 25 papers in Genetics and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Fadi F. Hamdan's work include Genetics and Neurodevelopmental Disorders (17 papers), Receptor Mechanisms and Signaling (17 papers) and Neuropeptides and Animal Physiology (11 papers). Fadi F. Hamdan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (17 papers), Receptor Mechanisms and Signaling (17 papers) and Neuropeptides and Animal Physiology (11 papers). Fadi F. Hamdan collaborates with scholars based in Canada, United States and France. Fadi F. Hamdan's co-authors include Guy A. Rouleau, Jacques L. Michaud, Jürgen Wess, Michel Bouvier, Julie Gauthier, Laurent Mottron, Amélie Piton, Sylvia Dobrzeniecka, Dan Spiegelman and Ridha Joober and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Biochemistry.

In The Last Decade

Fadi F. Hamdan

57 papers receiving 3.3k citations

Peers

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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20 of 20 papers shown

#	Work	Indexed citations
1	Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and Epilepsy 2017 ·The American Journal of Human Genetics ·Myriam Srour, Noriaki Shimokawa, Fadi F. Hamdan, Christina Nassif, Chantal Poulin, (unknown), Jill A. Rosenfeld, Noriyuki Koibuchi, Guy A. Rouleau, Aisha Al Shamsi, Jacques L. Michaud	24
2	Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changes 2016 ·American Journal of Medical Genetics Part A ·Farah Zahir, Tracy Tucker, Sonia Mayo, Carolyn J. Brown, Emilia L. Lim, Jonathan Taylor, Marco A. Marra, Fadi F. Hamdan, Jacques L. Michaud, Jan M. Friedman	12
3	CNIH4 Interacts with Newly Synthesized GPCR and Controls Their Export from the Endoplasmic Reticulum 2014 ·Traffic ·(unknown), Moulay Driss Rochdi, (unknown), Fadi F. Hamdan, Yann Percherancier, Jeremy C. Simpson, Rainer Pepperkok, Michel Bouvier	46
4	De Novo Mutations in Moderate or Severe Intellectual Disability 2014 ·PLoS Genetics ·Fadi F. Hamdan, Myriam Srour, José‐Mario Capo‐Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, Christine Massicotte, Amirthagowri Ambalavanan, Dan Spiegelman, Ousmane Diallo, Édouard Henrion, Alexandre Dionne‐Laporte, Anne Fougerat, Alexey V. Pshezhetsky, Sunita Venkateswaran, Guy A. Rouleau, Jacques L. Michaud	259
5	The genetic landscape of infantile spasms 2014 ·Human Molecular Genetics ·Jacques L. Michaud, Mathieu Lachance, Fadi F. Hamdan, Lionel Carmant, Anne Lortie, Paola Diadori, Philippe Major, Inge A. Meijer, Emmanuelle Lemyre, Patrick Cossette, Heather C. Mefford, Guy A. Rouleau, Elsa Rossignol	140
6	De novo deletion of FMN2 in a girl with mild non-syndromic intellectual disability 2013 ·European Journal of Medical Genetics ·(unknown), Fadi F. Hamdan, Géraldine Mathonnet, Bernard Rosenblatt, Myriam Srour	15
7	Recessive and Dominant Mutations in Retinoic Acid Receptor Beta in Cases with Microphthalmia and Diaphragmatic Hernia 2013 ·The American Journal of Human Genetics ·Myriam Srour, David Chitayat, Véronique Caron, Nicolas Chassaing, Pierre Bitoun, Lysanne Patry, Marie‐Pierre Cordier, José‐Mario Capo‐Chichi, Christine Francannet, Patrick Calvas, Nicola Ragge, Sylvia Dobrzeniecka, Fadi F. Hamdan, Guy A. Rouleau, André Tremblay, Jacques L. Michaud	74
8	De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism 2011 ·Biological Psychiatry ·Fadi F. Hamdan, Hussein Daoud, Amélie Piton, Julie Gauthier, Sylvia Dobrzeniecka, Marie‐Odile Krebs, Ridha Joober, Jean‐Claude Lacaille, Amélie Nadeau, Jeff M. Milunsky, Zhenyuan Wang, Lionel Carmant, Laurent Mottron, Miriam H. Beauchamp, Guy A. Rouleau, Jacques L. Michaud	130
9	A Population Genetic Approach to Mapping Neurological Disorder Genes Using Deep Resequencing 2011 ·PLoS Genetics ·Rachel A. Myers, Ferrán Casals, Julie Gauthier, Fadi F. Hamdan, Jon Keebler, Adam R. Boyko, Carlos D. Bustamante, Amélie Piton, Dan Spiegelman, Édouard Henrion, Martine Zilversmit, Julie Hussin, Jacklyn Quinlan, Yanlian Yang, Ronald G. Lafrenière, (unknown), Eric A. Stone, Guy A. Rouleau, Philip Awadalla	68
10	A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia 2011 ·Journal of Visualized Experiments ·(unknown), Fadi F. Hamdan, Guy A. Rouleau	9
11	De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment 2010 ·The American Journal of Human Genetics ·Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, (unknown), (unknown), Sylvia Dobrzeniecka, Marie‐Odile Krebs, Ridha Joober, Ronald G. Lafrenière, Jean‐Claude Lacaille, Laurent Mottron, Pierre Drapeau, Miriam H. Beauchamp, Michael Phillips, Éric Fombonne, Guy A. Rouleau, Jacques L. Michaud	170
12	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy 2009 ·Annals of Neurology ·Fadi F. Hamdan, Amélie Piton, Julie Gauthier, Anne Lortie, François Dubeau, Sylvia Dobrzeniecka, Dan Spiegelman, Anne Noreau, Stéphanie Pellerin, Mélanie Côté, Édouard Henrion, Éric Fombonne, Laurent Mottron, Claude Marineau, Pierre Drapeau, Ronald G. Lafrenière, (unknown), Guy A. Rouleau, Jacques L. Michaud	108
13	Mutations in the calcium-related gene IL1RAPL1 are associated with autism 2008 ·Human Molecular Genetics ·Amélie Piton, Jacques L. Michaud, Boon‐Peng Hoh, Swaroop Aradhya, J Gauthier, Laurent Mottron, Nathalie Champagne, Ronald G. Lafrenière, Fadi F. Hamdan, (unknown), Ridha Joober, Éric Fombonne, Claude Marineau, Patrick Cossette, Marie‐Pierre Dubé, Parviz Haghighi, Pierre Drapeau, Philip A. Barker, S. Carbonetto, Guy A. Rouleau	149
14	Unraveling G Protein-coupled Receptor Endocytosis Pathways Using Real-time Monitoring of Agonist-promoted Interaction between β-Arrestins and AP-2 2007 ·Journal of Biological Chemistry ·Fadi F. Hamdan, Moulay Driss Rochdi, Billy Breton, Delphine Fessart, (unknown), Pascale G. Charest, Stéphane A. Laporte, Michel Bouvier	66
15	Identification of an Agonist-induced Conformational Change Occurring Adjacent to the Ligand-binding Pocket of the M3 Muscarinic Acetylcholine Receptor 2005 ·Journal of Biological Chemistry ·Sung‐Jun Han, Fadi F. Hamdan, Soo‐Kyung Kim, Kenneth A. Jacobson, Lanh M. Bloodworth, Bo Li, Jürgen Wess	40
16	High-Throughput Screening of G Protein-Coupled Receptor Antagonists Using a Bioluminescence Resonance Energy Transfer 1-Based β-Arrestin2 Recruitment Assay 2005 ·SLAS DISCOVERY ·Fadi F. Hamdan, Martin Audet, Philippe Garneau, Jerry Pelletier, Michel Bouvier	150
17	A Schistosoma mansoni Pad1 homologue stabilizes c-Jun 2002 ·Molecular and Biochemical Parasitology ·Joseph F. Nabhan, Fadi F. Hamdan, Paula Ribeiro	13
18	Functional expression of M₁, M₃ and M₅ muscarinic acetylcholine receptors in yeast 2001 ·Journal of Neurochemistry ·(unknown), Evi Kostenis, Clarice Schmidt, Fadi F. Hamdan, Mark H. Pausch, Jürgen Wess	47
19	Cloning, Sequencing, and Developmental Expression Levels of a Novel Glutamate-Gated Chloride Channel Homologue in the Parasitic NematodeHaemonchus contortus 1999 ·Biochemical and Biophysical Research Communications ·Sean G. Forrester, Fadi F. Hamdan, Roger K. Prichard, Robin N. Beech	35
20	Cloning and sequence analysis of a lysophospholipase homologue from Schistosoma mansoni 1998 ·Parasitology Research ·Fadi F. Hamdan, Paula Ribeiro	6

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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